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INSTRUMENTATION SCIENCE & TECHNOLOGY · 2020 · IF 1.418

High quality factor D-type fiber surface plasmon resonance (SPR) sensor based on the modification of gold nanoshells

Li-Ye Niu,Qi Wang,Wan-Ming Zhao,Jian-Ying Jing

A D-type optical fiber surface plasmon resonance (SPR) sensor based on gold film and Au nanoshells is described. The sensor has a smaller full width at half maximum (FWHM) and a higher quality factor. The influence of the coupling effect between the Au nanoshells and gold film with different internal and external diameter ratios on the sensor was investigated by the finite element method. The simulation results show that the coupling effect between the SPR of the gold film and the localized surface plasmon resonance (LSPR) of the Au nanoshells effectively improved the electric field strength of the sensing region. The refractive index measurements show that the sensitivity of the D-type fiber/gold film/Au nanoshell (50/40 AuNS) SPR sensor is 3064 nm/RIU, which is 993 nm/RIU higher than for the D-type fiber/gold film SPR sensor. The D-type fiber/gold film/Au nanoshell (50/40 AuNS) SPR sensor also provides good linearity with a value of 99.4%. The sensor reported in this paper can be used for reference in the development of high performance biosensors.

CAS / MDL: 1191-43-1
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POLYMER BULLETIN · 2020 ·Vol. 78 ·期 1 ·147-163 · IF 2.014

The crystallization behavior of poly(l-lactide)/poly(d-lactide) blends: effect of stirring time during solution mixing

Shao Jun,Xu Lanli,Pu Shouzhi,Hou Haoqing

Blending of poly( l -lactide) and poly( d -lactide) (PLLA, PDLA) results in the formation of poly(lactide) stereocomplex crystallites (SC). For the preparation method, numerous reports employed solution mixing and stirring to receive a product with uniform performance. However, the effect of stirring time during solution mixing on the subsequent crystallization behavior did not clear yet, and which is important for solution crystallization, casting and spinning. In this paper, linear PLLA and PDLA with various molecular weights were synthesized. The PLLA and PDLA solutions were mixed together and stirred for different times before casting. Results revealed that the structures of PLA SC and homochiral crystallites (HC) did not vary with change in the stirring time. More amount of content of SC with uniform structure and less amount of content of HC were produced in the specimens stirred for longer time. When the specimens crystallized either from the melt or from the melt-quenching, less amount of content of crystallites (total crystallinity of SC and HC) was produced and the melting temperature of SC and HC depressed in the specimens that were stirred for longer time. With the increase in molecular weights, the effect of stirring time on the crystallization behaviors declined. This investigation provides a route to tailor the crystallization behavior of PLLA/PDLA specimens.

CAS / MDL: 67-63-0 301-10-0
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BIORESOURCE TECHNOLOGY · 2019 · IF 6.669

Functionalized polyhydroxyalkanoate nano-beads as a stable biocatalyst for cost-effective production of the rare sugar d-allulose

Ganqiao Ran,Dan Tan,Jiping Zhao,Fan Fan,Qiang Zhang,Xingjuan Wu,Peiyao Fan,Xinlei Fang,Xiaoyun Lu

d -Allulose is a promising low-calorie sweetener especially for diabetes and obesity patients. The functionalized polyhydroxyalkanoate (PHA) nano-beads decorated with d -tagatose 3-epimerase (DTE) was produced in recombinant endotoxin-free ClearColi , whereby the expression, purification, and immobilization of the active DTE were efficiently combined into one step. The immobilized DTE exhibited remarkable enzyme activity of 649.3 U/g beads and extremely high stability at a harsh working condition (pH 7.0–8.0, 65 °C). When DTE-PHA beads were subjected to enzymatic synthesis of d -allulose, a maximum conversion rate of 33% can be achieved at pH 7.0 and 65 °C for 3 h, and DTE-PHA beads retained about 80% of its initial activity after 8 continuous cycles. Moreover, the d -allulose/ d -fructose binary mixture can be simply separated by a single cation exchange resin-equipped chromatography. Taken together, DTE-PHA beads are promising and robust nano-biocatalysts that will remarkably simplify the production procedures of d -allulose, contributing to its cost-effective production.

CAS / MDL: 6104-59-2
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COLLOIDS AND SURFACES B-BIOINTERFACES · 2019 · IF 3.973

Injected laquinimod D-α-tocopheryl polyethylene glycol-1000 succinate polymeric micelles for the treatment of inflammatory bowel disease

Lifen Wang,Pengpeng Xue,Mengqi Tong,Rui Chen,Waigeng Yang,Deli ZhuGe,Jiandong Yuan,Qing Yao,Yingzheng Zhao,Helin Xu

Inflammatory bowel diseases (IBDs) are chronic relapsing disorders of the gastrointestinal tract characterized pathologically by intestinal inflammation and epithelial injury. Laquinimod (LAQ), a poorly water-soluble compound, was proved to be effective for colitis remission at low dose of 0.5 mg/kg in patients with Crohn’s disease. Due to its extremely low solubility in water, it was difficult to develop an injectable liquid dosage form. Herein, D-α-Tocopheryl polyethylene glycol-1000 succinate (TPGS) polymeric micelles were developed as a delivery vehicle of LAQ for the management of inflammatory bowel disease. Using the LAQ/TPGS ratio of 1:100, LAQ-loaded micelles were successfully prepared by thin-film dispersion method. The solubility of LAQ in water was significantly increased from 10.5 μg/mL in pure water to 500 μg/mL in TPGS micelles. LAQ-loaded micelles of TPGS exhibited the fine particle size of 34.6 nm and Zeta potential of -0.67 mV. Moreover, the good stability of LAQ-loaded micelles in physiology-mimicking medium was confirmed by detecting their particle size, zeta potential and leakage of the loading drug. Therapeutic effect of LAQ-loaded micelles on DSS-induced mice was proved by detecting DAI score, colon length and loss of body weight. Moreover, the morphology and colonic mucosal barrier of the injured colon of DSS-induced mice was largely recovered after treatment with LAQ-loaded micelles. Meanwhile, the inflammation of colitis colon was also obviously alleviated by LAQ-loaded micelles. Conclusively, polymeric micelles of TPGS may be a promising delivery vehicle of LAQ for the management of inflammatory bowel disease.

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Food Science & Nutrition · 2019 ·Vol. 7 ·期 6 ·2043-2049 · IF 1.747

Effects of power ultrasound on the activity and structure of β-D-glucosidase with potentially aroma-enhancing capability

Yujing Sun,Li Zeng,Yuanzhong Xue,Tianbao Yang,Zongming Cheng,Peilong Sun

β- d -glucosidase can release aroma precursors to improve the flavor of plant food, but the hydrolysis efficiency of the enzyme is low; the purpose of this study was to improve the enzyme activity using ultrasound. The effects of ultrasound parameters on β- d -glucosidase activity were investigated, and the respective structures of enzyme activated and enzyme inhibited were further analyzed. Low temperature (20–45°C), low ultrasonic intensity (<181.53 W/cm 2 ), and short treatment time (<15 min) led to the activation of β- d -glucosidase, whereas high temperature (45–60°C), high ultrasonic intensity (>181.53 W/cm 2 ), and long treatment time (>15 min) led to its inhibition. Application of ultrasound lowered the optimum temperature for β- d -glucosidase activity from 50 to 40°C. Ultrasound did not change the primary structures of the enzyme, but changed the secondary structures. When ultrasound activated β- d -glucosidase, the α-helix contents were increased, the β-fold and irregular coil content were reduced. When ultrasound inhibited β- d -glucosidase, the contents of β-folds were increased, the α-helix and irregular coil contents were reduced.. In summary, activation or inhibition of β- d -glucosidase under ultrasound was determined by the ultrasound conditions. This study suggests that ultrasound combined with β-D-glucosidase can be used in aroma-enhancing.

CAS / MDL: 3150-24-1
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APPLIED MICROBIOLOGY AND BIOTECHNOLOGY · 2018 ·Vol. 102 ·期 14 ·6039-6046 · IF 3.34

A highly active pantothenate synthetase from Corynebacterium glutamicum enables the production of d-pantothenic acid with high productivity

Tigu Fitsum,Zhang Junli,Liu Guoxia,Cai Zhen,Li Yin

d -Pantothenic acid (vitamin B 5 ) has wide applications in the feed, food, chemical, and pharmaceutical industries. Its biological production routes which employ pantothenate synthetase (PS) as the key enzyme are attractive since they avoid the tedious and time-consuming optical resolution process. However, little data is available on the activity and kinetics of this enzyme, hampering the rational selection of an efficient enzyme for the biological production of d -pantothenic acid. In this study, six phylogenetically distant PS-encoding genes, from Escherichia coli , Corynebacterium glutamicum , Bacillus subtilis , Bacillus thuringiensis , Bacillus cereus , and Enterobacter cloacae , were expressed in E. coli . The PS from C. glutamicum exhibited a specific activity of 205.1 U/mg and a turnover number of 127.6 s -1 , which to our best knowledge are the highest values ever reported. The addition of substrates ( d -pantoic acid and β-alanine) to the E. coli strain harboring this enzyme during the early log phase of fermentation resulted in the production of 97.1 g/L of d -pantothenic acid within 32 h, corresponding to a conversion yield of 99.1% and a productivity of 3.0 g/L/h. To the best of our knowledge, this is the highest productivity reported to date.

CAS / MDL: 50-99-7
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ANALYTICAL CHEMISTRY · 2018 · IF 6.042

Phospholipid-Tailored Titanium Carbide Nanosheets as a Novel Fluorescent Nanoprobe for Activity Assay and Imaging of Phospholipase D

Xiaohua Zhu,Lin Fan,Shigong Wang,Chunyang Lei,Yan Huang,Zhou Nie,Shouzhuo Yao

As one of the emerging inorganic graphene analogues, two-dimensional titanium carbide (Ti3C2) nanosheets have attracted extensive attention in recent years because of their remarkable structural and electronic properties. Herein, a sensitive and selective nanoprobe to fluorescently probe phospholipase D activity was developed on the basis of an ultrathin Ti3C2 nanosheets-mediated fluorescence quenching effect. Ultrathin Ti3C2 nanosheets with ∼1.3 nm in thickness were synthesized from bulk Ti3AlC2 powder by a two-step exfoliation procedure and further modified by a natural phospholipid that is doped with rhodamine B-labeled phospholipid (RhB-PL-Ti3C2). The close proximity between RhB and Ti3C2 leads to efficient fluorescence quenching (>95%) of RhB by energy transfer. Phospholipase D-catalyzed lipolysis of the phosphodiester bond in RhB-PL results in RhB moving away from the surface of Ti3C2 nanosheets and subsequent fluorescence recovery of RhB, providing a fluorescent “switch-on” assay for the phospholipase D activity. The proposed nanoprobe was successfully applied to quantitatively determine phospholipase D activity with a low limit of detection (0.10 U L–1) and to measure its inhibition. Moreover, in situ monitoring and imaging the activity of phospholipase D in living cells were achieved using this biocompatible nanoprobe. These results reveal that Ti3C2 nanosheets-based probes exhibit great potential in fluorometric assay and clinical diagnostic applications.

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NEUROTOXICOLOGY · 2018 · IF 3.076

Saikosaponin d causes apoptotic death of cultured neocortical neurons by increasing membrane permeability and elevating intracellular Ca2+ concentration

Jing Zheng,Juan Chen,Xiaohan Zou,Fang Zhao,Mengqi Guo,Hongbo Wang,Tian Zhang,Chunlei Zhang,Wei Feng,Isaac N. Pessah,Zhengyu Cao

Saikosaponins (SSs) are a class of naturally occurring oleanane-type triterpenoid saponins found in Radix bupleuri that has been widely used in traditional Chinese medicine. As the main active principals of Radix bupleuri , SSs have been shown to suppress mouse motor activity, impair learning and memory, and decrease hippocampal neurogenesis. In the present study, we investigated the effect of five SSs (SSa, SSb1, SSb2, SSc, and SSd) on neuronal viability and the underlying mechanisms in cultured murine neocortical neurons. We demonstrate that SSa, SSb1 and SSd produce concentration-dependent apoptotic neuronal death and induce robust increase in intracellular Ca 2+ concentration ([Ca 2+ ] i ) at low micromolar concentrations with a rank order of SSd > SSa > SSb1, whereas SSb2 and SSc have no detectable effect on both neuronal survival and [Ca 2+ ] i . Mechanistically, SSd-induced elevation in [Ca 2+ ] i is the primary result of enhanced extracellular Ca 2+ influx, which likely triggers Ca 2+ -induced Ca 2+ release through ryanodine receptor activation, but not SERCA inhibition. SSd-induced Ca 2+ entry occurs through a non-selective mechanism since blockers of major neuronal Ca 2+ entry pathways, including L-type Ca 2+ channel, NMDA receptor, AMPA receptor, Na + -Ca 2+ exchanger, and TRPV1, all failed to attenuate the Ca 2+ response to SSd. Further studies demonstrate that SSd increases calcein efflux and induces an inward current in neocortical neurons. Together, these data demonstrate that SSd elevates [Ca 2+ ] i due to its ability to increase membrane permeability, likely by forming pores in the surface of membrane, which leads to massive Ca 2+ influx and apoptotic neuronal death in neocortical neurons.

CAS / MDL: 148504-34-1
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MATERIALS SCIENCE FORUM · 2019 · IF 0

Facile Fabrication of N-Methyl-D-Glucamine Grafted HDPE Particle as Adsorbent for Boron Removal from Aqueous Solution

Ji Fu Du,Zhen Dong,Xin Yang,Long Zhao

Glycidyl methacrylate (GMA) was grafted onto the surface of HDPE particles by radiation grafting and emulsion graft copolymerization. And subsequent ring-opening reaction of expoxy groups in poly-GMA graft chains with N-methylglucamine (NMG) was conducted to synthesis the boron adsorbent. The synthesis condition (radiation dose and NMG concentration) was optimized and characterized by IR and SEM. Adsorption behaviors of the boron adsorbent for boron removal presented that adsorption kinetics was well described by pseudo-second-order kinetic mode. The adsorption isothermal was well fitted with both Langmuir and Freundlich isotherm models. The adsorption capacity for boron reached 15.63 mg/g at optimal pH 8. Dynamic experiment revealed that boron could be efficiently adsorbed by the boron adsorbent and fully desorbed using 13 BV of 1 mol/L HCl.

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JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY · 2019 · IF 3.571

d-chiro-Inositol Ameliorates High Fat Diet-Induced Hepatic Steatosis and Insulin Resistance via PKCε-PI3K/AKT Pathway

Feier Cheng,Lin Han,Yao Xiao,Chuanying Pan,Yunlong Li,Xinhui Ge,Yao Zhang,Shaoqing Yan,Min Wang

d-chiro-Inositol (DCI) is a biologically active component found in tartary buckwheat, which can reduce hyperglycemia and ameliorate insulin resistance. However, the mechanism underlying the antidiabetic effects of DCI remains largely unclear. This study investigated the effects and underlying molecular mechanisms of DCI on hepatic gluconeogenesis in mice fed a high fat diet and saturated palmitic acid-treated hepatocytes. DCI attenuated free fatty acid uptake by the liver via lipid trafficking inhibition, reduced diacylglycerol deposition, and hepatic PKCε translocation. Thus, DCI could improve insulin sensitivity by suppressing hepatic gluconeogenesis. Subsequent analyses revealed that DCI decreased hepatic glucose output and the expression levels of PEPCK and G6 Pase in insulin resistant mice through PKCε-IRS/PI3K/AKT signaling pathway. Likewise, such effects of DCI were confirmed in HepG2 cells with palmitate-induced insulin resistance. These findings indicate a novel pathway by which DCI prevents hepatic gluconeogenesis, reduces lipid deposition, and ameliorates insulin resistance via regulation of PKCε-PI3K/AKT axis.

CAS / MDL: 50-99-7
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Journal of Functional Foods · 2019 · IF 3.197

Kinetic study of d-limonene release from finger citron essential oil loaded nanoemulsions during simulated digestion in vitro

Ze-hua Li,Ming Cai,Kai Yang,Pei-long Sun

Nanoemulsion loading finger citron essential oil (FCEO) can maintain bioactivities of FCEO and increase its water solubility. In this study, stability of FCEO nanoemulsions during digestion in vitro were evaluated and the release kinetics of d-limonene (the main component in the oil) were developed. Compared with free oil released to maximum for 6 min, all nanoemulsions kept sustainably releasing for 300 min or longer. Droplet size of the nanoemulsions increased from 10–18 nm of initial to 105–1106 nm after digestion, indicating coalescence or aggregation occurred. Zero-order, Hixcon-Crowell, Higuchi, Ritger-Peppas and Niebergull models were used to describe the release kinetics. The results showed zero-order and Ritger-Peppas models were the best fit models at mouth and intestinal stage, respectively. Both zero-order and Higuchi models were appropriate at gastric stage. This study could demonstrate the digestion mechanisms of FCEO loaded nanoemulsion and facilitate the design of hydrophobic nutraceuticals delivery systems in food industry.

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Polymer Chemistry · 2019 ·Vol. 10 ·期 21 ·2706-2715 · IF 4.76

Synthesis, properties and photo-responsive behavior of luminescent side chain polymers containing D–π-A α-cyanostilbene units

Yongjie Yuan,Lifang He,Jindi Li,Hailiang Zhang

A series of luminescent side chain polymers containing a D–π-A structure and different flexible spacer lengths, namely, poly[(Z)-ω-(4-(1-cyano-2-(4-cyanophenyl)vinyl)phenoxy)alkyl methacrylate]s (PMmPVPCN, m = 2, 4, 6, 8), were successfully prepared. With the combination of aggregation-induced emission enhancement (AIEE) luminogens and mesogens, the resultant polymers are expected to possess both liquid crystal characteristics and AIEE characteristics. The phase structure of PMmPVPCN was explored by differential scanning calorimetry (DSC), polarized optical microscopy (POM), and one-dimensional wide-angle X-ray diffraction (1D WAXD). Photophysical properties of PMmPVPCN were studied by UV spectra and fluorescence spectra. Test results suggested that the phase structure of PMmPVPCN transformed from the amorphous phase (PMmPVPCN, m = 2, 4) to the nematic phase (PMmPVPCN, m = 6, 8) with the increase of polymer spacer length. All the synthetic monomers and polymers exhibited AIEE properties and the luminescence behavior of PMmPVPCN was associated with their chemical structure. The solid fluorescence quantum yields of PMmPVPCN increased from 22.4% to 42.7% with increasing spacer length. The polymer films also showed reversible fluorescence photo-responsive properties. The emission color and the emission intensity of polymer films changed when exposed to a 365 nm UV lamp. The change process was reversible and they could turn back to their original state when irradiated with a 254 nm UV lamp or heated at higher temperature.

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