School of Pharmacy, University of Eastern Finland, PO Box 1627, FI-70211, Kuopio, Finland.
J Pharm Biomed Anal. 2010 Jun 5;52(2):181-9. doi: 10.1016/j.jpba.2010.01.011. Epub 2010 Jan 15.
Monitoring systems providing fast and reliable, even on-line data, from a distinct process stage or final product are needed in drug development, from the early stages of drug discovery until the drug product manufacturing procedures. This includes also processes involving solid particles, such as drug dissolution. However, the existing in vitro drug dissolution test methods suffer limitations, such as long sampling times of 30-60s and thus the inability to be adapted to continuous monitoring, time consuming sample preparation and consumption of large amounts of reagents. In this study, an optical method for monitoring the dissolution rate of pharmaceutical powders was evaluated with model drugs having different dissolution rates. The measuring system consisted of a laser source, light detector, oscilloscope, magnetic stirrer and sample vessel. The intensity of laser light transmitted through the dissolution medium was recorded and displayed by the oscilloscope. Dissolution curves were produced by fitting the raw data with mathematical functions. The optical method was found to be resource-saving, reliable and capable of detecting differences in even rapid dissolution rates of drug compounds. This technique might have targets of application in real-time monitoring of processes in many different sectors, including the pharmaceutical industry.
在药物开发过程中,从药物发现的早期阶段到药物产品制造过程,都需要监测系统提供快速、可靠的,甚至是在线数据,以跟踪特定工艺阶段或最终产品的情况。这包括涉及固体颗粒的过程,例如药物溶出度。然而,现有的体外药物溶出度测试方法存在局限性,例如 30-60 秒的长采样时间,因此无法适应连续监测、耗时的样品制备和大量试剂的消耗。在这项研究中,评估了一种用于监测药物粉末溶出率的光学方法,该方法使用具有不同溶出率的模型药物进行了评估。测量系统由激光源、光探测器、示波器、磁力搅拌器和样品容器组成。通过示波器记录和显示穿过溶解介质的激光强度。通过将原始数据拟合到数学函数来生成溶出曲线。研究发现,该光学方法具有节省资源、可靠且能够检测药物化合物快速溶出率差异的特点。该技术可能适用于许多不同领域(包括制药行业)的实时过程监测。