New Jersey Institute of Technology, Newark, New Jersey 07102.
New Jersey Institute of Technology, Newark, New Jersey 07102.
J Pharm Sci. 2019 Jan;108(1):234-242. doi: 10.1016/j.xphs.2018.11.025. Epub 2018 Nov 22.
The effect of particle size on the dissolution behavior of the particles of amorphous solid dispersions (ASDs) of griseofulvin (GF), with 0%-50% Kollidon VA 64 as a crystallization inhibitor is investigated. Both the final dissolved GF concentration and the dissolution rate of GF ASDs were found to be inversely proportional to the particle size. The solution concentrations for the smallest (45-75 μm) size group with different polymer loadings were significantly higher than those for the largest (250-355 μm) group regardless of the initial GF amount. Specifically, the dissolution rate of GF ASDs with 50% polymer loading for the finest group was 2.7 times higher than for the largest group under supersaturating conditions. The rates of dissolution and recrystallization were assessed through surface concentration (C) and Avrami recrystallization rate kinetics, where the solid-state recrystallization was confirmed using Raman spectroscopy. Outcomes indicated that particle size reduction enhanced ASD drug loading by reducing the amount of polymer necessary as finest size ASDs initially dissolve faster, negating their higher recrystallization rate. Kollidon® VA 64 at 30% loading was sufficient to inhibit the GF recrystallization. Overall, the combination of particle size reduction and recrystallization inhibition is effective for improved dissolution behavior of GF ASDs.
研究了粒径对灰黄霉素(GF)无定形固体分散体(ASD)的溶解行为的影响,其中 0%-50% 的共聚维酮(Kollidon VA 64)作为结晶抑制剂。GF ASDs 的最终溶解 GF 浓度和溶解速率都发现与粒径成反比。无论初始 GF 量如何,具有不同聚合物负载的最小(45-75μm)粒径组的溶液浓度明显高于最大(250-355μm)粒径组。具体而言,在过饱和条件下,具有 50%聚合物负载的 GF ASDs 的最细粒径组的溶解速率比最大粒径组高 2.7 倍。通过表面浓度(C)和 Avrami 结晶动力学评估了溶解和再结晶的速率,其中使用拉曼光谱证实了固态再结晶。结果表明,通过减少作为最细粒径 ASDs 最初更快溶解所需的聚合物量,减少粒径可以提高 ASD 药物负载量,从而抵消其较高的再结晶速率。共聚维酮(Kollidon VA 64)的 30%负载量足以抑制 GF 的再结晶。总的来说,粒径减小和再结晶抑制的结合对于改善 GF ASDs 的溶解行为是有效的。