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An enteric-coated dry emulsion formulation for oral insulin delivery

机译:用于口服胰岛素递送的肠溶衣干乳剂

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摘要

A novel oral dosage formulation of insulin consisting of a surfactant, a vegetable oil, and a pH-responsive polymer has been developed. First, a solid-in-oil (S/O) suspension containing a surfactant-insulin complex was prepared. Solid-in-oil-in-water (S/O/W) emulsions were obtained by homogenizing the S/O suspension and the aqueous solution of hydroxypropylmethylcellulose phthalate (HPMCP). A microparticulate solid emulsion formulation was successfully prepared from the S/O/W emulsions by extruding them to an acidic aqueous solution, followed by lyophilization. The insulin release from the resultant dry emulsion responded to the change in external environment simulated by gastrointestinal conditions, suggesting that the new enteric-coated dry emulsion formulation is potentially applicable for the oral delivery of peptide and protein drugs. (c) 2005 Elsevier B.V. All rights reserved.
机译:已经开发了由表面活性剂,植物油和pH响应性聚合物组成的胰岛素的新型口服剂型。首先,制备包含表面活性剂-胰岛素复合物的油包固体(S / O)悬浮液。通过将S / O悬浮液和羟丙基甲基纤维素邻苯二甲酸酯(HPMCP)水溶液均化,可以获得水包油型固体(S / O / W)乳液。通过将S / O / W乳液挤出到酸性水溶液中,然后冻干,可以成功地制备出微粒状固体乳液制剂。从产生的干乳剂中释放的胰岛素对胃肠道条件模拟的外部环境变化作出了响应,这表明这种新型肠溶衣干乳剂配方可能适用于肽和蛋白质药物的口服给药。 (c)2005 Elsevier B.V.保留所有权利。

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