Reconstitution of Low-Density Lipoproteins with Fatty Acids for the Targeted Delivery of Drugs into Cancer Cells

被引:49
|
作者
Zhu, Chunlei [1 ,2 ]
Pradhan, Pallab [1 ,2 ,4 ]
Huo, Da [1 ,2 ]
Xue, Jiajia [1 ,2 ]
Shen, Song [1 ,2 ]
Roy, Krishnendu [1 ,2 ,4 ]
Xia, Younan [1 ,2 ,3 ]
机构
[1] Georgia Inst Technol, Wallace H Coulter Dept Biomed Engn, Atlanta, GA 30332 USA
[2] Emory Univ, Atlanta, GA 30332 USA
[3] Georgia Inst Technol, Sch Chem & Biochem, Sch Chem & Biomol Engn, Atlanta, GA 30332 USA
[4] Georgia Inst Technol, Parker H Petit Inst Bioengn & Biosci, Ctr ImmunoEngn Georgia Tech, Atlanta, GA 30332 USA
基金
美国国家卫生研究院;
关键词
cancer therapy; drug delivery; eutectic mixtures; fatty acids; low-density lipoproteins; SOLID LIPID NANOPARTICLES; APOLIPOPROTEIN B-100; CHOLESTEROL; ATHEROSCLEROSIS; RECEPTOR; BIOLOGY; MICE;
D O I
10.1002/anie.201704674
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Low-density lipoproteins (LDLs) are a class of nanocarriers for the targeted delivery of therapeutics into aberrant cells that overexpress the LDL receptor. A facile procedure is used for reconstituting the hydrophobic core of LDLs with a binary fatty acid mixture. Facilitated by the tumor targeting capability of the apolipoprotein, the reconstituted, drug-loaded LDLs can effectively target cancer cells that overexpress the LDL receptor while showing minor adverse impact on normal fibroblasts. According to a hypothesized mechanism, the reconstituted LDLs can also enable metabolism-iriggered drug release while preventing the payloads from lysosomal degradation. This study demonstrates that LDLs reconstructed with fatty acids hold great promise to serve as effective and versatile nanocarriers fur targeted cancer therapy.
引用
收藏
页码:10399 / 10402
页数:4
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