کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1220792 1494621 2015 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Strategy for design NIR calibration sets based on process spectrum and model space: An innovative approach for process analytical technology
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
پیش نمایش صفحه اول مقاله
Strategy for design NIR calibration sets based on process spectrum and model space: An innovative approach for process analytical technology
چکیده انگلیسی


• Stepwise pharmaceutical quality control by near infrared spectroscopy.
• A novel methodology for preparation of calibration set is proposed.
• Establishment of model space by Hotelling's T2 and Q-residuals statistics.
• Calibration sets prepared based on process spectrum and model space as an innovative tool for process analytical technology (PAT).

The pharmaceutical industry is under stringent regulations on quality control of their products because is critical for both, productive process and consumer safety. According to the framework of “process analytical technology” (PAT), a complete understanding of the process and a stepwise monitoring of manufacturing are required.Near infrared spectroscopy (NIRS) combined with chemometrics have lately performed efficient, useful and robust for pharmaceutical analysis. One crucial step in developing effective NIRS-based methodologies is selecting an appropriate calibration set to construct models affording accurate predictions.In this work, we developed calibration models for a pharmaceutical formulation during its three manufacturing stages: blending, compaction and coating. A novel methodology is proposed for selecting the calibration set –“process spectrum”–, into which physical changes in the samples at each stage are algebraically incorporated.Also, we established a “model space” defined by Hotelling's T2 and Q-residuals statistics for outlier identification – inside/outside the defined space – in order to select objectively the factors to be used in calibration set construction.The results obtained confirm the efficacy of the proposed methodology for stepwise pharmaceutical quality control, and the relevance of the study as a guideline for the implementation of this easy and fast methodology in the pharma industry.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Pharmaceutical and Biomedical Analysis - Volume 114, 10 October 2015, Pages 28–33
نویسندگان
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