Abstract

A near infrared (NIR) method able to directly quantify the active content in pharmaceutical powder blends used for manufacturing meloxicam tablets, without any sample preparation, was developed and fully validated. To develop calibration models for the assay of meloxicam in powder blends for tableting, the NIR reflectance spectra of different meloxicam powder blends prepared according to a calibration protocol was analysed using different preprocessing methods by partial last-square regression (PLS) and principal component regression (PCR).The best calibration model was found when partial last-square regression (PLS) was used as regression algorithm in association with Smoothing-Savitsky as pre-processing spectrum method. The trueness, precision (repeatability and intermediate precision), accuracy, linearity and range of application of the developed NIR method were validated according to the International Conference of Harmonization (ICH) and Medicine European Agency (EMA) guidelines and found to be fit for its intended purpose.

Highlights

  • To ensure appropriate quantitative results, the set of calibration samples has to be representative of the changes in the properties of samples that will be found in routine analysis

  • A near infrared method was developed for the quantification of meloxicam in powder blends for tableting

  • Different calibration models were evaluated for the quantification of meloxicam in powder blends for tableting, ranging from 10–15%, using Near Infrared (NIR)-chemometic technique

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Summary

Objectives

The aim of this work was to develop and validate a NIR-chemometric method for the assay of meloxicam in powder blends for tableting, based on laboratory made samples, in order to be used for in-line/at-line meloxicam pharmaceutical process monitoring. The aim of our research was to develop a NIR-chemometric method suitable for the direct quantification of meloxicam in powder blends for tableting, without any sample preparation

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