Department of Chemistry, Analytical and Biological Chemistry Research Facility (ABCRF), University College Cork, Ireland.
BARDS Acoustic Science Labs, Bio-Innovation Centre, UCC, Ireland.
Int J Pharm. 2018 Jun 10;544(1):31-38. doi: 10.1016/j.ijpharm.2018.04.018. Epub 2018 Apr 12.
There are no rapid dissolution based tests for determining coating thickness, integrity and drug concentration in controlled release pellets either during production or post-production. The manufacture of pellets requires several coating steps depending on the formulation. The sub-coating and enteric coating steps typically take up to six hours each followed by additional drying steps. Post production regulatory dissolution testing also takes up to six hours to determine if the batch can be released for commercial sale. The thickness of the enteric coating is a key factor that determines the release rate of the drug in the gastro-intestinal tract. Also, the amount of drug per unit mass decreases with increasing thickness of the enteric coating. In this study, the coating process is tracked from start to finish on an hourly basis by taking samples of pellets during production and testing those using BARDS (Broadband Acoustic Resonance Dissolution Spectroscopy). BARDS offers a rapid approach to characterising enteric coatings with measurements based on reproducible changes in the compressibility of a solvent due to the evolution of air during dissolution. This is monitored acoustically via associated changes in the frequency of induced acoustic resonances. A steady state acoustic lag time is associated with the disintegration of the enteric coatings in basic solution. This lag time is pH dependent and is indicative of the rate at which the coating layer dissolves. BARDS represents a possible future surrogate test for conventional USP dissolution testing as its data correlates directly with the thickness of the enteric coating, its integrity and also with the drug loading as validated by HPLC.
目前,还没有基于快速溶解的测试方法来检测控释丸在生产或生产后的包衣厚度、完整性和药物浓度。丸剂的制造需要根据配方进行多个包衣步骤。次包衣和肠溶包衣步骤通常每个步骤需要长达六个小时,然后是额外的干燥步骤。生产后的监管溶解测试也需要长达六个小时的时间来确定批能否放行用于商业销售。肠溶包衣的厚度是决定药物在胃肠道中释放速度的关键因素。此外,随着肠溶包衣厚度的增加,单位质量的药物量减少。在这项研究中,通过在生产过程中每隔一小时取丸剂样品,并使用 BARDS(宽带声振溶解光谱法)对其进行测试,从开始到结束跟踪包衣过程。BARDS 提供了一种快速的方法来表征肠溶包衣,其测量基于溶剂由于溶解过程中空气的演化而产生的可压缩性的可重复变化。这通过与感应声共振频率相关的变化在声学上进行监测。与基本溶液中肠溶包衣崩解相关的稳态声滞后时间。该滞后时间与 pH 值有关,表明涂层溶解的速度。BARDS 代表了未来可能替代常规 USP 溶解测试的替代测试方法,因为其数据与肠溶包衣的厚度、完整性以及通过 HPLC 验证的药物载量直接相关。