Novel pH-triggered biocompatible polymeric micelles based on heparin-alpha-tocopherol conjugate for intracellular delivery of docetaxel in breast cancer

(2020) Novel pH-triggered biocompatible polymeric micelles based on heparin-alpha-tocopherol conjugate for intracellular delivery of docetaxel in breast cancer. Pharmaceutical Development and Technology. pp. 492-509. ISSN 1083-7450

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Abstract

In this study, pH-triggered polymeric micelle comprising alpha-tocopherol (TOC) and heparin (HEP) was developed and loaded with docetaxel (DTX). The amphiphilic copolymer was synthesized by grafting TOC onto HEP backbone by a pH-cleavable bond. DTX-loaded micelles were characterized in terms of critical micelle concentration (CMC), particle size, zeta potential, entrapment efficiency (EE), pH-responsive behavior, and drug release. In vitro cytotoxicity of the micelles against breast cancer cells was investigated by MTT assay. The cellular uptake of coumarin-loaded micelles was also evaluated. Furthermore, the pharmacokinetics of DTX-loaded micelles was evaluated and compared with that of Taxotere (R). HEP-CA-TOC copolymers showed low CMC values and high EE. At pH 7.4, the micelles remained stable in size and shape, whereas considerable changes in particle size and morphology were observed at pH 5.5. DTX-loaded micelles showed pH-dependent drug release profiles. Coumarin-loaded micelles showed higher cellular uptake than free coumarin. Therefore, the DTX-loaded micelles showed more toxicity against breast cancer cells than free DTX. A significant increase in T-1/2 beta, AUC(0-infinity) and MRT was observed in DTX-loaded micelle treated group as compared to the group treated with Taxotere (R). The results suggest that the pH-sensitive HEP-modified micelles could be promising for enhanced intracellular drug delivery of DTX for cancer treatment.

Item Type: Article
Keywords: Polymeric micelle heparin tocopherol pH-sensitive breast cancer docetaxel SELF-ASSEMBLED NANOPARTICLES DRUG-DELIVERY TARGETED DELIVERY PLURONIC NANOGELS CO-DELIVERY ACID RELEASE PACLITAXEL SYSTEM OPTIMIZATION
Subjects: QV Pharmacology
QZ Pathology > QZ 200-380 Neoplasms
Divisions: Faculty of Pharmacy and Pharmaceutical Sciences
Faculty of Pharmacy and Pharmaceutical Sciences > Department of Pharmaceutical Biotechnology
Faculty of Pharmacy and Pharmaceutical Sciences > گروه شیمی دارویی
Faculty of Pharmacy and Pharmaceutical Sciences > Department of Pharmacotherapy
Page Range: pp. 492-509
Journal or Publication Title: Pharmaceutical Development and Technology
Journal Index: ISI
Volume: 25
Number: 4
Identification Number: https://doi.org/10.1080/10837450.2019.1711395
ISSN: 1083-7450
Depositing User: Zahra Otroj
URI: http://eprints.mui.ac.ir/id/eprint/12437

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