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The influence of lecithin on in vitro release and in vivo absorption of paracetamol from suppositories

机译:卵磷脂对体外释放和寄生酵母的体内吸收的影响

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In vitro release study revealed that lecithin (2% w/w) decreases significantly the release rate of paracetamol from lipid-type suppositories. The in vitro results can not be correlated with in vivo pharmacokinetics since no difference was observed between suppositories with and without lecithin regarding the concentration profiles of paracetamol in saliva
机译:体外释放研究表明,卵磷脂(2%w / w)显着降低了亚乙酰氨基酚的释放率来自脂质型栓剂。体外结果不能与体内药代动力学相关,因为在唾液中栓剂和没有卵磷酰胺的栓剂之间没有观察到差异,关于唾液中扑热息醇的浓度曲线

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