| Literature DB >> 29376322 |
Jin Yan, Wangxiao He1, Siqi Yan, Fan Niu, Tianya Liu, Bohan Ma, Yongping Shao, Yuwei Yan, Guang Yang2, Wuyuan Lu1, Yaping Du, Bo Lei, Peter X Ma3.
Abstract
Developing a sophisticated nanomedicine platform to deliver therapeutics effectively and safely into tumor/cancer cells remains challenging in the field of nanomedicine. In particular, reliable peptide drug delivery systems capable of overcoming biological barriers are still lacking. Here, we developed a simple, rapid, and robust strategy to manufacture nanoclusters of ∼90 nm in diameter that are self-assembled from lanthanide-doped nanoparticles (5 nm), two anticancer peptides with different targets (BIM and PMI), and one cyclic peptide iNGR targeted to cancer cells. The peptide-lanthanide nanoclusters (LDC-PMI-BIM-iNGR) enhanced the resistance of peptide drugs to proteolysis, disassembled in response to reductive conditions that are present in the tumor microenvironment and inhibited cancer cell growth in vitro and in vivo. Notably, LDC-PMI-BIM-iNGR exhibited extremely low systemic toxicity and side effects in vivo. Thus, the peptide-lanthanide nanocluster may serve as an ideal multifunctional platform for safe, targeted, and efficient peptide drug delivery in cancer therapy.Entities:
Keywords: multifunctional nanocluster; p53 activator; peptides; safe cancer therapy; stimuli-responsive; targeted delivery
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Year: 2018 PMID: 29376322 DOI: 10.1021/acsnano.8b00081
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881