Department of Chemical Engineering and Biotechnology, University of Cambridge, Cambridge, UK.
University of Strathclyde, Strathclyde Institute of Pharmacy and Biomedical Sciences, Glasgow, UK; EPSRC Future Manufacturing Research Hub for Continuous Manufacturing and Advanced Crystallisation (CMAC), University of Strathclyde, Technology and Innovation Centre, Glasgow, UK.
J Pharm Sci. 2021 May;110(5):2083-2092. doi: 10.1016/j.xphs.2020.11.041. Epub 2020 Dec 8.
There is a clear need for a robust process analytical technology tool that can be used for on-line/in-line prediction of dissolution and disintegration characteristics of pharmaceutical tablets during manufacture. Tablet porosity is a reliable and fundamental critical quality attribute which controls key mass transport mechanisms that govern disintegration and dissolution behavior. A measurement protocol was developed to measure the total porosity of a large number of tablets in transmission without the need for any sample preparation. By using this fast and non-destructive terahertz spectroscopy method it is possible to predict the disintegration and dissolution of drug from a tablet in less than a second per sample without the need of a chemometric model. The validity of the terahertz porosity method was established across a range of immediate release (IR) formulations of ibuprofen and indomethacin tablets of varying geometries as well as with and without debossing. Excellent correlation was observed between the measured terahertz porosity, dissolution characteristics (time to release 50% drug content) and disintegration time for all samples. These promising results and considering the robustness of the terahertz method pave the way for a fully automated at-line/on-line porosity sensor for real time release testing of IR tablets dissolution.
显然需要一种强大的过程分析技术工具,用于在线/在线预测药物片剂在制造过程中的溶出度和崩解特性。片剂孔隙率是一种可靠且基本的关键质量属性,控制着控制崩解和溶解行为的关键传质机制。已经开发了一种测量协议,用于在传输中测量大量片剂的总孔隙率,而无需任何样品制备。通过使用这种快速且无损的太赫兹光谱法,有可能在不到一秒的时间内预测药物从片剂中的崩解和溶解,而无需化学计量模型。太赫兹孔隙率方法的有效性已经在布洛芬和吲哚美辛的各种即时释放(IR)制剂的片剂以及有和没有压痕的片剂中得到了验证。所有样品的太赫兹孔隙率、溶解特性(释放 50%药物含量的时间)和崩解时间之间都观察到了极好的相关性。这些有希望的结果以及太赫兹方法的稳健性为实时释放测试的全自动在线/在线孔隙率传感器铺平了道路,用于即时释放片剂的溶解。