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通过固态 NMR 光谱学揭示固体分散体配方中药物溶出度与抗水致相分离能力之间的相关性。

Correlation between drug dissolution and resistance to water-induced phase separation in solid dispersion formulations revealed by solid-state NMR spectroscopy.

机构信息

Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba 260-8675, Japan.

Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba 260-8675, Japan.

出版信息

Int J Pharm. 2020 Mar 15;577:119086. doi: 10.1016/j.ijpharm.2020.119086. Epub 2020 Jan 25.

Abstract

We aimed to elucidate the dissolution mechanism of solid dispersions (SDs) according to the carrier polymers used. Nifedipine (NIF) and polymers dissolved simultaneously from NIF/Eudragit® S (EUD-S), NIF/Eudragit® L (EUD-L), and NIF/hypromellose (HPMC)/EUD-S spray-dried samples (SPDs). In contrast, NIF dissolved separately from polymers from NIF/HPMC and NIF/HPMC/EUD-L SPDs due to the formation of an amorphous NIF-rich interface. Solid-state NMR spectroscopy indicated that NIF-EUD interactions were stronger than NIF-HPMC interactions. NIF/HPMC SPD exhibited weak interactions; thus, it failed to inhibit phase separation during the dissolution process and control NIF dissolution. The hygroscopicity of SPDs was higher with HPMC mixing and increased substitution ratio of methacrylic acid in EUD. Moreover, solid-state NMR spectroscopy revealed that the NIF-EUD interactions were hindered to a large extent by the absorbed water. During the dissolution process of NIF/HPMC/EUD-L SPD, the introduction of water to the NIF-EUD-L interaction site could induce the phase separation and poor controllability of NIF dissolution. Water-induced phase separation should be considered based on molecular-level characterization to obtain SDs with enhanced drug dissolution. An investigation of the molecular state change caused by the absorbed water using solid-state NMR spectroscopy will be helpful in understanding the dissolution mechanism of SDs.

摘要

我们旨在根据所使用的载体聚合物阐明固体分散体(SD)的溶解机制。硝苯地平(NIF)和聚合物从 NIF/Eudragit® S(EUD-S)、NIF/Eudragit® L(EUD-L)和 NIF/羟丙甲纤维素(HPMC)/EUD-S 喷雾干燥样品(SPD)中同时溶解。相比之下,由于形成无定形富 NIF 界面,NIF 从 NIF/HPMC 和 NIF/HPMC/EUD-L SPD 中的聚合物中分别溶解。固态 NMR 光谱表明,NIF-EUD 相互作用强于 NIF-HPMC 相互作用。NIF/HPMC SPD 表现出较弱的相互作用;因此,它未能在溶解过程中抑制相分离并控制 NIF 溶解。HPMC 混合和 EUD 中甲基丙烯酸取代率增加会增加 SPD 的吸湿性。此外,固态 NMR 光谱表明,NIF-EUD 相互作用在很大程度上受到吸收水的阻碍。在 NIF/HPMC/EUD-L SPD 的溶解过程中,水进入 NIF-EUD-L 相互作用位点会导致相分离和 NIF 溶解的可控性差。应根据分子水平的表征考虑水诱导的相分离,以获得增强药物溶解的 SD。使用固态 NMR 光谱研究吸收水引起的分子状态变化将有助于理解 SD 的溶解机制。

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