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VD20 broken rice, a byproduct of rice milling, shows significant potential for value-added applications, particularly in functional beverage production. This study investigates the impact of homogenization and pasteurization on the quality and stability of VD20 broken rice-based beverages. Homogenization at speeds 6000 to 12,000 rpm for 5 to 20 min improved product stability, while pasteurization between 80 and 95 °C for up to 20 min ensured microbial safety and extended shelf life. Optimal processing conditions were achieved with homogenization at 10,000 rpm for 15 min and pasteurization at 90 °C for 15 min, maintaining a microbial count below 102 CFU/mL to meet health standards. Bioactive compounds were effectively preserved, with total flavonoid content at 47.19 ± 5.30 mgQE/mL, total phenolic content at 177.12 ± 0.39 mg GAE/mL, and antioxidant activities of DPPH and ABTS at 90.87 ± 1.12 mg AAE/mL and 50.42 ± 2.05 mg AAE/mL, respectively. The final product exhibited a viscosity of 4.00 ± 0.06 cP and color values of L*: 68.21 ± 0.06, a*: 3.08 ± 0.06, b*: −2.96 ± 0.15, and ΔE: 3.21 ± 0.06. These results offer an optimized process for producing a high-quality, nutritious beverage from VD20 broken rice, enhancing its economic potential and product diversity.

To reduce the hazards brought by water hyacinth, many applications of water hyacinth have been studied and continuously expanded. The large biomass of water hyacinth is applied in many fields such as for wastewater treatment, wastewater purification, biological raw material sources, animal feed production, medicine, antioxidants, agriculture, and household appliances. This research investigates the desalination capacity of freshwater hyacinths, raw materials from water hyacinths, biochar, and activated carbon materials from water hyacinth stems. Results have shown that the suitable temperature for charring fresh water hyacinth is 420 °C. The activated carbon from the water hyacinth stems with a BET surface area of 200.4 ± 1.9 m²/g can be desalinated under the conditions of 0.4 g of activated carbon mass, 15 min of reaction time, 2.0 ppt of salt concentration, and at neutral pH. In contrast, raw materials from water hyacinths and biochar were unable to desalinate. This study evaluates the desalination ability of the activated carbon material of water hyacinth.

Innovations for product preservation have attracted interest as they may increase the shelf-life of items when stored properly. In this study, the effects of various storage conditions, including four types of packaging (paper packaging, paper combined PE packaging, aluminum combined PE packaging, and plastic jar packaging) and temperatures (5, 15, 30, and 45 °C) on the quality of dried soursop were evaluated. The results demonstrated that the combination of plastic jar packaging and a storage temperature of 15 °C retained a significant portion of the initial total ascorbic acid content, total polyphenol content, and total flavonoid content. After four weeks of storage, the dried soursop preserve packaged in a plastic jar and stored at 15 °C exhibited a moisture content of 22.977 ± 0.093 %, total ascorbic acid content of 9.7 ± 0.46 mg/100gDW, total polyphenol content of 8.12 ± 0.06 mgGAE/gDW, total flavonoid content of 0.18 ± 0.02 mgQE/gDW, DPPH and ABTS scavenging activity of 0.69 ± 0.01 mgAA/gDW and 0.82 ± 0.01 mgAA/gDW, respectively. Moreover, the product meets the requirements of decision 46/2007/QD-BYT regulating the limits on biological and chemical contamination in food. The study offers valuable insights for the food industry in optimizing packaging and storage conditions to ensure the storage of quality and health-beneficial properties of this product.

In this study, the heat pump drying technique was applied to develop the production process of dried mango from Tu Quy mango sources, Ben Tre province, Vietnam. The experiment was performed in three steps. First, mango slices were treated through the blanching process. Samples were pretreated with sizes from 6 to 12 mm at 80–95°C for 3–6 min, and then the mango slices were soaked in a syrup solution concentration range of 25–40°Bx, citric acid of 0.5–2%, and glycerol of 0.1–0.4% at 35–65°C for 90–180 min. Finally, the samples were dried using a pilot-scale heat pump dryer until the moisture content reached 14–16%. The results showed that the blanching and osmosis processes were carried out under optimal conditions to inactivate the Polyphenol oxidase (PPO) enzyme, obtain maximum polyphenol compounds, and conform to the product appearance. Additionally, the drying process was carried out at 30°C for 1,080 min with the polyphenol content retaining 11.71 mgGAE/gDW—This signifies a successful endeavor in developing production methodologies and expanding the range of mango-derived products. Employing innovative technological processes enhances both the quantity and quality of the products. Moreover, the manufacturing procedure was executed on a pilot device, streamlining the synchronization of large-scale production processes effortlessly. This advancement not only enhances economic value but also addresses the issue of congestion prevalent in the current state of the mango industry in Vietnam.

Coptosapelta flavescens Korth. is one of the medicinal plants used as a traditional medicine in Vietnam for a long time. However, few documents proved its safety for a long time. Therefore, the study aimed to determine the toxicity effects of the aqueous extract of C. flavescens by determining its effects after subchronic oral administration in Swiss albino mice. The toxicity of C. flavescens extract was tested at doses of 400 and 1200 mg/kg, respectively, over 30 and 60 days on an in vivo model. Animal weight, behavior, and condition changes were monitored throughout the process. At the end of the observation periods, hematological indices and histopathological features of the animal specimens were analyzed. The administration of C. flavescens extract at doses of 400 and 1200 mg/kg caused a weight difference in male mice after 30 days and in both sexes after 60 days of administration compared to the control group. There were no significant changes in hematological parameters and biochemical indexes of the liver and kidney compared with the control group. The histological structure of the liver showed changes when treated with C. flavescens at both doses after 60 days, whereas the histological structure of the kidneys exhibited differences only at the dose of 400 mg/kg. Overall, the findings of this study indicate that Coptosapelta flavescens Korth. is unlikely to have subacute and subchronic oral toxicity. However, there are some minor effects on the liver and kidneys.

In this study, we proposed and tested a green method for producing microcrystalline cellulose (MCC) with high quality from waste banana pseudo-stem (BPS) after fruit harvesting. The MCC was synthesized by treating BPS with sulfuric acid, sodium hydroxide, and H2O2solution.The produced MCC material was then characterized by scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, and thermogravimetric analysis to explore its properties. The removal of methylene blue (MB) in aqueous solution was conducted by batch adsorption method to evaluate the applicability of MCC for wastewater treatment. The results showed that the adsorption using MCC reached equilibrium after 15 min. The highest MB adsorption capacity of MCC reached 16.6mg/g at pH 6. The adsorption kinetics data were best described by the pseudo second order rate equation. Equilibrium isotherm data of adsorption were well fitted to the linear Langmuir isotherm model. Affecting factors such as adsorbent dosage, initial concentration of MB, and temperature were also investigated. These results suggest a great potential use of MCC for advanced wastewater treatment.

Dangshen Codonopsis javanica exhibits invaluable medicinal properties in herbal remedies; however, there has currently not been much specific analysis of the phytochemicals and bioactivities of this plant. The root ethanol extract of C. javanica contains substances such as saponins, phenolic acids, terpenoids, and alkaloids. It displays an antibacterial effect against Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, and Bacillus cereus with the IC50 values of 150, 100, 150, and 90 μg/mL, respectively. The antioxidant capacity of the root extract was also observed with an IC50 value of 46.8 ± 6.8 μg/mL. Furthermore, the extract exhibits activity on human cancer cell lines HepG2 (IC50 = 83.6 ± 2.7 μg/mL) and MCF-7 (IC50 = 95.3 ± 2.3 μg/mL). Hence, this study provides the basic data for further research on the bioactivities of natural compounds of Dangshen C. javanica for the first time.

Introduction. Codonopsis javanica L. root is a gingsen-like medicinal material with valuable bioactive compounds and alkaloids in its composition. However, the diversification of commercial products from Codonopsis javanica root extract is limited and poorly represented on the market. This study presents a new production process of an instant tea product from Codonopsis javanica root extract, which involved spray drying with maltodextrin as a drying additive. Study objects and methods. The research featured different process parameters including a drying additive concentration, a drying temperature, and a feed flow rate. Moisture content and drying yield were selected as the main outcomes. Results and discussion. In general, the improved drying yield was associated with an increased drying additive concentration, a lower drying temperature, and a higher feed flow rate. The best drying yield (78.35%) was obtained at the drying additive concentration of 30% (w/w), the drying temperature of 140°C, and the feed flow rate of 300 mL/h. The total saponin content in the product was 0.29% (w/w), and the ABTS free radical scavenging ability reached 59.48 μgAA/g. The obtained powder was spherical and exhibited fairly uniform particle morphology with shriveled and concave outer surface. Conclusion. The research results justified the use of Codonopsis javanica as an ingredient in beverage industry and suggested maltodextrin as an appropriate substrate for spray-drying natural extracts.

For a long time, ethnic minorities in Ninh Thuan province have combined ''Day Khai'' (Coptosapelta flavescens Korth) with many other medicinal herbs, creating an esoteric remedy called ''Cao Khai''-an aqueous extract from Day Khai. This study tested an aqueous extract from ''Day Khai'' for total phenolics, total flavonoids, antioxidant, and anti-inflammatory activity in an in vivo mice model. The aqueous extracts of raw materials C. flavescens collected in different regions were found to have phenolics, flavonoids, and antioxidant capacity in vitro according to DPPH, ABTS, RP, TAC, and FRAP methods. This study evaluated the effect of C. flavescens on arthritis of Complete Freund's adjuvant (CFA) induced-mice by observing changes in the degree of edema in the leg joints blood index and histology. The findings indicated that the ''Cao Khai'' had anti-inflammatory benefits and lowered the inflammatory symptoms in mice equivalent to Mobic medications (p < 0.05) while also limiting cartilage tissue damage after 14 days of usage. As a result, it is clear that ''Cao Khai'' can be considered a medicinal herb with tremendous potential for usage as an addition to illness therapy that should be protected and cultivated.

Bưởi là loài cây không chỉ có giá trị cao về mặt dinh dưỡng mà còn có giá trị cao về mặt kinh tế và được trồng phổ biến ở Việt Nam. Ngoài ra, tinh dầu bưởi chứa nhiều hợp chất có hoạt tính sinh học cao. Tinh dầu bưởi được chiết xuất bằng phương pháp chưng cất lôi cuốn hơi nước và thành phần hóa học được phân tích bằng phương pháp GC-MS. Thành phần chính của tinh dầu gồm limonene (91,19%), b-myrcene (2,92%), a-phellandrene (1,98%) và a-pinene (1,19%). Hoạt tính kháng vi sinh vật của tinh dầu được khảo sát với vi khuẩn Gram dương (Bacillus cereus, Staphylococcus aureus), Gram âm (Escherichia coli) và nấm mốc Aspergillus flavus ở nồng độ 5, 10, 25 và 50% bằng phương pháp khuếch tán giếng thạch. Tinh dầu có khả năng kháng B. cereus, S. aureus và E. coli với đường kính vòng kháng khuẩn lần lượt là 8,3–11,3, 10,3–18,7 và 9,0–11,7 mm và ức chế sự phát triển của A. flavus (18,9–65,0%).

Microwave-assisted hydro-distillation (MAHD) is preferred to traditional extraction methods due to shorter extraction time, the inability of volatile components to be damaged or decomposed which in turn improve the efficiency and quality of essential oils. In this research, we investigated the parameters that affect the extraction of lemongrass oil process by MAHD method and compare with those of hydro-distillation (HD) method. Four parameters were identified which are: raw material size, raw material to water ratio, extraction time and microwave power. The results show that the optimum condition for determining the lemongrass essential oil content is 20 mm in the 90 min extraction time with a microwave power of 450 W at raw material to water ratio of 1:3 (g/mL). When compared to the HD method, we found that the yield lemongrass oil of MAHD method is 0.35% on 90 min and the yield of HD method is 0.2% on 360 min. The quality of oil samples at different extraction method was evaluated by determining their chemical constituents through GC-MS. The highest identified component is Citral with 93.28% for MAHD, while the HD was 83.85%. Therefore, MAHD method is highly efficient and shorten the time needed for the extraction of essential oils.

The worm-like exfoliated graphite (EG) based adsorbents prepared from low-cost natural graphite flakes via facile synthesis processes have been found to be efficient adsorbents when it comes to removing Pb (II) from aqueous solution. EG was fabricated by chemical intercalation and microwave assisted exfoliation. Furthermore, the magnetic exfoliated graphite (MEG) was developed by incorporating CoFe2O4 particles into the EG layers using the citric acid based sol-gel technique. Adsorption behaviour of Pb (II) on the as-prepared adsorbents was investigated by taking several experimental conditions into consideration such as contact time, initial concentration, adsorbent dosage, and pH value. The results with initial neutral pH indicated that the adsorption isotherms for Pb (II) on the EG and MEG were well consistent with the Langmuir isotherm model revealing the maximum adsorption capacity of 106 mg/g and 68 mg/g for EG and MEG, respectively. The adsorption kinetics of Pb (II) was found to adhere to the pseudo-second-order kinetic model. The chemical interaction between ? electrons on graphite sheets and Pb (II) ions was suggested to play an essential role in the adsorption mechanism. The introduction of magnetic CoFe2O4 to the EG was found to induce the shift of optimal pH value to a more basic condition. The characterization of the adsorbents was performed using relevant analysis techniques such as Scanning electron microscope (SEM), X–ray powder diffraction (XRD), vibrating-sample magnetometer (VSM), and Fourier-transform infrared (FTIR). The results of this work suggest a high possibility for application of the as-prepared modified graphite to remove hazardous substances in practical wastewater treatment systems. ABSTRAK: Penyerap Pengelupas Grafit (EG) yang berupa seperti cacing dihasilkan dari grafit semulajadi yang murah melalui proses sintesis serpihan, ia juga merupakan penyerap yang bagus dalam mengasingkan Pb (II) daripada larutan akues. EG direka dengan tindak balas interkalasi kimia dan pengelupasan melalui gelombang mikro. Tambahan, pengelupas grafit magnet (MEG) telah dihasilkan dengan memasukkan zarah CoFe2O4 ke dalam lapisan EG menggunakan teknik sol-gel yang berasaskan asid sitrik. Tindak balas penyerapan Pb (II) pada penyerap yang disiapkan ini, dikaji dengan mengambil kira beberapa keadaan eksperimen seperti waktu disentuh, konsentrasi awal, dos penyerap dan nilai pH. Hasil keputusan pH neutral awal menunjukkan bahawa isoterm penyerapan bagi Pb (II) pada EG dan MEG adalah konsisten dengan model isoterm Langmuir. Ini menunjukkan kapasiti penyerapan maksimum 106 mg/g dan 68 mg/g bagi EG dan MEG, masing-masing. Penyerapan kinetik Pb (II) didapati mematuhi model kinetik pesudo-order-kedua. Interaksi kimia antara elektron ? pada helaian grafit dan ion Pb (II) memainkan peranan penting dalam mekanisme penyerapan. Pengenalan magnet CoFe2O4 kepada EG didapati telah mengubah nilai pH optimum kepada keadaan asal. Pengelasan penyerapan dilakukan menggunakan teknik analisis yang relevan seperti Mikroskop Elektron Pengimbasan (SEM), Difraksi Serbuk sinar-X (XRD), Magnetometer Sampel-Getaran (VSM) dan Inframerah Perubahan-Fourier (FTIR). Hasil kerja ini mencadangkan kemungkinan besar bagi penggunaan grafit ubah suai yang disediakan bagi membuang bahan berbahaya dalam sistem rawatan air sisa praktikal.

A number of harmful effects on the ecosystem, the life of humankind, and living species caused by dye-contaminated wastewater have urged the development for an efficient and cost-efficient treatment method for colored effluents. The cellulose-based adsorbents have been considered as a facile and efficient approach to remove hazardous pollutants because of the abundance of inexpensive agricultural wastes in Viet Nam. This study aims to investigate the elimination of methylene blue (MB) and crystal violet (VL) from wastewater using a fixed-bed column of pre-treated durian peel. Examined variables in the process are bed depths (2–6 cm), flow rate (5–20 mL/min), and influent dye concentrations (200–600 mg/L). The highest adsorption amount of pre-treated DP was 235.80 mg/g and 527.64 mg/g, respectively, on a 600 mg/L of methylene blue and crystal violet achieved within a bed height of 4 cm and a flow rate of 10 mL/min. Accordingly, the breakthrough curves were constructed and modeled using the relevant theoretical models under the effects of different experimental conditions. Pre-treated durian peel was found to exhibit high adsorption capacity for cationic dye in an initial concentration of 200–600 mg/L with complete removal being obtained.

Recently, plenty of interesting studies on improvement of bioavailability for poorly soluble drugs were implemented with different approaches such as using of combined biopolymers as a delivery system that allowed to enhancing drug solubility and bioavailability. In this work, alginate and chitosan were blended together in the form of polymeric particles, loaded with both lovastatin and ginsenoside Rb1 to producing the four-component nanoparticles by ionic gelation method. CaCl2 and sodium tripolyphosphate were used as gelation agent and cross-linking agent, respectively. The characteristics of obtained nanoparticles were studied by means of infrared spectra (IR), scanning electron microscopy (SEM), differential scanning calorimetry (DSC), and dynamic light scattering (DLS). In combination, ginsenoside Rb1 and lovastatin both interacted with each other to improve the drug release ability of the polymer particles. The change of initial content of drugs in the nanoparticles has a negligible effect on the functional groups in the structure of the nanoparticles but has a significant impact on drug release process of both lovastatin and ginsenoside Rb1 from the nanoparticles in selective simulated body fluids. In addition, the synergistic interaction of lovastatin and ginsenoside Rb1 could be also observed through the modification of relative crystal degree and drug release efficiency.

Essential oils (EOs) are known as any aromatic oily organic substances which are naturally synthesized in plants. Exhibiting a broad range of biological activities, EOs have played a key role in numerous industries for ages, including pharmaceutical, textile, and food. However, the volatility and high sensitivity to environmental influences pose challenges to the application of EOs on industrial scale. Microencapsulation via the spray-drying method is one of the promising techniques to overcome these challenges, thanks to the presence of wall materials that properly protect the core EOs from oxidation and evaporation. By optimization of key factors related to the infeed emulsion properties and spray-drying process, the encapsulation efficiency and retention of encapsulated EOs could be significantly improved, thus allowing a wide range of EO applications. This review attempts to discuss on different determining factors of the spray-drying process to develop an effective encapsulation formula for EOs. Furthermore, recent applications of encapsulated EOs in the fields of foods, pharmaceuticals, and textile industries are also thoroughly addressed.

We report a numerical study on the design of a broadband metamaterial absorber (MMA) with a single layer of metal–dielectric–metal based on an FR-4 substrate for X-band applications. The MMA structure consists of a periodic array of a split circle ring and lumped resistors coupled within split segments. The MMA structure achieves a broadband absorption response in the frequency range of 7.8–12.6 GHz with an absorptivity of above 90% under normal incidence for all polarization angles. The absorptivity remains above 70% in the frequency range of 6.8–11.8 GHz at wide incident angles from 0° to 30° for both transverse electric and transverse magnetic polarizations. The physical mechanism of the absorber is explained by the electric and the surface current distributions that, in turn, are significantly affected by magnetic resonance.

Propranolol is one of the first medications of the beta-blocker used for antihypertensive drugs. This study reports the facile route for the synthesis of propranolol and its novel derivatives. Herein, propranolol synthesis proceeded from 1-naphthol and isopropylamine under mild and less toxic conditions. Novel propranolol derivatives were designed by reactions of propranolol with benzoyl chloride, pyridinium chlorochromate, and n-butyl bromide through esterification, oxidation reduction, and alkylation, respectively. The isolation and purity of compounds were conducted using column chromatography and thin-layer chromatography. Mass spectrometry and 1H-NMR spectroscopy were applied to identify new compounds structure. Propranolol derivatives from 2-chlorobenzoyl chloride (compound 3), 2-fluorobenzoyl chloride (compound 5), and especially acetic anhydride (compound 6) manifested high yields and significantly increased water solubility. Six semisynthetic propranolol derivatives promise to improve antioxidative and biological activities.

In this study, mixed oxides of Mn-Cu and Fe-Cu on OMS-2 support having an octahedral structure were synthesized by the refluxing and impregnation methods. The characteristics of the materials were analyzed by XRD, FTIR, SEM, EDX, and H2-TPR. In the CO oxidation test, CuFeOx/OMS-2 had slightly higher catalytic activity but is significantly more stable than CuMnOx/OMS-2 and CuO/OMS-2. Due to its lower reduction temperature in H2-TPR analysis, the Mars-Van-Krevelen mechanism for CuFeOx/OMS-2 (Cu2+–O–Fe3+ ↔ Cu+–□–Fe2+) could take place more energetically than CuO/OMS-2 and CuMnOx/OMS-2 (Cu2+–O2−–Mn4+ ↔ Cu+–□–Mn3+). In addition, the interaction between Fe and Cu in the catalyst could improve the durability of the surface oxides structure in comparison with that between Mn and Cu. With the high specific rate and TOF of 28.6 mmol/h.g and 0.508, respectively, CuFeOx/OMS-2 has a great potential as an effective catalyst for low-temperature oxidation application in CO and possible VOCs removal.

TiO2-based photocatalysts still have some limitations such as large bandgap and low surface area, leading to low efficiency in the photocatalytic degradation of VOCs and limiting it to use in sunlight. Here we report that the nanostructured Ir-doped TiO2 as an efficient photocatalyst generates an excellent risk-reduction material of gaseous toluene. We have succeeded in developing a nanostructured Ir-doped TiO2 and initially found that excellent efficient photocatalytic VOC decomposition can be achieved in our materials The nanostructured Ir-doped TiO2 was synthesized by a one pot, low temperature hydrothermal process with different ratios of Ir doped into the TiO2. It exhibited a high surface area, uniformly spherical morphology of 10–15 nm. Its activity for the photocatalytic degradation of gaseous toluene exhibited up to 97.5% under UV light. This enhancement could be explained by iridium doping which created a high concentration oxygen vacancy and changed the recombination rate of the photogenerated charge carriers. More generally, our study indicates a strategic way to develop the novel nanostructured material for numerous applications.

Herein, we described a tunable method for synthesis of novel hollow mesoporous carbon (MPC) via direct pyrolysis (800oC) of MIL-53 (Fe) as a self-sacrificed template. The structural characterization revealed a hollow, amorphous, defective and mesoporous MPC along with high surface area (approx. 200 m2 g−1). For the experiments of ibuprofen adsorption onto MPC, effects of contact time, MPC dosage, ionic strength, concentration and temperature were systematically investigated. The optimal conditions consisted of pH = 3, concentration 10 mg l−1 and dose of 0.1 g l−1 for the highest ibuprofen removal efficiency up to 88.3% after 4 h. Moreover, adsorption behaviour, whereby chemisorption and monolayer controlled the uptake of ibuprofen over MPC, were assumed. Adsorption mechanisms including H-bonding, π–π interaction, metal–oxygen, electrostatic attraction were rigorously proposed. In comparison to several studies, the MPC nanocomposite in this work obtained the outstanding maximum adsorption capacity (206.5 mg g−1) and good reusability (5 cycles); thus, it can be used as a feasible alternative for decontamination of ibuprofen anti-inflammatory drug from water.

Recently, organic contaminants from textile and dye industry have adversely affected on human’s health and living things. Hence, the development of effective contaminated water treatment is one of the most crucial tasks. Expanded Graphite (EG) has been considered as efficient platforms to remove of organic dyes from aqueous solution due to its excellent performance. The main objective of the present work is to investigate adsorption behavior of methylene blue (MB) and Congo Red (CO) on exfoliated graphite fabricated using flake graphite from Yen Bai province. The exfoliation of graphite was carried out using potassium permanganate and perchloric acid as oxidant agent and anhydride acetic as intercalating agent via microwave-assisted technique. The properties of EG were characterized by X-ray diffraction, scanning electron microscopy, Fourier-transform infrared spectroscopy and nitrogen adsorption/desorption analysis. In batch adsorption experiments, various factors including initial dye concentration (50–600 ppm), adsorbent dosage (0.5–3 g/L), contact time (10–120 min) and pH of solution (4–10) were also studied. It is found that as-prepared EG provided high removal efficiency and fast adsorption rate for MB and CO. The maximum adsorption capacity of EG for CO and MB was found at 201.21 and 47.62 mg/g, respectively. These results demonstrate that the as-synthesized EG appears as an efficient and low-cost platform for remediation of colored effluents via adsorption route.

This paper shows a comparison of porous properties of aminopropyl-MCM-41 materials functionalised via the direct and indirect methods. The obtained materials were characterised using X-ray powder diffraction (XRD), transmission electron microscopy (TEM), thermogravimetric analysis-differential scanning calorimeter (TGA-DSC), adsorption/desorption isotherms of nitrogen, and Fourier-transfer infrared (FT-IR) spectroscopy. The results showed that the direct method provided the aminopropyl-MCM-41 material with well-ordered pores and high surface areas but with a lower quantity of grafted 3-aminopropyltriethoxysilane than the indirect method. To remove the organic template in the indirect method, solvent extraction with HCl/C2H5OH and calcination at 500°C were used, and the former gave a higher quantity of grafted 3-aminopropyltriethoxysilane in the resulting aminopropyl-MCM-41 materials. The experimental data were applied to the isotherm models of adsorption including Langmuir, Freundlich, Redlich–Peterson, and Sips either in the linear or nonlinear form. In order to avoid the bias of the determination coefficient and the error function method, the paired-samples t-test as an alternative method was first proposed to look for the most appropriate adsorption isotherms. The maximum adsorption capacity of Cd(II) and Pb(II) was 14.08 mg·g−1 and 64.21 mg·g−1, respectively. The mechanism of complexation and isoelectric interaction was suggested to explain the adsorption of Pb(II) and Cd(II) from aqueous solutions on aminopropyl functionalised MCM-41 in the range of pH from 2 to 9.

Ibuprofen contamination from water sources has been increasingly alarming due to its environmentally accumulative retention; however, the strategies for ibuprofen-containing water treatment are still an enormous challenge. Herein, we described the utilization of metal-organic frameworks MIL-53(Fe) (MIL = Materials of Institute Lavoisier) for the adsorption of ibuprofen in synthetic solution. Firstly, the MIL-53(Fe) was solvothemally synthesized and then characterized using the X-ray diffraction and Fourier-transform infrared spectroscopy techniques. The optimization of ibuprofen adsorption over MIL-53(Fe) was performed with three independent variables including ibuprofen concentration (1.6–18.4 mg/L), adsorbent dosage (0.16–1.84 g/L), and pH (2.6–9.4) according to the experimental design from response surface methodology. Under the optimized conditions, more than 80% of ibuprofen could be eliminated from water, indicating the promising potential of the MIL-53(Fe) material for treatment of this drug. Kinetic and isotherm models also were used to elucidate the chemisorption and monolayer behavior mechanisms of ibuprofen over MIL-53(Fe).

In this study, we adopted the solution combustion method to synthesize magnesium ferrite (MgFe2O4) using urea as the fuel. Various techniques including TGA, XRD, SEM, TEM, FTIR, UV-Vis DRS, and EDS were employed to characterize the synthesized MgFe2O4 nanoparticles. The XRD analysis revealed that single-phase MgFe2O4 was formed at a calcination temperature of at 500–600°C for 3 hours in the absence of an intermediate phase. TEM analysis also revealed the formation of monodisperse magnesium ferrite nanoparticles, averaged at 30 nm in size. The photocatalytic activity of the synthesized MgFe2O4 nanoparticles against methylene blue dye under visible light was investigated, showing the efficiency of 89.73% after 240 minutes of light irradiation with the presence of H2O2.

Highly porous KOH–activated carbon was successfully synthesized from rice husk by chemical activation with KOH. The products were characterized by IR, SEM, and BET. The response surface methodology (RSM) was employed to determine the optimum fabrication conditions of AC with respect to the simultaneous effects of activation temperature (T), impregnation rate (IR) and activation time (t) to maximize the yield of activated carbon and removal efficiency of Ni2+. The optimum synthesis conditions were T = 522 oC, IR = 1.3 and t = 360 min with a maximum AC yield of 28.5 % and a maximum Ni2+ removal of 28.5 %. The results indicated that highly porous structure, high surface area as well as the surface functional groups are key impacts in the adsorptive capacity of activated carbons for Ni2+.

Porous nanosilica (PNS) has been regarded as a promising candidate for controlled delivery of anticancer drugs. Unmodified PNS-based nanocarriers, however, showed a burst release of encapsulated drugs, which may limit their clinical uses. In this report, PNS was surface conjugated with adamantylamine (ADA) via disulfide bridges (-SS-), PNS-SS-ADA, which was further modified with cyclodextrin-poly(ethylene glycol) methyl ether conjugate (CD-mPEG) to form a core@shell structure PNS-SS-ADA@CD-mPEG for redox triggered delivery of doxorubicin (DOX), DOX/PNS-SS-ADA@CD-mPEG. The prepared PNS-SS-ADA@CD-mPEG nanoparticles were spherical in shape with an average diameter of 55.5 ± 3.05 nm, a little larger than their parentally PNS nanocarriers, at 49.6 ± 2.56 nm. In addition, these nanoparticles possessed high drug loading capacity, at 79.2 ± 3.2%, for controlled release. The release of DOX from DOX/PNS-SS-ADA@CD-mPEG nanoparticles was controlled and prolonged up to 120 h in PBS medium (pH 7.4), compared to less than 40 h under reducing condition of 5 mM DTT. Notably, the PNS-SS-ADA@CD-mPEG was a biocompatible nanocarrier, and the toxicity of DOX was dramatically reduced after loading drugs into the porous core. This redox-sensitive PNS-SS-ADA@CD-mPEG nanoparticle could be considered a potential candidate with high drug loading capacity and a lower risk of systemic toxicity.

The present study focused on the use of the magnetic nanocomposite NiFe2O4/GO (GO - Graphene oxide) as an efficient adsorbent for the removal of congo red (CR). The NiFe2O4/GO was synthesized from NiFe2O4 and GO via a facile route, and the structure of this nanocomposite was analyzed by X-ray powder diffraction (XRD), scanning electron microscope (SEM), and Vibrating sample magnetometer (VSM). By applying the response surface methodology, the profound relationship was found between variables (initial concentration, adsorbent dosage, and pH) and CR removal efficiency. Moreover, the model was optimized to give a favourable condition for the adsorption. Up to 94.7% of CR removal was obtained via a confirmation test, and this result indicated that the magnetic NiFe2O4/GO was a promising material in terms of treatment for CR-contaminated wastewater.

In the present article, the optimization of removal of Cu 2+ , Ni 2+ , and Pb 2+ using sugarcane-based activated carbon was studied. The activated carbon synthesized from low-cost sugarcane bagasse via ZnCl 2 activation process was found to possess surprisingly high surface area (>1500 m 2 /g). In adsorption study, the individual and interactive effects of three critical parameters including initial concentration, pH of solution, and activated carbon dosage on removal efficiency of Cu 2+ , Ni 2+ , and Pb 2+ were assessed by applying the response surface methodology combined with central composite design. The established second-order polynomial regression models provided an excellent interpretation of experimental data with acceptable coefficients of determination ( R 2 ) and analysis of variance demonstrated statistical significance of the model terms. In the examined region, the predicted maximum removal efficiency and adsorption capacity were found in the order: Ni 2+ (66.4%, 2.99 mg/g)

Carboplatin (CAR) is a second generation platinum-based compound emerging as one of the most widely used anticancer drugs to treat a variety of tumors. In an attempt to address its dose-limiting toxicity and fast renal clearance, several delivery systems (DDSs) have been developed for CAR. However, unsuitable size range and low loading capacity may limit their potential applications. In this study, PAMAM G3.0 dendrimer was prepared and partially surface modified with methoxypolyethylene glycol (mPEG) for the delivery of CAR. The CAR/PAMAM G3.0@mPEG was successfully obtained with a desirable size range and high entrapment efficiency, improving the limitations of previous CAR-loaded DDSs. Cytocompatibility of PAMAM G3.0@mPEG was also examined, indicating that the system could be safely used. Notably, an in vitro release test and cell viability assays against HeLa, A549, and MCF7 cell lines indicated that CAR/PAMAM G3.0@mPEG could provide a sustained release of CAR while fully retaining its bioactivity to suppress the proliferation of cancer cells. These obtained results provide insights into the potential of PAMAM G3.0@mPEG dendrimer as an efficient delivery system for the delivery of a drug that has strong side effects and fast renal clearance like CAR, which could be a promising approach for cancer treatment.

In this study, a minimum-run resolution IV and central composite design have been developed to optimize tetracycline removal efficiency over mesoporous carbon derived from the metal-organic framework MIL-53 (Fe) as a self-sacrificial template. Firstly, minimum-run resolution IV, powered by the Design–Expert program, was used as an efficient and reliable screening study for investigating a set of seven factors, these were: tetracycline concentration (A: 5–15 mg/g), dose of mesoporous carbons (MPC) (B: 0.05–0.15 g/L), initial pH level (C: 2–10), contact time (D: 1–3 h), temperature (E: 20–40 °C), shaking speed (F: 150–250 rpm), and Na+ ionic strength (G: 10–90 mM) at both low (−1) and high (+1) levels, for investigation of the data ranges. The 20-trial model was analyzed and assessed by Analysis of Variance (ANOVA) data, and diagnostic plots (e.g., the Pareto chart, and half-normal and normal probability plots). Based on minimum-run resolution IV, three factors, including tetracycline concentration (A), dose of MPC (B), and initial pH (C), were selected to carry out the optimization study using a central composite design. The proposed quadratic model was found to be statistically significant at the 95% confidence level due to a low P-value (2 (0.9078), and the AP ratio (11.4), along with an abundance of diagnostic plots (3D response surfaces, Cook’s distance, Box-Cox, DFFITS, Leverage versus run, residuals versus runs, and actual versus predicted). Under response surface methodology-optimized conditions (e.g., tetracycline concentration of 1.9 mg/g, MPC dose of 0.15 g/L, and pH level of 3.9), the highest tetracycline removal efficiency via confirmation tests reached up to 98.0%–99.7%. Also, kinetic intraparticle diffusion and isotherm models were systematically studied to interpret how tetracycline molecules were absorbed on an MPC structure. In particular, the adsorption mechanisms including “electrostatic attraction„ and “π–π interaction„ were proposed.

This study aims to analyze compositions of fatty acids and phospholipid molecular species in the hard clams Meretrix lyrata (Sowerby, 1851) harvested from Cua Lo beach, Nghe An province, Viet Nam. Total lipid of hard clams Meretrix lyrata occupied 1.7 ± 0.2% of wet weight and contained six classes: hydrocarbon and wax (HW), triacylglycerol (TAG), free fatty acids (FFA), sterol (ST), polar lipid (PoL), and monoalkyl diacylglycerol (MADAG). Among the constituents, the proportion of PoL accounted was highest, at 45.7%. In contrast, the figures for MADAG were lowest, at 1.3%. Twenty-six fatty acids were identified with the ratios of USAFA/SAFA was 2. The percentage of n-3 PUFA (ω-3) and n-6 PUFA (ω-6) was high, occupying 38.4% of total FA. Among PUFAs, arachidonic acid (AA, 20:4n-6), eicosapentaenoic acid (EPA, 20:5n-3), docosapentaenoic acid (DPA, 22:5n-3), and docosahexaenoic acid (DHA, 22:6n-3) accounted for 3.8%, 7.8%, 2.2% and 12.0% of total lipid of the clam respectively. Phospholipid molecular species were identified in polar lipids of the clams consisting six types: phosphatidylethalnolamine (PE, with 28 molecular species), phosphatidylcholine (PC, with 26 molecular species), phosphatidylserine (PS, with 18 molecular species), phosphatidylinositol (PI, with 10 molecular species), phosphatidylglycerol (PG, with only one molecular species), and ceramide aminoethylphosphonate (CAEP, with 15 molecular species). This is the first time that the molecular species of sphingophospholipid were determined, in Meretrix lyrata in particular, and for clams in general. Phospholipid formula species of PE and PS were revealed to comprise two kinds: Alkenyl acyl glycerophosphoethanolamine and Alkenyl acyl glycerophosphoserine occupy 80.3% and 81.0% of total PE and PS species, respectively. In contrast, the percentage of diacyl glycero phosphatidylcholine was twice as high as that of PakCho in total PC, at 69.3, in comparison with 30.7%. In addition, phospholipid formula species of PI and PG comprised only diacyl glycoro phospholipids. PE 36:1 (p18:0/18:1), PC 38:6 (16:0/22:6), PS 38:1 (p18:0/20:1), PI 40:5 (20:1/20:4), PG 32:0 (16:0/16:0) and CAEP 34:2 (16:2/d18:0) were the major molecular species.

Polymer coating has drawn increasing attention as a leading strategy to overcome the drawbacks of superparamagnetic iron oxide nanoparticles (SPIONs) in targeted delivery of anticancer drugs. In this study, SPIONs were modified with heparin-Poloxamer (HP) shell to form a SPION@HP core-shell system for anticancer drug delivery. The obtained formulation was characterized by techniques including transmission electron microscopy (TEM), Fourier transform infrared spectra (FT-IR), vibration sample magnetometer (VSM), proton nuclear magnetic resonance (1H-NMR), and powder X-ray diffraction (XRD). Results showed the successful attachment of HP shell on the surface of SPION core and the inability to cause considerable effects to the crystal structure and unique magnetic nature of SPION. The core-shell system maintains the morphological features of SPIONs and the desired size range. Notably, Doxorubicin (DOX), an anticancer drug, was effectively entrapped into the polymeric shell of SPION@HP, showing a loading efficiency of 66.9 ± 2.7% and controlled release up to 120 h without any initial burst effect. Additionally, MTT assay revealed that DOX-loaded SPION@HP exerted great anticancer effect against HeLa cells and could be safely used. These results pave the way for the application of SPION@HP as an effective targeted delivery system for cancer treatment.

Chloramphenicol (CAP) is commonly employed in veterinary clinics, but illegal and uncontrollable consumption can result in its potential contamination in environmental soil, and aquatic matrix, and thereby, regenerating microbial resistance, and antibiotic-resistant genes. Adsorption by efficient, and recyclable adsorbents such as mesoporous carbons (MPCs) is commonly regarded as a “green and sustainable„ approach. Herein, the MPCs were facilely synthesized via the pyrolysis of the metal⁻organic framework Fe3O(BDC)3 with calcination temperatures (x °C) between 600 and 900 °C under nitrogen atmosphere. The characterization results pointed out mesoporous carbon matrix (MPC700) coating zero-valent iron particles with high surface area (~225 m2/g). Also, significant investigations including fabrication condition, CAP concentration, effect of pH, dosage, and ionic strength on the absorptive removal of CAP were systematically studied. The optimal conditions consisted of pH = 6, concentration 10 mg/L and dose 0.5 g/L for the highest chloramphenicol removal efficiency at nearly 100% after 4 h. Furthermore, the nonlinear kinetic and isotherm adsorption studies revealed the monolayer adsorption behavior of CAP onto MPC700 and Fe3O(BDC)3 materials via chemisorption, while the thermodynamic studies implied that the adsorption of CAP was a spontaneous process. Finally, adsorption mechanism including H-bonding, electrostatic attraction, π⁻π interaction, and metal⁻bridging interaction was proposed to elucidate how chloramphenicol molecules were adsorbed on the surface of materials. With excellent maximum adsorption capacity (96.3 mg/g), high stability, and good recyclability (4 cycles), the MPC700 nanocomposite could be utilized as a promising alternative for decontamination of chloramphenicol antibiotic from wastewater.

We have explored the effective approach to fabricate GZO/ZnO films that can make the pyramidal surface structures of GZO films for effective light scattering by employing a low temperature ZnO buffer layer prior to high temperature GZO film growth. The GZO thin films exhibit the typical preferred growth orientations along the (002) crystallographic direction at deposition temperature of 400°C and SEM showed that column-like granule structure with planar surface was formed. In contrast, GZO films with a pyramidal texture surface were successfully developed by the control of (110) preferred orientation. We found that the light diffuse transmittance of the film with a GZO (800 nm)/ZnO (766 nm) exhibited 13% increase at 420 nm wavelength due to the formed large grain size of the pyramidal texture surface. Thus, the obtained GZO films deposited over ZnO buffer layer have high potential for use as front TCO layers in Si-based thin film solar cells. These results could develop the potential way to fabricate TCO based ZnO thin film using MOCVD or sputtering techniques by depositing a low temperature ZnO layer to serve as a template for high temperature GZO film growth. The GZO films exhibited satisfactory optoelectric properties.

Nanogel-based systems loaded with single anticancer drugs display miscellaneous effectiveness in tumor remission, gradually circumventing mutation and resistance in chemotherapy. Hence, the existence of dual-drug delivered nano-sized systems has been contemporaneous with drug development and preceded the conventional-dose chemotherapy. Among outstanding synergistic drug nanoplatforms, thermosensitive copolymer heparin-Pluronic F127 (Hep-F127) co-delivering cisplatin (CDDP) and curcumins (Cur) (Hep-F127/CDDP/Cur) has emerged as a notable candidate for temperature-responsive drug delivery. The procedure was based on the entrapment of curcumin into the hydrophobic core of bio-degradable co-polymer Hep-F127 while the hydrophilic drug CDDP subsequently conjugated to the backbone heparin to form the core-shell structure. The copolymer was characterized by Fourier transform infrared (FT-IR) spectrophotometry, Transmission Electron Microscopy (TEM), and Dynamic Light Scattering (DLS), to corroborate the successful synthesis and via HPLC along with AES-ICP to evaluate the high drug loading along with a controllable release from the nano-gels. A well-defined nano-shell with size in the 129.3 ± 3.8 nm size range could enhance higher the efficacy of the conjugated-CDDP to Hep-F127 than that of single doses. Moreover, the considerable amount of dual-drug released from thermosensitive nanogels between different conditions (pH = 7.4 and pH = 5.5) in comparison to CDDP from Hep-F127 partially indicated the significantly anti-proliferative ability of Hep-F127/CDDP/Cur to the MCF-7 cell line. Remarkably, drug testing in a xenograft model elucidates the intricate synergism of co-delivery in suppressing tumor growth, which remedies some of the problems affecting in cancer chemotherapy.

UV light, especially UVB, is known as a trigger of allergic reaction, leading to mast cell degranulation and histamine release. In this study, phlorotannin Fucofuroeckol-A (F-A) derived from brown algal Ecklonia stolonifera Okamura was evaluated for its protective capability against UVB-induced allergic reaction in RBL-2H3 mast cells. It was revealed that F-A significantly suppress mast cell degranulation via decreasing histamine release as well as intracellular Ca2+ elevation at the concentration of 50 μM. Moreover, the inhibitory effect of F-A on IL-1β and TNF-α productions was also evidenced. Notably, the protective activity of F-A against mast cell degranulation was found due to scavenging ROS production. Accordingly, F-A from brown algal E. stolonifera was suggested to be promising candidate for its protective capability against UVB-induced allergic reaction.

Polyvinyl alcohol/agar/maltodextrin composite membranes at different ratios are investigated for the removal of the antibiotic ciprofloxacin from water. The factors affecting the adsorption capacity of the as-synthesized membranes include time, pH, temperature, concentration, and dosage of film. The PAM244 and PAM433 membranes are subjected to optimization using response surface methodology model employing the Box-Behnken experimental design model. The optimal model has shown compatibility between the experimental value and the predicted value of the model. The correlation coefficients of PAM244 and PAM433 are recorded as R² = 0.999 and R² = 0.991, respectively. The model also proposes the optimal parameters. For PAM244, the adsorption capacity predicted from the model is 11.52 mg g-1 (42% of efficiency) at pH 5.89, a concentration of 41.28 mg L-1, over a time period of 19.87 min, and dosage of film 2.08 g L-1 For PAM433, the adsorption capacity predicted from the model is 10.46 mg g-1 (40% of efficiency) at pH 6.07, a concentration of 41.24 mg L-1, over a time period of 19.59 min, and dosage of film 2.16 g L-1 To enhance the potential of the material, the membrane reusability is also examined with the number of reuses being three times with the PAM244 membrane and twice with the PAM433 membrane. [ABSTRACT FROM AUTHOR]

In this study, we used a synthetic aerogel based on PVA/agar/maltodextrin to remove the antibiotic ciprofloxacin (CFX) from aqueous media. Response surface method (RSM) is used to study the relationship between the factors affecting the adsorption process, thereby optimizing the adsorption efficiency, and making decisions on improving the adsorption process better sub. The research results obtained are as follows: pH2, initial CFX concentration 51 mg L-1, adsorbent dosage 0.16 g L-1, adsorption time 120 min, and temperature 51.5 °C reached the maximum adsorption capacity. The maximum additive is 38.63 mg g-1. The experimental data agree with the pseudo-quadratic kinetic model and the Langmuir and Temkin isotherm models. The composite aerogel adsorbent (AE) in this study is a potential candidate for adsorbent to remove antibiotic contamination in aqueous media. [ABSTRACT FROM AUTHOR]