Journal
JOURNAL OF CONTROLLED RELEASE
Volume 272, Issue -, Pages 107-113Publisher
ELSEVIER
DOI: 10.1016/j.jconrel.2018.01.011
Keywords
Polypeptides; Liposomes; Polymersomes; Lung cancer; Targeted chemotherapy
Funding
- National Natural Science Foundation of China [NSFC 51773145, 51473110, 51633005, 51603138]
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Doxil (R) is the first FDA-approved anti-cancer nano-drug. Notably, no targeted liposomal formulation has advanced to clinical stage despite tremendous work undertaken, partly due to a low stability of liposomes. Here, we report on novel lipopepsomes self-assembled from poly(ethylene glycol)-b-poly(alpha-aminopalmitic acid) as a stable and versatile alternative to liposomes for highly efficient encapsulation and tumor-targeted delivery of doxorubicin hydrochloride (Dox center dot HCl). Interestingly, lipopepsomes could be easily decorated with 20 mol% cRGD peptide and loaded with 17.4 wt% Dox center dot HCl, giving cRGD-LPP-Dox with a small size of similar to 80 nm. cRGD-LPP-Dox exhibited a high stability against 10% FBS and restrained drug release under physiological conditions. Flow cytometry, confocal microscopy and MTT assays using alpha(v)beta(3)-overexpressing A549 tumor cells showed obviously more efficient uptake and higher anticancer activity for cRGD-LPP-Dox than for non-targeted LPP-Dox and clinically used liposomal Dox (Lipo-Dox) controls. Notably, cRGD-LPP-Dox exhibited markedly enhanced toleration and tumor accumulation than Lipo-Dox. The therapeutic studies demonstrated that cRGD-LPP-Dox achieved effective suppression of orthotopic A549 human lung tumor in nude mice, resulting in significantly improved survival rate as compared to LPP-Dox and Lipo-Dox groups. Lipopepsomes with small size, efficient loading of Dox center dot HCl, high stability and versatile ligand decoration have appeared as a highly attractive nano-platform for targeted tumor chemotherapy.
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