pH-sensitive carbon nanotubes graft polymethylacrylic acid self-assembly nanoplatforms for cellular drug release

被引:2
|
作者
Han, Mei [1 ]
Zhou, Zi-Hao [1 ]
Luo, Yan-Ling [1 ]
Xu, Feng
Chen, Ya-Shao [1 ]
机构
[1] Shaanxi Normal Univ, Sch Chem & Chem Engn, Key Lab Macromol Sci Shaanxi Prov, Xian, Peoples R China
基金
中国国家自然科学基金;
关键词
Carbon nanotubes; controlled release; polymethylacrylic acid; pH responsiveness; self-assembly micelles; POLYMERIC MICELLES; RESPONSIVE NANOPARTICLES; NANOCARRIERS; DELIVERY; NANOCOMPOSITES; HYDROGELS;
D O I
10.1177/08853282221107156
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
pH-Sensitive carbon nanotubes graft polymethylacrylic acid hybrids (CNTs-g-PMAA) were prepared through a three-step process, and self-assembled into core-shell micelle nanoparticles. The chemical structure of the hybrids were characterized by FTIR, H-1 NMR and TGA. The critical micelle concentration (CMC) was measured by surface tension, and the value hinged on the Mn values or chain lengths of PMAA segments. The UV-vis transmittance, dynamical light scattering (DLS), and zeta potential measurements indicated that the hybrid self-assembly exhibited pH-sensentive responsiveness. The self-assembly was used to load an anticancer drug, paclitaxel (PTX), with an encapsulation efficiency of 77%. The PTX-loaded hybrid drug preparations were applied for cancer-cellular drug release, finding that the release rate was dependent on pH environments, and faster in acidic media of pH < 6.8 than in pH 7.4. MTT and hemolysis assays manifested that the blank hybrid drug carriers were nontoxic and safe, whereas the PTX-loaded drug preparations possessed comparable and even higher anticancer activity in comparison with free PTX. Consequently, the developed hybrid drug nanocarriers can be used for cancer therapy as a promising candidate.
引用
收藏
页码:737 / 750
页数:14
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