Simultaneous in-line particle size distribution determination of drug and excipient from their powder blend using endoscopic imaging and AI.

IF 4.7 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Máté Benczúr, Máté Ficzere, Orsolya Péterfi, Áron Kálnai, Zsombor Kristóf Nagy, Dorián László Galata
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引用次数: 0

Abstract

This paper presents a method capable of simultaneously measuring component-based particle size distribution and API concentration via direct, in situ measurements in bulk powders. The method uses real-time imaging with a probe connected to a digital camera, and machine vision combined with artificial intelligence to process the images. The pharmaceutical processing environment was simulated with a conveyor belt. The blends consisted of acetylsalicylic acid (ASA) and calcium hydrogen phosphate (CHP). The determined component-based particle size distributions were compared to references measured using a microscope, and the results showed good correlation. The method not only proved effective in real-time component-based particle size distribution determination but was also able to provide information about the API concentration of the blends. This technique could provide valuable, real-time information about bulk powders used in pharmaceutical processing environments. Therefore, the method has the potential to play a central role in monitoring product quality in bulk powder processing providing assistance in the development of pharmaceutical quality control.

利用内窥镜成像和人工智能同时在线测定混合粉末中药物和赋形剂的粒度分布。
本文提出了一种方法,能够同时测量组分为基础的粒度分布和API浓度通过直接,在散装粉末的原位测量。该方法使用连接数码相机的探头进行实时成像,并将机器视觉与人工智能相结合来处理图像。采用传送带模拟制药加工环境。共混物由乙酰水杨酸(ASA)和磷酸氢钙(CHP)组成。将测定的基于组分的粒度分布与显微镜测量的参考文献进行比较,结果显示出良好的相关性。该方法不仅在基于组分的粒度分布实时测定中被证明是有效的,而且能够提供有关共混物API浓度的信息。该技术可以为制药加工环境中使用的散装粉末提供有价值的实时信息。因此,该方法有潜力在散装粉末加工过程中监测产品质量方面发挥核心作用,为药品质量控制的发展提供帮助。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.60
自引率
2.20%
发文量
248
审稿时长
50 days
期刊介绍: The journal publishes research articles, review articles and scientific commentaries on all aspects of the pharmaceutical sciences with emphasis on conceptual novelty and scientific quality. The Editors welcome articles in this multidisciplinary field, with a focus on topics relevant for drug discovery and development. More specifically, the Journal publishes reports on medicinal chemistry, pharmacology, drug absorption and metabolism, pharmacokinetics and pharmacodynamics, pharmaceutical and biomedical analysis, drug delivery (including gene delivery), drug targeting, pharmaceutical technology, pharmaceutical biotechnology and clinical drug evaluation. The journal will typically not give priority to manuscripts focusing primarily on organic synthesis, natural products, adaptation of analytical approaches, or discussions pertaining to drug policy making. Scientific commentaries and review articles are generally by invitation only or by consent of the Editors. Proceedings of scientific meetings may be published as special issues or supplements to the Journal.
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