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通过甲基丙烯酸-丙烯酸乙酯共聚物(1:1)与羟丙基纤维素在三元无定形固体分散体中的协同相互作用提高塞来昔布的溶解度和过饱和度

Boost of solubility and supersaturation of celecoxib via synergistic interactions of methacrylic acid-ethyl acrylate copolymer (1:1) and hydroxypropyl cellulose in ternary amorphous solid dispersions.

作者信息

Pöstges Florian, Kayser Kevin, Stoyanov Edmont, Wagner Karl G

机构信息

Department of Pharmaceutical Technology and Biopharmaceutics, University of Bonn, Gerhard-Domagk-Str. 3, 53121 Bonn, Germany.

Nisso Chemical Europe GmbH, Berliner Allee 42, 40212 Düsseldorf, Germany.

出版信息

Int J Pharm X. 2022 Mar 24;4:100115. doi: 10.1016/j.ijpx.2022.100115. eCollection 2022 Dec.

Abstract

A current trend in the development of amorphous solid dispersions (ASDs) is the combination of two polymers for synergistic enhancement in supersaturation of poorly soluble drugs. We investigated the supersaturation potential of celecoxib (CXB) using combinations of methacrylic acid-ethyl acrylate copolymer (1:1) (EL 100-55) and hydroxypropyl cellulose (HPC) SSL. Initially, the supersaturation potential of single polymers and combinations in various ratios was assessed. While EL 100-55 and HPC SSL alone showed limited potential in solubility enhancement of CXB the combination of both polymers led to a boost of CXB solubility, whereby most promising results were obtained using a 50:50 polymer ratio. Binary and ternary CXB ASDs (10% drug load) were prepared via vacuum compressing molding (VCM) and hot melt extrusion (HME). ASDs were studied by exploring the miscibility and intermolecular interactions and tested for their dissolution performance. HPC SSL was identified to be a suitable precipitation inhibitor when added to a fast dissolving CXB: EL 100-55 ASD. Ternary ASDs showed even further dissolution improvement, when processed by HME. The combination of heat and shear stress led to a homogeneous and intimate mixture of EL 100-55 and HPC SSL, resulting in formation of synergistic interactions with pronounced impact on CXB supersaturation.

摘要

无定形固体分散体(ASD)开发的当前趋势是将两种聚合物结合起来,以协同增强难溶性药物的过饱和度。我们使用甲基丙烯酸-丙烯酸乙酯共聚物(1:1)(EL 100-55)和羟丙基纤维素(HPC)SSL的组合研究了塞来昔布(CXB)的过饱和潜力。最初,评估了单一聚合物和各种比例组合的过饱和潜力。虽然单独的EL 100-55和HPC SSL在提高CXB溶解度方面潜力有限,但两种聚合物的组合导致CXB溶解度提高,其中使用50:50的聚合物比例获得了最有前景的结果。通过真空压缩成型(VCM)和热熔挤出(HME)制备了二元和三元CXB ASD(药物载量为10%)。通过探索混溶性和分子间相互作用对ASD进行了研究,并测试了它们的溶解性能。当添加到快速溶解的CXB:EL 100-55 ASD中时,HPC SSL被确定为一种合适的沉淀抑制剂。当通过HME加工时,三元ASD显示出进一步的溶解改善。热和剪切应力的组合导致EL 100-55和HPC SSL形成均匀且紧密的混合物,从而形成对CXB过饱和度有显著影响的协同相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dc5/8968008/d7dd9cb7c4b2/ga1.jpg

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