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首页> 外文期刊>International Current Pharmaceutical Journal >Dissolution rate and bioavailability enhancement of co-ground mixtures of paliperidone, with different hydrophilic carriers
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Dissolution rate and bioavailability enhancement of co-ground mixtures of paliperidone, with different hydrophilic carriers

机译:具有不同亲水性载体的帕潘立酮共研磨混合物的溶出度和生物利用度的提高

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Co-ground mixtures of poorly water soluble drug Paliperidone (PAL) with different hydrophilic carriers [Polyvinylpyrrolidine (Plasdone K-25 and Plasdone S-630), Hydroxypropyl methyl cellulose (HPMC), Hydroxypropylcellulose (HPC) and Sodium alginate were prepared to improve the dissolution rate of PAL. Co-grinding with PVP, especially with PVP- S630 (Vinyl pyrrolidone/ vinyl acetate co-polymer), was more effective in reduction of particle size than milling of drug alone. DSC studies indicated that crystalline nature of drug was reduced after co-grinding with PVP grades as compared to their corresponding physical mixtures. The hydrophilic carriers other than PVP did not reduce the crystalline nature of the drug significantly. X-ray diffraction (XRD) was carried out for selected batches to confirm DSC results. Significant enhancement in dissolution rate as well as extent was observed with co-ground mixtures of drug and PVP. Among all the prepared batches in this study, co-ground mixture of PAL and Plasdone S-630 in 1:1 ratio showed best results in terms of extent of dissolution as well as dissolution rate in water. This effect was not only due to particle size reduction, but also loss of crystalline nature of the drug during co-grinding. PVP was found to be a better carrier among the different hydrophilic carriers used in the study for improving the dissolution characteristics of PAL. The extent of the mean plasma exposures of PAL was 7-fold higher in animals treated with co-ground mixture of PAL, Plasdone S630 (1:1) compared to animals treated with Pure PAL.DOI:?http://dx.doi.org/10.3329/icpj.v2i3.13632 International Current Pharmaceutical Journal, February 2013, 2(3): 70-77
机译:制备水溶性差的药物帕潘立酮(PAL)和不同的亲水性载体[聚乙烯基吡咯烷(Plasdone K-25和Plasdone S-630),羟丙基甲基纤维素(HPMC),羟丙基纤维素(HPC)和海藻酸钠)的共研磨混合物。 PAL的溶出度。与PVP共同研磨,特别是与PVP-S630(乙烯基吡咯烷酮/乙酸乙烯酯共聚物)共同研磨比单独研磨药物更有效地减小了粒径。 DSC研究表明,与相应的物理混合物相比,与PVP等级共研磨后,药物的结晶性降低了。除PVP以外的亲水性载体并未显着降低药物的结晶性。对选定的批次进行了X射线衍射(XRD),以确认DSC结果。使用药物和PVP的共研磨混合物,观察到溶出速率和程度的显着提高。在该研究的所有制备批次中,PAL和Plasdone S-630的1:1比例共研磨混合物在溶解度和在水中的溶解速率方面均显示出最佳结果。这种作用不仅是由于粒径减小,而且还因为共研磨过程中药物结晶性的丧失。在本研究中使用的不同亲水性载体中,PVP是改善PAL溶解特性的较好载体。与纯PAL处理的动物相比,用PAL共混的Plasdone S630(1:1)处理的动物的PAL平均血浆暴露程度高7倍。 .org / 10.3329 / icpj.v2i3.13632国际最新药学杂志,2013年2月,2(3):70-77

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