标题:Huperzine A-phospholipid complex-loaded biodegradable thermosensitive polymer gel for controlled drug release
作者:Cai, Xiaoqing; Luan, Yuxia; Jiang, Yue; Song, Aixin; Shao, Wei; Li, Zhonghao; Zhao, Zhongxi
作者机构:[Cai, Xiaoqing; Luan, Yuxia; Jiang, Yue; Shao, Wei; Zhao, Zhongxi] Shandong Univ, Sch Pharmaceut Sci, Jinan 250012, Shandong, Peoples R China.; [Cai 更多
通讯作者:Luan, YX
通讯作者地址:[Luan, YX]Shandong Univ, Sch Pharmaceut Sci, Jinan 250012, Shandong, Peoples R China.
来源:INTERNATIONAL JOURNAL OF PHARMACEUTICS
出版年:2012
卷:433
期:1-2
页码:102-111
DOI:10.1016/j.ijpharm.2012.05.009
关键词:Huperzine-A; Phospholipid complex; PLGA-PEG-PLGA thermogel; Drug release
摘要:The huperzine A-phospholipid complex loaded biodegradable thermosensitive PLGA-PEG-PLGA polymer gel was studied as injectable implant system for controlled release of huperzine-A (HA). First, HA molecules were successfully incorporated into the soybean phosphatidylcholine (SP) molecules to form the huperzine-A-soybean phosphatidylcholine complexes (HA-SPC), which was proved by FT-IR, DSC, XRD, solubility study, TEM, etc. The results indicated that hydrogen bonds and electrostatic interaction between HA and SP molecules play an important role in the formation of HA-SPC. Secondly, the HA-SPC was loaded into biodegradable PLGA-PEG-PLGA thermosensitive gel as injectable implant material to control the release of HA. The in vitro and in vivo drug release behaviors of the prepared products were studied. The in vitro release studies demonstrated that the HA-SPC-loaded gel significantly reduced the initial burst of drug release and extended the release period to about 2 weeks. The in vivo pharmacokinetics study of HA-SPC-loaded gel in rabbits showed that plasma concentration of HA (2.54-0.15 ng/mL) was detected for nearly 2 weeks from delivery systems upon single subcutaneous injection. What's more, the in vitro release pattern correlated well with the in vivo pharmacokinetics profile. The present study indicates that HA-SPC loaded PLGA-PEG-PLGA thermal gel may be an attractive candidate vehicle for controlled HA release. (C) 2012 Elsevier B. V. All rights reserved.
收录类别:SCOPUS;SCIE
WOS核心被引频次:22
Scopus被引频次:26
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84862905693&doi=10.1016%2fj.ijpharm.2012.05.009&partnerID=40&md5=3874b419270e0215d4e0c3510b277bff
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