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通过粉末混合来测量混合物的均匀性和溶解性,以预测药物团聚体分解的程度。

The measurement of mixture homogeneity and dissolution to predict the degree of drug agglomerate breakdown achieved through powder mixing.

作者信息

de Villiers M M, Van der Watt J G

机构信息

Research Institute for Industrial Pharmacy, Potchefstroom University for Christian Higher Education, South Africa.

出版信息

Pharm Res. 1994 Nov;11(11):1557-61. doi: 10.1023/a:1018997418322.

Abstract

Interactive mixing of agglomerates of small, cohesive particles with coarse carrier particles facilitate the deaggregation of agglomerates. In this study dispersion of agglomerates of microfine furosemide particles by such a mixing process was followed by measuring changes in the content uniformity and area under the dissolution curve. Interactive mixtures between agglomerates of different sized furosemide particles and coarse sodium chloride particles were prepared using different mixers, mixing times and mixer speeds. The dissolution rate of the drug from and content uniformity of the mixtures were measured, and degrees of dispersion were calculated. These degrees of dispersion were compared to the dispersion values obtained from the decrease in agglomerate size after mixing. An increase in mixing time led to an increase in dispersion. An initial fast deagglomeration, indicated by an increase in dissolution, increase in content uniformity and a decrease in particle size, was followed by substantially slower deaggregation of remaining agglomerates and smaller aggregates. For all mixtures studied the degree of dispersion estimated from dissolution measurements, when compared to equivalent content uniformity measurements, agreed closely with the degree of dispersion as indicated by the decrease in particle size. The use of the area under the dissolution curve to predict agglomerate breakdown proved useful and may find application in situations where it is impossible to follow directly deagglomeration through particle size measurements.

摘要

小的、有粘性的颗粒聚集体与粗载体颗粒的交互混合有助于聚集体的解聚。在本研究中,通过测量含量均匀度和溶出曲线下面积的变化,跟踪了通过这种混合过程对微粉速尿颗粒聚集体的分散情况。使用不同的混合器、混合时间和混合器速度,制备了不同大小速尿颗粒聚集体与粗氯化钠颗粒之间的交互混合物。测量了混合物中药物的溶出速率和含量均匀度,并计算了分散度。将这些分散度与混合后聚集体尺寸减小所获得的分散值进行比较。混合时间的增加导致分散度增加。最初快速的解聚表现为溶出增加、含量均匀度增加和粒径减小,随后剩余聚集体和较小聚集体的解聚速度大幅减慢。对于所有研究的混合物,从溶出测量估计的分散度与等效的含量均匀度测量相比,与粒径减小所表明的分散度密切一致。利用溶出曲线下面积来预测聚集体的分解被证明是有用的,并且可能在无法通过粒径测量直接跟踪解聚的情况下得到应用。

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