Isolation of plant-derived exosome-like nanoparticles (PDENs) from Solanum nigrum L. berries and Their Effect on interleukin-6 expression as a potential anti-inflammatory agent.

Inflammation is a temporary response of the immune system that can be treated using common anti-inflammatory drugs. However, prolonged use of these drugs increases the risk of adverse side effects. Accordingly, there is an increasing need for alternative treatments for inflammation with fewer side effects. Exosomes are extracellular vesicles secreted by most eukaryotic cells and have been studied as a candidate for cell-free therapy for inflammatory diseases due to their immunomodulatory and anti-inflammatory properties. In recent years, the focus of exosome research has shifted from animal cell-derived exosomes to plant-derived exosome-like nanoparticles (PDENs). Plant-derived exosome-like nanoparticles (PDENs) are easier to obtain, have minimal safety concerns, and can be produced in higher quantities and lower cost than exosomes derived from animal cells. In this study, the isolation and analysis of the anti-inflammatory potential of PDENs from black nightshade berries (Solanum nigrum L.) were carried out. The results of isolation and characterization showed that PDENs had a spherical morphology, measuring around 107 nm with zeta potential of -0.6 mV, and had a protein concentration of 275.38 µg/mL. PDENs were also shown to be internalized by RAW264.7 macrophage cell line after 2 hours of incubation and had no cytotoxicity effect up to the concentration of 2.5 µg/mL. Furthermore, exposure to several doses of PDENs to the LPS-stimulated RAW264.7 cell significantly decreased the expression of pro-inflammatory cytokine gene IL-6, as well as the expression of IL-6 protein up to 97,28%. GC-MS analysis showed the presence of neral, a monoterpene compound with known anti-inflammatory properties, which may contribute to the anti-inflammatory activity of PDENs isolated from Solanum nigrum L. berries. Taken together, the present study was the first to isolate and characterize PDENs from Solanum nigrum L. berries. The results of this study also demonstrated the anti-inflammatory activity of PDEN by suppressing the production of IL-6 in LPS-stimulated RAW264.7 cells.

Jackfruit peel cellulose nanocrystal - Alginate hydrogel for doripenem adsorption and release study.

As a natural raw material to replace synthetic chemicals, cellulose and its derivatives are the most popular choices in the pharmaceutical industry. For drug delivery applications, cellulose is usually used as a cellulose nanocrystal (CNC). CNC-based hydrogels are widely utilized for drug delivery because drug molecules can be encapsulated in their pore-like structures. This study aims to develop CNC hydrogels for the delivery of doripenem antibiotics. CNC was obtained from jackfruit peel extraction, and alginate was used as a network polymer to produce hydrogels. Ionotropic gelation was used in the synthesis of CNC-alginate hydrogel composites. The maximum adsorption of doripenem by CNC was 65.7 mg/g, while the maximum adsorption by CNC-alginate was 98.4 mg/g. One of the most challenging aspects of drug delivery is predicting drug release from a solid matrix using simple and complex mathematical equations. The sigmoidal equation could represent the doripenem release from CNC, while the Ritger-Peppas equation could describe the doripenem release from CNC-Alginate. The biocompatibility testing of CNC and CNC-alginate against a 7F2 cell line indicates that both materials were non-toxic.

Polysaccharides gums in drug delivery systems: A review.

For the drug delivery system, drug carriers' selection is critical to the drug's success in reaching the desired target. Drug carriers from natural biopolymers are preferred over synthetic materials due to their biocompatibility. The use of polysaccharide gums in the drug delivery system has received considerable attention in recent years. Polysaccharide gums are renewable resources and abundantly found in nature. They could be isolated from marine algae, microorganisms, and higher plants. In terms of carbohydrates, the gums are water-soluble, non-starch polysaccharides with high commercial value. Polysaccharide gums are widely used for controlled-release products, capsules, medicinal binders, wound healing agents, capsules, and tablet excipients. One of the essential applications of polysaccharide gum is drug delivery systems. The various kinds of polysaccharide gums obtained from different plants, marine algae, and microorganisms for the drug delivery system application are discussed comprehensively in this review paper.

Cellulose Nanocrystals (CNCs) and Its Modified Form from Durian Rind as Dexamethasone Carrier.

In this study, CNCs were extracted from durian rind. Modification to CNCs with saponin was conducted at 50 °C for one h. CNCs and CNCs-saponin were employed as dexamethasone carriers. Modification to CNCs using saponin did not change the relative crystallinity of CNCs. CNCs' molecular structure and surface chemistry did not alter significantly after modification. Both nanoparticles have surface charges independently of pH. Dexamethasone-released kinetics were studied at two different pH (7.4 and 5.8). Higuchi, Ritger-Peppas, first-order kinetic and sigmoidal equations were used to represent the released kinetic data. The sigmoidal equation was found to be superior to other models. The CNCs and CNCs-saponin showed burst release at 30 min. The study indicated that cell viability decreased by 30% after modification with saponin.

Facile Synthesis of Silane-Modified Mixed Metal Oxide as Catalyst in Transesterification Processes.

The fast depletion of fossil fuels has attracted researchers worldwide to explore alternative biofuels, such as biodiesel. In general, the production of biodiesel is carried out via transesterification processes of vegetable oil with the presence of a suitable catalyst. A mixed metal oxide has shown to be a very attractive heterogeneous catalyst with a high performance. Most of the mixed metal oxide is made by using the general wetness impregnation method. A simple route to synthesize silane-modified mixed metal oxide (CaO-CuO/C6) catalysts has been successfully developed. A fluorocarbon surfactant and triblock copolymers (EO)106(PO)70(EO)106 were used to prevent the crystal agglomeration of carbonate salts (CaCO3-CuCO3) as the precursor to form CaO-CuO with a definite size and morphology. The materials show high potency as a catalyst in the transesterification process to produce biodiesel. The calcined co-precipitation product has a high crystallinity form, as confirmed by the XRD analysis. The synthesized catalyst was characterized using Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy-dispersive X-ray (EDX). The mechanism of surface modification and the effects of the catalytic activity were also discussed. The biodiesel purity of the final product was analyzed by gas chromatography. The optimum biodiesel yield was 90.17% using the modified mixed metal oxide CaO-CuO/C6.

Low-cost structured alginate-immobilized bentonite beads designed for an effective removal of persistent antibiotics from aqueous solution.

The removal of persistent antibiotics from the water bodies can be quite challenging. The present study deals with the removal of doripenem, one of the most stable and persistent antibiotics, from aqueous solution via adsorption technique using the low-cost structured alginate-immobilized bentonite (Alg@iB) beads which can be easily recovered after the process. Alg@iB possesses a porous interior and higher basal spacing compared with the acid-activated bentonite (iB). Its adsorption/desorption isotherm corresponds to type IV IUPAC classification and H4-type hysteresis loops, implying the presence of slit- or plane-shaped pores. The influences of four independent adsorption parameters, e.g., pH, initial doripenem concentrations (md), temperature (T), and Alg@iB loading (mc), on the removal rate of doripenem (Yd) are investigated. The maximum Yd (95.8% w/w) is obtained at pH = 5, mc = 1.4% w/v, T = 50 °C, and md = 250 mg/l. The study suggests that the adsorption of doripenem is spontaneous and endothermic. Further analysis using the multi-linear intra-particle diffusion (IPD) model indicates that the rate-governing step in this adsorption process is the physical diffusion from the bulk solution to the boundary layer of Alg@iB. However, the mechanism study also considers the chemical hydrogen binding between the hydronium ions of Alg@iB and hydroxyl groups of doripenem as one of the driving forces that promote adsorption. Alg@iB shows good reusability with Yd > 90% w/w up to five adsorption cycles. Based on the study, the Alg@iB beads exhibit excellent affinity to doripenem, indicating that an effective doripenem removal can be achieved using this sorbent material.

Effects of acute and chronic nuts consumption on energy metabolism: a systematic review of randomised clinical trials.

Nuts are high-energy density foods and are associated with beneficial effects on health, including weight control. Effects on resting energy expenditure, respiratory quotient, and diet-induced thermogenesis are suggested mechanisms behind the effects of nuts consumption on weight control. Thus, we revised the randomised clinical trials that assessed acute and chronic nuts consumption effects on energy metabolism. Walnuts (22.1 g to 56 g) consumption appears to modulate energy metabolism markers differently depending on the dose and profile of the evaluated subject. In its turn, 56 g of high-oleic peanuts increased postprandial energy expenditure and thermic effect of food after three hours postprandial compared to consumption of conventional peanuts. Almonds, hazelnuts, peanuts, and a mix of nuts were the nuts studies in the chronic studies, which does not seem to influence energy metabolism markers. Further studies are needed to elucidate the effects of other types of nuts consumption on energy metabolism.

TiO2/guar gum hydrogel composite for adsorption and photodegradation of methylene blue.

The development of porous adsorbent materials from renewable resources for water and wastewater treatment has received considerable interest from academia and industry. This work aims to synthesize composite hydrogel from the combination of guar gum (a neutral galactomannan polysaccharide) and TiO2. The TiO2-embedded guar gum hydrogel (TiO2@GGH) was utilized to remove methylene blue through adsorption and photodegradation. The presence of TiO2 particles in the hydrogel matrix (TiO2@GGH) was confirmed by scanning electron microscopy-energy dispersive X-ray and X-ray photoelectron spectroscopy analysis. The mercury intrusion and N2 sorption isotherm indicate the macroporous structure of the TiO2@GGH composite, showing the presence of pore sizes ~420 µm. The dye removal efficiency of the GGH and TiO2@GGH was evaluated in batch mode at ambient temperature under varying pH. The effect of UV radiation on the dye removal efficiency was also assessed. The results demonstrated that the highest dye removal was recorded at pH 10, with the equilibrium condition achieved within 5 h. UV radiation was shown to enhance dye removal. The maximum adsorption capacity of TiO2@GGH is 198.61 mg g-1, while GGH sorbent is 188.53 mg g-1. The results imply that UV radiation gives rise to the photodegradation effect.

Nanocelluloses: Sources, Pretreatment, Isolations, Modification, and Its Application as the Drug Carriers.

The 'Back-to-nature' concept has currently been adopted intensively in various industries, especially the pharmaceutical industry. In the past few decades, the overuse of synthetic chemicals has caused severe damage to the environment and ecosystem. One class of natural materials developed to substitute artificial chemicals in the pharmaceutical industries is the natural polymers, including cellulose and its derivatives. The development of nanocelluloses as nanocarriers in drug delivery systems has reached an advanced stage. Cellulose nanofiber (CNF), nanocrystal cellulose (NCC), and bacterial nanocellulose (BC) are the most common nanocellulose used as nanocarriers in drug delivery systems. Modification and functionalization using various processes and chemicals have been carried out to increase the adsorption and drug delivery performance of nanocellulose. Nanocellulose may be attached to the drug by physical interaction or chemical functionalization for covalent drug binding. Current development of nanocarrier formulations such as surfactant nanocellulose, ultra-lightweight porous materials, hydrogel, polyelectrolytes, and inorganic hybridizations has advanced to enable the construction of stimuli-responsive and specific recognition characteristics. Thus, an opportunity has emerged to develop a new generation of nanocellulose-based carriers that can modulate the drug conveyance for diverse drug characteristics. This review provides insights into selecting appropriate nanocellulose-based hybrid materials and the available modification routes to achieve satisfactory carrier performance and briefly discusses the essential criteria to achieve high-quality nanocellulose.

One-step synthesis of nitrogen-grafted copper-gallic acid for enhanced methylene blue removal.

Nitrogen-grafting through the addition of glycine (Gly) was performed on a metal- phenolic network (MPN) of copper (Cu2+) and gallic acid (GA) to increase its adsorption capacity. Herein, we reported a one-step synthesis method of MPN, which was developed according to the metal-ligand complexation principle. The nitrogen grafted CuGA (Ng-CuGA) MPN was obtained by reacting Cu2+, GA, and Gly in an aqueous solution at a molar ratio of 1:1:1 and a pH of 8. Several physicochemical measurements, such as Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), N2 sorption, X-ray diffraction (XRD), and thermal gravimetry analysis (TGA), were done on Ng-CuGA to elucidate its characteristics. The analysis revealed that the Ng-CuGA has non-uniform spherical shaped morphology with a pore volume of 0.56 cc/g, a pore size of 23.25 nm, and thermal stability up to 205 °C. The applicational potential of the Ng-CuGA was determined based on its adsorption capacity against methylene blue (MB). The Ng-CuGA was able to adsorb 190.81 mg MB per g adsorbent at a pH of 6 and temperature of 30 °C, which is 1.53 times higher than the non-grafted CuGA. Detailed assessment of Ng-CuGA adsorption properties revealed their pH- and temperature-dependent nature. The adsorption capacity and affinity were found to decrease at a higher temperature, demonstrating the exothermic adsorption behavior.

Efficient One-Step Conversion of a Low-Grade Vegetable Oil to Biodiesel over a Zinc Carboxylate Metal-Organic Framework.

In this study, a metal-organic framework, namely, Zn3(BTC)2 (BTC = 1,3,5-benzenetricaboxylic acid), was solvothermally synthesized and employed as a catalyst for biodiesel production from degummed vegetable oil via a one-step transesterification and esterification reaction. The resulting Zn3(BTC)2 particles exhibit a well-defined triclinic structure with an average size of about 1.2 µm, high specific surface area of 1176 m2/g, and thermal stability up to 300 °C. The response surface methodology-Box-Behnken design (RSM-BBD) was employed to identify the optimal reaction conditions and to model the biodiesel yield in relation to three important parameters, namely, the methanol/oil molar ratio (4:1-8:1), temperature (45-65 °C), and time (1.5-4.5 h). Under the optimized reaction conditions (i.e., 6:1 methanol/oil molar ratio, 65 °C, 4.5 h), the maximum biodiesel yield reached 89.89% in a 1 wt % catalyst, which agreed very well with the quadratic polynomial model's prediction (89.96%). The intrinsic catalytic activity of Zn3(BTC)2, expressed as the turnover frequency, was found to be superior to that of other MOF catalysts applied in the transesterification and esterification reactions. The reusability study showed that the as-synthesized Zn3(BTC)2 catalyst exhibited good stability upon three consecutive reuses without a noticeable decrease in the methyl ester yield (∼4%) and any appreciable metal leaching (<5%). Furthermore, a preliminary technoeconomic analysis showed that the total direct operating cost for the kilogram-scale production of Zn3(BTC)2 is estimated to be US$50, which may sound economically attractive.

Fabrication of cellulose carbamate hydrogel-dressing with rarasaponin surfactant for enhancing adsorption of silver nanoparticles and antibacterial activity.

Bacterial contamination on external wounds is known to be a factor that prevents wound healing and triggers tissue damage. Hydrogel-dressings with antibacterial activity is a useful medical device to avoid this contamination, wherein the antibacterial activity can be provided via incorporation of silver nanoparticles (AgNPs). Contrary to the conventional two-step preparation of an AgNPs-loaded hydrogel (AgNPs@hydrogel), this work aims to establish a new and facile synthesis method employing the adsorption principle. Once AgNO3 adsorbed into active sites of the hydrogels, in situ reductions using NaBH4 was employed to produce AgNPs@hydrogel. The effect of surfactant addition on the AgNO3 loading and the antibacterial activity of the resulting hydrogel dressing was investigated. The outcome of this work indicates that the addition of rarasaponin not only can increase the loading of AgNPs on cellulose carbamate hydrogel (CCH) but also significantly enhance the antibacterial activity of the resulted hydrogel-dressing. Superior to the other studied surfactant, the loading capacity (LC) of AgNPs is found to be 10.15, 9.94, and 7.53 mg/g for CCH modified with rarasaponin, CTAB, and Tween80, respectively. These findings conclude that the addition of surfactant, especially rarasaponin, can effectively improve the loading of AgNPs onto hydrogel-dressing via adsorption and promote the antibacterial activity. Furthermore, the cytotoxic test shows that the hydrogel-dressings have good biocompatibility toward skin fibroblast cells.

Hydrophobic Cetyltrimethylammonium Bromide-Pillared Bentonite as an Effective Palm Oil Bleaching Agent.

To promote a minimal use of acid in the activation of bentonite and to maintain oil quality during refinery and storage, a new class of bleaching agent, cetyltrimethylammonium bromide (CTAB)-pillared bentonite (CTAB@Bent), is fabricated. The influences of three independent intercalation variables, including temperature T (40, 50, and 60 °C), time t (2, 4, and 6 h), and CTAB loading m c (0.2, 0.25, 0.33, 0.50, and 1.00%, w/w), on the ß-carotene removal rate are studied. The multilevel factorial design combined with the response surface methodology and three-way analysis of variance is employed to design and optimize experiments in regard to the three independent variables. Based on the optimization results, the highest ß-carotene removal rate is monitored at 71.04% (w/w) using CTAB@Bent obtained at optimum intercalation conditions (CTAB@Ben-Opt): T = 40 °C, t = 3.2 h, m c = 1.00% (w/w). The mechanism study shows that the adsorption of ß-carotene onto CTAB@Bent-Opt is spontaneous and endothermic, with the governing steps of physical interaction and ion exchange between ß-carotene and the cationic head of CTAB. CTAB@Bent-Opt also exhibits characteristics superior to those of commercial raw bentonite and acid-activated bentonite, indicating that a more efficient ß-carotene removal can be achieved using this new bleaching agent.

Hydrothermal Synthesize of HF-Free MIL-100(Fe) for Isoniazid-Drug Delivery.

Sustainable development of drug delivery materials with good biocompatibility and controlled-release is a popular topic among researchers. In this research study, we demonstrated the potential of the metal-organic framework, that is MIL-100(Fe), as a drug delivery platform for isoniazid (INH). The MIL-100(Fe) was prepared by using the hydrofluoric acid-free hydrothermal method. Several physical measurements were conducted to characterize the MIL-100(Fe), including x-ray diffraction (XRD), scanning electron microscopy (SEM), nitrogen sorption, and thermal-gravimetric (TG). The synthesized MIL-100(Fe) has octahedron-shaped particles with superior properties, that is large surface area (1456.10 m2/g) and pore volume (1.25 cm3/g). The drug loading rate and capacity were determined by means of adsorption kinetic and isotherm. The studied INH@MIL-100(Fe) adsorption system kinetics follow the pseudo-first-order model, while the isotherm system follows the Langmuir model with the maximum adsorption capacity of 128.5 mg/g at 30 °C. MIL-100(Fe) shows adequate biocompatibility, also exhibits a reasonable and controlled drug release kinetics. The results obtained show that MIL-100 (Fe) can be a good choice of drug delivery platform among other available platforms.