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一种用于提高溶出性能的阿苯达唑新型热熔挤出制剂。

A novel hot-melt extrusion formulation of albendazole for increasing dissolution properties.

作者信息

Martinez-Marcos Laura, Lamprou Dimitrios A, McBurney Roy T, Halbert Gavin W

机构信息

EPSRC Centre for Innovative Manufacturing in Continuous Manufacturing and Crystallisation (CMAC), University of Strathclyde, Technology and Innovation Centre, 99 George Street, G1 1RD Glasgow, United Kingdom; Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, 161Cathedral Street, G4 0RE Glasgow, United Kingdom.

EPSRC Centre for Innovative Manufacturing in Continuous Manufacturing and Crystallisation (CMAC), University of Strathclyde, Technology and Innovation Centre, 99 George Street, G1 1RD Glasgow, United Kingdom; Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, 161Cathedral Street, G4 0RE Glasgow, United Kingdom.

出版信息

Int J Pharm. 2016 Feb 29;499(1-2):175-185. doi: 10.1016/j.ijpharm.2016.01.006. Epub 2016 Jan 6.

Abstract

The main aim of the research focused on the production of hot-melt extrusion (HME) formulations with increased dissolution properties of albendazole (ABZ). Therefore, HME was applied as a continuous manufacturing technique to produce amorphous solid dispersions of the poorly water soluble drug ABZ combined with the polymer matrix polyvinylpyrrolidone PVP K12. HME formulations of ABZ-PVP K12 comprised a drug content of 1%, 5% and 10% w/w. The main analytical characterisation techniques used were scanning electron microscopy (SEM), micro-computed tomography (μ-CT), X-ray powder diffraction (XRPD), differential scanning calorimetry (DSC) and dissolution profile studies. The application of SEM, XRPD and DSC evidenced drug physical transformation from crystalline to amorphous state and therefore, the achievement of an amorphous solid dispersion. The introduction of a novel technique, μ-CT, to characterise the internal structure of these materials revealed key information regarding materials distribution and void content. Dissolution profile studies evidenced a high increase in drug release profile compared to pure ABZ. These promising results can lead to a great enhancement of the oral bioavailability of ABZ dosage forms. Therefore, HME is a potential continuous manufacturing technique to overcome ABZ poor solubility properties and lead to a significant increase in the therapeutic effect.

摘要

该研究的主要目的集中在制备具有提高阿苯达唑(ABZ)溶解性能的热熔挤出(HME)制剂。因此,HME作为一种连续制造技术,用于制备难溶性药物ABZ与聚合物基质聚乙烯吡咯烷酮PVP K12的无定形固体分散体。ABZ-PVP K12的HME制剂的药物含量为1%、5%和10%(w/w)。使用的主要分析表征技术有扫描电子显微镜(SEM)、微计算机断层扫描(μ-CT)、X射线粉末衍射(XRPD)、差示扫描量热法(DSC)和溶出曲线研究。SEM、XRPD和DSC的应用证明了药物从结晶态到无定形态的物理转变,从而实现了无定形固体分散体。引入一种新技术μ-CT来表征这些材料的内部结构,揭示了有关材料分布和孔隙率的关键信息。溶出曲线研究表明,与纯ABZ相比,药物释放曲线有显著提高。这些有前景的结果可极大提高ABZ剂型的口服生物利用度。因此,HME是一种潜在的连续制造技术,可克服ABZ的低溶解性,并显著提高治疗效果。

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