Palladium responsive liposomes for triggered release of aqueous contents

被引:3
|
作者
Chasteen, Jordan L. [1 ]
Padilla-Coley, Sasha [1 ]
Li, Dong-Hao [1 ]
Smith, Bradley D. [1 ]
机构
[1] Univ Notre Dame, Dept Chem & Biochem, 251 Nieuwland Sci Hall, Notre Dame, IN 46556 USA
关键词
Caged phospholipid; Palladium; Dioleoylphosphoethanolamine; Fluorescent liposome leakage; Membrane mixing; INDUCED DESTABILIZATION; DRUG-DELIVERY; FUSION; PHASE;
D O I
10.1016/j.bmcl.2023.129215
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Palladium (Pd) is a promising metal catalyst for novel bioorthogonal chemistry and prodrug activation. This report describes the first example of palladium responsive liposomes. The key molecule is a new caged phos-pholipid called Alloc-PE that forms stable liposomes (large unilamellar vesicles,-220 nm diameter). Liposome treatment with PdCl2 removes the chemical cage, liberates membrane destabilizing dioleoylphosphoethanol-amine (DOPE), and triggers liposome leakage of encapsulated aqueous contents. The results indicate a path towards liposomal drug delivery technologies that exploit transition metal triggered leakage.
引用
收藏
页数:5
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