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Selected Pharmaceutical Excipients:Physicochemical Properties and their Excipient-Excipient Interactions

机译:选定的药物辅料:理化性质及其与辅料的相互作用

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Excipients are secondary ingredients added to a formulation to aid the delivery, processing andstability of the active drug/ drugs. Formulation stability largely depends on interaction of excipients orlack of interaction of excipients with the active drug and other excipients. The objective of this study wasto analyze any excipients- excipient interactions within the selected pharmaceutical excipients.Forty of the most commonly used excipients, selected on the basis of their utilization informulations were organized into seven categories: Alcohols, Carbohydrates, Sugars, Acid and Salts,Polymers, Oils and Waxes and Inorganics. The excipients selected for this study included polyethyleneglycol 1450, polyethylene glycol 4000, polyethylene glycol 8000, Mannitol, Sorbitol, Corn Starch,Microcrystalline Cellulose, Ethyl Cellulose, Stearic acid, Magnesium stearate, and Benzoic acid. Binarymixtures of the excipients were prepared in the ratio of 1:1 w/w and studied by Differential ScanningCalorimetry (DSC), Thermal Gravimetric Analysis (TGA) and Powder X-ray Diffraction Analysis(PXRD). The properties obtained from the binary mixtures were compared with the individual excipientsto predict any deviant behaviour and thus probable interactions.The binary mixtures which showed no interactions in both DSC and PXRD studies included PEGs:PEGs, PEGs: Sorbitol, PEGs: Stearic acid, PEGs: Benzoic acid, mannitol: sorbitol, mannitol: ethylcellulose, mannitol: magnesium stearate, and sorbitol: benzoic acid. These mixtures are suggested to becompatible for formulation purpose.
机译:赋形剂是添加到配方中的辅助成分,有助于输送,加工和 活性药物的稳定性。制剂的稳定性在很大程度上取决于赋形剂或 赋形剂与活性药物和其他赋形剂之间缺乏相互作用。这项研究的目的是 分析所选药物辅料中的任何辅料-辅料相互作用。 40种最常用的赋形剂,是根据它们在下列物质中的利用而选择的 配方分为七个类别:酒精,碳水化合物,糖,酸和盐, 聚合物,油,蜡和无机物。本研究选择的赋形剂包括聚乙烯 乙二醇1450,聚乙二醇4000,聚乙二醇8000,甘露醇,山梨糖醇,玉米淀粉, 微晶纤维素,乙基纤维素,硬脂酸,硬脂酸镁和苯甲酸。二进位 以1:1 w / w的比例制备赋形剂的混合物并通过差示扫描研究 量热法(DSC),热重分析(TGA)和粉末X射线衍射分析 (PXRD)。从二元混合物获得的性质与单独的赋形剂进行比较 预测任何异常行为,从而预测可能的相互作用。 在DSC和PXRD研究中均未显示相互作用的二元混合物包括PEG: PEG,PEG:山梨醇,PEG:硬脂酸,PEG:苯甲酸,甘露醇:山梨醇,甘露醇:乙基 纤维素,甘露醇:硬脂酸镁,山梨糖醇:苯甲酸。这些混合物建议是 兼容配方用途。

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