湿法球磨过程中研磨球对缩小阿瑞匹坦粒度的影响

IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pharmaceutical Development and Technology Pub Date : 2024-04-01 Epub Date: 2024-04-08 DOI:10.1080/10837450.2024.2334754
Dourna Memarvar, Shadi Yaqoubi, Hamed Hamishehkar, Matthew Lam, Ali Nokhodchi
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引用次数: 0

摘要

减小粒径是改善水溶性差药物溶解性的一种广泛应用的方法。球磨是一种自上而下的机械技术,用于减小粒度。本研究评估了球数、球大小和研磨速度对研磨阿瑞匹坦特性的影响。采用全因子设计研究了影响因素对粒度减小的影响。使用辅料将药物悬浮在蒸馏水中制成初始悬浮液,然后在行星式球磨机中进行研磨。球的大小、球的数量和研磨速度调节了阿瑞匹坦的粒度分布。将每种球径的球数从最少增加到最多,可使平均粒径减少约 28%,D90% 减少 37%,体积平均粒径与数值平均粒径之比减少 25%。平均而言,使用 10 毫米的球而不是 30 毫米的球可使平均粒径减少 1.689 微米。因此,球尺寸、球数和研磨速度是球磨过程中的三个有效因素。通过增加球数和减小球径,可以有效地使药物颗粒微粉化,而且粒度更加均匀。
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Impact of grinding balls on the size reduction of Aprepitant in wet ball milling procedure.

One of the widely used approaches for improving the dissolution of poorly water-soluble drugs is particle size reduction. Ball milling is a mechanical, top-down technique used to reduce particle size. The effect of ball number, ball size, and milling speed on the properties of milled Aprepitant is evaluated. A full factorial design was employed to investigate the influence of affecting factors on particle size reduction. The initial suspension was made by suspending the drug in distilled water using excipients followed by milling in a planetary ball mill. Ball size, ball number, and milling speed modulated particle size distribution of Aprepitant. Increasing the number of balls from minimum to maximum for each ball size led to approximately a 28% reduction in mean particle size, a 37% decrease in D90%, and a 25% decrease in the ratio of volume mean particle diameter to numeric mean particle diameter. On average, using 10 mm balls instead of 30 mm balls reduced mean particle size by 1.689 µm. As a result, ball size, ball number, and milling speed are three effective factors in the process of ball milling. By increasing the ball number and decreasing the ball size, efficient micronization of drug particles takes place and the particle size is more uniform.

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来源期刊
CiteScore
5.90
自引率
2.90%
发文量
82
审稿时长
1 months
期刊介绍: Pharmaceutical Development & Technology publishes research on the design, development, manufacture, and evaluation of conventional and novel drug delivery systems, emphasizing practical solutions and applications to theoretical and research-based problems. The journal aims to publish significant, innovative and original research to advance the frontiers of pharmaceutical development and technology. Through original articles, reviews (where prior discussion with the EIC is encouraged), short reports, book reviews and technical notes, Pharmaceutical Development & Technology covers aspects such as: -Preformulation and pharmaceutical formulation studies -Pharmaceutical materials selection and characterization -Pharmaceutical process development, engineering, scale-up and industrialisation, and process validation -QbD in the form a risk assessment and DoE driven approaches -Design of dosage forms and drug delivery systems -Emerging pharmaceutical formulation and drug delivery technologies with a focus on personalised therapies -Drug delivery systems research and quality improvement -Pharmaceutical regulatory affairs This journal will not consider for publication manuscripts focusing purely on clinical evaluations, botanicals, or animal models.
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