Fugit Kyle D, Jyoti Amar, Upreti Meenakshi, Anderson Bradley D
Department of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, Lexington, KY 40536, USA.
Department of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, Lexington, KY 40536, USA.
J Control Release. 2015 Jan 10;197:10-9. doi: 10.1016/j.jconrel.2014.10.011. Epub 2014 Oct 25.
A non-invasive fluorescence method was developed to monitor liposomal release kinetics of the anticancer agent topotecan (TPT) in physiological fluids and subsequently used to explore the cause of accelerated release in plasma. Analyses of fluorescence excitation spectra confirmed that unencapsulated TPT exhibits a red shift in its spectrum as pH is increased. This property was used to monitor TPT release from actively loaded liposomal formulations having a low intravesicular pH. Mathematical release models were developed to extract reliable rate constants for TPT release in aqueous solutions monitored by fluorescence and release kinetics obtained by HPLC. Using the fluorescence method, accelerated TPT release was observed in plasma as previously reported in the literature. Simulations to estimate the intravesicular pH were conducted to demonstrate that accelerated release correlated with alterations in the low intravesicular pH. This was attributed to the presence of ammonia in plasma samples rather than proteins and other plasma components generally believed to alter release kinetics in physiological samples. These findings shed light on the critical role that ammonia may play in contributing to the preclinical/clinical variability and performance seen with actively-loaded liposomal formulations of TPT and other weakly-basic anticancer agents.
开发了一种非侵入性荧光方法,用于监测生理流体中抗癌药物拓扑替康(TPT)的脂质体释放动力学,并随后用于探究血浆中加速释放的原因。荧光激发光谱分析证实,未包封的TPT在pH值升高时其光谱会发生红移。利用这一特性监测从低囊内pH值的主动载药脂质体制剂中释放的TPT。建立了数学释放模型,以提取通过荧光监测的水溶液中TPT释放的可靠速率常数以及通过HPLC获得的释放动力学。使用荧光方法,观察到血浆中TPT的释放加速,正如文献中先前报道的那样。进行了估计囊内pH值的模拟,以证明加速释放与低囊内pH值的变化相关。这归因于血浆样品中存在氨,而不是通常认为会改变生理样品中释放动力学的蛋白质和其他血浆成分。这些发现揭示了氨在导致TPT和其他弱碱性抗癌药物的主动载药脂质体制剂出现临床前/临床变异性和性能方面可能发挥的关键作用。