| Literature DB >> 29624828 |
Fuwu Zhang1, Qianqian Ni1,2, Orit Jacobson1, Siyuan Cheng1, Arthur Liao1, Zhantong Wang1, Zhimei He1, Guocan Yu1, Jibin Song1, Ying Ma1, Gang Niu1, Longjiang Zhang2, Guizhi Zhu1, Xiaoyuan Chen1.
Abstract
Polymeric micelle-based drug delivery systems have dramatically improved the delivery of small molecular drugs, yet multiple challenges remain to be overcome. A polymeric nanomedicine has now been engineered that possesses an ultrahigh loading (59 %) of a glutathione (GSH)-sensitive heterodimeric multifunctional prodrug (HDMP) to effectively co-deliver two synergistic drugs to tumors. An HDMP comprising of chemotherapeutic camptothecin (CPT) and photosensitizer 2-(1-hexyloxyethyl)-2-devinyl pyropheophorbide-α (HPPH) was conjugated via a GSH-cleavable linkage. The intrinsic fluorogenicity and label-free radio-chelation (64 Cu) of HPPH enabled direct drug monitoring by fluorescence imaging and positron emission tomography (PET). Through quantitative PET imaging, HDMP significantly improves drug delivery to tumors. The high synergistic therapeutic efficacy of HDMP-loaded NPs highlights the rational design of HDMP, and presents exciting opportunities for polymer NP-based drug delivery.Entities:
Keywords: dimeric prodrugs; drug delivery; nanomedicine; pharmacoimaging; synergistic therapy
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Year: 2018 PMID: 29624828 DOI: 10.1002/anie.201801984
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336