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首页> 外文期刊>Powder Technology: An International Journal on the Science and Technology of Wet and Dry Particulate Systems >Huperzine A loaded multiparticulate disintegrating tablet: Drug release mechanism of ethyl cellulose microparticles and pharmacokinetic study
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Huperzine A loaded multiparticulate disintegrating tablet: Drug release mechanism of ethyl cellulose microparticles and pharmacokinetic study

机译:Huperzine一种负载的多颗粒崩解片剂:乙基纤维素微粒和药代动力学研究的药物释放机制

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Huperzine A loaded multiparticulate tablet with sustained release was developed to reduce dosing frequency and increase swallowing. The sustained release was provided by the ethyl cellulose/Poloxamer 127 (EC/F127) microparticles (MPs). F127 was added to facilitate drug release of EC MPs, and the enhanced dissolution mechanism was investigated regarding to the particle size, water uptake, and wettability of MPs. The greater wettability, which highly relied on the medium and formulation components, generated larger water uptake and faster drug release through improving the penetration of the medium into the internal space of MPs. The EC/F127 MPs were further compressed into tablets for dissolution and pharmacokinetic studies. The results demonstrated that the tablet remained unchanged release profile to the MPs, and exhibited profoundly sustained release with a relatively bioavailability of 125.18% to the commercial tablet. Therefore, the multiparticulate tablet was successfully designed based on the drug release mechanism and high compressibility of MPs. (C) 2019 Elsevier B.V. All rights reserved.
机译:Huperzine具有持续释放的负载的多颗粒片以减少给药频率并增加吞咽。乙基纤维素/泊洛沙姆127(EC / F127)微粒(MPS)提供持续释放。加入F127以促进EC MP的药物释放,并研究了MPS的粒度,水吸收和润湿性的增强溶解机制。通过改善培养基的渗透到MPS内部空间,较高依赖于培养基和配方组分,产生更大的水吸收和更快的药物释放的润湿性更大的润湿性。 EC / F127 MPS进一步压制成用于溶解和药代动力学研究的片剂。结果表明,该片剂对MPS保持不变的释放曲线,并具有125.18%的相对生物利用度的深刻持续释放。因此,基于药物释放机理和MPS的高可压力成功设计了多颗粒片。 (c)2019年Elsevier B.V.保留所有权利。

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