| Literature DB >> 28868145 |
Jing Tian1,2,3, Yuanzeng Min2,3, Zachary Rodgers2,4, Kin Man Au2,3, C Tilden Hagan2,5, Maofan Zhang2,3,6, Kyle Roche2,3, Feifei Yang2,3,7, Kyle Wagner2,3, Andrew Z Wang2,3.
Abstract
Chemoradiotherapy (CRT) with paclitaxel (PTX) and cisplatin (CP) is part of the standard of care for patients with locally advanced non-small cell lung cancer (NSCLC). Despite the high treatment intensity, many patients still develop local recurrence after treatment. Thus, there is a strong need to further improve CRT for lung cancer. One strategy is to co-deliver cytotoxic chemotherapy agents using biocompatible nanoparticles (NPs) which can limit off-target tissue toxicity and improve therapeutic efficacy. Herein, we report the development of dual-drug loaded nanoformulations that improve the efficacy of CRT for NSCLC by co-encapsulation of cisplatin (CP) and PTX in PLGA-PEG NPs. Mice bearing NSCLC xenografts given the dual-drug loaded NPs during CRT showed greater inhibition of tumor growth than free drug combinations or combinations of single-drug loaded NPs. These results indicate that using a NP co-delivery strategy for this common CRT regimen may improve clinical responses in NSCLC patients.Entities:
Year: 2017 PMID: 28868145 PMCID: PMC5576184 DOI: 10.1039/C7TB01370A
Source DB: PubMed Journal: J Mater Chem B ISSN: 2050-750X Impact factor: 6.331