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Synthesis and in vitro evaluation of pH-sensitive PEG-I-dC16 block polymer micelles for anticancer drug delivery

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成果类型:
期刊论文
作者:
Huang Rongbin;Xiang Lei;Liu Ying;Deng Xiangping;Cao Xuan;...
通讯作者:
Tang Guotao
作者机构:
[Huang Rongbin] First Peoples Hosp Xiangtan City, Xiangtan, Peoples R China.
[Deng Xiangping; Xiang Lei; Cao Xuan; Li Lanfang; Tang Guotao; Liu Ying; Yu Cuiyun] Univ South China, Learning Key Lab Pharmacoprote, Inst Pharm & Pharmacol, Hengyang 421001, Hunan, Peoples R China.
[Chen Yanming] Mu Dan Jiang You Bo Pharmacert Co Ltd, Mudanjiang, Peoples R China.
通讯机构:
[Tang Guotao] U
Univ South China, Learning Key Lab Pharmacoprote, Inst Pharm & Pharmacol, Hengyang 421001, Hunan, Peoples R China.
语种:
英文
关键词:
benzoic-imine bond;pH-sensitive;micelle;drug delivery system
期刊:
Journal of Pharmacy and Pharmacology
ISSN:
0022-3573
年:
2016
卷:
68
期:
6
页码:
751-761
基金类别:
construct programme of the key discipline in Hunan province; Cooperative Innovation Center for Molecular Target New Drug Study; research foundation of education Bureau of Hunan Province, China [13C833]
机构署名:
本校为通讯机构
院系归属:
药学与生物科学学院
摘要:
Objectives To develop an acid trigger release of antitumour drug delivery carriers, pH-sensitive amphiphilic poly (ethyleneglycol)-imine-benzoic-dipalmitate (PEG-I-dC16) polymers were designed and synthesized and the drug-loaded micelles were evaluated in vitro. Methods PEG-I-dC16 synthesized by Schiff base synthetic method and characterized by 1H-NMR. To determine the drug-loading capacity, doxorubicin (DOX) was encapsulated in the micelles using membrane dialysis method. Zeta potential, particle size, drug-loading capacity, in vitro drug rele...

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