Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
606589 | Journal of Colloid and Interface Science | 2015 | 10 Pages |
•Glycyrrhetinic acid decorated polymer (GA-CMCA) was used to deliver quercetin (QC).•QC-GA-CMCA had smaller size and narrower size distribution than unmodified ones.•GA modification on conjugates could alter the in vitro release pattern of QC.•QC-GA-CMCA showed enhanced cytotoxicity and cell apoptosis rate.•QC-GA-CMCA could prolong drug circulation time in rats.
Quercetin (QC), a type of plant-based chemical, has been reported to own anticancer activity in vivo. However, the poor water solubility limits its pharmaceutical application. In this study, two kinds of QC-loaded self-aggregates based on O-carboxymethyl chitosan-cholic acid conjugates (CMCA) were developed to improve the drug bioavailability in which glycyrrhetinic acid (GA) modification was utilized in the nanocarrier fabrication (QC-GA-CMCA) or not (QC-CMCA). These self-aggregates were prepared by a modified ultrasound-dialysis method and the role of GA modification on the evaluation of QC-loaded self-aggregates was investigated. Transmission Electron Microscopy (TEM) images revealed the formation of spherical particles of both self-aggregates. Dynamic Light Scattering (DLS) analysis and UV–VIS spectroscopy showed that the QC-GA-CMCA had smaller size, narrower size distribution, higher drug loading and entrapment efficiency than corresponding QC-CMCA aggregates. QC-GA-CMCA showed more obvious sensitivity to acidic pH condition based on the zeta potential measurements at various pHs, and fastest drug release was observed at pH 5.7 for QC-CMCA while at pH 6.5 for QC-GA-CMCA. In addition, QC-GA-CMCA demonstrated enhanced cell cytotoxicity and higher cell apoptosis rate in vitro, and also higher AUC value and a prolonged residence time of drug in vivo.
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