| Literature DB >> 25037431 |
Hua Guo1, Yuanyuan Liu2, Yan Wang3, Jing Wu4, Xiaoying Yang3, Rongshan Li3, Yinsong Wang5, Ning Zhang6.
Abstract
Urocanic acid was conjugated to pullulan to synthesize O-urocanyl pullulan (URPA) with degree of substitution (DS) of 8.2%. URPA nanoparticles prepared by dialysis method had spherical shapes and a mean diameter of 156.8 ± 16.8 nm. Adriamycin (ADR) was successfully loaded into URPA nanoparticles and exhibited pH-sensitive in vitro release property. MTT assay showed that ADR-loaded URPA (ADR/URPA) nanoparticles had a significant higher toxicity against drug resistant MCF-7/ADR cells than free ADR, and the reversal index reached up to 9.6. The results of flow cytometry and confocal microscopy showed that URPA nanoparticles efficiently enhanced accumulation and retention of ADR in MCF-7/ADR cells and successfully delivered ADR into cell nucleus. The reversal effect of ADR/URPA nanoparticles on the drug resistance of MCF-7/ADR cells was perhaps related with their cell entry and intracellular drug release mechanisms.Entities:
Keywords: Cancer; Drug resistance; Nanoparticle carrier; O-Urocanyl pullulan; pH-sensitive
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Year: 2014 PMID： 25037431 DOI： 10.1016/j.carbpol.2014.05.057
Source DB: PubMed Journal: Carbohydr Polym ISSN： 0144-8617 Impact factor: 9.381