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Development and application of a validated HPLC method for the analysis of dissolution samples of levothyroxine sodium drug products

✍ Scribed by J.W. Collier; R.B. Shah; A.R. Bryant; M.J. Habib; M.A. Khan; P.J. Faustino


Book ID
108189823
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
341 KB
Volume
54
Category
Article
ISSN
0731-7085

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## Abstract A fast and simple HPLC method has been developed and validated for the quantification of a completely new anti‐cancer drug during the manufacturing process. The combination of four compounds including α‐ketoglutaric acid, hydroxymethylfurfural, __N__‐acetyl‐L‐methionine and __N__‐acetyl