A Fast and Non-destructive Terahertz Dissolution Assay for Immediate Release Tablets

被引:32
作者
Bawuah, Prince [1 ]
Markl, Daniel [2 ,3 ]
Turner, Alice [2 ,4 ]
Evans, Mike [5 ]
Portieri, Alessia [5 ]
Farrell, Daniel [5 ]
Lucas, Ralph [6 ]
Anderson, Andrew [7 ]
Goodwin, Daniel J. [7 ]
Zeitler, J. Axel [1 ]
机构
[1] Univ Cambridge, Dept Chem Engn & Biotechnol, Cambridge, England
[2] Univ Strathclyde, Strathclyde Inst Pharm & Biomed Sci, Glasgow, Lanark, Scotland
[3] Univ Strathclyde, Technol & Innovat Ctr, EPSRC Future Mfg Res Hub Continuous Mfg & Adv Cry, Glasgow, Lanark, Scotland
[4] Univ Strathclyde, Technol & Innovat Ctr, EPSRC CMAC Future Mfg Res Hub, CMAC Natl Facil, 99 George St, Glasgow G1 1RD, Lanark, Scotland
[5] TeraView Ltd, 1 Enterprise,Cambridge Res Pk, Cambridge CB25 9PD, England
[6] Huxley Bertram Engn Ltd, 53 Pembroke Ave, Cambridge, England
[7] David Jack Ctr, Res & Dev, GSK, Pk Rd, Ware, Herts, England
基金
“创新英国”项目; 英国工程与自然科学研究理事会;
关键词
Terahertz spectroscopy; Pharmaceutical tablet; Porosity; disintegration; Dissolution; Real time release testing; Process analytical technology; PHARMACEUTICAL TABLETS; POROSITY MEASUREMENT; DISINTEGRATION TIME; TENSILE-STRENGTH; SPECTROSCOPY; PREDICTION; TRANSMISSION; PROFILES; COMPACTS;
D O I
10.1016/j.xphs.2020.11.041
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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. (c) 2021 American Pharmacists Association (R). Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:2083 / 2092
页数:10
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