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热熔挤出对聚乙烯醇压片行为的影响。

The impact of hot-melt extrusion on the tableting behaviour of polyvinyl alcohol.

作者信息

Grymonpré W, De Jaeghere W, Peeters E, Adriaensens P, Remon J P, Vervaet C

机构信息

Laboratory of Pharmaceutical Technology, Ghent University, Ghent, Belgium.

Laboratory of Pharmaceutical Process Analytical Technology, Ghent University, Ghent, Belgium.

出版信息

Int J Pharm. 2016 Feb 10;498(1-2):254-62. doi: 10.1016/j.ijpharm.2015.12.020. Epub 2015 Dec 12.

Abstract

There is evidence that processing techniques like hot-melt extrusion (HME) could alter the mechanical properties of pharmaceuticals, which may impede further processability (e.g. tableting). The purpose of this study was to evaluate if HME has an impact on the tableting behaviour of polyvinyl alcohol (PVA)-formulations. Mixtures of partially hydrolysed PVA grades (with a hydroxylation degree of 75 and 88%) and sorbitol (0, 10 and 40%) were extruded, (cryo-) milled and compressed into compacts of 350 ± 10 mg. Before compression all intermediate products were characterized for their solid-state (Tg, Tm, crystallinity) and material properties (particle size, moisture content, moisture sorption). Because both PVA-grades required higher extrusion temperatures (i.e. 180 °C), sorbitol was added to PVA as plasticizing agent to allow extrusion at 140 °C. Compaction experiments were performed on both physical mixtures and cryo-milled extrudates of PVA-sorbitol. By measuring tablet tensile strength and porosity in function of compaction pressure, tableting behaviour was compared before and after HME by means of the CTC-profiles (compressibility, tabletability, compactibility). A higher amorphous content in the formulation (as a result of HME) negatively influenced the tableting behaviour (i.e. lower tablet tensile strength). HME altered the mechanical properties towards more elastically deforming materials, thereby increasing tablet elastic recovery during decompression. The lower tensile strengths resulted from a combined effect of less interparticulate bonding areas (because of higher elastic recovery) and weaker bonding strengths per unit bonding area (between glassy particles).

摘要

有证据表明,诸如热熔挤出(HME)等加工技术可能会改变药物的机械性能,这可能会阻碍进一步的加工过程(例如压片)。本研究的目的是评估HME是否会对聚乙烯醇(PVA)制剂的压片行为产生影响。将部分水解的PVA等级(羟基化度分别为75%和88%)与山梨醇(0%、10%和40%)的混合物进行挤出、(冷冻)研磨并压制成350±10毫克的片剂。在压片之前,对所有中间产品的固态(玻璃化转变温度、熔点、结晶度)和材料性能(粒径、水分含量、吸湿率)进行表征。由于两种PVA等级都需要更高的挤出温度(即180°C),因此将山梨醇作为增塑剂添加到PVA中,以便在140°C下进行挤出。对PVA-山梨醇的物理混合物和冷冻研磨挤出物都进行了压片实验。通过测量片剂抗张强度和孔隙率随压片压力的变化,借助CTC曲线(压缩性、可压性、成型性)比较了HME前后的压片行为。制剂中较高的无定形含量(由于HME)对压片行为产生负面影响(即片剂抗张强度较低)。HME使材料的机械性能向更易发生弹性变形的方向转变,从而增加了减压过程中片剂的弹性回复率。较低的抗张强度是由颗粒间结合面积减少(由于较高的弹性回复率)和单位结合面积(玻璃态颗粒之间)的结合强度较弱共同作用的结果。

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