Yumin Yang

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Organization: Nantong University
Department: Jiangsu Key Laboratory of Neuroregeneration
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Co-reporter:Yinxin Zhao, Guicai Li, Yumin Yang
Journal of Controlled Release 2017 Volume 259(Volume 259) pp:
Publication Date(Web):10 August 2017
DOI:10.1016/j.jconrel.2017.03.101
Co-reporter:Yahong Zhao, Yongjun Wang, Jiahuan Gong, Liu Yang, Changmei Niu, Xuejun Ni, Yaling Wang, Su Peng, Xiaosong Gu, Cheng Sun, Yumin Yang
Biomaterials 2017 Volume 134(Volume 134) pp:
Publication Date(Web):1 July 2017
DOI:10.1016/j.biomaterials.2017.02.026
Chitosan-based artificial nerve grafts have been widely employed to repair peripheral nerve defects. Our previous study has shown that chitosan constructed nerve graft not only provides suitable scaffolds for nerve regeneration, its degradation products, chitooligosaccharides (COS), also promote nerve repair. However, the involved mechanisms are still not fully elucidated. In the present study, we observed that pro-inflammatory cytokines, as well as macrophage infiltration, were transiently up-regulated in the injured sciatic nerves which were bridged with silicon tubes filled with COS. Based upon transcriptome analysis, the axis of miR-327/CCL2 in Schwann cells (SCs) was identified as a potential target of COS. The following experiments have confirmed that COS stimulate CCL2 expression by down-regulating miR-327 in SCs. Consequently, the resulting CCL2 induces macrophage migration at injury sites to re-construct microenvironments and thus facilitates nerve regeneration. Collectively, our data provide a theoretical basis for the clinical application of chitosan-based grafts in peripheral nerve regeneration.
Co-reporter:Xiaoyu Liu;Su Peng;Yahong Zhao;Tingting Zhao;Meihong Wang
Molecular Neurobiology 2017 Volume 54( Issue 5) pp:3554-3564
Publication Date(Web):18 May 2016
DOI:10.1007/s12035-016-9913-3
The process of Schwann cells (SCs) forming a sheath around axons is termed as myelination, which plays a pivotal role for proper physiological function in the peripheral nervous system (PNS). The molecular mechanisms regulating SC myelination in the PNS remain to be elucidated. Here, we show that AMP-activated protein kinase (AMPK) in sciatic nerves was gradually decreased during the PNS myelination process. Pharmacological interventions showed that activation of AMPK by AICAR attenuated myelin gene expression in SCs, whereas inhibition of AMPK by Compound C (ComC) or AMPKα1 knockdown stimulated myelin gene expression. Following experiments revealed that c-Jun, a negative modulator of PNS myelination, was activated by AMPK in SCs. The application of ComC in newborn rats markedly downregulated c-Jun expression in sciatic nerves. The lipid and protein synthesis in sciatic nerves was greatly potentiated by ComC. As a consequence, myelin gene expression in sciatic nerves, as well as myelin sheath thickness, were promoted in the ComC-treated rats. All together, our data identify that AMPK is an important negative regulator of Schwann cell myelination in the PNS, and this regulation role may rely on c-Jun activation.
Co-reporter:Luzhong Zhang, Guicai Li, Ming Gao, Xin Liu, Bing Ji, Ruheng Hua, Youlang Zhou, Yumin Yang
Colloids and Surfaces B: Biointerfaces 2016 Volume 144() pp:81-89
Publication Date(Web):1 August 2016
DOI:10.1016/j.colsurfb.2016.03.077
•PH-dependent RGD conjugated EPB loaded inulin-ibuprofen nanoparticles were fabricated.•Nanoparticles increased the cellular uptake and cytotoxicity.•Nanoparticles show superior tumor growth inhibition and reduced systemic toxicity.•RGD conjugated EPB loaded inulin-ibuprofen nanoparticles have a great potential in chemo-therapy.Recently, chemotherapy-based polymeric nanoparticles have been extensively investigated for solid tumor treatment. Tumor targeted nanoparticles demonstrated great potential for improved accumulation in the tumor tissue, superior anticancer activity and reduced side effects. Thus, inulin-ibuprofen polymer was synthesized by esterification between inulin and ibuprofen, and RGD targeted epirubicin (EPB) loaded nanoparticles were prepared by the self-assembly of inulin-ibuprofen polymer and in situ encapsulation of EPB. RGD conjugated EPB loaded nanoparticles were characterized by dynamic light scattering (DLS) and transmission electron microscope (TEM). The EPB release from the nanoparticles showed pH-dependent profile and accelerated by the decreased pH value, which would favor the effective drug delivery in vivo. Intracellular uptake analysis suggested that RGD conjugated nanoparticles could be easily internalized by the cancer cells. In vitro cytotoxicity revealed that RGD conjugated EPB loaded nanoparticles exhibited the better antitumor efficacy compared with non-conjugated nanoparticles. More importantly, RGD conjugated EPB loaded nanoparticles showed superior anticancer effects and reduced toxicity than free EPB and non-conjugated nanoparticles by in vivo antitumor activity, EPB biodistribution and histology analysis.RGD conjugated EPB loaded inulin-ibuprofen nanoparticles were prepared to enhance tumor accumulation and reduce the systemic toxicity.
Co-reporter:Guicai Li, Yinxin Zhao, Luzhong Zhang, Ming Gao, Yan Kong, Yumin Yang
Colloids and Surfaces B: Biointerfaces 2016 Volume 143() pp:547-556
Publication Date(Web):1 July 2016
DOI:10.1016/j.colsurfb.2016.03.079
•GO/PAM composite hydrogel was successfully prepared by in-situ radical polymerization.•GO could obviously change the physical and chemical properties of PAM hydrogel.•GO with a suitable concentration could effectively promote Schwann cell growth.•The study will be beneficial and helpful for designing new peripheral nerve implants.Various hydrogel materials have been developed for improving the regeneration of peripheral nerve. Among which the graphene related hydrogels with excellent mechanical properties have attracted great attention. However, the effect of these hydrogels on peripheral nerve regeneration is still unclear. In the present study, the graphene oxide/polyacrylamide (GO/PAM) composite hydrogels were fabricated by in-situ free radical polymerization. The morphology, wettability, composition, swelling ratio, mechanical property and degradation behavior of the prepared GO/PAM composite hydrogels were separately characterized. The effect of GO/PAM hydrogel on the attachment and proliferation of Schwann cells was evaluated. Moreover, the release of biofactors by Schwann cells and adsorption of matrix proteins were further measured. The results showed that the color of the hydrogel became darker with the increased GO concentration, while the surface pore structure also displayed large variation when GO concentration was increased. The hydrophobicity and mechanical properties of hydrogel were increased with the ascending GO concentration. In addition, the variation of GO concentration displayed no obvious influence on the degradation of the composite hydrogel in different medium. The GO/PAM composite hydrogel with 0.4% GO (G0.4) could effectively enhance the attachment and proliferation of Schwann cells. Furthermore, the cells on G0.4 hydrogel displayed higher biofactors release and larger matrix adsorption than other samples. The results demonstrated that GO with suitable concentration in PAM hydrogel could effectively promote Schwann cell growth. The study may provide an important experimental basis for the design and development of new nerve grafts with potential application for peripheral nerve regeneration.Sketchmap of the preparation of GO/PAM composite hydrogel.
Co-reporter:Luzhong Zhang;Fan Liu;Guicai Li;Youlang Zhou
Journal of Pharmaceutical Sciences 2015 Volume 104( Issue 12) pp:4185-4196
Publication Date(Web):
DOI:10.1002/jps.24649

One major obstacle in the application of drug delivery systems for cancer chemotherapy is their poor penetration in tumor tissues. Conjugating active ligand moieties to the surface of nanoparticles may be a promising approach for enhancing the tumor accumulation and penetration of nanoparticles. Herein, the cell-penetrating peptide twin-arginine translocation (Tat)-conjugated epirubicin-loaded poly(lactic-glycolic acid) nanoparticles were prepared to achieve deep tumor penetration. The morphology and size of nanoparticles were characterized by scanning electron microscopy and dynamic light scattering, and the biological behaviors of nanoparticles were evaluated. It is demonstrated that Tat-conjugated nanoparticles have a significant improvement in antitumor activity and biodistribution compared with nonconjugated nanoparticles. Importantly, Tat conjugated on the surface of nanoparticles could facilitate the encapsulated drug penetration into deeper tumor tissue. Additionally, Tat-conjugated nanoparticles have good biocompatibility, as demonstrated by hemolytic tests, in vitro cytotoxicity, and histology study. These results suggested that the Tat-conjugated nanoparticles, as a powerful delivery system for chemotherapeutic drug, would have a promising application in human cancer therapy. © 2015 Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 104:4185–4196, 2015

Co-reporter:Guicai Li, Luzhong Zhang, Yumin Yang
Colloids and Surfaces B: Biointerfaces 2015 Volume 134() pp:413-422
Publication Date(Web):1 October 2015
DOI:10.1016/j.colsurfb.2015.07.012
•Chitosan scaffolds are successfully tailored by oppositely charged biomolecules.•APTE increased charge densities of chitosan scaffolds while heparin decreased.•Scaffolds with negative charged heparin can obviously promote Schwann cells growth.•Charge tailored chitosan scaffolds show potential for peripheral nerve regeneration.•The study will be beneficial and helpful for designing new peripheral nerve implants.Chitosan has been well known for promoting peripheral nerve regeneration, however, its effect is still not as good as that of autografts. In this study, the feasibility of using negatively charged heparin and positively charged γ-aminopropyltriethoxysilane (APTE) treatment as biocompatible modification of lyophilized porous chitosanscaffolds was evaluated. The morphology of the prepared chitosan scaffolds as a function of treatment with different charged molecules showed no significant differences, while a skin-like surface was observed for the scaffolds modified with high APTE concentration and heparin. The quantitative and qualitative characterization of heparin and amino densities by Toluidine Blue O (TBO) and Acid Orange (AO) assays confirmed the successful immobilization of heparin and APTE on the chitosan scaffolds. The measurement of surface charge densities indicated that the scaffolds treated with APTE showed increased charge densities while heparin decreased the cationic charge density. Moreover, the fabricated charge processed chitosan scaffolds were stable after immersion in phosphate buffer saline for more than ten days. Further on, the chitosan scaffolds processed with 2 mg/mL heparin did facilitate the attachment, proliferation and maintain the biological function of Schwann cells in vitro. The study demonstrates that chitosan scaffolds treated with suitable heparin concentration provides an effective selection for biomaterials surface modification and shows great potential for the application in peripheral nerve regeneration.Sketchmap of the preparation of positive and negative charge modified chitosan scaffolds by APTE and Heparin, respectively.
Co-reporter:Guicai Li;Xueying Zhao;Luzhong Zhang;Caiping Wang;Yunwei Shi
Macromolecular Bioscience 2014 Volume 14( Issue 8) pp:1067-1075
Publication Date(Web):
DOI:10.1002/mabi.201400098

To address the effect of chitosan micropatterning on nerve regeneration, two sizes of parallel microstripes of chitosan are fabricated on the surface of coverslips using a micromodeling method. The morphology of the prepared polydimethylsiloxane stamps and chitosan micropatterning is observed by scanning electron microscopy and the wettability of the prepared micropatterning is evaluated using water contact-angle measurements. Schwann cell (SC) culture is used to evaluate the effect of chitosan micropatterning on cell behavior. The results show that the stripe-like chitosan micropatterning can be successfully fabricated on coverslip surfaces. SCs on 30/30 μm chitosan micropatterning shows the most obvious cell orientation. Moreover, the secretion of nerve growth factor by SCs indicate that the chitosan micropatterning has no negative influence on the normal physiological function of the cells. Thus, the study suggests that chitosan micropatterning can induce and regulate the growth of SCs well, which may have potential application in peripheral nerve regeneration.

Co-reporter:Guicai Li;Xueying Zhao;Luzhong Zhang;Caiping Wang;Yunwei Shi
Macromolecular Bioscience 2014 Volume 14( Issue 8) pp:
Publication Date(Web):
DOI:10.1002/mabi.201470028
Co-reporter:Guicai Li, Luzhong Zhang, Caiping Wang, Xueying Zhao, Changlai Zhu, Yanhong Zheng, Yaling Wang, Yahong Zhao, Yumin Yang
Carbohydrate Polymers 2014 Volume 101() pp:718-726
Publication Date(Web):30 January 2014
DOI:10.1016/j.carbpol.2013.09.064
•APTE silanized chitosan scaffolds were successfully prepared.•Silanization treatment changed the morphology of original CS scaffolds.•Silanization treatment increased the porosity while reduced the swelling ratio of CS scaffolds.•The silanized CS scaffolds possessed improved stability in PBS and HCl.•The silanized scaffolds could promote the proliferation of Schwann cells.The aim of this study was to evaluate the feasibility of using 3-aminopropyltriethoxysilane (APTE) silanization treatment for modification and biocompatibility of lyophilized chitosan porous scaffolds. The process is beneficial for biomaterial development due to its low toxicity and simplicity. The silanization treatment with low APTE concentration showed no significant influence on the morphology of chitosan scaffolds, while a skin-like surface was observed for the silanized scaffolds treated with high APTE concentration. The porosity and surface amino densities were increased after silanization whereas the swelling ratio was reduced, and the degradation ratio in PBS and anti-acid degradation properties of the silanized chitosan scaffolds were significantly improved. The in vitro Schwann cells culture demonstrated that the silanized scaffolds with 8% APTE could obviously facilitate the attachment and proliferation of Schwann cells, indicating great potential for the application in peripheral nerve regeneration.
Co-reporter:Luzhong Zhang, Yue Li, Caiping Wang, Guicai Li, Yahong Zhao, Yumin Yang
Materials Science and Engineering: C 2014 Volume 42() pp:111-115
Publication Date(Web):1 September 2014
DOI:10.1016/j.msec.2014.05.025
•Methylprednisolone loaded nanoparticles was prepared for drug delivery.•In vitro cytotoxicity tests revealed the nanoparticles have good biocompatibility.•Nanoparticles would have great potential in synergetic effect treatment for spinal cord injury.Ibuprofen modified inulin was synthesized through a direct esterification linkage in which the in situ activation of the carboxylic acid with N,N′-carbonyldiimidazole was carried out. The critical aggregation concentration of the ibuprofen modified inulin was determined by using pyrene as the fluorescence probe. Methylprednisolone loaded nanoparticles were prepared by the self-assembly of the ibuprofen modified inulin copolymer and methylprednisolone. In vitro release of the methylprednisolone and the cytotoxicity of the methylprednisolone loaded nanoparticles against RSC-96 cells were evaluated. Since the ibuprofen and methylprednisolone could stimulate a significant neurite growth and diminish the human neurological deficits after the spinal cord injury, the methylprednisolone loaded nanoparticles based on the ibuprofen modified inulin copolymer may have a great potential in the synergetic effect treatment for spinal cord injury.
Co-reporter:Guicai Li, Xueying Zhao, Weixin Zhao, Luzhong Zhang, Caiping Wang, Maorong Jiang, Xiaosong Gu, Yumin Yang
Biomaterials 2014 35(30) pp: 8503-8513
Publication Date(Web):
DOI:10.1016/j.biomaterials.2014.05.093
Co-reporter:Yun Gu, Jianbin Zhu, Chengbin Xue, Zhenmeiyu Li, Fei Ding, Yumin Yang, Xiaosong Gu
Biomaterials 2014 35(7) pp: 2253-2263
Publication Date(Web):
DOI:10.1016/j.biomaterials.2013.11.087
Co-reporter:LuZhong Zhang;YouLang Zhou;GuiCai Li;YaHong Zhao
Science China Life Sciences 2014 Volume 57( Issue 2) pp:256-262
Publication Date(Web):2014 February
DOI:10.1007/s11427-014-4606-5
Peripheral nerve functional recovery after nerve injury generally requires multiple growth factors by synergistic effect. However, the optical combination of multiple synergistic growth factors for axonal regeneration has been scarcely considered up to now. Meanwhile, the use of growth factors in promoting nerve regeneration was limited by its short biological half-life in vivo, its vulnerability to structure disruption or hydrolyzation, leading to loss of bioactivity. Herein, a novel polymeric nanoparticle delivery system composed of heparin and ɛ-poly-L-lysine (PL) was prepared for control release of nerve growth factor (NGF) and basic fibroblast growth factor (bFGF). The nanoparticles were synthesized by polyelectrolyte complexation in aqueous solution at room temperature, followed by cross-linking with biological genipin. The obtained nanoparticles had a spherical shape, with a mean diameter of about 246 nm, and high growth factors encapsulation efficiency as well as good stability. NGF and bFGF were encapsulated in the nanoparticles and showed a continuous and slow release behavior in vitro. The bioactivities of the released growth factors were evaluated, and exhibited the synergistic effect. The controlled release of the dual synergistic growth factors would improve the treatment of peripheral nerve injury to mimic the natural cellular microenvironments.
Co-reporter:Yahong Zhao;Yong Ling;Jing Zhao;Ying Yuan;Yibin Guo;Qiong Liu;Bingxin Wu;Zuoyou Ding
Archiv der Pharmazie 2013 Volume 346( Issue 4) pp:300-307
Publication Date(Web):
DOI:10.1002/ardp.201200444

Abstract

Salidroside is a natural product isolated from Rhodiola rosea L. which possesses a wide range of biological activities, especially neuroprotective effects in the treatment of ischemic stroke. In an attempt to improve its neuroprotective effects, a series of novel salidroside analogues were synthesized and their neuroprotective activities were evaluated against the glucose and serum depletion-induced cell death in differentiated PC12 cells. Most target compounds displayed protective effects on the cell viability, especially for compound 6, which had a great potency superior to salidroside. MTT assay and Hoechst 33342 staining collectively showed that pretreatment with 6 attenuated cell viability loss and reduced apoptotic death in cultured PC12 cells with glucose and serum depletion. And its neuroprotective effects might be associated with the increase of the apoptosis-related protein Bcl-2/Bax expression ratio, and also with the inhibition of caspase-3 activation. Therefore, our new findings may provide potentially important information for further development of salidroside analogues and lay the basis for further studies on the cerebral ischemic stroke and neurodegenerative diseases for human clinical treatment.

Co-reporter:Yin Guibo;Zhao Qing;Zhao Yahong;Yuan Yin;Yang Yumin
Journal of Applied Polymer Science 2013 Volume 128( Issue 2) pp:1061-1069
Publication Date(Web):
DOI:10.1002/app.38211

Abstract

In this article, polyamide (PA) 6 was dissolved in 98 wt % formic acids with a concentration of 13 wt %, and then the electrospun PA 6 nanofiber membranes were prepared. The filtration potential of the nanofiber membranes were firstly analyzed based on the scanning electron microscope images and pore size measurements, and then the effects of thermal treatment on the dimensional stability were studied. Subsequently, the continuous production process based on the above experiments and the deposition areas of the nanofibers on the collecting meshes was designed. Finally, the mechanical properties and the filtration performances of the electrospun PA 6 nanofiber membranes were assessed. The results showed the membranes with a thickness of 71 μm (electrospinning for 15 min) had good filtration potential for the microparticles with 0.3 μm diameter. After being treated by tension and relaxation heat setting, the membranes demonstrated excellent dimensional stability, the breaking tenacity, and the elongation reached 4.71 ± 1.66 MPa and (69.97 ± 6.56)%, respectively. The permeability decreased with the increase of the membranes thickness. However, the permeability of membranes with (72.9 ± 1.04) μm thickness still maintained 516 L/m2 s, and the actual filtration efficiency of 0.3 μm particles reached 99.98%. The above results showed that the membranes fabricated by the continuous production process could meet the demands of high efficiency filtration and provide a reference for the industrial use of electrospun nanofiber membranes. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013

Co-reporter:Youlang Zhou, Luzhong Zhang, Weixin Zhao, Yafang Wu, Changlai Zhu, Yumin Yang
Biomaterials 2013 34(33) pp: 8269-8278
Publication Date(Web):
DOI:10.1016/j.biomaterials.2013.07.072
Co-reporter:Luzhong Zhang, Sufeng Dou, Yan Li, Ying Yuan, Yawei Ji, Yaling Wang, Yumin Yang
Materials Science and Engineering: C 2013 Volume 33(Issue 5) pp:2626-2631
Publication Date(Web):1 July 2013
DOI:10.1016/j.msec.2013.02.024
The films of poly(glycolic acid) grafted chitosan were prepared without using a catalyst to improve the degradable property of chitosan. The films were characterized by Fourier transform-infrared spectroscopy and X-ray photoelectron spectroscopy (XPS). The degradation of the poly(glycolic acid) grafted chitosan films were investigated in the lysozyme solution. In vitro degradation tests revealed that the degradation rate of poly(glycolic acid) grafted chitosan films increased dramatically compared with chitosan. The degradation rate of poly(glycolic acid) grafted chitosan films gradually increased with the increasing of the molar ratio of glycolic acid to chitosan. Additionally, the poly(glycolic acid) grafted chitosan films have good biocompatibility, as demonstrated by in vitro cytotoxicity of the extraction fluids. The biocompatible and biodegradable poly(glycolic acid) grafted chitosan would be an effective material with controllable degradation rate to meet the diverse needs in biomedical fields.Highlights► Chitosan-g-poly(glycolic acid) copolymer was prepared without using a catalyst. ► Degradation rate of copolymer increased dramatically compared with that of chitosan. ► Degradation rate was controlled by the molar ratio of glycolic acid to chitosan. ► In vitro cytotoxicity tests revealed that the copolymer has good biocompatibility. ► The copolymer has a great potential to meet diverse needs in biomedical fields.
Co-reporter:Yun Gu, Yawei Ji, Yahong Zhao, Yan Liu, Fei Ding, Xiaosong Gu, Yumin Yang
Biomaterials 2012 33(28) pp: 6672-6681
Publication Date(Web):
DOI:10.1016/j.biomaterials.2012.06.006
Co-reporter:Xin Tang, Chengbin Xue, Yaxian Wang, Fei Ding, Yumin Yang, Xiaosong Gu
Biomaterials 2012 33(15) pp: 3860-3867
Publication Date(Web):
DOI:10.1016/j.biomaterials.2012.02.008
Co-reporter:Ying Meng, Yibing Guo, Yong Ling, Yahong Zhao, Qi Zhang, Xinyang Zhou, Fei Ding, Yumin Yang
Bioorganic & Medicinal Chemistry 2011 Volume 19(Issue 18) pp:5577-5584
Publication Date(Web):15 September 2011
DOI:10.1016/j.bmc.2011.07.031
Neuroprotective agents have been in the focus of attention in the treatment of ischemic stroke. Salidroside, a phenylpropanoid glycoside isolated from Rhodiola rosea L., possessed a wide range of biological activities, especially neuroprotection. In an attempt to improve neuroprotective effects of new salidroside analogs for ischemic stroke, a series of novel aralkyl alcoholic 2-acetamido-2-deoxy-β-d-pyranosides were synthesized and their protective activities against the hypoglycemia and serum limitation induced cell death in rat pheochromocytoma cells (PC12 cells) were studied. Most compounds showed strong neuroprotective effects, especially for 4g and 4h, which exhibited a great potency superior to salidroside. MTT assay, Hoechst 33342 staining, and flow cytometry with annexin V/PI staining collectively showed that pretreatment with 4g and 4h attenuated cell viability loss and apoptotic cell death in cultured PC12 cells. Caspase-3 colorimetric assay and Rhodamine 123 staining revealed the changes in expression levels of caspase-3 and mitochondrial membrane potential in PC12 cells on exposure to hypoglycemia and serum limitation with and without 4g and 4h pretreatment, respectively. All the results suggested that 4g and 4h protects the PC12 cells against hypoglycemia and serum limitation induced apoptosis possibly by modulation of apoptosis-related gene expression and restoration of the mitochondrial membrane potential. Therefore, these novel findings may provided a new framework for the design of new aralkyl alcoholic 2-acetamido-2-deoxy-β-d-pyranosides as neuroprotective agents for treating cerebral ischemic stroke and neurodegenerative diseases.Most compounds showed strong neuroprotective effects, especially for 4g and 4h, which attenuated cell viability loss and apoptotic cell death in cultured PC12 cells.
Co-reporter:Shanqin Xu;Xiaoli Yan;Yahong Zhao;Wei Wang
Journal of Applied Polymer Science 2011 Volume 119( Issue 6) pp:3490-3494
Publication Date(Web):
DOI:10.1002/app.32996

Abstract

In this study, electrospinning was used to fabricate silk-fibroin (SF)-based mats, which served as substrates for the culturing of rat Schwann cells. Microscopic observation and physical parameter measurements revealed that the electrospun SF mats had a nanofibrous structure with favorable physical properties. Fourier transform infrared analysis provided chemical characterization of the molecular confirmation of the SF proteins in the mats. The morphology and immunocytochemistry showed that the mats supported the survival and growth of the cultured Schwann cells, and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide analysis indicated that the electrospun SF mat extract had no cytotoxic effects on Schwann cell proliferation. Collectively, all of the results suggest that the electrospun SF mats might become a candidate scaffold for tissue-engineered nerve grafts to promote peripheral nerve regeneration. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011

Co-reporter:Hui Chen;Zhi Zhao;Yahong Zhao
Journal of Materials Science: Materials in Medicine 2010 Volume 21( Issue 10) pp:2887-2895
Publication Date(Web):2010 October
DOI:10.1007/s10856-010-4141-2
The traditional nonabsorbable silicone buckling implant (buckle) may cause some long-term complications when it is used in the retinal detachment surgery. In this study we fabricated a chitosan–gelatin based buckling implant to replace the traditional one. We evaluated its biocompatibility with human scleral fibroblasts (HSF) in vitro and its cytotoxicity with L929 cell. To evaluate elasticity and hardness of the blends buckle, the mechanical properties of the chitosan–gelatin buckle were compared with the traditional silicone buckle. The light and electron microscopy coupled with immunocytochemistry demonstrated that chitosan–gelatin blends supported the survival and growth of primarily cultured HSF without significant cytotoxic effects. MTT analysis and cell cycle analysis indicated that chitosan–gelatin blends promoted the proliferation of HSF. A preliminary in vivo implantation test indicated that chitosan–gelatin buckling implant were compatible with the surrounding tissue. The results collectively demonstrated that chitosan–gelatin blends could be a candidate biodegradable material for scleral buckling surgery.
Co-reporter:Yaling Wang;Jian Shao;Ying Meng
Medicinal Chemistry Research 2010 Volume 19( Issue 9) pp:1055-1063
Publication Date(Web):2010 December
DOI:10.1007/s00044-009-9251-3
Chitosan membranes loaded with bovine serum albumin (BSA; BSA/chitosan membranes) were prepared by either oven-drying or lyophilization. The encapsulation of BSA was mostly >80%. Controlled release of BSA from the membranes into phosphate-buffered saline (PBS; pH 7.4) was determined with Coomassie brilliant blue at different time periods. The highest cumulative amount of released BSA was 17.30% after 20 days. The optimized chitosan concentration was found to range from 10 to 20 g/l. The most favorable drying temperature for the membrane preparation was 55°C. And membranes made by lyophilization were more porous and uniform than those made by oven-drying.
Co-reporter:Jian Shao;Ling-Ling Huang;Yu-Min Yang
Journal of Chemical Technology and Biotechnology 2009 Volume 84( Issue 4) pp:633-635
Publication Date(Web):
DOI:10.1002/jctb.2086

Abstract

An organic/inorganic hybrid gel of alginate–SiO2 (ALG–SiO2) was used to immobilize the partially purified potato polyphenol oxidase (PPO) for the treatment of phenolic wastewater. The influences of alginate concentration, quantity of both enzyme and tetramethoxysilane (TMOS) on immobilization were investigated. The Michaelis constant for immobilized PPO was determined as 14.7 mmol L−1 at 25 °C, and the highest activity of immobilized PPO was achieved at pH 7.0. The ALG–SiO2 immobilized PPO was more stable than the free PPO or ALG(alone) immobilized PPO. This study suggests that ALG–SiO2 immobilized PPO might be a potential tool for the removal of phenolic compounds from industrial wastewater. Copyright © 2008 Society of Chemical Industry

Co-reporter:Jian Shao;Huimin Ge
Biotechnology Letters 2007 Volume 29( Issue 6) pp:901-905
Publication Date(Web):2007 June
DOI:10.1007/s10529-007-9329-2
A partially purified potato polyphenol oxidase (PPO) was immobilized in a cross-linked chitosan–SiO2 gel and used to treat phenol solutions. Under optimized conditions (formaldehyde 20 mg/ml, PPO 4 mg/ml and pH 7.0), the activity of immobilized PPO was 1370 U/g and its Km value for catechol was 12 mm at 25°C. The highest activity of immobilized enzyme was at pH 7.4. Immobilization stabilized the enzyme with 73 and 58% retention of activity after 10 and 20 days, respectively, at 30°C whereas most of the free enzyme was inactive after 7 days. The efficiency of removing phenol (10 mg phenol/l) by the immobilized PPO was 86%, and about 60% removal efficiency was retained after five recycles. The immobilized PPO may thus be a useful for removing phenolic compounds from industrial waste-waters.
Co-reporter:Luzhong Zhang, Fan Liu, Guicai Li, Youlang Zhou, Yumin Yang
Journal of Pharmaceutical Sciences (December 2015) Volume 104(Issue 12) pp:4185-4196
Publication Date(Web):1 December 2015
DOI:10.1002/jps.24649
One major obstacle in the application of drug delivery systems for cancer chemotherapy is their poor penetration in tumor tissues. Conjugating active ligand moieties to the surface of nanoparticles may be a promising approach for enhancing the tumor accumulation and penetration of nanoparticles. Herein, the cell-penetrating peptide twin-arginine translocation (Tat)-conjugated epirubicin-loaded poly(lactic-glycolic acid) nanoparticles were prepared to achieve deep tumor penetration. The morphology and size of nanoparticles were characterized by scanning electron microscopy and dynamic light scattering, and the biological behaviors of nanoparticles were evaluated. It is demonstrated that Tat-conjugated nanoparticles have a significant improvement in antitumor activity and biodistribution compared with nonconjugated nanoparticles. Importantly, Tat conjugated on the surface of nanoparticles could facilitate the encapsulated drug penetration into deeper tumor tissue. Additionally, Tat-conjugated nanoparticles have good biocompatibility, as demonstrated by hemolytic tests, in vitro cytotoxicity, and histology study. These results suggested that the Tat-conjugated nanoparticles, as a powerful delivery system for chemotherapeutic drug, would have a promising application in human cancer therapy.
Co-reporter:Ya Wei JI, Yan KONG, Ya Hong ZHAO, Ya Ling WANG, Jing ZHAO, Lu Zhong ZHANG, Yu Min YANG
Biomedical and Environmental Sciences (December 2014) Volume 27(Issue 12) pp:
Publication Date(Web):1 December 2014
DOI:10.3967/bes2014.139
Co-reporter:Hua Xian, Jing Zhao, Yuan Zheng, Meihong Wang, Jun Huang, Bingxin Wu, Cheng Sun, Yumin Yang
Life Sciences (8 May 2014) Volume 103(Issue 1) pp:34-40
Publication Date(Web):8 May 2014
DOI:10.1016/j.lfs.2014.02.040
AimsTo investigate the anti-apoptotic effect of MADP, an analog of salidroside, against glutamate induced apoptosis in the cultured rat hippocampal neurons.Main methodsCytotoxicity was determined by the MTT method and lactate dehydrogenase release to the medium. Cell apoptosis was evaluated by Hoechst 33342 staining, TUNEL assay and flow cytometric analysis. Western blotting was applied for detecting protein levels of cellular signaling molecules.Key findingsOur results showed that glutamate exposure significantly induces cell apoptosis, whereas the pretreatment of salidroside or MADP remarkably improves cell viability. Most importantly, the anti-apoptotic effect of MADP against glutamate insult is superior to salidroside. To explore the involved mechanisms, we measured some pro-apoptotic and anti-apoptotic protein levels, and several cell survival signaling pathways were analyzed as well. No visible alterations in Bcl-2 and Bax protein levels were observed by MADP or salidroside. Akt and JNK phosphorylation was robustly stimulated by MADP in the glutamate-treated neurons. Salidroside treatment results in a slight activation in Akt, while no significant alteration in JNK activity was observed.SignificanceMADP exhibits higher capacity to attenuate glutamate induced cell apoptosis in the cultured rat hippocampal neurons, suggesting that MADP might be a better candidate than salidroside for developing novel drugs treating neuron loss associated disorders.
L-Aspartic acid,L-arginylglycyl-
Epirubicin
Glycogen synthase kinase 3, GSK3β
Leptin