| Literature DB >> 28371012 |
Guoqing Yan1, Jun Wang1, Jiejie Qin1, Liefeng Hu1, Panpan Zhang1, Xin Wang1, Rupei Tang1.
Abstract
To compare the chemotherapeutic efficacy determined by extra- and intracellular drug release strategies, poly(ortho ester amide)-based drug carriers (POEAd-C) with well-defined main-chain lengths, are successfully constructed by a facile method. POEAd-C3-doxorubicin (DOX) can be rapidly dissolved to release drug at tumoral extracellular pH (6.5-7.2), while POEAd-C6-DOX can rapidly release drug following gradual swelling at intracellular pH (5.0-6.0). In vitro cytotoxicity shows that POEAd-C3-DOX exhibits more toxic effect on tumor cells than POEAd-C6-DOX at extracellular pH, but POEAd-C6-DOX has stronger tumor penetration and inhibition in vitro and in vivo tumor models. So, POEAd-C6-DOX with the intracellular drug release strategy has stronger overall chemotherapeutic efficacy than POEAd-C3-DOX with extracellular drug release strategy. It is envisioned that these poly(ortho ester amides) can have great potential as drug carriers for efficient chemotherapy with further optimization.Entities:
Keywords: antitumor; drug delivery; nanoparticles; ortho ester
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Year: 2017 PMID: 28371012 DOI: 10.1002/mabi.201600503
Source DB: PubMed Journal: Macromol Biosci ISSN: 1616-5187 Impact factor: 4.979