Microencapsulation of Lactobacillus plantarum with Improved Survivability Using Pufferfish Skin Gelatin-Based Wall Materials.

To improve the survivability of probiotics, Lactobacillus plantarum was microencapsulated using pufferfish skin gelatin (PSG)-based wall materials by spray-drying. This work investigated the protective effect of three different pH-dependent proteins (sodium caseinate (SC), soy protein isolate (SPI), and whey protein isolate (WPI)) combined with PSG on L. plantarum. The experimental results of spray-drying with an inlet temperature of 120 °C and an outlet temperature of 80 °C, storage at 4 °C for 6 months, simulated digestion, and turbidity indicated that PSG/SC had better stability and encapsulation effects and was more suitable to encapsulate L. plantarum than PSG/SPI and PSG/WPI. The optimum preparation conditions for L. plantarum microcapsules were a PSG/SC mass ratio of 2:1, an SC concentration of 20 g/L, and a cell concentration of 10 g/L. The encapsulation efficiency of the obtained microcapsules was 95.0%, and the survival rate was 94.2% in simulated gastric fluid for 2 h and 98.0% in simulated intestinal fluid for 2 h. Amino acid composition analysis exhibited that the imino acid and aspartic acid contents of PSG were 27.98 and 26.16 g/100 g protein, respectively, which was much higher than commercial bovine gelatin. This characteristic was favorable to the high encapsulation efficiency and stability of microcapsules. In vitro release experiments showed that the PSG/SC microcapsules did not disintegrate in simulated gastric fluid for 2 h but could completely release in simulated intestinal fluid for 2 h, which can maintain the high survivability of L. plantarum in simulated digestion. In general, this study demonstrated that microcapsules using PSG/SC as wall materials can effectively improve the survivability of probiotics and have great potential for application in probiotic products.

Efficient Preparation of High-Purity Fucoxanthinol by SpyTag-Tailored Active Cholesterol Esterase Aggregates.

A novel approach to producing high-purity fucoxanthinol (FXOH) was exploited as a sustainable method to maximize fucoxanthin (FX) utilization. Through fusing the genes of cholesterol esterase and SpyTag and then expressing them in Escherichia coli, the fusion chimera was self-assembled into insoluble active aggregates by SpyTag, which could be regarded as carrier-free immobilization. The immobilization yield of the active cholesterol esterase aggregates could reach 60%. They have expressed good activity retention at 92.48% and 60.13% after 3 and 12 cycles, respectively, which is an exciting finding. The conversion ratio of FX to FXOH is 95.02%, which is remarkably higher than those realized via the conventional chemical reduction method (55.86%) and the enzymatic hydrolysis method by free cholesterol esterases (84.51%). The purity of FXOH obtained by this method is as high as 98%, which is much higher than those obtained by other methods. Thus, a promising method for simultaneously purifying and immobilizing active cholesterol esterase aggregates is demonstrated in this study by SpyTag tailoring. In addition, this study provides an eco-friendly method for producing high-purity FXOH from FX in a highly efficient manner.

A Study of 11-[³H]-Tetrodotoxin Absorption, Distribution, Metabolism and Excretion (ADME) in Adult Sprague-Dawley Rats.

Tetrodotoxin (TTX) is a powerful sodium channel blocker that in low doses can safely relieve severe pain. Studying the absorption, distribution, metabolism and excretion (ADME) of TTX is challenging given the extremely low lethal dose. We conducted radiolabeled ADME studies in Sprague-Dawley rats. After a single dose of 6 µg/(16 µCi/kg) 11-[³H]TTX, pharmacokinetics of plasma total radioactivity were similar in male and female rats. Maximum radioactivity (5.56 ng Eq./mL) was reached in 10 min. [³H]TTX was below detection in plasma after 24 h. The area under the curve from 0 to 8 h was 5.89 h·ng Eq./mL; mean residence time was 1.62 h and t½ was 2.31 h. Bile secretion accounted for 0.43% and approximately 51% of the dose was recovered in the urine, the predominant route of elimination. Approximately 69% was recovered, suggesting that hydrogen tritium exchange in rats produced tritiated water excreted in breath and saliva. Average total radioactivity in the stomach, lungs, kidney and intestines was higher than plasma concentrations. Metabolite analysis of plasma, urine and feces samples demonstrated oxidized TTX, the only identified metabolite. In conclusion, TTX was rapidly absorbed and excreted in rats, a standard preclinical model used to guide the design of clinical trials.

Comparative evaluation of the radical-scavenging activities of fucoxanthin and its stereoisomers.

Fucoxanthin (Fuco) is a characteristic carotenoid of brown seaweeds. In the present study, Fuco and its stereoisomers 9'Z-Fuco, 13Z- and 13'Z-Fuco were extracted from Laminaria japonica Aresch. They were isolated and purified by silica gel column chromatography, Sephadex LH-20, and reversed-phase HPLC. The radical-scavenging activities of the three stereoisomers were evaluated toward 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical, 2-2'-azinobis-(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) radical, hydroxyl radical, and superoxide radical. The order of 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical-scavenging activity was 13Z- and 13'Z-Fuco > (all-E)-Fuco > 9'Z-Fuco. The order of 2-2'-azinobis-(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) and hydroxyl radical-scavenging activities were 9'Z-Fuco > (all-E)-Fuco > 13Z-and 13'Z-Fuco. The order of superoxide radical-scavenging activity was 13Z- and 13'Z-Fuco > (all-E)-Fuco > 9'Z-Fuco. The scavenging activities of Fuco and its stereoisomers toward the four radical types were all dose-dependent. The ABTS, DPPH, and superoxide radical-scavenging activities were all weaker than that of tocopherol (VE), while their hydroxyl radical-scavenging activities were stronger than that of VE. The results confirmed that Fuco and its stereoisomers have potent antioxidant activities.

Preparation and Embedding Characterization of Hydroxypropyl-ß-cyclodextrin/Menthyl Acetate Microcapsules with Enhanced Stability.

OBJECTIVE: Hydroxypropyl-ß-cyclodextrin (HP-ß-CD)/menthyl acetate (MA) microcapsules were developed to overcome the volatile and unstable defects of MA and improve the ease of use and storage. METHODS: MA microcapsules were prepared via spray drying using HP-ß-CD as the wall material. The embedding rate of MA microcapsules was determined through gas chromatography. The embedding characteristics were studied using phase solubility and nuclear magnetic resonance (NMR). The stability was characterized via differential scanning calorimetry (DSC) and the release and retention rates of MA microcapsules at different temperatures. RESULTS: The embedding rate of HP-ß-CD /MA microcapsules was 96.3%. The Gibbs free energy change, enthalpy change and entropy change of the embedding reaction between HP-ß-CD and MA were all less than zero, indicating that the embedding process was a spontaneous exothermic reaction. NMR spectra showed that MA entered the cavity of HP-ß-CD through the large opening end and interacted with the inner wall of the small opening end. DSC and the release and retention rates of MA microcapsules at different temperatures showed that the stability of MA was significantly enhanced after being embedded in HP-ß-CD. CONCLUSION: The HP-ß-CD/MA microcapsules are able to significantly improve the stability of MA and reduce the volatilization of MA.

Effect of Collagen Peptide-Chelated Zinc Nanoparticles From Pufferfish Skin on Zinc Bioavailability in Rats.

Small-molecular-weight collagen peptides (CPs) with high zinc-chelating ability were extracted from pufferfish skin. Chelation of CPs with zinc was performed to prepare novel CP-chelated zinc (CP-Zn) nanoparticles. CP-Zn nanoparticles were spherical, regular, and well dispersed with an average size of ∼100 nm. The zeta potential assay was used to explore the stability of CP-Zn nanoparticles. CP-Zn nanoparticles were much more stable in the pH range of 3-8. The structural properties of CP-Zn nanoparticles were characterized by matrix-assisted laser desorption-ionization time-of-flight mass spectrometry, Fourier transform infrared spectroscopy, and 1H nuclear magnetic resonance spectroscopy. The results indicated that CPs were chelated with Zn ions through the amino nitrogen and oxygen atoms from the carboxyl groups. Furthermore, the animal experiment results showed that CP-Zn nanoparticles were more effective in improving zinc bioavailability of Zn-deficient rats than zinc gluconate and zinc sulfate. The study demonstrated that CP-Zn nanoparticles were ideal for zinc supplementation.

A Facile Co-Deposition Approach to Construct Functionalized Graphene Quantum Dots Self-Cleaning Nanofiltration Membranes.

In this study, a novel photocatalytic self-cleaning nanofiltration (NF) membrane was fabricated by constructing aspartic acid-functionalized graphene quantum dots (AGQDs) into the polydopamine/polyethyleneimine (PDA/PEI) selective layer via the co-deposition method. The chemical composition, microstructure, and hydrophilicity of the prepared membranes were characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM), attenuated total reflection (ATR-FTIR), X-ray photoelectron spectroscopy (XPS), and water contact angle (WCA). Meanwhile, the effects of PEI molecular weight and AGQDs concentration on NF membrane structures and separation performance were systematically investigated. The photocatalytic self-cleaning performance of the PDA/PEI/AGQDs membrane was evaluated in terms of flux recovery rate. For constructing high-performance NF membranes, it is found that the optimal molecular weight of PEI is 10,000 Da, and the optimal concentration of AGQDs is 2000 ppm. The introduction of hydrophilic AGQDs formed a more hydrophilic and dense selective layer during the co-deposition process. Compared with the PDA/PEI membrane, the engineered PDA/PEI/AGQDs NF membrane has enhanced water flux (55.5 LMH·bar-1) and higher rejection (99.7 ± 0.3% for MB). In addition, the PDA/PEI/AGQDs membrane exhibits better photocatalytic self-cleaning performance over the PDA/PEI membrane (83% vs. 69%). Therefore, this study provides a facile approach to construct a self-cleaning NF membrane.

Constructing Positively Charged Thin-Film Nanocomposite Nanofiltration Membranes with Enhanced Performance.

Using polyethylenimine (PEI) as the aqueous reactive monomers, a positively charged thin-film nanocomposite (TFN) nanofiltration (NF) membrane with enhanced performance was developed by successfully incorporating graphene oxide (GO) into the active layer. The effects of GO concentrations on the surface roughness, water contact angle, water flux, salt rejection, heavy metal removals, antifouling property, and chlorine resistance of the TFN membranes were evaluated in depth. The addition of 20 ppm GO facilitated the formation of thin, smooth, and hydrophilic nanocomposite active layers. Thus, the TFN-PEI-GO-20 membrane showed the optimal water flux of 70.3 L·m-2·h-1 without a loss of salt rejection, which was 36.8% higher than the thin-film composite (TFC) blank membrane. More importantly, owing to the positively charged surfaces, both the TFC-PEI-blank and TFN-PEI-GO membranes exhibited excellent rejections toward various heavy metal ions including Zn2+, Cd2+, Cu2+, Ni2+, and Pb2+. Additionally, compared with the negatively charged polypiperazine amide NF membrane, both the TFC-PEI-blank and TFN-PEI-GO-20 membranes demonstrated superior antifouling performance toward the cationic surfactants and basic protein due to their hydrophilic, smooth, and positively charged surface. Moreover, the TFN-PEI-GO membranes presented the improved chlorine resistances with the increasing GO concentration.

A rapid and scalable integrated membrane separation process for purification of polysaccharides from Enteromorpha prolifera.

An integrated membrane separation process combining the tubular ceramic microfiltration (MF) membrane and the flat-sheet ultrafiltration (UF) membrane was developed to purify polysaccharides from Enteromorpha prolifera. The effects of membrane pore size, molecular weight cut-off (MWCO), transmembrane pressure (TMP) and adding-water multiples on membrane performance were in-depth studied. The results indicated that the optimal membrane pore size and TMP of the tubular ceramic MF process were found to be 1.2 µm and 0.225 MPa, and the optimal MWCO and TMP of the flat-sheet UF process were found to be 100 kDa and 0.3 MPa. The yields of polysaccharides were increased and optimized while the adding-water multiples was 1 during the diafiltration procedure. Furthermore, the water fluxes could be completely recovered using the specialized membrane cleaning methods, which ensured the reuse of membrane elements and satisfied the demands of industrial production. After purification by this integrated membrane separation process, the content of polysaccharides reached to 96.3%. The purified polysaccharides exhibited the superior moisture absorption and moisture retention properties compared to glycerol, polyethylene glycol (PEG) and luffa water.

A Novel Thin-Film Nanocomposite Nanofiltration Membrane by Incorporating 3D Hyperbranched Polymer Functionalized 2D Graphene Oxide.

In order to develop a high-performance thin-film nanocomposite (TFN) nanofiltration (NF) membrane, the functionalized graphene-based nanomaterial (GO-HBE-COOH) was synthesized by combining two-dimensional graphene oxide (GO) with a three-dimensional hyperbranched polymer, which was used as the novel nanofiller and successfully embedded into the polypiperazine-amide (PPA) active layers on polysulfone (PSU) substrates via interfacial polymerization (IP) process. The resultant NF membranes were characterized using ATR-FTIR, SEM, and AFM, while their performance was evaluated in terms of water flux, salt rejection, antifouling ability, and chlorine resistance. The influence of GO-HBE-COOH concentration on the morphologies, properties, and performance of TFN NF membranes was investigated. With the addition of 60 ppm GO-HBE-COOH, the TFN-GHC-60 NF membrane exhibited the optimal water flux without a sacrifice of the salt rejection. It was found that the introduction of GO-HBE-COOH nanosheets favored the formation of a thinner and smoother nanocomposite active layer with an enhanced hydrophilicity and negative charge. As a result, TFN NF membranes demonstrated a superior permeaselectivity, antifouling ability, and chlorine resistance over the conventional PPA thin-film composite (TFC) membranes.