Kinetics of acoustic release of doxorubicin from stabilized and unstabilized micelles and the effect of temperature

被引:12
作者
Husseini, Ghaleb A. [1 ,2 ]
de la Rosa, Mario A. Diaz [2 ]
AlAqqad, Emad O. [1 ]
Al Mamary, Saif [1 ]
Kadimati, Yaman [1 ]
Al Baik, Abdullah [1 ]
Pitt, William G. [2 ]
机构
[1] Amer Univ Sharjah, Dept Chem Engn, Sharjah, U Arab Emirates
[2] Brigham Young Univ, Dept Chem Engn, Provo, UT 84602 USA
来源
JOURNAL OF THE FRANKLIN INSTITUTE-ENGINEERING AND APPLIED MATHEMATICS | 2011年 / 348卷 / 01期
基金
美国国家卫生研究院;
关键词
Pluronic (R) P105; Polymeric micelles; Ultrasound; Kinetic constants; Stabilized micelles; DRUG-DELIVERY; P105; MICELLES; IN-VITRO; CAVITATION; ULTRASOUND; VIVO;
D O I
10.1016/j.jfranklin.2009.02.007
中图分类号
TP [自动化技术、计算机技术];
学科分类号
0812 ;
摘要
Ultrasound is being investigated as a trigger mechanism to deliver high concentrations of chemotherapy drugs to cancerous tissues using polymeric micelles. In this paper, we examined the kinetics of acoustic release of doxorubicin using stabilized and non-stabilized micelles. Kinetic models were used to regress release and re-encapsulation time constants for three different compounds, namely non-stabilized Pluronic (R) P105 micelles, P105 micelles stabilized using an interpenetrating network of N,N-diethylacrylamide and micelles formed by PEO-b-poly(NIPAAm-co-HEMA-lactate(n)). Results showed that the kinetic release constant (k(r)) depends on the micellar system under investigation. On the other hand, there is no statistically significant difference between re-encapsulation rate constants for stabilized and unstabilized micelles. We hypothesize that k(r) depends on the degree of cross-linking or stabilization. (C) 2009 Published by Elsevier Ltd. on behalf of The Franklin Institute.
引用
收藏
页码:125 / 133
页数:9
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