Self-assembly of Amphiphilic Tripeptides into Nanoparticles for Drug Delivery

被引:0
作者
Tu, Zhaoxu [1 ]
Xu, Xianghui [1 ]
Jian, Yeting [1 ]
Zhong, Dan [1 ]
He, Bin [1 ]
Gu, Zhongwei [1 ]
机构
[1] Sichuan Univ, Natl Engn Res Ctr Biomat, Chengdu 610064, Sichuan, Peoples R China
基金
美国国家科学基金会;
关键词
Amphiphilic tripeptide; controlled release; cytotoxicity; drug delivery; nanoparticles; self-assembly; BLOCK-COPOLYMER; IN-VITRO; CARRIERS; ELLIPTICINE; DENDRIMERS; MICELLES; DESIGN; SYSTEM;
D O I
暂无
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
Peptide-based nanomaterials are widely used as nanocarriers for catalysis, drug delivery, and gene delivery. In this paper, we designed and synthesized the amphiphilic tripeptides through solution phase synthesis. The tripeptides were purified by column chromatography and the molecular structures were confirmed by H-1 NMR and TOF-MS. The tripeptides could self-assemble into spherical nanoparticles in aqueous media with a low critical aggregation concentration. The size and morphology of the nanoparticles were performed by dynamic light scattering, scanning electron microscopy and transmission electron microscope. The peptide-based nanoparticles were used as biocompatible nanocarriers for encapsulating hydrophobic doxorubicin (DOX) to achieve controlled release. The CCK-8 assay indicated that the peptide-based nanocarriers could enhance cellular uptake and drug efficacy of DOX to A549 tumor cell line. These results showed that the self-assembly of amphiphilic tripeptides provided a facile strategy to fabricate nanoparticles for anti-tumor drug delivery.
引用
收藏
页码:194 / 199
页数:6
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