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首页> 外文期刊>Chemical Engineering & Technology: Industrial Chemistry -Plant Equipment -Process Engineering -Biotechnology >Amoxicillin and Ethyl Cellulose Precipitation by Two Supercritical Antisolvent Processes
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Amoxicillin and Ethyl Cellulose Precipitation by Two Supercritical Antisolvent Processes

机译:两种超临界反溶剂法沉淀阿莫西林和乙基纤维素

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Composites of amoxicillin and ethyl cellulose in the micrometer range were precipitated by supercritical antisolvent (SAS) processes using carbon dioxide as anti-solvent and a mixture of dichloromethane and dimethylsulfoxide as solvents. Morphologies and mean diameter ranges were analyzed by scanning electron microscopy. X-ray photoelectron spectroscopy (XPS) and high-performance liquid chromatography were carried out in order to ensure successful coprecipita-tion and to determine the amoxicillin contents in the final products. The SAS processes used differ mainly in the way in which the solutions are introduced: through a normal or a coaxial nozzle. The XPS results provided proof that amoxicillin was not distributed in the same way in all the samples. The release behavior of the composites obtained was evaluated in two biological fluids, i.e., simulated gastric and simulated intestinal fluids. The different systems led to the release of the drug in different ways; but in all cases slower solubilization was obtained than for the pure drug.
机译:阿莫西林和乙基纤维素的微米范围内的复合物通过超临界抗溶剂(SAS)工艺沉淀,使用二氧化碳作为反溶剂,二氯甲烷和二甲基亚砜的混合物作为溶剂。形态和平均直径范围通过扫描电子显微镜分析。进行X射线光电子能谱(XPS)和高效液相色谱法以确保成功共沉淀并确定最终产品中阿莫西林的含量。所使用的SAS工艺的主要区别在于引入解决方案的方式不同:通过普通喷嘴或同轴喷嘴。 XPS结果提供了证据,证明在所有样品中阿莫西林的分布都不相同。在两种生物流体,即模拟的胃液和模拟的肠液中,评价了所得复合材料的释放行为。不同的系统导致药物的释放方式不同。但在所有情况下,溶解速度都比纯药物慢。

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