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Co-precipitation of amoxicillin and ethyl cellulose microparticles by supercritical antisolvent process

机译:超临界反溶剂法共沉淀阿莫西林和乙基纤维素微粒

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摘要

Microparticles of ethyl cellulose (EC) and amoxicillin (AMC) have been precipitated by a supercritical antisolvent process (SAS) using CO2 as the antisolvent and a mixture of dichloromethane (DCM) and dimethyl sulfoxide (DMSO) as solvents. Combinations of three temperatures (308, 323 and 333 K) and four pressures (100, 150, 200 and 250 bar) were assessed in the vessel and the rest of the variables were held constant (i.e. CO2 flow rate, sample flow rate, washing time, nozzle diameter and the amoxi-cillimethyl cellulose ratio). Scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and elemental analysis (EA) were used to determine the particle size and shape and to confirm the presence of both compounds in the resulting precipitates. In most cases, mixed amoxicillin and ethyl cellulose particles were produced with sizes in the micrometer range. Pressure and temperature effects on the co-precipitation were investigated. The release behaviour of the microparticles precipitated by the SAS process was evaluated in two biological fluids - simulated gastric and simulated intestinal fluids. Co-precipitated materials allowed a slower drug release rate than pure drug.
机译:乙基纤维素(EC)和阿莫西林(AMC)的微粒已通过超临界抗溶剂工艺(SAS)沉淀,使用的是CO2作为反溶剂,二氯甲烷(DCM)和二甲基亚砜(DMSO)的混合物作为溶剂。在容器中评估了三个温度(308、323和333 K)和四个压力(100、150、200和250 bar)的组合,其余变量保持恒定(即,CO2流量,样品流量,洗涤时间,喷嘴直径和阿莫西-甲基纤维素比率)。使用扫描电子显微镜(SEM),X射线光电子能谱(XPS)和元素分析(EA)来确定粒径和形状,并确认所得沉淀物中两种化合物的存在。在大多数情况下,生产的阿莫西林和乙基纤维素混合颗粒的尺寸在微米范围内。研究了压力和温度对共沉淀的影响。在两种生物流体(模拟胃液和模拟肠液)中评估了通过SAS工艺沉淀的微粒的释放行为。共沉淀的材料使药物的释放速度比纯药物慢。

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