聚磷腈
乙二醇
磷腈
两亲性
化学
盐酸阿霉素
高分子化学
共聚物
小泡
胶体金
聚合物
盐酸盐
氯仿
纳米颗粒
有机化学
化学工程
膜
阿霉素
外科
化疗
工程类
医学
生物化学
出处
期刊:Langmuir
[American Chemical Society]
日期:2017-10-04
卷期号:33 (43): 12291-12299
被引量:7
标识
DOI:10.1021/acs.langmuir.7b02745
摘要
Polymeric graft polyphosphazene containing 4-aminobenzoic acid diethylaminoethyl ester (DEAAB) as hydrophobic side groups was rationally designed and named PDEP. PDEP can self-assemble into a nanovesicle in water. More importantly, when compared with the amphiphile poly[(methoxy-poly(ethylene glycol))(ethyl p-aminobenzoate)]phosphazene (PEP) copolymer containing benzene rings and the amphiphile poly[(methoxy-poly(ethylene glycol)(N,N-diisopropylethylenediamine)]phosphazene (PDP) copolymer containing tertiary amino groups, the coexistence of benzene and tertiary amino groups in PDEP enabled it to effectively load water-soluble small-molecule doxorubicin hydrochloride (DOX·HCl) into the vesicle and efficiently induce in situ transformation of gold tetrachloroaurate (HAuCl4) to gold nanoparticles (AuNPs) as both a reductant and a stabilizer. By optimizing the reduction conditions, such as the temperature, reaction time, and hydrophobic group in polymer/HAuCl4 molar ratio, the AuNP complex PDEP vesicles significantly inhibited the DOX·HCl burst release at pH 7.4 while displaying a fast release responsive to pH 5.5.
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