Applicability of the Monocyte Activation Test (MAT) in Brazil: the importance of its use as a test for the detection of pyrogens in the quality control of injectable products
DOI:
https://doi.org/10.3395/2317-269x.00519Keywords:
Monocyte Activation Test, Rabbit Pyrogen Test, Pharmacopoeias, Biological productsAbstract
Monocyte Activation Test (MAT) is thought to be a good replacement for rabbit pyrogen test (RPT); however, MAT remains controversial. MAT was not adequately evaluated in a sufficient number of products, and there is no sufficient data that support the ability of MAT to detect non-endotoxin pyrogens. Furthermore, MAT was used subject to validation for each specific product. The aim of this study was to identify in main pharmacopoeias, whose monographs require pyrogenicity tests, and propose those products for which only the rabbit pyrogen test is required to be used as a kick-off study for future studies. Products’ monographs in pharmacopeias in the United States, Europe, and Brazil that are recommended for RPT or Bacterial Endotoxins Test (BET) are as follows. RPT: 20 in American, 37 in European, and 28 in Brazilian pharmacopoeias. BET: 619 in American, 157 in European, and 41 in Brazilian pharmacopoeias. Four products require pyrogenicity testing in three pharmacopoeias. Both RPT and BET are recommended by six monographs in Brazilian pharmacopeias and 15 in European pharmacopoeias. In Brazilian pharmacopoeias most are biological. These products should be the first to be tested for their applicability to MAT because they are currently tested mainly by RPT.Downloads
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