Management of validation of HPLC method for determination of acetylsalicylic acid impurities in a new pharmaceutical product.

M, Kowalska; M, Woźniak; M, Kijek; P, Mitrosz; J, Szakiel; P, Turek

doi:10.1038/s41598-021-99269-x

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Management of validation of HPLC method for determination of acetylsalicylic acid impurities in a new pharmaceutical product.

Shared by NobleBlocks on Jan 6, 2022 • 12:00 AM UTC

Authors:

Kowalska M

Woźniak M

Kijek M

Abstract

The work mainly focused on a validation of the method for determining the content of salicylic acid and individual unknown impurities in new pharmaceutical product-tablets containing: 75, 100 or 150 mg of acetylsalicylic acid and glycine in the amount of 40 mg for each dosage. The separation of the ...

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