| Literature DB >> 32626854 |
Zi Fu1, Gareth R Williams2, Shiwei Niu1, Jianrong Wu3, Feng Gao4, Xuejing Zhang1, Yanbo Yang1, Yu Li1, Li-Min Zhu1.
Abstract
In this work, an innovative boron-based multifunctional nanoplatform was developed for synergistic chemotherapy/low temperature photothermal therapy (PTT). This platform is functionalized with a cRGD peptide to allow the targeting of αvβ3 integrin, which is over-expressed in the cells of tumors. The nanoparticles were further loaded with the chemotherapeutic drug doxorubicin (DOX) and a heat shock protein inhibitor (17AAG), and high loading capacities for both DOX (603 mg g-1 B-PEG-cRGD) and 17AAG (417 mg g-1) were obtained. The resultant DOX-17AAG@B-PEG-cRGD system shows both pH-controlled and near-infrared (NIR)-induced DOX and 17AAG release. It also provides significantly enhanced cellular uptake in cancerous cells over healthy cells. The presence of 17AAG allows low-temperature PTT to be combined with chemotherapy with DOX, resulting in highly effective anti-cancer activity. This has been confirmed by both in vitro assays and using an in vivo murine cancer model. It is expected that such a multifunctional nanoplatform can serve as a promising candidate for cancer therapy.Entities:
Mesh:
Substances:
Year: 2020 PMID: 32626854 DOI: 10.1039/d0nr02291h
Source DB: PubMed Journal: Nanoscale ISSN: 2040-3364 Impact factor: 7.790