Research Center Pharmaceutical Engineering (RCPE) GmbH, Inffeldgasse 13, 8010 Graz, Austria.
Research Center Pharmaceutical Engineering (RCPE) GmbH, Inffeldgasse 13, 8010 Graz, Austria; Institute for Process and Particle Engineering, Graz University of Technology, Inffeldgasse 13, 8010 Graz, Austria.
Int J Pharm. 2022 Apr 25;618:121680. doi: 10.1016/j.ijpharm.2022.121680. Epub 2022 Mar 18.
Enteric coatings are designed to protect active pharmaceutical ingredients (APIs) against untimely release in the stomach. Acid protection of such coatings depends on the coating layer thickness and integrity, which must be determined in an accurate and reliable way to ensure the final product's desired performance. Our work addresses the use of optical coherence tomography (OCT) for characterizing the coating thickness and variability of an enteric-coated drug product and linking them to resistance against gastric fluid. In this study, three batches of enteric-coated tablets drawn during the manufacturing process were investigated. An industrial OCT system was used to establish the coating thickness variability of single tablets (intra-tablet), all tablets in a batch (inter-tablet) and between the batches (inter-batch). Based on the large amount of OCT data, we calculated a critical coating thickness for the investigated film coating, which was found to be 27.4 µm. The corresponding distribution has a mean coating thickness of 44.3 µm ± 7.8 µm. The final coated product has a final mean coating thickness of 63.4 µm ± 8.7 µm, guaranteeing that all tablets meet the quality criterion (i.e., acid protection). Based on the measured thickness distributions, already known distribution functions were considered and an additional, new function was proposed for characterizing the coating thickness distributions in the early stages of industrial coating processes. The proposed approach can be transferred to in-line monitoring of the tablet coating processes, which could drastically improve the production efficiency by ultimately allowing real-time release testing (RTRT).
肠溶性包衣旨在保护药物活性成分(APIs)免受胃部过早释放。这种涂层的酸保护取决于涂层的厚度和完整性,必须以准确可靠的方式来确定,以确保最终产品的预期性能。我们的工作涉及使用光学相干断层扫描(OCT)来表征肠溶性药物产品的涂层厚度和变化,并将其与抵抗胃液的能力联系起来。在这项研究中,研究了制造过程中抽取的三个批次的肠溶性片剂。工业 OCT 系统用于建立单个片剂(片剂内)、一批片剂(片剂间)和批次间(批间)的涂层厚度变化。基于大量的 OCT 数据,我们计算了所研究的薄膜涂层的临界涂层厚度,发现为 27.4 µm。相应的分布具有 44.3 µm ± 7.8 µm 的平均涂层厚度。最终涂覆的产品具有最终的平均涂层厚度为 63.4 µm ± 8.7 µm,保证了所有片剂都符合质量标准(即酸保护)。基于测量的厚度分布,考虑了已知的分布函数,并提出了一个新的函数来描述工业涂层过程早期的涂层厚度分布。所提出的方法可以转移到片剂涂层过程的在线监测,这最终可以通过实时释放测试(RTRT)极大地提高生产效率。