Bio-inspired keratin-based core-crosslinked micelles for pH and reduction dual-responsive triggered DOX delivery

被引:31
|
作者
Zhang, Huifang [1 ,2 ]
Liu, Peng [1 ,2 ]
机构
[1] Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Gansu, Peoples R China
[2] Lanzhou Univ, Coll Chem & Chem Engn, Key Lab Nonferrous Met Chem & Resources Utilizat, Lanzhou 730000, Gansu, Peoples R China
关键词
Drug delivery system; Chicken feather keratin; pH and reduction dual-responsive; Core-crosslinked micelles; Enhanced anti-tumor efficacy; NANOPARTICLES; DOXORUBICIN; EXTRACTION; CARRIERS;
D O I
10.1016/j.ijbiomac.2018.11.178
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Facile bio-inspired approach has been developed to prepare novel DOX-loaded chicken feather keratin-based core-crosslinked micelles (DOX/Ker-PEG CCMs) for pH and reduction dual-responsive tumor-specific intracellular triggered DOX delivery, by oxidation crosslinking the DOX/Ker-PEG micelles which were simply self assembled by adjusting solution pH value to 10. The final DOX/Ker-PEG CCMs with a mean hydrodynamic diameter of 152 nm were obtained with a drug loading capacity (DLC) of 24.8%. The in vitro controlled release profiles demonstrated the pH and reduction dual-responsive triggered release of DOX from the developed bio-inspired drug delivery system (DDS), with a cumulative release of 58% within 3 days in a sustained release manner in the stimulated tumor intracellular microenvironment, while a low premature drug leakage of 14% occurred in the normal physiological medium. Furthermore, the MTT assays demonstrated that the graft copolymer Ker-PEG(58) possessed excellent cytocompatibility, while the DOX/Ker-PEG CCMs exhibited an enhanced anti-tumor efficacy on the HepG2 cells than the free DOX. 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:1150 / 1156
页数:7
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