摘要
Quercetin (QCT) has important functions such as antioxidant, anti-inflammatory and anticancer. However, its applications in food and in drug are restricted owing to its poor water solubility. In this work, a novel amphiphilic wall-material chitosan was synthesized via grafting of chitosan with deoxycholic acid (DA) as hydrophobic group and modified N-acetyl-L-cysteine (NAC) as hydrophilic group. Amphiphilic chitosan was self-assembled to load QCT as nanomicelles by a low-cost and inorganic solvent procedure. Both the encapsulation efficiencies (EE) and drug-loading rates (DL) increased when increasing the grafting rate of DA. There was a bursting release of QCT for the QCT-loaded nanomicelles (CS-DA-NAC-QNMs) from 0 to 8 h, and then the release rate decreased gradually. After releasing for 72 h, the final cumulative release percentages were more than 40%. All the QCT-loaded nanomicelles samples showed good hemocompatibility, and their water solubility and biocompatibility increased evidently. What's more, they exhibited an obvious inhibition rate of A549 cells.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 519-526 |
| 页数 | 8 |
| 期刊 | Colloids and Surfaces B: Biointerfaces |
| 卷 | 179 |
| DOI | |
| 出版状态 | 已出版 - 1 7月 2019 |
学术指纹
探究 'Self-assembled amphiphilic chitosan nanomicelles to enhance the solubility of quercetin for efficient delivery' 的科研主题。它们共同构成独一无二的学术指纹。引用此
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