| Literature DB >> 31788896 |
Junchao Xu1,2, Yinlong Zhang1,2, Jiaqi Xu1,2, Guangna Liu1,3, Chunzhi Di1,2, Xiao Zhao1,2, Xiang Li4, Yao Li1, Ningbo Pang5, Chengzhi Yang6, Yanyi Li4, Bozhao Li1,3, Zefang Lu1,2, Meifang Wang1,3, Kesheng Dai5, Rong Yan5, Suping Li1,2, Guangjun Nie1,2.
Abstract
Rapid cut-off of blood supply in diseases involving thrombosis is a major cause of morbidity and mortality worldwide. However, the current thrombolysis strategies offer limited results due to the therapeutics' short half-lives, low targeting ability, and unexpected bleeding complications. Inspired by the innate roles of platelets in hemostasis and pathological thrombus, platelet membrane-camouflaged polymeric nanoparticles (nanoplatelets) are developed for targeting delivery of the thrombolytic drug, recombinant tissue plasminogen activator (rt-PA), to local thrombus sites. The tailor-designed nanoplatelets efficiently accumulate at the thrombi in pulmonary embolism and mesenteric arterial thrombosis model mice, eliciting a significantly enhanced thrombolysis activity compared to free rt-PA. In addition, the nanoplatelets exhibit improved therapeutic efficacy over free rt-PA in an ischemic stroke model. Analysis of in vivo coagulation indicators suggests the nanoplatelets might possess a low risk of bleeding complications. The hybrid biomimetic nanoplatelets described offer a promising solution to improve the efficacy and reduce the bleeding risk of thrombolytic therapy in a broad spectrum of thrombosis diseases.Entities:
Keywords: nanoplatelets; plasminogen activators; targeted drug delivery; thrombus
Year: 2019 PMID: 31788896 DOI: 10.1002/adma.201905145
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849