D'Souza Susan S, Faraj Jabar A, DeLuca Patrick P
University of Kentucky College of Pharmacy, Lexington, KY 40536, USA.
AAPS PharmSciTech. 2005 Oct 31;6(4):E553-64. doi: 10.1208/pt060470.
The purpose of this study was to determine the feasibility of applying accelerated in vitro release testing to correlate or predict long-term in vitro release of leuprolide poly(lactide-co-glycolide) microspheres. Peptide release was studied using a dialysis technique at 37 degrees C and at elevated temperatures (50 degrees C-60 degrees C) in 0.1M phosphate buffered saline (PBS) pH 7.4 and 0.1M acetate buffer pH 4.0. The data were analyzed using a modification of the Weibull equation. Peptide release was temperature dependent and complete within 30 days at 37 degrees C and 3 to 5 days at the elevated temperatures. In vitro release profiles at the elevated temperatures correlated well with release at 37 degrees C. The shapes of the release profiles at all temperatures were similar. Using the modified Weibull equation, an increase in temperature was characterized by an increase in the model parameter, alpha, a scaling factor for the apparent rate constant. Complete release at 37 degrees C was shortened from approximately 30 days to 5 days at 50 degrees C, 3.5 days at 55 degrees C, 2.25 days at 60 degrees C in PBS pH 7.4, and 3 days at 50 degrees C in acetate buffer pH 4.0. Values for the model parameter beta indicated that the shape of the release profiles at 55 degrees C in PBS pH 7.4 (2.740) and 50 degrees C in 0.1M acetate buffer pH 4.0 (2.711) were similar to that at 37 degrees C (2.677). The E(a) for hydration and erosion were determined to be 42.3 and 19.4 kcal/mol, respectively. Polymer degradation was also temperature dependent and had an E(a) of 31.6 kcal/mol. Short-term in vitro release studies offer the possibility of correlation with long-term release, thereby reducing the time and expense associated with long-term studies. Accelerated release methodology could be useful in the prediction of long-term release from extended release microsphere dosage forms and may serve as a quality control tool for the release of clinical or commercial batches.
本研究的目的是确定应用加速体外释放试验来关联或预测亮丙瑞林聚(丙交酯-共-乙交酯)微球的长期体外释放的可行性。在37℃以及50℃至60℃的高温下,于pH 7.4的0.1M磷酸盐缓冲盐水(PBS)和pH 4.0的0.1M醋酸盐缓冲液中,使用透析技术研究肽的释放。数据采用修正的威布尔方程进行分析。肽的释放取决于温度,在37℃下30天内完成,在高温下3至5天内完成。高温下的体外释放曲线与37℃下的释放曲线相关性良好。所有温度下释放曲线的形状相似。使用修正的威布尔方程,温度升高的特征是模型参数α增加,α是表观速率常数的比例因子。在pH 7.4的PBS中,37℃下的完全释放从约30天缩短至50℃时的5天、55℃时的3.5天、60℃时的2.25天,在pH 4.0的醋酸盐缓冲液中50℃时为3天。模型参数β的值表明,在pH 7.4的PBS中55℃(2.740)和pH 4.0的0.1M醋酸盐缓冲液中50℃(2.711)时释放曲线的形状与37℃(2.677)时相似。水合和侵蚀的活化能分别确定为42.3和19.4千卡/摩尔。聚合物降解也取决于温度,活化能为31.6千卡/摩尔。短期体外释放研究提供了与长期释放相关联的可能性,从而减少了与长期研究相关的时间和费用。加速释放方法可用于预测长效微球剂型的长期释放,并可作为临床或商业批次释放的质量控制工具。