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7篇 您的检索式:作者名="Yanzuo"
    题名 作者 年代 出处 被引量
1Multifunctional Pluronic P123/F127mixed polymeric micelles loaded with paclitaxel for the treatment of multidrug resistant tumors显示文摘Wei Zhang Yuan Shi Yanzuo Chen 2011Biomaterials2011,,32:1
2Multifunctional Pluronic P123/F127 mixed polymeric micelles loaded with paclitaxel for the treatment of muhidrug resistant tumors 显示文摘ZHANG WEI SHI YUAN YANZUO CHEN 2011B iomaterials2011,32,11:1
3In vivo distribution and antitumor activity of doxorubicin-loaded N-isopropylacrylamide-co-methacrylic acid coated mesoporous silica nanoparticles and safety evaluation显示文摘Yanzuo Chen Wuli Yang Baisong Chang Hangting Hu Xiaoling Fang Xianyi Sha 2013European Journal of Pharmaceutics and Biopharmaceutics2013,,:1
4Angiopep-conjugated poly(ethylene glycol)-co-poly(ε-caprolactone) nanoparticles as dual-targeting drug delivery system for brain glioma显示文摘Hongliang Xin Xinyi Jiang Jijin Gu Xianyi Sha Liangcen Chen Kitki Law Yanzuo Chen Xiao Wang Ye Jiang Xiaoling Fang 2011Biomaterials2011,,18:1
5Solid tumor penetration by integrin-mediated pegylated poly(trimethylene carbonate) nanoparticles loaded with paclitaxel显示文摘Xinyi Jiang Hongliang Xin Jijin Gu Ximing Xu Weiyi Xia Shuo Chen Yike Xie Liangcen Chen Yanzuo Chen Xianyi Sha Xiaoling Fang 2013Biomaterials2013,,6:1
6Enhanced antitumor efficacy by paclitaxel-loaded pluronic P123/F127 mixed micelles against non-small cell lung cancer based on passive tumor targeting and modulation of drug resistance 显示文摘WEI ZHANG YUAN SHI YANZUO CHEN 2010European Journal of Pharmaceutics and Biopharmaeeu- tics2010,75,3:1
7Cyclodextrin/chitosan nanoparticles for oral ovalbumin delivery: Preparation, characterization and intestinal mucosal immunity in mice显示文摘A novel oral protein delivery system with enhanced intestinal penetration and improved antigen stability based on chitosan(CS) nanoparticles and antigen-cyclodextrin(CD) inclusion complex was prepared by a precipitation/coacervation method. Ovalbumin(OVA) as a model antigen was firstly encapsulated by cyclodextrin, either β-cyclodextrin( β-CD) or carboxymethyl-hydroxypropyl-β-cyclodextrin(CM-HP-β-CD) and formed OVA-CD inclusion complexes, which were then loaded to chitosan nanoparticles to form OVA loaded β-CD/CS or CM-HP-β-CD/CS nanoparticles with uniform particle size(836.3 and 779.2 nm, respectively) and improved OVA loading efficiency(27.6% and 20.4%, respectively). In vitro drug release studies mimicking oral delivery condition of OVA loaded CD/CS nanoparticles showed low initial releases at p H 1.2 for 2 h less than 3.0% and a delayed release which was below to 30% at p H 6.8 for further 72 h. More importantly, after oral administration of OVA loaded β-CD/CS nanoparticles to Balb/c mice, OVA-specific sIgA levels in jejunum of OVA loaded β-CD/CS nanoparticles were 3.6-fold and 1.9-fold higher than that of OVA solution and OVA loaded chitosan nanoparticles, respectively. In vivo evaluation results showed that OVA loaded CD/CS nanoparticles could enhance its efficacy for inducing intestinal mucosal immune response. In conclusion, our data suggested that CD/CS nanoparticles could serve as a promising antigen-delivery system for oral vaccination.Muye He Chen Zhong Huibing Hu Yu Jin Yanzuo Chen Kaiyan Lou Feng Gao 2019Asian Journal of Pharmaceutical Sciences2019,14,2:0
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