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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.
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页码:737 / 750
页数:14
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