IIUM Repository (IREP)

Development of chitosan-α-mangostin loaded nanoparticles as an anticancer agent

Elsaid Ali, Aimen Abdo and Bakhtiar, M. Taher and Mohamed, Farahidah (2011) Development of chitosan-α-mangostin loaded nanoparticles as an anticancer agent. In: International Postgraduate Conference on Biotechnology (IPBC) 2011, 15-18 Dec 2011, Kuala Terengganu.

[img] PDF (Development of chitosan-α-mangostin loaded nanoparticles as an anticancer agent) - Presentation
Restricted to Repository staff only

Download (962kB) | Request a copy

Abstract

α-Mangostin is one of the main active constituents that can be isolated from the stem bark of Garcinia malaccensis (GM) and has been documented to exert different cytotoxic activities against many cancerous cell lines. Due to its non selective distribution into the tissue, this study had attempted to encapsulate the α-mangostin into biodegradable PLGA copolymer using colloidal extraction solvent evaporation method. The polysaccharide Chitosan was incorporated with the loaded nanoparticles to improve their affinity towards lung cancer cells. The resultant nanoparticles were characterized for their size distribution and external morphology by laser diffractometry and scanning electron microscope (SEM), respectively. The concentration of entrapped α-mangostin was determined by HPLC. Our data demonstrated that the encapsulation efficiency for Chitosan-α-mangostin-loaded PLGA nanoparticles (CM-NP) was higher than those without Chitosan (M-NP). The in vitro release from (CM-NP) and (NPM) was carried out in PBS containing 0.1% tween 20 over three weeks. Whereas, in vitro anti-cancer activities of (CM-NP) and (M-NP) were evaluated against lung cancer cell line (A549) and compared to the free α-mangostin. Our data revealed that (CM-NP) showed higher cytotoxic effect compared to (M-NP) and both had lower cytotoxicity than free α-mangostin. In conclusion, PLGA nanoparticles in combination with Chitosan may be used as a promising composite micro-carrier system to deliver α-mangostin to the lung cancer tissue.

Item Type: Conference or Workshop Item (Poster)
Additional Information: 5209/12374
Uncontrolled Keywords: Chitosan
Subjects: R Medicine > RM Therapeutics. Pharmacology > RM300 Drugs and their action
R Medicine > RS Pharmacy and materia medica
Kulliyyahs/Centres/Divisions/Institutes: Kulliyyah of Pharmacy > Department of Pharmaceutical Technology
Depositing User: Assoc Prof Farahidah Mohamed
Date Deposited: 14 Jan 2013 14:25
Last Modified: 09 Dec 2014 09:31
URI: http://irep.iium.edu.my/id/eprint/12374

Actions (login required)

View Item View Item

Downloads

Downloads per month over past year