The Life Quality Engineering Interest Group, School of Chemical and Environmental Engineering, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou, 215123, China.
School of Chemical Engineering, UNSW Sydney, Sydney, NSW, 2052, Australia.
AAPS PharmSciTech. 2022 Sep 1;23(7):246. doi: 10.1208/s12249-022-02401-x.
Compared to traditional drug release monitoring with manual sampling and testing procedures, low-field nuclear magnetic resonance (LF-NMR) imaging is a one-step, visual, non-destructive, and non-invasive measurement method. Here, we reported the application of LF-NMR to image the morphology, component, sub-diffusion, and spatial distribution of a solid oral formulation, Biyankang tablets, during dissolution in vitro. The drug ingredients with characteristic relaxation times were distinguished and localized based on the signal of standards, such as patchouli oil, Xanthium strumarium extract, and starch. The hydration, swelling, disintegration, and sub-diffusion of tablets in simulated gastric fluids (SGF) were visualized statically. All tablets showed similar expansion (37.4-42.0%) along the direction of thickness at 25 min and reached a full disintegration at 145 min, at pH 1.80-6.15, indicating pH-independent swelling and disintegration. Compared to that static immersion within 20 mL SGF, the tablet disintegration time was shortened by ~ 11% in 30 mL SGF. The application of shear reduced the time by ~ 28%, suggesting a major role of hydrodynamic condition in tablet dissolution. The ability to simultaneously visualize, distinguish, and localize drug ingredients using LF-NMR is expected to provide valuable information to develop drug release monitoring systems in vitro and potentially in vivo using small animal studies.
与传统的药物释放监测方法相比,低场核磁共振(LF-NMR)成像技术是一种一步式、可视化、无损、非侵入性的测量方法。在这里,我们报告了 LF-NMR 在体外溶解过程中对固体口服制剂比炎康片的形态、成分、亚扩散和空间分布进行成像的应用。根据标准(如薄荷油、苍耳提取物和淀粉)的信号,对具有特征弛豫时间的药物成分进行区分和定位。通过静态可视化,观察片剂在模拟胃液(SGF)中的水合、膨胀、崩解和亚扩散。在 pH 值为 1.80-6.15 时,所有片剂在 25 分钟内沿厚度方向显示出相似的膨胀(37.4-42.0%),并在 145 分钟时完全崩解,表明片剂在膨胀和崩解过程中不受 pH 影响。与在 20 毫升 SGF 中静态浸泡相比,在 30 毫升 SGF 中片剂崩解时间缩短了约 11%。剪切的应用将时间缩短了约 28%,这表明流体动力学条件在片剂溶解中起着主要作用。LF-NMR 能够同时可视化、区分和定位药物成分,有望为开发体外药物释放监测系统提供有价值的信息,并有可能通过小动物研究进行体内研究。