Husseinil Ghaleb A, Kherbeckl Laura, Pitt William G, Hubbell Jeffrey A, Christensen Douglas A, Velluto Diana
J Nanosci Nanotechnol. 2015 Mar;15(3):2099-104. doi: 10.1166/jnn.2015.9498.
To minimize the adverse side effects of conventional chemotherapy, a targeted micellar drug carrier was investigated that retains hydrophobic drugs in its core and then releases the drug via ultrasonic activation. This paper compares the percent drug release from folated versus non-folated micelles by insonation at 70 kHz and different acoustic power densities. The encapsulated drug is Doxoru- bicin (Dox). A physical model of zero-order release with first-order re-encapsulation was used to fit the experimental kinetic data. Additionally, the acoustic activation power density and Gibbs free energy were introduced and calculated for folated and non-targeted micelles. The data suggests an important role of inertial cavitation in drug release and the presence of a power density threshold for inertial cavitation.
为了将传统化疗的不良副作用降至最低,研究了一种靶向胶束药物载体,该载体将疏水性药物保留在其核心部位,然后通过超声激活释放药物。本文比较了在70kHz和不同声功率密度下,经超声处理后叶酸化胶束与非叶酸化胶束的药物释放百分比。包封的药物是阿霉素(Dox)。采用具有一级再包封的零级释放物理模型来拟合实验动力学数据。此外,还引入并计算了叶酸化胶束和非靶向胶束的声激活功率密度和吉布斯自由能。数据表明惯性空化在药物释放中起重要作用,且存在惯性空化的功率密度阈值。