Sutananta W, Craig D Q, Newton J M
Centre for Materials Science, School of Pharmacy, University of London, UK.
J Pharm Pharmacol. 1995 Mar;47(3):182-7. doi: 10.1111/j.2042-7158.1995.tb05775.x.
A series of dispersions containing theophylline in Gelucires 43/01, 54/02, 50/02, 50/13 and 55/18 was prepared and the physical structures studied using differential scanning calorimetry. The dissolution, erosion and swelling profiles of the drug dispersions were assessed. Gelucire 43/01 and 54/02 systems were found to release the drug by a simple diffusion mechanism, with no evidence for erosion or swelling being noted. Gelucire 55/18, however, showed a more complex mechanism involving both diffusion and erosion. On increasing the drug load within the matrices, the predominance of the erosion mechanism increased. Drug release from Gelucire 50/13 matrices took place principally by erosion, although the process was dominated by swelling and subsequent disintegration of the matrix, rather than simple dissolution of the base as was found for Gelucire 55/18. Gelucire 50/02 matrices also exhibited swelling, although drug release occurred predominantly via diffusion. The study, therefore, demonstrates that Gelucires may release incorporated drugs by a number of mechanisms depending on the chemical composition of the base.
制备了一系列含有氨茶碱的Gelucire 43/01、54/02、50/02、50/13和55/18的分散体,并使用差示扫描量热法研究其物理结构。评估了药物分散体的溶解、侵蚀和溶胀曲线。发现Gelucire 43/01和54/02体系通过简单扩散机制释放药物,未观察到侵蚀或溶胀迹象。然而,Gelucire 55/18显示出一种更复杂的机制,涉及扩散和侵蚀。随着基质中药物载量的增加,侵蚀机制的主导作用增强。Gelucire 50/13基质中的药物释放主要通过侵蚀发生,尽管该过程以基质的溶胀和随后的崩解为主导,而不是像Gelucire 55/18那样以基质的简单溶解为主导。Gelucire 50/02基质也表现出溶胀,尽管药物释放主要通过扩散发生。因此,该研究表明,根据基质的化学成分,Gelucire可能通过多种机制释放包封的药物。