Macroporous Resin Research Articles

A green method for decolorization of polysaccharides from alfalfa by S-8 macroporous resin and their characterization and antioxidant activity.

In this study, the decolorization conditions of polysaccharides extracted from alfalfa by S-8 macroporous adsorption resin were optimized through the response surface method, and the physicochemical properties and antioxidant activity of decolorized polysaccharides were investigated. The optimal decolorization conditions were determined to be as follows: the amount of S-8 macroporous adsorption resin was 1.4 g, the adsorption time was 2 h, and the adsorption temperature was 58 °C. Under these optimal conditions, a decolorization ratio of 71.43 ± 0.23% was achieved, which was consistent with the model hypothesis. The adsorption curve showed that S-8 macroporous adsorption resin adsorption of pigment molecules in alfalfa polysaccharides (APS) agreed with the Freundlich and pseudo-second-order equations, and the adsorption was a spontaneous endothermic process. High-performance liquid chromatography (HPLC) analysis of monosaccharide composition showed that APS was composed of mannose, glucose, galactose, arabinose and glucuronic acid in a molar ratio of 1.18 : 8.04 : 1.22 : 0.92 : 1. The results of antioxidant activity studies showed that APS had strong scavenging activity against ABTS, DPPH and hydroxyl radicals. This study will help to further understand the adsorption mechanism of macroporous resin on polysaccharide pigment molecules and lay a basis for evaluating their physiological activity.

Towards furfural and biomass char production from Camellia oleifera husks using dilute hydrochloric acid pretreatment: a comprehensive investigation on adsorption performance

The whole component utilization of lignocellulose was achieved, and hemicellulose was used to prepare FF which was adsorbed with S-8 macroporous resin and purified. The residue including cellulose and lignin was converted to biomass char, which was used for the adsorption of methylene blue dye.

Enrichment of rosmarinic acid from Salvia przewalskii Maxim. leaves using macroporous resin: Adsorption/desorption behavior, process optimization followed by scale-up

To valorize Salvia przewalskii Maxim. leaves as a renewable source of rosmarinic acid, an efficient macroporous resin enrichment technology was established in this work. X-5 resin was considered as the most appropriate adsorbent in view of its highest adsorption/desorption capacity for rosmarinic acid, and the adsorption data were best expounded by Langmuir isotherm model and pseudo-second-order kinetics model. The influences of sample volume, loading and elution flow rates, eluent type and volume were evaluated to obtain the optimum enrichment procedure, which was as follows: for adsorption, the rosmarinic acid concentration, loading flow rate and sample volume were respectively 0.24 mg/mL, 3 BV/h, and 12 BV; for desorption, the eluent type, elution flow rate and volume were respectively 50% ethanol, 3 BV/h and 9 BV. Furthermore, an enrichment process scale-up of rosmarinic acid was performed under optimal procedure. After one-step large-scale enrichment, the content of rosmarinic acid improved 3.65-fold from 12.41% to 45.30% with a satisfactory recovery of 80.17%. Results suggested that X-5 resin chromatographic enrichment technique developed in the present study offered a feasible scheme for the industrial enrichment of rosmarinic acid from S. przewalskii leaves. • X-5 reisn was the optimum resin for the enrichment of rosmarinic acid. • Adsorption/desorption behavior of rosmarinic acid on X-5 reisn was studied. • An effective resin chromatography to enrich rosmarinic acid was developed. • The enrichment method showed a promising prospect for industrial application.

Extraction, Characterization, and In Vitro Hypoglycemic Activity of a Neutral Polysaccharide from the New Medicinal Mushroom Cantharellus yunnanensis (Agaricomycetes).

Polysaccharides serve as promising ingredients for health-beneficial functional foods, while there were no investigations into the structural characterizations and bioactivities of an edible mushroom Cantharellus yunnanensis. In the study, crude polysaccharides from this mushroom were extracted by hot water and isolated by ethanol precipitation. Then, a neutral polysaccharide (named CY-1) was purified from the crude polysaccharide by deproteinization with Sevag reagent, decolorization with a kind of macroporous adsorption resin SP-825, DEAE-52 cellulose column chromatography and dialysis. The physicochemical properties of CY-1 were characterized by UV, IR, SEM, NMR, and HPLC analyses. Structural characterizations revealed that CY-1 is a homogeneous heteropolysaccharide with an average molecular weight of 3.06 × 104 Da. CY-1 exhibited a honeycomb structure with an irregular branching shape, and it was composed of mannose, glucose, fucose, xylose, arabinose, galactose, rhamnose, and glucuronic acid, with molar fractions of 54.83%, 25.11%, 10.28% 4.53%, 2.12%, 1.64%, 0.83%, and 0.64%, respectively. In vitro hypoglycemic tests showed that CY-1 had an inhibitory effect on α-glucosidase. In addition, CY-1 of 160 µg/mL promoted glucose consumption in normal HepG2 cells. These results suggested that CY-1 may be a potential hypoglycemic agent.

A combination of surface-initiated atom transfer radical polymerization and photo-initiated “thiol-ene” click chemistry: Fabrication of functionalized macroporous adsorption resins for enrichment of glycopeptides

A hydrophilic adsorbent (Cys@poly(AMA)@MAR) was successfully prepared for the enrichment of N-glycopeptides via surface-initiated atom transfer radical polymerization (SI-ATRP) and photo-initiated “thiol-ene” reaction using monodisperse macroporous adsorbent resin (MAR) as adsorption matrix. Due to the presence of electron-deficient acrylic groups and electron-rich vinyl groups in allyl methacrylate (AMA), both of them can participate in free radical reaction. Therefore, the polymerization time of SI-ATRP was optimized. The resulting poly(AMA)@MAR was modified with l-cysteine (L-Cys) via photo-initiated “thiol-ene” reaction, and the amount of vinyl retained was determined by measuring the adsorption of Cu2+. The Cys@poly(AMA)@MAR pendant brushes with high density of amine and carboxyl groups could capture N-glycopeptides from IgG digest and human serum digest by hydrophilic interaction. The 22 N-glycopeptides were identified from IgG digest and the limit of detection reached 10 fmol. The 319 N-glycosylation sites and 583 N-glycopeptides were identified from 2 μL human serum digest and mapped to 147 glycoproteins. It demonstrates great potential and commercialization prospects for the enrichment of N-glycopeptides.

Deactivation of macroporous ion-exchange resins by acetonitrile and inhibition by water in the simultaneous synthesis of ethyltert-butyl ether (ETBE) andtert-amyl ethyl ether (TAEE)

The deactivating effect of acetonitrile (ACN) and ACN/water mixtures on the feed stream has been investigated for the simultaneous syntheses of ethyltert-butyl ether andtert-amyl ethyl ether over Amberlyst™35 and Purolite®CT-275 ion-exchange resins.

Separation of flavonoids with significant biological activity from Acacia mearnsii leaves.

Acacia mearnsii leaves, which are a rich source of flavonoids, were used to separate and purify myricitrin (W3) and myricetin-3-O-glucoside (W1). Further, the antioxidant and hypoglycemic activities of the two purified flavonoids were evaluated. The flavonoids were separated using solvent partition, macroporous adsorbent resin column, and Sephadex column chromatography, and purified using preparative reverse-phase high-performance liquid chromatography (HPLC). The purified flavonoids were characterized using HPLC, mass spectrometry, and nuclear magnetic resonance methods. A high yield (7.3 mg g-1 of crude extract) of W3 was obtained, with a high purity of 98.4%. Furthermore, the purity of W1 was over 95%. W1 and W3 showed strong antioxidant activity and significantly inhibited α-glucosidase. W3 also demonstrated substantial α-amylase inhibitory capacity. This study indicated that A. mearnsii leaves, which are discarded in significant amounts, can be used as a source of myricitrin, thus providing more adequate material for the production of antioxidants and type II diabetes inhibitors. Hence, A. mearnsii leaves have the potential to create great market economic value and environmental benefits.

Effects of a Macroporous Resin Extract of Dendrobium officinale Leaves in Rats with Hyperuricemia Induced by Anthropomorphic Unhealthy Lifestyle.

Hyperuricemia (HUA) has received increased attention in the last few decades due to its global prevalence. Our previous study found that administration of a macroporous resin extract of Dendrobium officinale leaves (DoMRE) to rats with HUA that was induced by exposure to potassium oxazine combined with fructose and a high-purine diet led to a significant reduction in serum uric acid (SUA) levels. The aim of this study was to explore the effects of DoMRE on hyperuricemia induced by anthropomorphic unhealthy lifestyle and to elucidate its possible mechanisms of action. Dosages (5.0 and 10.0 g/kg/day) of DoMRE were administered to rats daily after induction of HUA by anthropomorphic unhealthy lifestyle for 12 weeks. The levels of UA in the serum, urine, and feces; the levels of creatinine (Cr) in the serum and urine; and the levels of aspartate aminotransferase (AST) and alanine aminotransferase (ALT) in serum were all measured using an automatic biochemical analyzer. The activities of xanthine oxidase (XOD) and adenosine deaminase (ADA) in the serum, liver, and intestine tissue supernatant were measured using appropriate kits for each biological target. The expressions levels of UA transporters (ABCG2 and GLUT9), tight junction (TJ) proteins (ZO-1 and occludin), and inflammatory factors (IL-6, IL-8, and TNF-α) in the intestine were assayed by immunohistochemical (IHC) staining. Hematoxylin and eosin (H&E) staining was used to assess histological changes in the renal and intestinal tissues. DoMRE treatment significantly reduced SUA levels and concomitantly increased fecal UA (FUA) levels and the fractional excretion of UA (FEUA) in HUA rats. Furthermore, DoMRE significantly reduced both the XOD activity in the serum, liver, and intestine and the ADA activity in the liver and intestine. DoMRE also effectively regulated the expression of GLUT9 and ABCG2 in the intestine, and it significantly upregulated the expression of the intestinal TJ proteins ZO-1 and occludin. Therefore, DoMRE reduced the damage to the intestinal barrier function caused by the increased production of inflammatory factors due to HUA to ensure normal intestinal UA excretion. DoMRE demonstrated anti-HUA effects in the HUA rat model induced by an anthropomorphic unhealthy lifestyle, and the molecular mechanism appeared to involve the regulation of urate transport-related transporters (ABCG2 and GLUT9) in the intestine, protection of the intestinal barrier function to promote UA excretion, and inhibition of XOD and ADA activity in the liver and intestine to inhibit UA production in the HUA-induced rats.

Biochemical and physical investigations on detoxification of ginkgo kernel juice using probiotic fermentation with macroporous resin addition

Biochemical and physical investigations on detoxification of ginkgo kernel juice using probiotic fermentation with macroporous resin addition

Effective adsorption of In(iii) from hydrochloric acid solution using hyperbranched polyethyleneimine and sodium chloroacetate modified weakly acidic macroporous resin

CM-HPEI-HD-1, prepared by modifying HD-1 resin with HPEI and sodium chloroacetate, is a promising adsorbent with good performance and good stability for adsorption of In(iii).

Separation and Purification of Antioxidant Peptide from Fermented Whey Protein by Lactobacillus rhamnosus B2-1.

In this study, a antioxidant activity peptide fraction was separated and purified from metabolites of whey protein fermented by Lactobacillus rhamnosus B2-1. The fermentation sample was separated by macroporous resin D101 and Sephadex G-15. The collected fractions were tested for antioxidant and antitumor activities. In order to test the antioxidant activity of fractions, Hydroxyl (·OH), 2,2'-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid (ABTS), and Oxygen Radical Absorbance Capacity (ORAC) were used. The final purified peptide B11 showed highest ABTS and ·OH radical scavenging rate by 84.36±1.89% and 62.43±2.64%, respectively, and had an ORAC activity of 1,726.44± 2.76 μM Trolox equivalent/g. Further, the inhibitory effect of B11 on the proliferation of LoVo human colon cancer cells, KB and Cal-27 human oral cancer cells were enhanced with increasing concentrations of B11. B11 contains 51.421% amino acids, with Glu and Asp being the major constituents. In this study, we obtained peptide fraction B11 with antioxidant activity, which is promising for development.

Controlled release and antibacterial properties of nanofiber membrane loaded with tea saponin

The controlled release packaging system has been considered as an efficient strategy for drug delivery, but the contradiction of instability and release difficulty after encapsulation of natural active compound is unsolved. In this research, tea saponin was embedded into the cavity of β-cyclodextrin polymer (β-CDP) to form a stable inclusion complex and then successfully constructed the nanofibers by electrospinning. The optimal polymer substrates (polyacrylonitrile, 0.1 g β-CDP, 0.03 g tea saponin, dendritic mesoporous silica nanoparticles (DMSNs) 3.75 wt% of the mass of PAN) were obtained to fabricate the TS/PAN@ β-CDP-DMSNs with a typical nanofiber structure with uniform diameter distribution and high porosity. The nanofiber exhibited a better thermal stability (270 °C), higher moisture resistance (water contact angle 126.4°) and relatively larger specific surface area. Results of the FTIR and XPS characterization indicate chemical interactions of TS/PAN@ β-CDP-DMSNs via van der Waals forces and hydrogen bonds. As a result, the tea saponin release efficiency increased from 69.30% of liposome to 81.16% of nanofiber at 36 h. Simultaneously, the antibacterial rates against Escherichia coli and Staphylococcus aureus were significantly improved compared with tea saponin and PAN@ β-CDP-DMSNs. This research provides a feasible strategy for the application of the drug delivery systems to both solve the stability and release efficiency of natural active compounds. • A novel TS/PAN@ β-CDP-DMSNs nanofiber was prepared via electrospinning. • Tea saponin with 94.23% purity is obtained by AB-8 macroporous resin. • The PAN@ β-CDP-based nanofiber improves drug stability and release efficiency. • The prepared nanofiber exhibits the remarkable synergistic bacteriostatic effects.

Rapid determination of rebaudioside A content in the macroporous resin elution process using a portable near-infrared spectrometer

Portable NIR spectroscopy is used to monitor the macroporous resin elution process. The PLSR and SVMR models displayed good performance for determining the RA content. The PLSR model displayed higher predictive accuracy than the SVMR model.

Method development for the identification, extraction and characterization of melanoidins in thermal hydrolyzed sludge

Melanoidins, the brown late-stage Maillard reaction products, are responsible for color development and refractoriness in thermal hydrolyzed sludge (THS), causing negative effects on wastewater treatment. This study aimed to develop a methodology for the identification, isolation and preliminary characterization of the THS melanoidins. After thermal hydrolysis, the formation of melanoidins were confirmed by physicochemical indicators and excitation-emission matrix fluorescence analysis. The macroporous resin adsorption method was adopted to successfully extract melanoidins from THS with high recovery and selectivity. The main chemical components of the extracted melanoidins were carbohydrate (23.1 %), protein (43.8 %) and phenol (13.7 %), and the C/N was 4.5. In addition, furans, alcohols and sulfur-containing volatile substances were detected by pyrolysis-gas chromatography–mass spectrometry. Fourier transform infrared spectroscopy determined that functional groups such as CO, CN, NH, C-O-C, amide I and phenyl were present in the structure of THS melanoidins, and nuclear magnetic resonance spectroscopy indicated the formation of heterocyclic macromolecular structures. Their formation pathways were speculated to involve the cross-linkage of low-molecular-weight components (e.g. proteins, Amadori and Schiff base compounds) and the polymerization of heterocyclic units (e.g. furans, pyroles and pyrazines). The above results clarify the fundamental characteristics of the melanoidins formed during sludge thermal hydrolysis and will help improve subsequent research on melanoidins control.

Yangqing Chenfei formula attenuates silica-induced pulmonary fibrosis by suppressing activation of fibroblast via regulating PI3K/AKT, JAK/STAT, and Wnt signaling pathway

BackgroundYangqing Chenfei formula (YCF) has been demonstrated its clinical efficiency on silicosis patients. However, the effect of YCF against silicotic fibrosis and its mechanism remain unclear. PurposeThis study is aimed to investigate active compounds and molecular mechanism of YCF in treating silicosis. MethodYCF was orally administrated to silicosis rats induced by crystalline silica. The effective fraction of YCF and the compounds was isolated and identified by using macroporous resin and HPLC-MS, respectively. The targets and potential molecular mechanism of YCF against silicotic fibrosis were investigated through pharmacological network and RNA-sequencing analysis and in vitro-experimental validation. ResultsYCF could remarkably improve the lung function and pathological changes of silicotic rats, reduce the aggregation of fibrocytes and deposition of ECM, such as collagen I, III, FN, and α-SMA, and suppress the TGF-β/Smad3 signaling. Furthermore, YCF6, the effective fraction derived from YCF, could significantly inhibit fibroblast activation induced by TGF-β. Then, 135 compounds were identified from YCF6 by using HPLC-MS, and Network pharmacology analysis predicted total 941 targets for these compounds. Moreover, 409 differentially expressed genes of fibroblast activation induced by TGF-β were identified. Then, integrated analysis of the 941 targets with 409 differentially expressed genes showed that YCF6 contains multiple compounds, such as tangeretin, L-Malic acid, 2-Monolinolein etc., which inhibits fibroblast activation probably by targeting different proteins, such as PIK3CA, AKT1, JAK2, STAT3, GSK3β, leading to regulate the signal network, such as PI3K/AKT signaling pathway, JAK/STAT signaling pathway, and Wnt signaling pathway. Finally, in vitro experiment indicated that tangeretin, the active compound contained in YCF6, could significantly inhibit TGF-β induced fibroblast activation. Moreover, YCF6 and tangeretin could markedly inhibit the activation of PI3K/AKT, JAK/STAT, and Wnt pathway. ConclusionYCF contained multiple compounds and targeted various proteins that regulated the fibroblast activation, which might be the molecular mechanisms of it in treating silicosis.

Useful separation and purification of anthocyanin compounds from grape skin pomace Alicante Bouschet using macroporous resins

Useful separation and purification of anthocyanin compounds from grape skin pomace Alicante Bouschet using macroporous resins

Removal and destruction of perfluoroalkyl ether carboxylic acids (PFECAs) in an anion exchange resin and electrochemical oxidation treatment train

Perfluoroalkyl ether carboxylic acids (PFECAs) are a group of emerging recalcitrant contaminants that are being developed to replace legacy per- and polyfluoroalkyl substances (PFAS) in industrial applications and that are generated as by-products in fluoropolymer manufacturing. Here, we report on the removal and destruction of four structurally different PFECAs using an integrated anion exchange resin (AER) and electrochemical oxidation (ECO) treatment train. Results from this work illustrated that (1) flow-through columns packed with PFAS-selective AERs are highly effective for the removal of PFECAs and (2) PFECA affinity is strongly correlated with their hydrophobic features. Regeneration of the spent resin columns revealed that high percentage (e.g., 80%) of organic cosolvent is necessary for achieving 60-100% PFECA release, and regeneration efficiency was higher for a macroporous resin than a gel-type resin. Treatment of spent regenerants showed (1) >99.99% methanol removal was achieved by distillation, (2) >99.999% conversion of the four studied PFECAs was achieved during the ECO treatment of the still bottoms after 24 hours with an energy per order of magnitude of PFECA removal (EE/O) <1.03 kWh/m3 of total groundwater treated, and (3) >85% of the organic fluorine was recovered as inorganic fluoride. Trifluoroacetic acid (TFA), perfluoropropionic acid (PFPrA), and perfluoro-2-methoxyacetic acid (PFMOAA) were confirmed via high-resolution mass spectrometry as transformation products (TPs) in the treated still bottoms, and two distinctive degradation schemes and four reaction pathways are proposed for the four PFECAs. Lastly, dissolved organic matter (DOM) inhibited uptake, regeneration, and oxidation of PFECAs throughout the treatment train, suggesting pretreatment steps targeting DOM removal can enhance the system's treatment efficiency. Results from this work provide guidelines for developing effective separation-concentration-destruction treatment trains and meaningful insights for achieving PFECA destruction in impacted aquatic systems.

Adsorption Properties and Preparative Separation of Flavonoids from Rhizoma Smilacis Glabrae Using Macroporous Resins

Astilbin (AST), isoastilbin (ISO), and engeletin (ENG) are the main flavonoids in Rhizoma Smilacis Glabrae (RSG) and have many biological activities. In this study, the adsorption kinetics of AST, ISO, and ENG on HPD-300 resin was investigated and their adsorption processes conformed to a pseudo-second-order kinetics equation. The fitting curves of the intraparticle diffusion model showed three linear stages and did not pass through the origin, meaning the adsorption process of the three flavonoids was controlled by boundary layer diffusion and intraparticle diffusion. Their adsorption isotherms were also constructed and could be well-fitted by the Langmuir equation. A low temperature was favorable for their adsorption. The relative adsorption capacity of ENG was significantly higher than those of the other two compounds, indicating that the substitution pattern on ring B has an important impact on the adsorption of flavonoids with resin. The separation process was optimized by dynamic adsorption/desorption experiments. After separation, the purities of AST, ISO, and ENG increased from 5.55%, 1.22%, and 0.45% to 27.46%, 6.14%, and 2.27%, respectively, and all the recoveries exceeded 75%. After that, the three compounds were further separated by preparative HPLC and silica gel chromatography. In the final product, the purities of AST, ISO, and ENG could reach above 98%.

Extraction and purification of antioxidative flavonoids from Chionanthus retusa leaf.

In this work, flavonoids from the leaves of Chionanthus retusa were extracted using alcohol, and the extraction yield was optimized by single-factor and orthogonal experiments. Then, the extracted solution with flavonoids was purified via macroporous resin by elution with different concentrations of ethanol. The antioxidative activity of total flavonoid in purified extracted solution was evaluated by detecting its ability to scavenge DPPH free radicals. The results demonstrated that ethanol with a concentration of 60%, ultrasonic power of 140W, liquid-solid ratio of 25:1ml g-1, and water-bath temperature of 80°C were the optimal conditions for the extraction of total flavonoids from C. retusa leaf, achieving a yield of 121.28mg g-1. After purification by macroporous resin using different concentrations of ethanol, the highest content of total flavonoids (88.51%) in the extracted solution can be obtained with the 50% ethanol eluant. The results of scavenging DPPH free radicals suggest that the purified flavonoids in the 50% ethanol eluant had the best antioxidant capacity over the flavonoids in other ethanol eluants. In addition, it is confirmed the antioxidant capacity of the extractives was associated with the content of total flavonoids and kinds of flavonoids. These results may provide a feasible pathway to make full use of total flavonoids from C. retusa leaf.

Detoxification of hemicellulose-enriched hydrolysate from sugarcane bagasse by activated carbon and macroporous adsorption resin

Detoxification of hemicellulose-enriched hydrolysate from sugarcane bagasse by activated carbon and macroporous adsorption resin