首页> 外文会议>Annual meeting exposition of the Controlled Release Society >Influence of Particle Size on Bioavailability and Rate of Absorption For Oral Dosage Forms Prepared From Poorly Water Soluble Drugs: A Comparison Between in-silico, in-vitro and invivo Pharmacokinetic Data.
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Influence of Particle Size on Bioavailability and Rate of Absorption For Oral Dosage Forms Prepared From Poorly Water Soluble Drugs: A Comparison Between in-silico, in-vitro and invivo Pharmacokinetic Data.

机译:粒度对水溶性药物不良制备的口服剂型生物利用度的影响及其吸收率:硅,体外和Invivo药代动力学数据的比较。

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The influence of particle size on oral bioavailability was evaluated in terms of the rate of dissolution of poorly soluble drugs and in-vivo PK results. The in-vitro dissolution corroborated a new theoretical model for dissolution of sub-micron colloidal suspensions. The invivo data clearly demonstrated the influence of particle size which could be readily explained in terms of the theoretical model.
机译:粒度对口服生物利用度的影响是在溶解差的药物和体内PK结果的溶解速率方面评价的。体外溶解证实了亚微米胶体悬浮液溶解的新理论模型。 Invivo数据清楚地证明了粒度的影响,这可以在理论模型方面容易地解释。

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