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Human milk oligosaccharides (HMOs) are a set of complex carbohydrates and the third largest solid component of human milk, after lactose and lipids. To date, over 150 HMOs have been identified and the diversity of structures produced by lactating women is influenced by maternal genetics as well as other maternal, infant, and environmental factors. While the concentrations of individual HMOs have been shown to vary between individuals and throughout the course of lactation, the variability of HMO concentration profiles following different pregnancies occurring in the same woman is presently unknown. As such, the objective of this study was to compare HMO concentrations in human milk samples provided by the same women (n = 34) following repeat pregnancies. We leveraged existing human milk samples and metadata from the UC San Diego Human Milk Research Biorepository (HMB) and measured the concentrations of the 19 most abundant HMOs using high-performance liquid chromatography with fluorescence detection (HPLC-FL). By assessing dissimilarities in HMO concentration profiles, as well as concentration trends in individual structures between pregnancies of each participant, we discovered that HMO profiles largely follow a highly personalized and predictable trajectory following different pregnancies irrespective of non-genetic influences. In conclusion, this is the first study to assess the interactions between parity and time following delivery on variations in HMO compositions.

Glycosaminoglycans (GAGs), including hyaluronic acid (HA), chondroitin sulfate (CS)/dermatan sulfate (DS), heparan sulfate (HS)/heparin (HP), and keratan sulfate (KS), play pivotal roles in living organisms. Generally, GAGs are analyzed after enzymatic digestion into unsaturated or saturated disaccharides. Due to high structural similarity between disaccharides, however, separation during analysis is challenging. Additionally, little is known about the structures of GAGs and their functional relationships. Elucidating the function of GAGs requires highly sensitive quantitative analytical methods. We developed a method for the simultaneous analysis of 18 types of disaccharides derived from HA (1 type), CS/DS (7 types), HS/HP (8 types), and KS (2 types) potentially detectable in analyses of human urine. The simple method involves HPLC separation with fluorescence detection following derivatization of GAG-derived disaccharides using 4-aminobenzoic acid ethyl ester (ABEE) as a pre-labeling agent and 2-picoline borane as a reductant. The ABEE derivatization reaction can be performed under aqueous conditions, and excess derivatization reagents can be easily, rapidly, and safely removed. This method enables highly sensitive simultaneous analysis of the 18 abovementioned types of GAG-derived disaccharides using HPLC with fluorescence detection in small amounts of urine (1 mL) in a single run. The versatile method described here could be applied to the analysis of GAGs in other biological samples. [ABSTRACT FROM AUTHOR]

Sixteen color additives (tar colors) were detected in 128 food samples (macarons, meringue cookies, and coque macarons) using HPLC with a photodiode array detector at 420 nm, 520 nm, and 620 nm for the yellow, red, and blue and green color types, respectively. The tar color recovery rates ranged from 81.3 to 95.6%, and their limits of detection (LOD) and quantification (LOQ) were 0.001–0.049 mg/kg and 0.004–0.147 mg/kg, respectively. Seven tar colors (Y4, Y5, R3, R40, R102, B1, and B2) were detected in 129 samples. All the samples did not contain nine tar colors (R2, G3, Azo, R106, QY, ORII, BBN, PBV, and GS). The quantity of tar colors (Y4, Y5, R40, and B1) in 15 samples exceeded the Korean Ministry of Food and Drug Safety (MFDS) standard. Ninety samples (70%) used a mixture of two or more tar colors, and the amount used was 11.0–1643.3 mg/kg. The quantity of combined tar colors in 15 samples exceeded 300 mg/kg. Through these findings, this study aims to contribute to the development of safer and more reliable desserts containing tar colors, by enhancing safety measures and ensuring improved quality control for consumer protection. [ABSTRACT FROM AUTHOR]

Two simple, valid and green chromatographic based techniques are developed in the present work for first time to simultaneously analyze the recently approved combination of Aspirin (ASP) with the novel gastro-protective agent Vonoprazan (VON). First method is an HPLC-DAD "diode array detection", where separation was successful using C18 (250 × 4.6 mm) column with isocratic elution of phosphate buffer-pH 6.8 and acetonitrile in ratio of 63:37 with detection at 230 nm. Second method is an HPTLC method on HPTLC silica plates using ethyl acetate: ethanol (75%): ammonia (5:5:0.05 v/v) mobile phase followed by densitometric scanning at 230 nm. The methods were applied successfully for analysis of VON and ASP mixture in laboratory-prepared tablets and the methods were validated in regards to linearity, precision, accuracy and selectivity. The proposed methods are assessed for their greenness and whiteness as well using the "Analytical GREEnness Metric Approach", "Complementary Modified Green Analytical Procedure Index" and the new algorithm "RGB 12 model" (Red-Green-Blue) and proved the greenness and the sustainability of the methods in the routine assay of the newly marketed formulation. [ABSTRACT FROM AUTHOR]

Background Results Conclusion Lead (Pb) is a metal that affects many body systems, primarily the male reproductive system. This study aimed to examine the phytochemical profiling and beneficial effects of Juglans regia oil (JRO) in alleviating lead‐induced reprotoxicity‐associated oxidative injury in rats. Adult male Wistar rats were randomly divided into four groups as follows: control group received no treatment, Pb group was exposed to 0.344 g kg−1 bw of Pb acetate, Pb + JRO group was co‐treated with Pb plus walnut oil (0.9 g kg−1 bw) and JRO group received walnut oil only.Pb‐treated rats showed significantly decreased gonado‐somatic index, count and viability of sperm. Testosterone levels decreased in Pb‐treated animals. Besides, Pb disrupted the oxidative/antioxidative status, the plasmatic lipase activity and testicular Pb content. Furthermore, Pb produced testis histopathological features, especially cell degeneration, atrophy and tubular disarrangement. Co‐treatment with JRO was found to be effective for recovering the increased testicular oxidative damage‐associated histological features in the Pb group. This was supported by the in silico modeling results.The in silico analyses revealed that JRO compounds bound androgen receptor and RAC‐alpha serine/threonine kinase with high affinities, which together with pharmacokinetic properties and molecular interactions satisfactorily support the beneficial in vivo findings in the Pb + JRO group of rats. © 2024 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

Congenital disorders of glycosylation (CDG) are a family of rare inherited metabolic disorders. This study aimed to examine the carbohydrate-deficient transferrin (CDT) screening results of 1,328 patients with suspected CDG by using transferrin- high pressure liquid chromatography (Tf- HPLC) method and to evaluate the performance of the method as a reference diagnostic tool.Relative CDT levels (CDT concentrations expressed as percent of total transferrin) were determined in serum samples by HPLC. The method sensitivity, specificity and positive predictive value (PPV) were further calculated.Abnormal transferrin isoform profile consistent with CDG Type-I and CDG Type-II were determined in 50 cases; in 44 cases asiolo-Tf (7.63 ± 5.44 %) and disialo-Tf (36.29 ± 9.04 %), in six cases monosialo-Tf (3.95 ± 0.95 %) and trisialo-Tf (25.05 ± 4.46 %) were determined and decreased tetrasialo-Tf (49.75 ± 11.59 %) was identified in all cases. Two cases having abnormal CDT pattern were molecularly diagnosed with hereditary fructose intolerance and galactosemia and 11 cases diagnosed with CDG based on clinical and molecular analysis showed a normal pattern. The sensitivity, specificity and positive predictive values of Tf-HPLC method were 81.96 %, 99% and 96 %, respectively.Tf-HPLC is a useful, highly sensitive, cost-advantageous and reliable method for the detection and preliminary diagnosis of CDG for laboratories working with large sample series. [ABSTRACT FROM AUTHOR]

AbstractOlopatadine Hydrochloride, a H1-receptor antagonist, widely used for Allergic Conjunctivitis. A HPLC method was created and validated for the quantification of olopatadine hydrochloride and its related substances in eye formulation in accordance with ICH standards. The separation of olopatadine hydrochloride was done by using a 4.6-mm 15-cm; 5 µm packing USP L7 column with a mobile phase made up of a mixer of phosphate buffer, pH 3.0: Acetonitrile (72:28) ratio at a flow rate of 1.0 mL/min and injection volume 30 µL. A photodiode array detector was used at a wavelength of 299 nm. The validation parameters including specificity, LOD/LOQ, linearity, accuracy, precision, robustness, and solution stability, were verified for performance of the method. The linearity ranges were 0.02–0.40, 0.0004–0.008 and 0.0001–0.002 mg/mL for olopatadine hydrochloride, olopatadine-related compound B and olopatadine carbaldehyde, respectively. The % recovery was within the 80–120%. When the column temperature and flow rate were changed, the system suitability resolution was still within the acceptable range. The solutions were stable after 24 hr at both room temperature and 5°C temperature. For the analysis of olopatadine hydrochloride and its impurity in pharmaceutical finished eye dosage form, the confirmed HPLC method can be a workable analytical approach. [ABSTRACT FROM AUTHOR]

Introduction: Ferroptosis is a crucial process contributing to neuronal damage following intracerebral hemorrhage (ICH). Didang Tang (DDT), a traditional therapeutic, has been used clinically to manage ICH for many years, yet the molecular mechanisms by which by DDT protects neurons from ferroptosis after ICH remain elusive. Methods: This study utilized high-performance liquid chromatography-based fingerprint analysis to characterize DDT's chemical composition. An ICH rat model and hemin and erastin-induced PC12 cell ferroptosis models were developed to investigate DDT's neuroprotective mechanisms. Histological assessments of brain tissue morphology and iron deposition were performed using hematoxylin-eosin, Nissl, and Perl's blue staining. Neurological function was evaluated using Longa and Berderson scores, while lipid peroxidation was measured using biochemical assays and flow cytometry. Protein expression levels of ferroptosis- and endoplasmic reticulum stress (ERS)-related markers were analyzed via Western blotting and immunofluorescence. Results: Our results demonstrated that DDT reduced hematoma volume, decreased iron deposition, lowered malondialdehyde (MDA) levels, and upregulated glutathione peroxidase (GPX4) and SLC7A11 expression in affected brain regions. Furthermore, DDT downregulated GRP78 expression and inhibited the PERK/eIF2α/ATF4/CHOP/GPX4 pathway, exerting strong neuroprotective effects. The fluorescence staining results of MAP2/GPX4 and MAP2/CHOP suggested that DDT may regulate neuronal ferroptosis and ERs to exert the protective effect. In vitro experiments using hemin- and erastin-induced neuron-derived PC12 cells as neuronal ferroptosis models developed in our laboratory corroborated these in vivo findings, showing increased survival and reduced lipid peroxidation in DDT-treated cells, along with similar inhibitory effects on ferroptosis and ERS. Molecular docking suggested that DDT components, such as sennoside B, amygdalin, rhein, and emodin, interact favorably with PERK/eIF2α/ATF4/CHOP signaling pathway proteins, highlighting their potential role in DDT's anti-ferroptosis effects. Conclusion: DDT alleviates neuronal ferroptosis after ICH by modulating the PERK/eIF2α/ATF4/CHOP/GPX4 signaling pathway. Overall, this study provides novel insights into DDT's protective mechanisms against ICH-induced neuronal injury by modulating ferroptosis and ERS pathways, underscoring its potential as an effective therapeutic strategy. [ABSTRACT FROM AUTHOR]

Retinoids (vitamin A) and tocopherols (vitamin E) are essential for key biological functions in vertebrates, including cell growth, cell death and differentiation, embryonic development, reproduction and vision. In fish, however, much less is known about the retinoid functions, although retinoic acid has been shown to be involved in embryonic development. In this study, we quantified the levels of different retinoids, carotenoids and vitamin E in various tissues of both adult and embryos of the viviparous fish eelpout (Zoarces viviparus). Our results demonstrate clear seasonal differences in the levels of these vitamins in the liver of the female fish as well as in its ovarian tissues, eggs and/or embryos. Overall, this study is a baseline assessment and describes the annual variations in the vitamin status by comparing the tissue distribution of retinoids, carotenoids and vitamin E. This baseline study investigates the natural background levels of these compounds and relates their seasonal fluctuations to the reproductive cycle in the viviparous eelpout. The results of this study strengthen the current evidence base necessary to understand retinoid pathways during fish development. This understanding is crucial for utilizing retinoid composition in fish as a biological response to exposure to environmental pollution with hazardous substances in the marine environment. [ABSTRACT FROM AUTHOR]

The experiment was conducted from April to May 2024 at the Centre for Excellence in Biotechnology Research and Training (CEBRT) lab of Amicable Knowledge Solution University (AKS) University, Satna. In the present study, a simple, routine, and reproducible RP-HPLC method was employed for estimating the levels of Ferulic acid (FA) in different treatments of maize that is essential in the phytochemical analysis of this plant, has been assessed based on ferulic acid (FA). The method used in this study was based on HPLC on a C18 column using a gradient of water, methanol, and acetic acid. The calibration curve showed optimum linearity from 10 to 100 µg ml-1, with R²=0.981. This method is used to quantify the concentration of FA. This methodology was used to detect FA in maize plants with different treatments: T1: control plants, T2: drought-induced plants, T3: plants inoculated with PKR1, T4: plants inoculated with PKR5, T5: plants inoculated with PKR6. An increase in FA was observed in all three Plant Growth-Promoting Rhizobacteria (PGPR)-treated plants (T3, T4, and T5) compared to T1 (control plants) and T2 (drought-induced plants). Among these, maximum FA was found in T4 treatment, and the maximum peak height and area of T4 were 229259 and 10884, respectively. The validated RP-HPLC method provided a reliable approach for analyzing FA content in maize leaves, supporting phytochemical studies and quality assurance across various plant treatments and derived products. [ABSTRACT FROM AUTHOR]

TATB as an insensitive high explosive, has wide applications in both civil and military areas. High performance liquid chromatography (HPLC) is a crucial tool to analyze the purity for quality control of TATB. However, current HPLC method for TATB has several drawbacks resulted by its poor solubility. A deep eutectic solvent (CS-1) has high solubility toward TATB, so it has been used as the pretreatment solvent and mobile phase to develop a new HPLC method for TATB in this work. When CS-1 was used as the pretreatment solvent for TATB prior to HPLC analysis, it displayed greater efficiency, less dosage, and shorter time compared to conventional solvents such as dimethyl sulfoxide (DMSO) and dimethyl formamide (DMF). Compared to the pretreatment time of 240 min by using DMSO, the pretreatment time of TATB by using CS-1 is significantly shortened to 20 min. Meanwhile, the carrying capacity of mobile phase for TATB became stronger after CS-1 was added into the mobile phase. The concentration of TATB with 40 mg·100 mL−1 is successfully analyzed by the HPLC based on the mobile phase containing CS-1, which is 10 times higher than that of DMSO with 4.0 mg·100 mL−1. Therefore, a new HPLC method based on CS-1 as one of the deep eutectic solvents is first established to improve the efficiency and representation of analyzing high concentration of TATB. [ABSTRACT FROM AUTHOR]

Background Glycated hemoglobin, or hemoglobin A1c (HbA1c), serves as a crucial marker for diagnosing diabetes and monitoring its progression. We aimed to assess the interference posed by common Hb variants on popular HbA1c measurement systems. Methods A total of 63 variant and nonvariant samples with target values assigned by the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC)-calibrated methods were included. We assessed 6 methods for measuring HbA1c in the presence of HbS, HbC, HbD, HbE, and fetal hemoglobin (HbF): 2 cation-exchange high-performance liquid chromatography (HPLC) methods (Bio-Rad D-100 and HLC-723 G8), a capillary electrophoresis (CE) method (Sebia Capillarys 3 TERA), an immunoassay (Roche c501), an enzyme assay system (Mindray BS-600M), and a boronate affinity method (Primus Premier Hb9210). Results The HbA1c results for nonvariant samples from the 6 methods were in good agreement with the IFCC-calibrated method results. The Bio-Rad D-100, Capillarys 3, Mindray BS-600M, Premier Hb9210, and Roche c501 showed no interference from HbS, HbC, HbD, and HbE. Clinically significant interference was observed for the HLC-723 G8 standard mode. Elevated HbF levels caused significant negative biases for all 6 methods, which increased with increasing HbF concentration. Conclusion Elevated levels of HbF can severely affect HbA1c measurements by borate affinity, immunoassays, and enzyme assays. [ABSTRACT FROM AUTHOR]

The insecticidal and repellent activities of the four wild plant extracts: stinging nettle, Urtica dioica L., white henbane, Hyoscyamus albus L., camphorweeds, Pluchea dioscoridis L., and cocklebur, Xanthium strumarium L. were tested compared to the insecticide spirotetramat against the 3rd nymphal instar of Aphis gossypii Glover and adult females of Phenacoccus solenopsis Tinsley after 24 and 48 h of treatment. Their effects on acetylcholinesterase (AChE) and glutathione-S-transferase (GST) enzyme activities were also assessed to explore their possible mechanisms of action. The phenolic compounds of the plant extracts were investigated by high-performance liquid chromatography (HPLC) analysis. The most abundant compounds in the methanol extract from P. dioscoridis were gallic acid (14.45 µg/mL), and cinnamic acid (11.44 µg/mL); from U. dioica were caffeic acid (15.32 µg/mL) and syringic acid (13.47 µg/mL); from H. albus were syringic acid (7.12 µg/mL) and catechol (5.33 µg/mL); and from X. strumarium were p-coumaric acid (24.53 µg/mL) and pyrogallol (18.35 µg/mL). According to the LC50 values, the contact toxicity of U. dioica, H. albus, P. dioscoridis, and X. strumarium against A. gossypii was 40.3, 60.6, 56.2, and 32.3 mg/L, whereas, the contact toxicity against P. solenopsis was 56.4, 67.5, 64.3, and 36.2 mg/L, compared to the spirotetramat (17.2 and 24.5 mg/L), respectively, at 48 h of treatment. The highest repellency rates were observed with LC50 values for X. strumarium (63.2 and 60.3%), followed by U. dioica (46.2 and 43.5%), P. dioscoridis (45.3 and 42.8%), and H. albus extract (38.8 and 35.2%) compared to the spirotetramat (78.5 and 76.2%) against A. gossypii and P. solenopsis at 24 h, but decreased with time. The AChE and GST activities in pests were significantly inhibited, compared to control and spirotetramat, with dose and time-dependent effects. These findings indicate that tested wild extracts may be suggested as viable alternatives for aphids and mealybugs control. [ABSTRACT FROM AUTHOR]

Micronutrient deficiency is wide spread and highly affects morbidity, mortality, and well-being of human beings. Micronutrient deficiency gradually manifests into diseases, which effects pathophysiology directly or indirectly. There is an imprecision in the diagnosis of micronutrient deficiency because of two causes; the selection of the standard biomarker and the diagnostic technique used. In appropriate diagnosis could increase the severity of the disorder. Instead of a single a combination of biomarkers can give more stringent results for micronutrient testing. Several traditional analytical techniques are used for diagnosis but HPLC, ELISA & LCMS/MS are most sensitive and reliable methods used by CLSIA-certified labs. However, these techniques require well-equipped, centralized laboratory facilities. The diagnostic era moves toward the Point of Care Testing (POCT), a boon in emerging diagnostics, breaking all paradigms of traditional analytical techniques. POCT led us toward the development of biosensors, which encompasses many techniques like paper-based sensors, microfluidic chip, wearable devices, and smartphone-assisted diagnostics, which become more popular diagnostic tools. This outlook summarizes the micronutrients like vitamins A, B5, B6, B7, B9, B12 C, D, and E and Minerals like iron, calcium, zinc, magnesium, and sodium; along with its biomarkers, analytical techniques, and point of care innovation in micronutrients. [ABSTRACT FROM AUTHOR]

Inborn errors of monoamine neurotransmitter metabolism are rare diseases characterized by nonspecific neurological symptoms. These symptoms appear in early childhood and correspond to movement disorders, epilepsy, sleep disorders and/or mental disability. Cerebrospinal fluid biomarkers have been identified and validated to allow specific diagnosis of these diseases. Biomarkers of inborn errors of monoamine neurotransmitter metabolites are divided in two groups: monoamine neurotransmitter metabolites and pterins. Biomarkers quantification in cerebrospinal fluid is based on high-performance liquid chromatography separation coupled to electrochemical detection, fluorescence detection, or mass spectrometry. The following article reviews the advances in the proposed routine methods for the measurement of these analytes in cerebrospinal fluid. The purpose of this review is to compare the various proposed methods in terms of sample preparation, chromatographic conditions and detection modes. Despite the broad range of proposed methods, quantification of inborn errors of monoamine neurotransmitter biomarkers remains a great challenge, given the complexity of biological fluids and the low amounts of analytes that are present in cerebrospinal fluid. [ABSTRACT FROM AUTHOR]

Curcumol, a significant bioactive molecule, requires accurate detection methods due to its extensive pharmacological properties. This study develops high‐performance liquid chromatography (HPLC) methods to detect curcumol and constructs sample pretreatment techniques using salt‐assisted liquid‐liquid microextraction (SALLME). The optimization process focuses on conditions for acetonitrile (ACN) anhydrous sodium sulfate‐assisted liquid‐liquid microextraction. By adding excess anhydrous sodium sulfate to an ACN aqueous solution, ACN precipitates, forming a saturated saline solution and resulting in a two‐phase system. Curcumol, being highly soluble in ACN, separates into and enriches within the ACN phase, achieving effective matrix separation. SALLME demonstrated an enrichment factor of up to 12.4 for curcumol. The extracted ACN is then injected into an HPLC instrument for quantitative detection and analysis. The method exhibited a good linear range (0.5–10.0 µg/mL) and a low detection limit (0.05 µg/mL). The results indicate that curcumol can be effectively separated from complex matrices using this technique. By optimizing salt concentration and temperature, the HPLC method for determining curcumol in biological samples was successfully established, achieving recoveries between 86.2% and 137.6% in spiked urine and blood samples. Furthermore, this method offers rapid, efficient, and environmentally friendly sample preparation, promising significant applications in pharmacological and clinical settings. [ABSTRACT FROM AUTHOR]

• Oryza coarctata (Roxb.), a mangrove plant in Bangladesh, was screened to identify active chemicals in the plant. • The phytochemical investigation, GC-MS, and HPLC analysis detected distinct phytochemicals. • The ethanol extract of O. coarctata showed marked antidiarrheal activities in vivo through a novel intestinal antisecretory mechanism. • Molecular docking and dynamics simulation revealed the structural stability of the complexes of selected phytochemicals, suggesting antidiarrheal activity through neprilysin inhibition. Plants are a rich source of medicinal compounds. The Sundarbans in Bangladesh, the largest deltaic swamp forest in the world, are home to many plant species, but research on the bioactivities of many of these plants is still lacking. The current study aims to explore the antioxidative and antidiarrheal effects of Oryza coarctata (common name: wild rice) and the responsible pharmacophores through in silico approaches. Ethanol extract of the experimental plant was subject to preliminary phytochemical screening, GC-MS, and HPLC analysis to identify secondary metabolites. In vitro antioxidant test and in vivo antidiarrheal assay was done. Moreover, molecular docking and dynamics simulation were performed on neprilysin protein to corroborate in vivo observational results. In the phytochemical tests, different secondary metabolites were found to be present. The result of the GC-MS ascertained 21 compounds having the highest yield of bicyclo[4.1.0]heptane-7-carboxylic acid-4-acetylphenyl ester (22.38%), and HPLC identified seven polyphenols with the most significant amount of (-) epicatechin (39.48 mg/100 g of dry extract). The quantitative measurement of total polyphenol, flavonoid, and terpenoid contents resulted in 158 mg GAE/g, 257 mg QE/g, and 19.85 mg UAE/g of dry extract. The SC 50 (50% scavenging capacity) of the extract in the DPPH and hydrogen peroxide scavenging assay was 56 µg/mL and 63.52 µg/mL as compared to 4 µg/mL and 11.07 µg/mL of ascorbic acid, respectively. The extract also posed ferric-reducing antioxidant capacity, which varied with concentration. In the acute toxicity study on mice, the extract produced no toxicity up to 3,000 mg/kg. The extract significantly (p<0.001) attenuated 72.59% and 79.04% diarrhea in castor oil- and 67.83% and 78.27% in magnesium sulfate-induced diarrheal models at 200 and 400 mg/kg oral doses in comparison to 83.88% reduction in castor oil- and 86.09% reduction in magnesium sulfate-induced model by the standard racecadotril at 20 mg/kg dose. In silico studies confirmed the structural stability of the docked complexes, and (-) epicatechin of all compounds revealed the best binding poses with the neprilysin (an enkephalinase) throughout a molecular dynamics simulation of 100 ns. Therefore, our findings provide a solid pharmacological basis for the antioxidant and antidiarrheal properties of O. coarctata and suggest that (-) epicatechin, 2,4-difluorobenzoic acid-2-propylphenyl ester (DE), bicyclo[4.1.0]heptane-7-carboxylic acid-4-acetylphenyl ester (BE), and 3-benzylsulfanyl-3-fluoro-2-trifluoromethyl-acrylonitrile (BA) could be the potential leads against neprilysin for antidiarrheal drug development. [ABSTRACT FROM AUTHOR]

Sustainable catalyst synthesis offers a fundamental development via utilizing plants reducing the dependency on synthetic chemicals and minimizing environmental impact. This study presents a sustainable approach to catalysis through the synthesis of MnO2 using oak bark as a precursor. The catalyst synthesis was characterized using various analytical techniques including Fourier Transform Infrared Spectroscopy (FT-IR), X-ray Diffraction (XRD), Scanning Electron Microscopy with Energy Dispersive X-ray Spectroscopy (SEM–EDX), and High-Performance Liquid Chromatography (HPLC). FT-IR analysis confirmed the chemical structure and functional groups peak observed at 1709 cm−1 is indicative of the stretching vibration of conjugated alkenes' C–C bonds. XRD revealed the crystalline nature and phase purity, confirming the formation of MnO2. HPLC analysis demonstrated the catalytic activity of MnO2 catalyst organic transformations derived from oak bark includes polyphenolic compounds such as gallic acid (RT 9.2 min; C7H6O5), condensed tannins like proanthocyanidin (RT 21.7 min; C31H28O12), quercetin derivatives such as quercetin-3-O-glucoside (RT 32.2 min; C21H20O12), and flavonoids such as kaempferol (RT 35.3 min; C15H10O6). This study emphasizes the feasibility and effectiveness of using natural sources like oak bark for synthesizing eco-friendly catalysis with promising applications in green chemistry. [ABSTRACT FROM AUTHOR]

Background and Objectives: The aims of this study were to assess the functional and phytochemical characteristics, as well as the antioxidant properties, of bran from five distinct rice varieties. Additionally, it evaluated the impact of extrusion cooking on the composition and quantity of individual phytochemicals in both free and bound states in the bran of these varieties. Findings: The functional properties and phytochemical profiles of raw and extruded rice bran from different rice varieties differed significantly. The extrusion process significantly influenced the color, protein solubility, foaming properties, polyphenolics, and amino acid composition of rice bran. Total phenolics ranged from 3.18 to 4.80 mg GAE/g, increased by 12.6%–17% postextrusion. Similarly, total flavonoid content ranged from 15.22 to 17.37 mg RTE/100 g, with a 30%–33% increase after extrusion cooking. Throughout the extrusion process, a rise in the concentration of free phenolics accompanied by a decrease in the concentration of bound phenolics was observed. Conclusion: The study revealed the impact of extrusion cooking on the distribution of total phytochemicals, particularly phenolics and flavonoids, and the levels of antioxidant activity in free and bound phenolics, as well as amino acid composition and functional properties. The extrusion cooking increased levels of free phenolics and 2,2‐diphenyl‐1‐picrylhydrazyl activity, while bound forms decreased. Extrusion cooking variably impacted the functionality and phytochemical content of bran from different rice varieties, thus influencing their likely applications. Significance and Novelty: This study established the foundation for producing food products using extruded rice bran, offering health benefits and meeting the growing demand in the functional food sector. [ABSTRACT FROM AUTHOR]

This study aims to investigate the seasonal and spatial distribution of surface phytoplankton communities in the Baltic Sea, using pigment analysis and hydrological parameters. Data were collected during six oceanographic campaigns between 2005 and 2008, including high-performance liquid chromatography (HPLC) pigment characterization and hydrological measurements. The first part of this comprehensive study was focused on the HPLC phytoplankton pigment dataset in relation to hydrological conditions. The research highlighted the importance of high-quality input data for accurate taxonomic analysis. Several unsupervised machine learning approaches, such as hierarchical cluster analysis (HCA), principal component analysis (PCA), and network-based community detection analysis (NCA), were used to analyze the data and identify phytoplankton communities based on biomarker pigments. Five main phytoplankton communities were identified: diatoms, dinoflagellates, cryptophytes, green algae, and cyanobacteria. The results evidenced distinct seasonal patterns, with diatom blooms dominating in spring, cyanobacterial blooms in mid-summer, and haptophyte and dinoflagellate peaks occurring in late summer and autumn. While PCA and NCA provided consistent insights into community structure, HCA offered less clarity in distinguishing between groups. The results of the statistical analysis were then compared with those of traditional approaches such as CHEMTAX and region-specific bio-optical algorithms, providing new perspectives on the taxonomic composition of phytoplankton groups. This study provides valuable insights into phytoplankton dynamics in the Baltic Sea and the effectiveness of different analytical approaches in understanding community structure, providing metrics that can enhance current and future advancements in remote sensing, including support for hyperspectral ocean color remote sensors. [ABSTRACT FROM AUTHOR]

In this study, isothermal decomposition kinetic of a triple-base propellant (TBP) has been investigated by vacuum stability test (VST). The volumes of the evolved gas have been recorded step by step to monitor gas evolution in VST at 80°C, 90°C, 100°C, 110°C, 120°C, and 150°C. This semi-continuous data-recording mode makes it possible to use the Berthelot equation for shelf-life prediction of TBP. Activation energy has been calculated in both model-free and model-fitting methods, and F0/R1 is determined as the best model for thermal decomposition of TBP at VST. High-performance liquid chromatography has been used to determine stabilizer (methyl centralite) content of the TBP at various extents of reactions (α). The critical amount of stabilizer was specified at 2% α. Arrhenius average temperatures have been calculated at various climate categories and used as actual storage temperatures. Molecular weight (Mw) reductions of nitrocellulose were determined by gel permeation chromatography during aging. According to the results, the shelf-life of TBP has been estimated using the Berthelot equation at 2% α in various climate categories. Shelf-life of studied TBP differs from 14 to about 36 (years) in extremely hot dry (A1) to intermediate (A3) climate categories. [ABSTRACT FROM AUTHOR]

In vitro transcription (IVT) reaction is an RNA polymerase‐catalyzed production of messenger RNA (mRNA) from DNA template, and the unit operation with highest cost of goods in the mRNA drug substance production process. To decrease the cost of mRNA production, reagents should be optimally utilized. Due to the catalytic, multicomponent nature of the IVT reaction, optimization is a multi‐factorial problem, ideally suited to design‐of‐experiment approach for optimization and identification of design space. We derived a data‐driven model of the IVT reaction and explored factors that drive process yield (in g/L), including impact of nucleoside triphosphate (NTP) concentration and Mg:NTP ratio on reaction yield and how to optimize the main cost drivers RNA polymerase and DNA template, while minimizing dsRNA formation, a critical quality attribute in mRNA products. We report a methodological approach to derive an optimum reaction design, with which cost efficiency of the reaction was improved by 44%. We demonstrate the validity of the model on mRNA construct of different lengths. Finally, we maximized the yield of the IVT reaction to 24.9 ± 1.5 g/L in batch, thus doubling the highest ever reported IVT yield. [ABSTRACT FROM AUTHOR]

The quality of amla fruits is greatly affected by post-harvest factors, especially storage temperature and time, which undergo rapid quality changes after harvest. Therefore, a detailed storage study was necessary for amla fruit. Hence, this study was conducted to determine the impact of different storage temperatures and durations on physicochemical, textural, bioactive, and microstructure properties of amla fruit. Storage analysis was performed at low (6 °C) and room temperature (25 °C) conditions. The results showed that fructose sugar significantly (p < 0.05) decreased by 15.79% during room temperature (RT) storage due to a higher respiration rate (14.32–45.98 mL kg− 1h− 1) in the RT environment, while it was non-significantly affected during low-temperature (LT) storage. Although, total soluble solid (TSS) of RT-stored amla increased by 76.67% due to moisture loss (7.82%). These results correlated that increased TSS is due to moisture loss, unrelated to ripening or starch degradation. In addition, total phenol content (TPC) of RT-amla was increased by 28.23%, while it slightly decreased by 6.58% for LT-amla. At the same time, variations in TSS, weight, and moisture were insignificant during LT storage, resulting in no significant changes in textural properties and SEM microstructures. Textural properties of RT and LT-stored amla exhibited opposite trends during storage, which can be correlated with reduced intercellular space and increased gumminess in SEM microstructure analysis. These findings provide new insights into governing amla fruit's characteristics during storage, which will be beneficial in enhancing shelf-life. [ABSTRACT FROM AUTHOR]

Chlorophyll b quantities of raw (control) and roasted rapeseed samples were specified to be higher than chlorophyll a. Additionally, total phenol, total flavonoid quantities and antioxidant activity (DPPH and FRAP assays) values of roasted powdered and whole rapeseed samples were observed to increase compared to the control. K232 and K270 values ​​of conventional oven roasted, ground and whole rapeseeds were slightly higher than the results in the microwave. The highest K232 value was observed in oil provided from the sample that was powdered and heat treated in conventional oven. The phenolic constituents of ground and whole rapeseeds were partially higher than those of their oils. The dominant fatty acids of the oils extracted from unroasted and roasted rapeseeds were oleic, linoleic, linolenic and palmitic acids in decreasing order. Oleic acid quantities of the oil provided from powdered and whole rapeseeds roasted in microwave and oven were defined as 62.00 and 61.97% to 61.48 and 62.06%, respectively. The main variables of PC1 for rapeseed were dedected as catechin (0.912), coumaric acid (0.840) and ferulic acid (0.733). [ABSTRACT FROM AUTHOR]

Overuse of artificial chemical fertilizers could be detrimental to the environment. Utilizing beneficial microorganisms as biofertilizers is a sustainable technique that promotes soil health, crop yield, and ecosystem preservation. Curcuma longa L. is utilized as a medication since it has its antibacterial, anti-microbial, and anti-tumor characteristics, which reduce inflammation and hasten wound healing. The effect of E. cloacae strain MSR1, which is common in the roots of alfalfa grown in the Al-Ahsaa region, on C. longa plants is being investigated. C. longa rhizomes were planted under greenhouse conditions after being submerged in a solution of E. cloacae strain MSR1 (OD 500) or water treatment as a control for 12 hours. After 240 days of growing, ten randomly selected plants from each treatment were collected, and the vegetative growth and yield metrics were assessed. To investigate how E. cloacae influences C. longa production and chemical composition (photosynthetic pigment, nitrogen, phosphorus, potassium, and curcuminoid), measurements were conducted as well as genes diketide-CoA and curcumin synthases genes. Our research showed that C. longa's growth and yield were favorably impacted by E. cloacae. Significant increases in the related plants' chlorophyll a,b, carotenoid, nitrogen, phosphorus, and potassium levels were likewise a reflection of the enhanced effects shown in the growth and yield parameters. Treatment with E. cloacae raised the curcuminoid's three sub-components' compositions to varying degrees: bisdemethoxycurcumin, demethoxycurcumin, and curcumin. Comparing E. cloacae treated plants to the control, high expression levels of the genes diketide-CoA and curcumin synthase-1, -2, and 3 were also found. The treatment of E. cloacae is a good biostimulant candidate for boosting growth and yield as well as raising the medicinal qualities of C. longa, according to the overall results. [ABSTRACT FROM AUTHOR]

Herbal medicine could be an option for atopic dermatitis (AD) treatment for those suffering from global public health. HMB is a new combination of three herb extracts, consisting of the Ha‐Rak (HR) remedy extract, Piper betle (PB) extract, and Garcinia mangostana (GM) extract in equal proportions, using Thai traditional medicine theory, that uses a combination of medications that can improve therapeutic efficacy and reduce side effects and toxicity. HMB extract has anti‐inflammatory and antiallergic properties, is a component for AD treatment, and tends to develop topical products. Drug registration requires stability data. Results from drug stability testing affect not only the efficacy of the drug but also its safety. The aim of this study was to investigate stability through forced degradation and an accelerated study of extracts. Chemical content analysis and in vitro biological activities such as anti‐inflammatory and antiallergic activities determined the effects of all examined samples. Anti‐inflammatory and antiallergic effects were assessed by inhibiting nitric oxide synthesis in RAW 264.7 cells and β‐hexosaminidase release in RBL‐2H3 cells, respectively. High‐performance liquid chromatography (HPLC) assessed content indicators. Moisture and temperature hydrolysis had no significant differences in the chemical or biological properties of the HMB. However, the HMB demonstrated sensitivity to alkaline hydrolysis, showed low anti‐inflammatory activity, and decreased hydroxychavicol, eugenol, and α‐mangostin contents. The contents of the three compounds also decrease with acid hydrolysis. For the accelerated study, anti‐inflammatory and antiallergic effects and hydroxychavicol amount were not significantly different after 180 days at 40°C and 75% RH. Therefore, the contents of eugenol and α‐mangostin were changed. Eugenol in HMB decreased significantly from the 15th day until the 180th day of storage. In addition, α‐mangostin amounts in HMB decreased slightly on 180th day. Fortunately, reducing the two chemicals did not affect anti‐inflammatory or antiallergic effects. For stability, combination extract should be stored in a closed container in the refrigerator at a low temperature and protected from light, high temperature, oxygen, and pH. Further HMB development should avoid pH or oxidation processes or components. [ABSTRACT FROM AUTHOR]

ABSTRACT Nanoparticles (NPs) are well‐known biostimulants in plant biotechnology, utilised to enhance the physical properties of plants and exhibit positive effects on them. The important key role is the most suitable type, effective dose and size of NP to be used in plant tissue culture systems. In this study, various concentrations of silver nanoparticles (AgNPs; 0, 25, 50, 75 and 100 μg L−1) were tested as elicitors in callus culture with the aim of enhancing secondary metabolite production in lemon balm (Melissa officinalis L.). According to the results obtained, callus formation rates have shown an increase in all applications compared to the control group. The highest callus formation, weight and diameter were observed in 50 μg L−1 application. In this application, the callus structure was compact and its colour was green. However, the aromatic compounds, neral and geranial increased significantly in 25 μg L−1 application. The maximum increase in phenolic compounds such as caffeic acid, chlorogenic acid, proto‐catechic acid, hesperidin and p‐coumaric acid was observed in the 75 μg L−1 AgNP and the highest increase in rosmarinic acid compound was determined in the 50 μg L−1 application. The study found that AgNP applications are an effective method for increasing the production of secondary metabolites in medicinal and aromatic plants, such as lemon balm, in vitro. [ABSTRACT FROM AUTHOR]

Background Results Conclusion Kenaf seeds are a rich source of protein; however, finding the best extraction method is crucial to obtaining high‐quality protein from these underutilized seeds. This research devised an optimized extraction process for best recovery of kenaf seeds protein using response surface methodology. The key parameters affecting the yield and protein content were optimized, including extraction pH (2–11), seed:water ratio (5:1–50:1), temperature (30–90 °C), and duration (20–360 min). The physicochemical and techno‐functional properties of kenaf seed protein isolates (KSPIs) were examined.A maximum protein yield of 12.05 g/100 g with purity level 91.94 g/100 g was obtained using an optimized extraction with pH 11.0, seed:water ratio 50:1, 360 min duration, and temperature 50 °C. The oil and water retention capacities of KSPI were 1.14 mL g−1 and 1.37 mL g−1 respectively. After 30 min at pH 7, KSPIs demonstrated remarkable emulsion capacity (83.12%) and stability (75.63%), along with high foaming capacity (106%) and stability (18.3%). As per high‐performance liquid chromatography analysis, arginine, glutamic acid, leucine, phenylalanine, and lysine were the most abundant amino acids detected in KPSIs. The KSPIs’ globular protein structure was successfully verified using analytical approaches, including Fourier transform infrared spectroscopy, protein fraction ratios, and differential scanning calorimetry. Sodium dodecyl sulfate polyacrylamide gel electrophoresis analysis revealed that KPSI has a molecular weight distribution ranging from 10 kDa to 50 kDa.The results of this study support the application of the proposed response‐surface‐methodology‐optimized extraction method for efficient recovery of high‐quality kenaf seed proteins that meet the necessary physicochemical and techno‐functional requirements. © 2024 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

1. The objective of this research was to compare the pharmacokinetics and bioavailability of tolfenamic acid, analgesic, antipyretic and anti-inflammatory compound, after administration through different routes to Pekin ducks. The investigation was carried out over four time periods using a randomised cross-pharmacokinetic design.2. Tolfenamic acid was administered to ducks intravenously, intramuscularly, subcutaneously and orally at a dose of 2 mg/kg. Tolfenamic acid analysis was performed using HPLC-UV and pharmacokinetic data were conducted by non-compartmental analysis.3. The total clearance, volume of distribution at steady state and terminal elimination half‐life after intravenous administration were 0.14 l/h/kg, 0.29 l/kg and 1.80 h, respectively. The peak plasma concentration and bioavailability for intramuscular, subcutaneous and oral administration were 4.59, 3.55 and 2.23 μg/ml and 93.62, 74.30 and 43.43%, respectively.4. Tolfenamic acid was absorbed rapidly, eliminated quickly and exhibited a small distribution volume in Pekin ducks. Pharmacokinetic parameters, including maximum concentration, area under the plasma concentration – time curve and bioavailability, were found to be different in ducks from other bird species. [ABSTRACT FROM AUTHOR]

Background and Objectives Materials and Methods Results Conclusion Sickle cell trait (SCT) persons are significant donors, and discarding these blood units reduces their supplies, mainly in the third‐world countries. This work focused on 12 metabolites associated with the red blood cell (RBC) storage lesion and 23 amino acids in the supernatants of packed RBC units from SCT and reference (non‐SCT) donors stored in the same conditions.All samples of RBC concentrates were collected and separated from the storage of Colsan (Beneficient Association of Blood Collection), where they were routinely processed and separated as packed RBC units and stored in the refrigerator (2°–6°C). The supernatant samples of each packed RBC bag were separated by centrifugation at days 1, 7, 14, 21, 28 and 35 of storage and kept at −80°C till the metabolite analysis together.The quantitation of metabolites and amino acids examined in the supernatant of SCT and reference donors showed no statistical differences along the cold storage. Lactic acid and malic acid releases occur in three phases during RBC storage. Basic and acid amino acids and corresponding amides have low and stable values during the first 14 days of storage, followed by a steep increase.Our metabolomic results give elements that seem not to contraindicate the transfusion of RBC with SCT, besides its more structural fragility. [ABSTRACT FROM AUTHOR]

The control of ergot alkaloids in biotechnological processes is important in the context of obtaining new strain producers and studying the mechanisms of the biosynthesis, accumulation and secretion of alkaloids and the manufacturing of alkaloids. In pharmaceuticals, it is important to analyze the purity of raw materials, especially those capable of racemization, quality control of dosage forms and bulk drugs, stability during storage, etc. This review describes the methods used for qualitative and quantitative chemical analysis of ergot alkaloids in tablets and pharmaceutic forms, liquid cultural media and mycelia from submerged cultures of ergot and other organisms producing ergoalkaloid, sclerotias of industrial Claviceps spp. parasitic strains. We reviewed analytical approaches for the determination of ergopeptines (including their dihydro- and bromine derivatives) and semisynthetic ergot-derived medicines such as cabergoline, necergoline and pergolide, including precursors for their synthesis. Over the last few decades, strategies and approaches for the analysis of ergoalkaloids for medical use have changed, but the general principles and objectives have remained the same as before. These changes are related to the development of new genetically improved strains producing ergoalkaloids and the development of technologies for the online control of biotechnological processes and pharmaceuticalmanufacturing ("process analytical technologies," PAT). Overall, the industry is moving toward "smart manufacturing." The development of approaches to production cost estimation and product quality management, manufacturing management, increasing profitability and reducing the negative impact on personnel and the environment are integral components of sustainable development. Analytical approaches for the analysis of ergot alkaloids in pharmaceutical rawmaterials should have high enough specificity for the separation of dihydro derivatives, enantiomers and R-S epimers of alkaloids, but low values of the quantitative detection limit are less frequently needed. In terms of methodology, detection methods based on mass spectrometry have become more developed and widespread, but NMR analysis remains in demand becauseof its high accuracy and specificity. Both rapid methods and liquid chromatography remain indemand in routine practice, with rapidanalysis evolving toward higher accuracy owing to improved analytical performance and new equipment. New composite electrochemical sensors (including disposable sensors) have demonstrated potential for real-time process control. [ABSTRACT FROM AUTHOR]

The production of indigo, primarily used by the denim industry, increases year by year, and is mainly of synthetic origin. The textile industry, on which its production depends, is responsible for 10% of greenhouse gases and 20% of water pollution. However, the source of this pigment/colorant, mainly based on petrochemistry, remains a key issue today. Extracting indigo from plants is becoming a popular answer and requires an understanding and evaluation of the entire process, from raw material to pigment recovery. In this study, the indigotin precursor, indoxyl, derived from the hydrolysis of O-glycosides biomass extracted in water, was oxidized to obtain the desired pigment. This step is the most sensitive, as variations have been observed during this phase. Consequently, the standardization of the oxidation process was established to determine the extract capacity to consistently produce the blue dye pigment. Partial hydrolysis of the O-glycosides, the indoxyl precursors, was identified as a factor causing this yield variability in the obtained extracts. Once the precursors were fully chemically hydrolyzed, plants harvested during summer and during a freezing period showed a similar capacity to produce indigotin, with values of 412 ± 25 ppm and 379 ± 0 ppm, respectively. This result showed that in freezing conditions, the enzymatic material was not available, resulting in the lack of indigotin formation. To address the use of oxidation in an alkaline medium, a spontaneous oxidation method was proposed. This method produced a purer indigotin pigment, with a 21.6% purity compared to 5.9% purity using air-mediated oxidation in an alkaline medium. [ABSTRACT FROM AUTHOR]

This work reports the synthesis method and various properties of four rod-like antiferroelectric (R) laterally substituted enantiomers, with or without fluorine atoms used as substituents in the benzene ring. The influence of fluorine substitution on the mesophase temperature range was determined. The synthesized compounds are three-ring rod-like smectics with a chiral center based on (R)-(−)-2-octanol. Their chemical and optical purity was checked using high-performance liquid chromatography (HPLC). Two newly synthesized enantiomers and three previously reported (R) enantiomers were used to formulate two antiferroelectric mixtures. The mesomorphic behavior was characterized by polarizing optical microscopy, differential scanning calorimetry, and X-ray diffraction (XRD). The helical pitch and tilt angle measurements were done using the selective light reflection phenomenon and the electro-optical method, respectively. All the enantiomers exhibit a wide temperature range of the antiferroelectric phase, with a high tilt angle. Furthermore, the enantiomer with lateral fluorine substitution in the ortho position has a very long helical pitch (more than 2.0 µm), relatively low enthalpy of melting point, and a tilt angle close to 45 degrees. The designed (R) enantiomers can be useful for formulating eutectic mixtures for further use in various devices, including photonics and optoelectronics. [ABSTRACT FROM AUTHOR]

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Copyright of Science & Technology of Food Industry is the property of Science & Technology of Food Industry Editorial Office and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Antibiotics can be effectively removed from wastewater using constructed wetlands (C.W.s). However, little is known about using attractive garden plants in C.W.s to eliminate antibiotics. Thus, the current study aims to treat amoxicillin (AMX)-contaminated wastewater through a Rhapis excelsa-based bioretention system (BS). The investigation was done at 15 days hydraulic retention time (HRT) under two conditions: set-1, varied AMX 5 to 25 ppm with constant NPK (nitrogen, phosphorus, potassium) source; and set-2, varied NPK sources with constant AMX (25 ppm). During the study, it was observed that in the set-1 condition with increasing AMX concentration, the removal of AMX through BS decreased; however, in the set-2 experiment, with enhancing NPK source, the performance of the BS treating 25-ppm AMX-contaminated wastewater increased. AMX removal of 2.3%, 66.3%, 60.6%, 52.2%, 46.7%, and 44.9% was achieved for control, BS-1, BS-2, BS-3, BS-4, and BS-5, respectively, during set-1 experiment. However, in the set-2 experiment, 23.4% (control), 43.3% (BS-1), 60.3% (BS-2), 75.9% (BS-3), 88.8% (BS-4), and 99% (BS-5) AMX removal were achieved. Removing pollutants like AMX, COD, PO43−-P, NO3−-N, and NH4+-N followed first-order kinetics. A positive correlation of COD with AMX was observed through principal component analysis and correlation matrix. The microbial community study was also covered to prioritize the role of microbes in treating AMX through BSs. The AMX treatment through Rhapis excelsa-based BS supported plant growth and development with increasing chlorophyll content, fresh weight, and C, H, N value. [ABSTRACT FROM AUTHOR]

The development of two eco-friendly analytical methods for the simultaneous determination of eight cardiovascular drugs; hydrochlorothiazide (HCT), captopril (CPL), lisinopril (LSP), valsartan (VAL), atorvastatin (ATR), bisoprolol (BSL), amlodipine (AML) and carvedilol (CVL); alongside with the nutraceutical vincamine (VIC) is essential for sustainable pharmaceutical analysis. This study explores the application of Micellar Electro Kinetic Chromatography (MEKC) and High-Performance Liquid Chromatography (HPLC) for this purpose. In MEKC method, the separation was done using fused silica capillary (41.5 cm × 50 µm id) and a back ground electrolyte consisting of 50 mM borate buffer (pH 9) containing 50 mM sodium lauryl sulphate (SLS) and 10% organic modifier (Acetonitrile). In HPLC method, separation was performed on a ZORBAX Extend-C18 (4.6 × 250 mm, 5 µm) column, using a gradient mobile phase consisting of 50 mM phosphate buffer pH 3 and methanol. Both methods attained good linearity (r ≥ 0.9996) with low values of LOD and LOQ. Both methods were successfully applied in the determination of co-administered single, binary and ternary dosage form of the studied drugs. Moreover, application of various combinations of co-administered dosage forms was achieved in rat plasma, confirming the applicability of these methods in different matrices. The use of micellar solutions in MEKC enhances separation efficiency while reducing the need for organic solvents, aligning with green chemistry principles. HPLC methods were optimized using environmentally benign solvents, ensuring reduced toxicity and waste production. The methodologies were evaluated through green, white, and blue metrics to ensure comprehensive sustainability, considering ecological impact, safety, and practical efficiency. These methods were not only cost-effective and time-saving but achieved high efficiency, sensitivity, and reproducibility making them ideal for routine use in pharmaceutical analysis. [ABSTRACT FROM AUTHOR]

Background: This study developed and validated a simple, robust, and cost-effective RP-HPLC bioanalytical method for the determination of nebivolol hydrochloride (NBH) and amlodipine besylate (AMB) in human plasma. Briefly, NBH and AMB were extracted from plasma through protein precipitation using 5% formic acid and acetonitrile. Chromatographic separation was achieved using an Inertsil ODS-3 V column (150 mm × 4.6 mm, 5 μm) with a mobile phase composed of acetonitrile and buffer (40:60, v/v). The analysis was conducted using UV detection at 215 nm. Results: The bioanalytical method demonstrated linearity for NBH (4.50–180.12 μg/mL) and AMB (3.50–140.06 μg/mL). It exhibited good selectivity and sensitivity, with LLOQ responses within ≤ 20% of the analyte signal. Accuracy and precision were within acceptable limits. The extraction recovery from human plasma showed a CV (%) of 1.15% for NBH and 1.35% for AMB, indicating consistent recovery rates. Stability studies on drug-spiked human plasma at LQC and HQC levels confirmed the stability of the drugs under various conditions. Conclusion: The present bioanalytical method successfully quantified NBH and AMB simultaneously in plasma samples. It demonstrated suitability, supported by high recovery rates and low relative standard deviations. With its proven linearity, accuracy, and precision, this technique is well suited for drug identification in plasma samples. [ABSTRACT FROM AUTHOR]

Green, selective and accurate high-performance liquid chromatography (HPLC) chromatographic method is presented for simultaneous separation and quantitation of the co-prescribed drugs in chemotherapy omeprazole, ondansetron and deflazacort in spiked human plasma. An isocratic HPLC separation was performed on X Bridge C18 (4.6 × 250 mm) column with 5 μm particle size using mobile phase consisting of methanol: ammonium acetate buffer pH 4 adjusted by acetic acid (60: 40, v/v). The injection volume was 20μL with UV detection wavelength at 237 nm at room temperature. Flow rate of the mobile phase was adjusted to be 2.0 ml/min. Dexamethasone was used as internal standard to correct the variation during sample pretreatment. FDA guidelines were followed to validate the developed method. Successful application of the developed method was revealed by simultaneous determination of omeprazole, ondansetron and deflazacort in spiked human plasma in ranges of 1–20, 0.1–8 and 0.2–8 μg mL−1 for omeprazole, ondansetron and deflazacort, respectively. Four greenness assessment tools were used to evaluate the greenness of the developed method and the results were accepted. This method permitted the accurate simultaneous determination of the studied drugs, thus it can be used during therapeutic drug monitoring in daily clinical practice. [ABSTRACT FROM AUTHOR]

Aflatoxin B1 (AFB1), the most potent toxic and carcinogenic secondary fungal metabolite, has frequently been reported in food/feed. Nowadays, herbal extracts are considered safe dietary additives to reduce the toxicity of such compounds. The protective capability of various combinations of hydro‐alcoholic extracts (HAEs) of ginger, turmeric, and Shirazi thyme, against the toxicity of AFB1 on the RAW264.7 cell line was investigated. The RAW264.7 cells were exposed to six different concentrations of AFB1 (0.09, 0.18, 0.37, 0.75, 1.5, and 3 μg mL−1) for 48 h to determine the IC50 of AFB1. AFB1 was estimated to have an IC50 of 1.5 μg mL−1 for RAW264.7 cells. Then, the cells were simultaneously incubated with 1.5 μg mL−1 AFB1 and the HAEs for 24 h. The HAEs significantly reduced the toxicity of AFB1 in RAW264.7 cells. HAE of Shirazi thyme showed the highest amount of total phenol content (TPC) and the highest DPPH• activity. In addition, a combination of ginger, turmeric, and Shirazi thyme extract showed the highest antioxidant activity. Rutin, quercetin, and apigenin were the main phenolic components of ginger HAE. A significantly positive correlation was observed between TPC of hydro‐alcoholic extract with ferric reducing antioxidant power (FRAP) and 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide (MTT) values. Consequently, the simultaneous consumption of such extracts is recommended to protect the cells against dietary toxins. [ABSTRACT FROM AUTHOR]

This study presents the development and validation of environmentally friendly analytical methods for quantifying Abiraterone Acetate (AA) in both its pure form and commercial pharmaceutical formulations. An optimized High-Performance Liquid Chromatography (HPLC) method was developed using an Agilent Extend C18 column (250 mm × 4.6 mm, 5 μm) at 25 °C. The mobile phase consisted of formic acid and ethanol in isocratic mode, with a flow rate of 1.0 mL min−1, and detection was performed at 253 nm. The spectrophotometric method involved a comprehensive evaluation of AA's spectral properties in various solvents, with ultrapure water providing the most suitable spectra for analysis at 253 nm. Both methods were validated according to ICH guidelines, demonstrating selectivity, linearity, accuracy, precision, detection and quantification limits, and robustness, with correlation coefficients exceeding 0.999 across the 5–30 μg mL−1 concentration range. Comparative statistical analysis using Student's t-test and Fisher's F-test showed no significant differences between the two methods. The environmental impact of both methods was assessed using AGREE and GAPI software, confirming their sustainability. These validated methods offer reliable and eco-friendly approaches for the quantitative analysis of AA in tablet formulations, promoting safer and greener laboratory practices in pharmaceutical analysis. [ABSTRACT FROM AUTHOR]

Introduction: A limited sampling strategy (LSS) for estimating the area under the plasma concentration–time curve (AUC0–12) of the immunosuppressant mycophenolic acid (MPA) is used for therapeutic drug monitoring (TDM) in clinical practice. Our study delves into the applicability of the MPA AUC0–12 LSS, originally developed using particle‐enhanced turbidimetric inhibition immunoassay (PETINIA) measurements, to those obtained via high‐performance liquid chromatography with ultraviolet detection (HPLC–UV). Methods: We developed an LSS for estimating MPA AUC0–12 based on PETINIA measurements in 32 adult kidney transplant patients who were receiving mycophenolate mofetil. Validation of this strategy was conducted in an additional 14 adult kidney transplant patients (validation sets) through measurements obtained by both PETINIA and HPLC–UV. Predictive performance was assessed using mean absolute error (MAE), root mean squared error (RMSE), and "good guess" defined as predicted AUC within observed AUC ± 15%. Results: The three time point equation (0, 2, and 6 h) emerged as optimal for estimating MPA AUC0–12, balancing predictive performance and usefulness in clinical settings. In validation sets, the coefficient of determination for observed versus predicted AUC0–12 was consistent between PETINIA (0.978) and HPLC–UV (0.958) measurements. Comparable MAE, RMSE, and "good guess" outcomes were observed for PETINIA (6.4%, 8.1%, and 85.7%, respectively) and HPLC–UV (7.6%, 9.4%, and 85.7%, respectively) measurements. Conclusion: Our findings support the application of the MPA AUC0–12 LSS, originally developed using PETINIA measurements, to those obtained via HPLC–UV. [ABSTRACT FROM AUTHOR]

This study describes the purification and preparation of tricin (5, 7, 4-trihydroxy-3, 5-dimethoxyflavone) from Carex Meyeriana Kunth via adsorption and desorption using macroporous resins and high-performance liquid chromatography. Six resins were tested to evaluate the static adsorption and desorption capacities. The HPD-300 resin was selected as the adsorption material to enrich tricin because of its suitable adsorption and desorption capacities. Adsorption thermodynamics and kinetics were studied on HPD-300 resin, and the results agreed with the Langmuir model and quasi-second-order kinetics model, respectively. The parameters of the dynamic adsorption and desorption tests were then optimized. The purity of tricin increased from 2.6 mg/g to 45.1 mg/g with a recovery yield of 76.4% after purification using HPD-300 resin. Then, Prep-HPLC was used to further purify tricin. The purity of tricin reached 99.4%, with a recovery yield of 78.0% thereafter. Tricin exerts an inhibitory effect on the proliferation of various tumor cells, including gastric cancer SGC-7901 cells. It significantly suppresses cell colony formation while also altering cell cycle progression metabolism by decreasing the proportion of cells in the G0/G1 phase and increasing the proportion in the S and G2/M phases. Additionally, tricin affects the efficiency of SGC-7901 cell lactate production, ATP content, and glucose uptake. These findings suggest that tricin may impede tumor cell proliferation through its impact on cell cycle progression and energy metabolism. [ABSTRACT FROM AUTHOR]

The enantioselective binding of three proton pump inhibitors (PPIs)—omeprazole, rabeprazole, and lansoprazole—to two key plasma proteins, α1-acid glycoprotein (AGP) and human serum albumin (HSA), was characterized. The interactions between PPI enantiomers and proteins were investigated using a multifaceted analytical approach, including high-performance liquid chromatography (HPLC), fluorescence and UV spectroscopy, as well as in silico molecular docking. HPLC analysis demonstrated that all three PPIs exhibited enantioseparation on an AGP-based chiral stationary phase, suggesting stereoselective binding to AGP, while only lansoprazole showed enantioselective binding on the HSA-based column. Quantitatively, the S-enantiomers of omeprazole and rabeprazole showed higher binding affinity to AGP, while the R-enantiomer of lansoprazole displayed greater affinity for AGP, with a reversal in the elution order observed between the two protein-based columns. Protein binding percentages, calculated via HPLC, were greater than 88% for each enantiomer across both transport proteins, with all enantiomers displaying higher affinity for AGP compared to HSA. Thermodynamic analysis indicated that on the HSA, the more common, enthalpy-controlled enantioseparation was found, while in contrast, on the AGP, entropy-controlled enantioseparation was observed. The study also identified limitations in using fluorescence titration due to the high native fluorescence of the compounds, whereas UV titration was effective for both proteins. The determined logK values were in the range of 4.47–4.83 for AGP and 4.02–4.66 for HSA. Molecular docking supported the experimental findings by revealing the atomic interactions driving the binding process, with the predicted enantiomer elution orders aligning with experimental data. The comprehensive use of these analytical methods provides detailed insights into the enantioselective binding properties of PPIs, contributing to the understanding of their pharmacokinetic differences and aiding in the development of more effective therapeutic strategies. [ABSTRACT FROM AUTHOR]

Crocus sativus L. is a widely cultivated traditional plant for obtaining dried red stigmas known as "saffron," the most expensive spice in the world. The response of C. sativus to pre-sowing processing of corms with cold plasma (CP, 3 and 5 min), vacuum (3 min), and electromagnetic field (EMF, 5 min) was assessed to verify how such treatments affect plant performance and the quality and yield of herbal raw materials. The results show that applied physical stressors did not affect the viability of corms but caused stressor-dependent changes in the kinetics of sprouting, growth parameters, leaf trichome density, and secondary metabolite content in stigmas. The effect of CP treatment on plant growth and metabolite content was negative, but all stressors significantly (by 42–74%) increased the number of leaf trichomes. CP3 treatment significantly decreased the length and dry weight of flowers by 43% and 60%, respectively, while EMF treatment increased the length of flowers by 27%. However, longer CP treatment (5 min) delayed germination. Vacuum treatment improved the uniformity of germination by 28% but caused smaller changes in the content of stigma compounds compared with CP and EMF. Twenty-six compounds were identified in total in Crocus stigma samples by the HPLC-DAD method, including 23 crocins, rutin, picrocrocin, and safranal. Processing of Crocus corms with EMF showed the greatest efficiency in increasing the production of secondary metabolites in saffron. EMF increased the content of marker compounds in stigmas (crocin 4: from 8.95 to 431.17 mg/g; crocin 3: from 6.27 to 164.86 mg/g; picrocrocin: from 0.4 to 1.0 mg/g), although the observed effects on growth were neutral or slightly positive. The obtained findings indicate that treatment of C. sativus corms with EMF has the potential application for increasing the quality of saffron by enhancing the amounts of biologically active compounds. [ABSTRACT FROM AUTHOR]

A sensitive analytical procedure for simultaneous extraction and determination of bisphenol A and alkyl phenols, namely, 4‐sec‐butylphenol, 4‐tert‐butylphenol, and 4‐tert‐amylphenol from aqueous samples with metal–organic framework (MOF)‐based dispersive micro‐solid‐phase extraction (D‐µSPE) and high‐performance liquid chromatography (HPLC) technique is developed. Sample contaminants were preconcentrated with amino‐functionalized aluminum MOF and later eluted with acetonitrile. The reconstituted sample was subjected to HPLC analysis. Various procedural parameters related to D‐µSPE were optimized. Under optimized preconcentration and chromatographic conditions, calibration curves with excellent linearity (R2 > 0.9986) in the working range of 0.25–100 ng mL−1 were prepared. Limit of detection (S/N = 3) for every analyte within the range of 0.020–0.022 ng mL−1 was obtained. Analyte's recovery 91.16%–97.01% (RSD = 1.02–3.01) for intraday and 89.86%–95.83% (RSD = 1.15–3.13) for inter‐day analysis was obtained from real water samples. [ABSTRACT FROM AUTHOR]

In the scope of vegetarian diets, cobalamin (CBL or vitamin B12) remains a particular concern, as it is mostly absent from natural, vegetarian foods. As such, vegetarians must rely on supplementation or enriched food products, to fulfil their recommended daily intake of the vitamin. The potential of microalgae is of extreme importance in this context, given the fact that they may absorb exogenous CBL and display significant levels of the vitamin. Therefore, it is crucial to establish fast and reliable B12 determination methods, to accurately characterize these products or ingredients and conclude about their role as CBL sources. To that extent, this work presents the application of the AOAC's final action method 2014.02 on the determination of total CBL in selected, commercial, microalgae and cyanobacteria powder samples. Four variants of Chlorella vulgaris, namely organic, smooth, white and honey, as well as Spirulina (Arthrospira platensis) were investigated. High-performance liquid chromatography coupled with ultraviolet (UV), diode-array detection (HPLC-DAD) was implemented in the analysis of microalgal extracts. After slight adaptation and optimisation of the extraction and analysis procedures, namely to allow lower sample amounts, it was determined that the different commercial Chlorella products, organic, smooth, white and honey have total CBL concentrations of 1063 ± 158 μg (100 g)-1, 482 ± 55 μg (100 g)-1, 681 ± 87 μg (100 g)-1 and 660 ± 68 μg (100 g)-1, respectively. Analysis of Spirulina did not yield any measurable levels of CBL in any of the purified extracts. Despite the obtained results displaying the same order of magnitude previously determined in similar microalgal products, these CBL values are amongst the highest concentrations found. Therefore, even considering the known limitations in bioaccessibility and bioavailability of CBL in microalgae, it is possible to conclude that these results stand for the inclusion of these products in vegetarian foods or as food supplements, as good potential sources of CBL, which is generally lacking in vegetarian diets. [ABSTRACT FROM AUTHOR]

Intractable inflammation plays a key role in the progression of autoimmune diseases such as rheumatoid arthritis. Oedema and angiogenesis are the hall marks of chronic inflammation. The current study was aimed to investigate the pharmacological effects of the methanolic extract of Viola odorata (Vo.Me) on inflammation induced oedema and angiogenesis, and to identify the active principles and explore the molecular mechanisms thereof. Various models of inflammation were utilized in rats, including carrageenan- and histamine-induced acute oedema, as well as chronic models of Complete Freund's Adjuvant (CFA)-induced arthritis and cotton pellet-induced granuloma. Anti-angiogenic activity was evaluated by CAM assay followed by quantification of phytoconstituents through HPLC. Effect of Vo.Me treatment on the expression of various mediators (PGE-2 and NO) and genes (IL-1β, TNF-α, NF-κB, and COX-2) were explored by qPCR and ELISA assays. HPLC analysis showed the presence of quercetin, chlorogenic acid, gallic acid, benzoic acid, m-coumaric acid, p-coumaric acid, synergic acid, caffeic acid, vanillic acid, sinapic acid, and cinnamic acid in Vo.Me. Significant dose-dependent inhibition of rats' paw oedema was observed in the Vo.Me administered groups (p < 0.05) in both acute and chronic inflammatory models. Moreover, at a dosage of 500 mg/kg, Vo.Me exhibited a comparable anti-inflammatory effect to indomethacin (p > 0.05). Additionally, Vo.Me demonstrated a remarkable anti-granulomatous activity. Histopathological findings demonstrated amelioration of inflammation in animal paws which were treated with Vo.Me and indomethacin. CAM assay also displayed significant inhibitory effect of Vo.Me on the blood vasculature growth. Vo.Me treatment also caused relatively less gastric irritation and hepatic damage as compared to indomethacin. At a molecular level, the down-regulation of NF-κB signalling leading to the decreased activation of pro-inflammatory mediators (such as IL-1β, TNF-α, and COX-2) and their downstream molecules including prostaglandin E-2 (PGE-2) and nitric oxide (NO), is suggested to be responsible for these diverse anti-inflammatory effects. These findings confirmed the promising anti-inflammatory and anti-angiogenic activities of Vo.Me, which warrant bench-to-bedside translational studies to assess its safety and suitability for clinical usage. [ABSTRACT FROM AUTHOR]

Tomato has antioxidant properties from polyphenols, but tomato by-products have been little studied, which can have significant added value for the pharmaceutical or food industry. Several polyphenol extraction processes cause variability in detected compounds and their concentrations, making it necessary to characterize each method for a suitable exploitation strategy. In this research, tomato by-products were first dried using an oven or a dehydrator, resulting in oven-dried extracts with higher polyphenols than dehydrator-dried ones. Four solid–liquid methods by Soxhlet extraction (SOX), stirring extraction (SE), ultrasound-assisted extraction (UAE), and microwave-assisted extraction (MAE) were developed and employed for obtaining oven-dried extracts. Suitable and green extraction processes were carried out using different ethanol/water extractants, sample–extractant ratios, extraction times, and exposing conditions to physical energies, depending on optimal conditions calculated by multivariate optimization. Total polyphenols and antioxidant capacity indices and gallic acid, caffeic acid, chlorogenic acid, quercetin, and kaempferol concentrations were determined in extracts. Principal component analysis found an excellent relationship between caffeic acid and total polyphenol index and gallic acid and antioxidant capacity. SE and UAE extracted more amounts of all polyphenols, but UAE was exhaustive at only 5 min. MAE was also fast, completing extraction at 20 min, but reducing phenol concentration by around 30% than SE and UAE. SOX showed the lowest indices and phenol concentrations after a long extraction time. To sum up, the present study evidences the importance of the extraction method on the quality and quantity of polyphenols in tomato by-product extracts. [ABSTRACT FROM AUTHOR]

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