Swedish NMR Centre, University of Gothenburg, SE-41390 Gothenburg, Sweden; Department of Chemistry and Chemical Engineering, Chalmers University of Technology, SE-412 96 Gothenburg, Sweden.
Pharmaceutical Technology and Development, AstraZeneca Gothenburg, SE-43183 Mölndal, Sweden.
J Control Release. 2019 Oct;311-312:117-124. doi: 10.1016/j.jconrel.2019.08.025. Epub 2019 Aug 24.
Polymer films based on mixtures of ethyl cellulose (EC) and hydroxypropyl cellulose (HPC) have been widely used to coat pellets and tablets to modify the release profile of drugs. For three different EC/HPC films we used H and F MRI in combination with a designed release cell to monitor the drug, polymer and water in 5 dimensional (5D) datasets; three spatial, one diffusion or relaxation and a temporal dimension, in real time. We observed that the water inflow through the films correlated with the initiation of the dissolution of the drug in the tablet beneath the film. Leaching of the pore forming HPC further accelerated water penetration and resulted in a drug release onset after a hydrostatic pressure was generated below the film indicated by positional changes of the film. For the more permeable film, both water ingress and drug egress showed a large variability of release over the film surface indicating the heterogeneity of the system. Furthermore, the H diffusion dataset revealed the formation of a gel layer of HPC at the film surface. We conclude that the setup presented provides a significant level of details, which are not achieved with traditional methods.
基于乙基纤维素(EC)和羟丙基纤维素(HPC)混合物的聚合物薄膜已被广泛用于包衣丸剂和片剂,以改变药物的释放曲线。对于三种不同的 EC/HPC 薄膜,我们使用 H 和 F MRI 结合设计的释放池,在实时的 5 维(5D)数据集中监测药物、聚合物和水;三维空间、一维扩散或弛豫和时间维度。我们观察到,水通过薄膜的流入与薄膜下片剂中药物溶解的开始相关。形成孔的 HPC 的浸出进一步加速了水的渗透,并导致薄膜下产生静水压力后药物释放开始,这可以通过薄膜的位置变化来指示。对于更具渗透性的薄膜,水的进入和药物的流出都显示出在薄膜表面上释放的高度可变性,表明该系统的不均匀性。此外,H 扩散数据集显示在薄膜表面形成了 HPC 的凝胶层。我们得出结论,所提出的设置提供了传统方法无法达到的详细程度。