作者: Jiang Yuan , Jian Shen , Jinsong Du , Jie Dou , Xiao Han
DOI: 10.1080/09205063.2021.1906074
关键词: Nanoparticle 、 Doxorubicin 、 Glutathione 、 Biophysics 、 Tannic acid 、 Chemistry 、 Drug carrier 、 Keratin 、 A549 cell 、 Tumor microenvironment
摘要: Drug-loaded nanoparticles have been widely used in the field of tumor treatment due to their low side effects and reduced frequency administration. In this study, pH glutathione (GSH) dual-responsive keratin-tannic acid (TA) complex were established trigger drug release under microenvironments. Reductive keratin was first extracted using a reduction method. Then, keratin-TA (KNPs) self-assembled via non-covalent interaction further stabilized by self-crosslinking thiols. This method facile green without chemicals during whole procedure. KNPs exhibited GSH dual responsiveness as well charge reversibility simulated microenvironment. The anticancer doxorubicin (DOX) loaded on hydrophobicity hydrogen bonds. accelerated mimicked microenvironments, performing high toxic against A549 cells while normal cells. Besides, drug-loaded could be endocytosed Based these results, may serve carriers for therapeutic delivery.