Preparation and characterization of two new forced degradation products of letrozole and development of a stability-indicating RP-LC method for its determination.

Publisher: Faculty of Pharmacy, University of Karachi Country of Publication: Pakistan NLM ID: 9426356 Publication Model: Print Cited Medium: Print ISSN: 1011-601X (Print) Linking ISSN: 1011601X NLM ISO Abbreviation: Pak J Pharm Sci Subsets: MEDLINE

Original Publication: Karachi : Faculty of Pharmacy, University of Karachi, [1988-

Chromatography, High Pressure Liquid*/standards ; Chromatography, Reverse-Phase*/standards ; Drug Contamination*; Aromatase Inhibitors/*chemistry ; Nitriles/*chemistry ; Technology, Pharmaceutical/*methods ; Triazoles/*chemistry; Aromatase Inhibitors/blood ; Calibration ; Chemistry, Pharmaceutical ; Drug Stability ; Hot Temperature ; Humans ; Hydrogen-Ion Concentration ; Hydrolysis ; Letrozole ; Linear Models ; Mass Spectrometry ; Nitriles/blood ; Oxidation-Reduction ; Photolysis ; Reference Standards ; Reproducibility of Results ; Technology, Pharmaceutical/standards ; Triazoles/blood

Two new hydrolytic products of letrozole were identified and proved to be true degradation products obtained by alkaline and acidic degradation of the drug. The acid and amide forms of the nitrile groups of letrozole were prepared and identified by IR and mass spectroscopic techniques. Subsequently, a simple, precise and selective stability-indicating RPLC method was developed and validated for the determination of letrozole in the presence of its degradation products. Letrozole was subjected to alkali and acid hydrolysis, oxidation, thermal degradation and photo-degradation. The degradation products were well isolated from letrozole. The chromatographic method was achieved using gradient elution of the drug and its degradation products on a reversed phase Zorbax Eclipse C18 column (100mm x 4.6mm, 3.5 μm) using a mobile phase consisting of 0.01M KH₂PO₄and methanol at a flow rate of 1 mL min⁻¹. Quantitation was achieved with UV detection at 230 nm. Linearity, accuracy and precision were found to be acceptable over the concentration range of 0.01-80 μgmL⁻¹. The proposed method was successfully applied to the determination of letrozole in bulk, plasma and in its pharmaceutical preparation.

0 (Aromatase Inhibitors)
0 (Nitriles)
0 (Triazoles)
7LKK855W8I (Letrozole)

Date Created: 20151208 Date Completed: 20160310 Latest Revision: 20191210

20250114

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