An efficient, maintenance free and approved method for spectroscopic control and monitoring of blend uniformity: The moving F-test.

J Pharm Biomed Anal

Pharmaceutical Sciences and Clinical Supplies, Merck/MSD, PO Box 20, 5340 BH Oss, The Netherlands; Currently at InProcess-LSP, Molenstraat 110, 5342 CC Oss, The Netherlands.

Published: October 2015

AI Article Synopsis

  • Dry powder mixing is important in the pharmaceutical industry, and the use of in-line Near Infrared (NIR) Spectroscopy is becoming more common for monitoring Blend Uniformity (BU), although it still faces challenges in routine application.
  • A new qualitative approach to NIR-BU is introduced that simplifies the process without heavy calibration or method maintenance, using a moving F-test to determine the mixing endpoint.
  • The method has been successfully used in commercial production for a low-dose product over five years, demonstrating its effectiveness and compliance with regulatory standards during over 100 batches.

Article Abstract

Dry powder mixing is a wide spread Unit Operation in the Pharmaceutical industry. With the advent of in-line Near Infrared (NIR) Spectroscopy and Quality by Design principles, application of Process Analytical Technology to monitor Blend Uniformity (BU) is taking a more prominent role. Yet routine use of NIR for monitoring, let alone control of blending processes is not common in the industry, despite the improved process understanding and (cost) efficiency that it may offer. Method maintenance, robustness and translation to regulatory requirements have been important barriers to implement the method. This paper presents a qualitative NIR-BU method offering a convenient and compliant approach to apply BU control for routine operation and process understanding, without extensive calibration and method maintenance requirements. The method employs a moving F-test to detect the steady state of measured spectral variances and the endpoint of mixing. The fundamentals and performance characteristics of the method are first presented, followed by a description of the link to regulatory BU criteria, the method sensitivity and practical considerations. Applications in upscaling, tech transfer and commercial production are described, along with evaluation of the method performance by comparison with results from quantitative calibration models. A full application, in which end-point detection via the F-test controls the blending process of a low dose product, was successfully filed in Europe and Australia, implemented in commercial production and routinely used for about five years and more than 100 batches.

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Source
http://dx.doi.org/10.1016/j.jpba.2015.06.019DOI Listing

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