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溶剂对通过珠磨法制备的无定形固体分散体的可制造性、相行为和形态的影响。

Solvent influence on manufacturability, phase behavior and morphology of amorphous solid dispersions prepared via bead coating.

机构信息

Department of Pharmaceutical and Pharmacological Sciences, Drug Delivery and Disposition Leuven 3000, Belgium.

出版信息

Eur J Pharm Biopharm. 2021 Oct;167:175-188. doi: 10.1016/j.ejpb.2021.07.013. Epub 2021 Jul 26.

Abstract

Bead coating or fluid-bed coating serves as an auspicious solvent-based amorphous solid dispersion (ASD) manufacturing technique in respect of minimization of potential physical stability issues. However, the impact of solvent selection on the bead coating process and its resulting pellet formulation is, to the best of our knowledge, never investigated before. This study therefore aims to investigate the influence of the solvent on the bead coating process itself (i.e. manufacturability) and on solid-state characteristics of the resulting ASDs coated onto beads. For this purpose, the drug-polymer system felodipine (FEL)-poly(vinylpyrrolidone-co-vinyl acetate) (PVP-VA) was coated onto microcrystalline cellulose (MCC) beads from acetonitrile (ACN), methanol (MeOH), ethanol (EtOH), acetone (Ac), 2-propanol (PrOH), dichloromethane (DCM) and ethyl acetate (EthAc). A drug loading screening approach with bead coating revealed analogous ability to manufacture high drug-loaded ASDs from the different organic solvents. The results show no correlation with crystallization tendency or with equilibrium solubility of the drug in the different solvents, nor with the solvent-dependent drug-polymer miscibility obtained from film casting experiments. Distinct coating morphologies were however observed for PVP-VA and FEL-PVP-VA ASDs deposited onto beads from the various solvents, which is attributed to differences in solvent evaporation kinetics.

摘要

包衣或流化床包衣是一种有前途的基于溶剂的无定形固体分散体(ASD)制造技术,可最大限度地减少潜在的物理稳定性问题。然而,就我们所知,溶剂选择对包衣过程及其所得丸剂配方的影响从未被研究过。因此,本研究旨在研究溶剂对包衣过程本身(即可制造性)和涂覆在丸剂上的所得 ASD 的固态特性的影响。为此,将药物-聚合物系统非洛地平(FEL)-聚(乙烯基吡咯烷酮-co-醋酸乙烯酯)(PVP-VA)从乙腈(ACN)、甲醇(MeOH)、乙醇(EtOH)、丙酮(Ac)、异丙醇(PrOH)、二氯甲烷(DCM)和乙酸乙酯(EthAc)涂覆到微晶纤维素(MCC)丸剂上。通过丸剂包衣进行的药物负载筛选方法表明,从不同有机溶剂中制造高载药量 ASD 的能力类似。结果与药物在不同溶剂中的结晶倾向或平衡溶解度、以及从薄膜浇铸实验获得的与溶剂相关的药物-聚合物混溶性均无相关性。然而,从不同溶剂中沉积到丸剂上的 PVP-VA 和 FEL-PVP-VA ASD 观察到明显不同的包衣形态,这归因于溶剂蒸发动力学的差异。

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