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This study explores a novel, eco-friendly approach to silver nanoparticle (AgNP) synthesis by using rose petal (RP) extracts. Unlike traditional chemical synthesis, this method reduces silver ions (Ag+) to elemental silver (Ag0) with RP, facilitating nanoparticle stabilization. RP-AgNPs were structurally characterized using UV/Vis (ultraviolet/visible) spectroscopy, Fourier transform infrared spectroscopy, dynamic light scattering, zeta potential, transmission electron microscopy, scanning electron microscopy, and energy dispersive X-ray spectroscopy which confirmed the synthesis of predominantly spherical to oval RP-AgNPs, with a distinct absorption peak at 410 nm as observed in UV/Vis spectra. The NPs demonstrated exceptional antibacterial efficacy against Escherichia coli and Staphylococcus aureus (inhibitory zones of 12.5 ± 0.20 and 14 ± 0.67 mm at 50 µg) and potent antibiofilm activity. Crucially, they also exhibited selective cytotoxicity toward HeLa cervical cancer cells when assessed by viability assays, fluorescence imaging, and flow cytometry. These findings underscore the potential of green synthesized AgNPs for future biomedical applications in areas such as infection control and cancer treatment.

Polymethyl methacrylate (PMMA) has garnered significant attention in the field of dentistry due to its wide applications. This paper proposes the incorporation of the nystatin coated copper oxide (CuO) particles having desirable conductivity and antifungal properties, as a filler in the PMMA denture to address their low thermal conductivity, low impact strength, low fatigue resistance, and microbial adhesion. The prepared nystatin coated CuO particles were characterized with several analytical techniques. The nystatin coated CuO particles were mixed in different ratios (0%, 1%, 2%, and 4%) in PMMA corresponding to groups C, E1, E2, and E3, respectively. The prepared samples of composite PMMA with nystatin coated CuO were evaluated to determine their transverse strength, impact strength, Vickers hardness (HV), and thermal conductivity. Furthermore, antifungal properties of CuO particles, nystatin coated CuO particles, and their acrylic composites were evaluated against Candida albicans. Scanning electron microscopy (SEM) analysis confirmed the particles' spherical and irregular shapes. The particle sizes range from nano to micron level. Fourier‐transform infrared spectroscopy (FTIR) and energy dispersive X‐ray spectroscopy (EDX) analysis confirmed the coating of nystatin on CuO. X‐ray diffraction (XRD) analysis showed the diffraction patterns and planes of CuO monoclinic shape structure. The composite prepared to have higher values of HV (19.53 ± 0.65, 20.16 ± 0.37, and 21.11 ± 0.75, respectively) as compared to the control. The impact strength values were measured high at 14.12 ± 5.55 kJ/m2 for 2% containing nystatin coated CuO acrylic resins compared to control and other groups. The conductivity increased linearly with the addition of CuO particles. The addition of CuO particles causes a reduction in flexural strength as compared to the control group. As the concentration of nystatin coated CuO (1%, 2%, and 4%) in acrylic samples increased, the antifungal properties were improved. Thus, the incorporation of optimized concentrations of nystatin coated CuO particles in acrylic resin resulted in the improved mechanical, thermal, and antifungal properties. [ABSTRACT FROM AUTHOR]

Pyridine derivatives are the most common and significant heterocyclic compounds, which play an important role in various fields ranging from medicinal to chemosensing applications. Pyridine derivatives possess different biological activities such as antifungal, antibacterial, antioxidant, antiglycation, analgesic, antiparkinsonian, anticonvulsant, anti-inflammatory, ulcerogenic, antiviral, and anticancer activity. Furthermore, these derivatives have a high affinity for various ions and neutral species and can be used as a highly effective chemosensor for the determination of different species. In this review article, generally used synthetic routes of pyridine, structural characterization, medicinal applications, and potential of pyridine derivatives in analytical chemistry as chemosensors have been discussed. We hope this study will support the new thoughts to design biological active compounds and highly selective and effective chemosensors for the detection of various species (anions, cations, and neutral species) in various samples (environmental, agricultural, and biological). [ABSTRACT FROM AUTHOR]

One of the most effective, rapid, and simple methods reversed-phase high-performance liquid chromatography (RP-HPLC) was used for simultaneous development and validation of Eletriptan hydrobromide (ELE HBR) and Itopride hydrochloride (ITP HCL) in combination. The method was validated based on the regulations of United States Pharmacopeia (USP) and International Conference on Harmonization (ICH) guidelines. Separation of both drugs was achieved within approximately 5 min by using a mobile phase made up of a 70:30 ratio of phosphate buffer and acetonitrile having a flow rate of 1 mL min−1. Furthermore, a comprehensive study was conducted on precision, accuracy, linearity, inter-day, intra-day studies, an assay of formulated films, and stability studies of combined prepared film. Co-efficient of correlation ranged between 0.9993, and 0.9965 for ELE HBR and ITP HCL respectively. The accuracy of the developed method was accurate as drug recoveries in both cases of ITP HCL, and ELE HBR falls between (99.87, 99.96, and 99.84%) to (99.81, 99.12, and 98.44%) respectively having a concentration range of solutions between 10, 30 and 50 μg mL−1 dilution. Films developed by using both drugs in combination were then validated for assay studies, and it was found that substantial results of 99.05%, and 99.87% were found in the case of ITP HCL and ELE HBR respectively. The stability of the solution and mobile phase showed the method's accuracy as the results were 97% for ITP HCL and 99% for ELE HBR. The proposed method developed for simultaneous determination of ITP HCL and ELE HBR was developed and validation and no interaction of any excipient were found. [ABSTRACT FROM AUTHOR]

Among the oral route, mouth dissolving tablets (MDTs) offer a benefit for drugs with slow dissolution and having low oral bioavailability. Epalrestat is one of the best effective diabetic neuropathy medication used for treating nerve pain. The problem associated with this drug is high first pass metabolism and low solubility in acidic media as well in basic media leads to short half-life, delayed dissolution and side effects. Therefore, the goal of the current work is to developed an epalrestat MDTs tablet that will provide quick drug dissolution and a quick onset of action for the treatment of nerve pain. MDTs of epalrestat were formulated by direct compression using natural superdisintegrants obtained from the various sources such as fenugreek, gum karaya and banana powder. All of the pre- and postcompression parameter results were shown to be in accordance with established specifications. In comparison to other formulations of MDTs, formulation F3 with 15 mg (7.5%) of banana powder displayed a higher rate of dissolution. It was determined that epalrestat MDTs containing natural superdisintegrant were successfully formulated with acceptable physical and chemical properties, quick oral cavity disintegration, a quick onset of action, and improved patient compliance. [ABSTRACT FROM AUTHOR]

Schiff bases, named after Hugo Schiff, are formed when primary amine reacts with carbonyl compounds (aldehyde or ketone) under specific conditions. Schiff bases are economical, simple synthetic routes, and easily accessible in laboratories. They have medicinal and biological applications such as antiviral, antioxidant, antifungal, anticancer, anthelmintic, antibacterial, antimalarial, anti-inflammatory, antiglycation, anti-ulcerogenic, and analgesic potentials. A number of Schiff bases are reported for the detection of various metal ions. They are also used as catalysts, polymer stabilizers, intermediates in organic synthesis, and corrosion inhibitors. In this review, we have highlighted the recent advancements in the development of bioactive Schiff base derivatives and their sensing applications for detecting metal cations. Additionally, various spectroscopic techniques for structural characterization, such as X-ray diffraction analysis (XRD), FT-IR, UV-vis, and NMR spectroscopy were also discussed. [ABSTRACT FROM AUTHOR]

The current studies were aimed to formulate ethyl cellulose (EC), beta-cyclodextrin β-CD facilitated EC based Ondansetron nanosponges (NS) using Response Surface Methodology (RSM) by employing One Factor Design. The NS were fabricated by Emulsion Solvent Diffusion method, followed by characterizations including, drug-polymer compatibility, entrapment efficiency, percentage yield, zeta size, zeta potential and in-vitro release of drug and Scanning Electron Microscopy (SEM) and X-Ray Diffractometry (XRD). The outcomes of Fourier Transformed Infra-Red Spectroscopy (FTIR) have confirmed the compatibility of the drug and excipients. It was found that NS have good entrapment efficiency along with their satisfactory percentage yield. Particle size analysis has confirmed the synthesis of nanosized NS (87.8nm to 108.2nm), having spongy surface, that was described by SEM results. Furthermore, the drug release studies have described a good sustained release of ondansetron for the period of 8 hours. The kinetic modeling has predicted that drug would follow the non fickian type of diffusion mechanism. The application of statistical approach was found helpful in designing and evaluating the NS, avoiding the laborious work, needs to be conducted while using hit and trial method. [ABSTRACT FROM AUTHOR]

Background: Thalassemia major has become a public health problem worldwide, mainly in developing and poor countries, while the role of educating the family and community has not been considered enough in patients' care. Purpose: This study was done to examine the impact of partnership care model on mental health of patients with beta-thalassemia major. Materials and Methods: This experimental study, with pretest and posttest design, was performed on patients with beta-thalassemia major in Jeddah city. 40 patients with beta-thalassemia major were assigned randomly into two groups of intervention (20 patients) and control (n=20) groups. Mental health of the participants was measured using the standard questionnaire before and after intervention in both groups. The intervention was applied to the intervention group for 6 months, based on the partnership care model. Results: There were significant differences between the scores of mental health and its subscales between the two groups after the intervention (P< 0.05). Conclusions: The findings of the study revealed the efficacy and usefulness of partnership care model on mental health of patients with beta-thalassemia major; thus, implementation of this model is suggested for the improvement of mental health of patients with beta-thalassemia major. [ABSTRACT FROM AUTHOR]

Pyridine derivatives are the most common and significant heterocyclic compounds, which show their fundamental characteristics to various pharmaceutical agents and natural products. Pyridine derivatives possess several pharmacological properties and a broad degree of structural diversity that is most valuable for exploring novel therapeutic agents. These compounds have an extensive range of biological activities such as antifungal, antibacterial, anticancer, anti-obesity, anti-inflammatory, antitubercular, antihypertensive, antineuropathic, antihistaminic, antiviral activities, and antiparasitic. The potent therapeutic properties of pyridine derivatives allow medicinal chemists to synthesize novel and effective chemotherapeutic agents. Consequently, the imperative objective of this comprehensive review is to summarize and investigate the literature regarding recent advancements in pyridine-based heterocycles to treat several kinds of cancer. Furthermore, the performances of pyridine derivatives were compared with some standard drugs, including etoposide, sorafenib, cisplatin, and triclosan, against different cancer cell lines. We hope this study will support the new thoughts to pursue the most active and less toxic rational designs., (Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.)

Atherosclerotic patients suffering with acute coronary disease are lying at high risk. This life-threatening problem can be curtailed by using statins e.g., ezetimibe (EZT), atorvastatin calcium (ATC). In this study, co-loaded Fast Dissolving oral films (FDOFs), of ATC-EZT with HPMC E5 prepared by solvent evaporation method. Prepared FDOFs were evaluated for physicochemical, thermal and mechanical properties. In-vivo animal studies were performed on albino rats against diet induced hyperlipidemia. Prepared FDOFs have rapid DT; 27sec, TDT >2min and in-vitro drug release 97% in a min. In DSC, FTIR and XRD analysis, prepared films were chemically compatible and no chemical interaction of drugs and excipient was found. In kinetic modeling, it was observed their EZT exhibited lowest R 2 value for zero order kinetic and best fit model was first order kinetic (n, 0.9823). The korsmeyer peppas model films (n, 0.016) indicate fickian type drug diffusion. The groups treated with marketed suspension of drug and FODPs were compared with normal group and high fats diet group. Study reviled that combination FDOPs of both ATC/EZT significantly reduce hyperlipemia as compared to high fat diet group. It can be concluded that ATC and EZT encapsulated in FODFs provide instant drug release and better therapeutic outcomes.

Hypothesis: This review article represents a brief layout of the risk factors and pathophysiology responsible for obesity, customary treatment strategies, and nanotechnology-based nutraceutical for the therapeutics of obesity., Experiments: An exhaustive search of the literature was done for this purpose, using Google Scholar, PubMed, and ScienceDirect databases. A literature study was conducted using publications published in peer-reviewed journals between 2000 and 2022., Findings: This was revealed that risk factors responsible for obesity were genetic abnormalities and environmental and socio-economic factors. Several research articles published between 2000 and 2022 were based on phytoconstituents-based nanoformulation for obesity therapeutics and, therefore, have been systematically compiled in this review. Various nutraceuticals like Garcinia cambogia, quercetin, resveratrol, capsaicin, Capsicum, Curcuma longa, Camella Sinensis, Zingiber officinalis, Citrus aurantium, Aegle marmelos, Coffea canephora, Asparagus officinalis, Gardenia jasminoides, Catha edulis, Clusia nemroisa, Rosmarinus officinalis, Cirsium setidens, Betula platyphylla, Tripterygium wilfordi possessing anti-obesity actions are discussed in this review along with their patents, clinical trials as well as their nanoformulation available., Conclusion: This review illustrates that nanotechnology has a great propensity to impart a promising role in delivering phytochemicals and nutraceuticals in managing obesity conditions and other related disorders., (Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.)