Nanodiscs: a versatile nanocarrier platform for cancer diagnosis and treatment

被引:88
作者
Bariwal, Jitender
Ma, Hairong
Altenberg, Guillermo A.
Liang, Hongjun [1 ]
机构
[1] Texas Tech Univ, Hlth Sci Ctr, Sch Med, Dept Cell Physiol & Mol Biophys, Lubbock, TX 79430 USA
基金
美国国家科学基金会;
关键词
HIGH-DENSITY-LIPOPROTEINS; IMMUNOGENIC CELL-DEATH; DRUG-DELIVERY SYSTEMS; VIVO SIRNA DELIVERY; MEMBRANE-PROTEINS; POLYMERIC MICELLES; TARGETED DELIVERY; BLOCK-COPOLYMERS; PARTICLE-SHAPE; RESPONSIVE POLYMERSOMES;
D O I
10.1039/d1cs01074c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cancer therapy is a significant challenge due to insufficient drug delivery to the cancer cells and non-selective killing of healthy cells by most chemotherapy agents. Nano-formulations have shown great promise for targeted drug delivery with improved efficiency. The shape and size of nanocarriers significantly affect their transport inside the body and internalization into the cancer cells. Non-spherical nanoparticles have shown prolonged blood circulation half-lives and higher cellular internalization frequency than spherical ones. Nanodiscs are desirable nano-formulations that demonstrate enhanced anisotropic character and versatile functionalization potential. Here, we review the recent development of theranostic nanodiscs for cancer mitigation ranging from traditional lipid nanodiscs encased by membrane scaffold proteins to newer nanodiscs where either the membrane scaffold proteins or the lipid bilayers themselves are replaced with their synthetic analogues. We first discuss early cancer detection enabled by nanodiscs. We then explain different strategies that have been explored to carry a wide range of payloads for chemotherapy, cancer gene therapy, and cancer vaccines. Finally, we discuss recent progress on organic-inorganic hybrid nanodiscs and polymer nanodiscs that have the potential to overcome the inherent instability problem of lipid nanodiscs.
引用
收藏
页码:1702 / 1728
页数:27
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