Laboratory of Food, Drug, and Cosmetics (LTMAC), School of Health Sciences, University of Brasilia, Brasilia, DF, 70910-900, Brazil.
Faculty of Ceilândia, University of Brasília (UnB), Brasilia, DF, 72220-900, Brazil.
AAPS PharmSciTech. 2019 Dec 3;21(1):8. doi: 10.1208/s12249-019-1554-1.
The subdivision of sustained release tablets is a controversial issue, especially concerning its impact on dissolution profiles. The purpose of this study was to elucidate the behavior upon subdivision of this class of tablets. For this, three common sustained release matrices containing different technologies were selected, e.g., a tablet comprised of a multiple-unit particulate system (MUPS), a lipid matrix tablet, and a polymeric inert matrix tablet. These tablets were studied concerning their physicochemical performance, dissolution rate, and kinetic profile before and after their subdivision. When subdivision occurred in the scoreline, mass variation and mass loss were below the mean values described in the literature. The dissolution of tablets with inert matrices and some lipid tablets that had their matrices preserved along the dissolution was influenced directly by tablet surface area, which increased after the subdivision. Such a result implies possible clinical consequences, especially in the case of drugs with a narrow therapeutic window, such as clomipramine. Conversely, the subdivision of MUPS tablets did not interfere in the dissolution profile since the drug was released from the granules that resulted from tablet disintegration. Hence, MUPS technology is the most recommended to produce sustained release matrix tablets intended for dose adjustment upon subdivision.
缓控释片剂的细分是一个有争议的问题,特别是其对溶出曲线的影响。本研究旨在阐明该类片剂细分后的行为。为此,选择了三种常见的包含不同技术的缓控释基质,例如由多单位颗粒系统(MUPS)组成的片剂、脂质基质片剂和聚合物惰性基质片剂。研究了这些片剂在细分前后的物理化学性能、溶出率和动力学特征。当在刻痕处进行细分时,质量变化和质量损失低于文献中描述的平均值。具有惰性基质的片剂和一些其基质在整个溶解过程中得以保留的脂质片剂的溶解直接受到片剂表面积的影响,细分后表面积增加。这样的结果意味着可能存在临床后果,特别是对于治疗窗较窄的药物,如氯米帕明。相反,MUPS 片剂的细分不会干扰溶出曲线,因为药物是从片剂崩解产生的颗粒中释放出来的。因此,MUPS 技术是最推荐用于生产旨在细分时进行剂量调整的缓控释基质片剂的技术。