Department of Pharmacy, Faculty of Health and Medical Sciences, University of Copenhagen, Universitetsparken 2, 2100 Copenhagen, Denmark.
Losan Pharma GmbH, Otto-Hahn-Str. 13, 79395 Neuenburg, Germany.
Int J Pharm. 2023 Feb 5;632:122564. doi: 10.1016/j.ijpharm.2022.122564. Epub 2022 Dec 28.
In this study, the stability and intrinsic dissolution of vacuum compression molded (VCM) amorphous solid dispersions (ASDs) of efavirenz (EFV) were investigated in relation to its solubility limits in seven polymers determined by the melting point depression (MPD) method. The extrapolated solubility limits of EFV at 22 °C ranged from 3 to 68% (w/w) with PVOH being the only polymer suggesting immiscibility with EFV according to both MPD and Hansen solubility parameters (HSPs). All ASDs with EFV loadings below or close to their calculated solubility limit did not show any signs of crystallization upon conditioning for 7 months at either 22 or 37 °C and 23 or 75% relative humidity. However, all ASDs with EFV loading above the solubility limit crystallized at high humidity, while the ASDs with cellulose derived carrier polymers proved kinetically stable at low humidity over 7 months. While the EFV intrinsic dissolution rates from the VCM ASDs were partly depending on the polymer dissolution rate, no correlation was observed between EFV matrix crystallization and its miscibility in the polymer. Altogether, the observations of the study underline the importance of combining preformulation miscibility determination and dissolution studies to rationally decide on both stability and viability of ASD formulations.
在这项研究中,通过熔点降低(MPD)法测定了埃法韦仑(EFV)在七种聚合物中的溶解度极限,研究了真空压缩成型(VCM)无定形固体分散体(ASD)的稳定性和内在溶解率与溶解度极限的关系。EFV 在 22°C 时的溶解度极限经外推得出,范围为 3%至 68%(w/w),其中只有聚乙烯醇(PVOH)根据 MPD 和 Hansen 溶解度参数(HSP)均表明与 EFV 不混溶。所有 EFV 载药量低于或接近计算溶解度极限的 ASD,在 22 或 37°C 和 23 或 75%相对湿度下放置 7 个月后,均未出现结晶迹象。然而,所有 EFV 载药量超过溶解度极限的 ASD 在高湿度下均结晶,而源自纤维素的载体聚合物的 ASD 在 7 个月的低湿度下证明具有动力学稳定性。尽管 VCM ASD 中的 EFV 内在溶解速率部分取决于聚合物的溶解速率,但未观察到 EFV 基质结晶与其在聚合物中的混溶性之间存在相关性。总之,研究中的观察结果强调了在合理决定 ASD 制剂的稳定性和可行性时,结合预配方混溶性测定和溶解研究的重要性。