Izvorni znanstveni članak

https://doi.org/10.2478/acph-2018-00019

A headspace-gas chromatography method for isopropanol determination in warfarin sodium products as a measure of drug crystallinity

ZIYAUR RAHMAN ; Division of Product Quality and Research, Center for Drug Evaluation and Research, Food and Drug Administration, Maryland, USA
SOHAIL AKHTAR ; Division of Product Quality and Research, Center for Drug Evaluation and Research, Food and Drug Administration, Maryland, USA
AKHTAR SIDDIQUI ; Division of Product Quality and Research, Center for Drug Evaluation and Research, Food and Drug Administration, Maryland, USA
ANTHONY B. CIAVARELLA ; Division of Product Quality and Research, Center for Drug Evaluation and Research, Food and Drug Administration, Maryland, USA
AGNES NGUYENPHO ; Division of Product Quality and Research, Center for Drug Evaluation and Research, Food and Drug Administration, Maryland, USA
PATRICK J. FAUSTINO ; Division of Product Quality and Research, Center for Drug Evaluation and Research, Food and Drug Administration, Maryland, USA
MANSOOR A. KHAN ; Division of Product Quality and Research, Center for Drug Evaluation and Research, Food and Drug Administration, Maryland, USA; Irma Lerma Rangel College of Pharmacy, Texas A&M Health Science Center, Texas A&M University, Reynolds Medical Building, Suite

Sažetak

Coumadin® and several generic products of warfarin sodium (WS) contain the crystalline form (clathrate) in which WS and isopropanol (IPA) are associated in a 2:1 molar ratio. IPA is critical in maintaining the WS crystalline structure. Physicochemical properties of the drug and drug product may change when the crystalline drug transforms to amorphous form. A headspace-gas chromatography (HS-GC) method was developed and validated for IPA determination in the WS drug product. n-propanol (NPA) was used as internal standard and the method was validated for specificity, system suitability, linearity, accuracy, precision, range, limits of detection and quantification, and robustness. The method was specific, with good resolution between IPA and NPA peaks. Chromatographic parameters (retention time, IPA/NPA area ratio, tailing factor, theoretical plates, USP symmetry, capacity factor, selectivity and resolution) were consistent over three days of validation. The analytical method was linear from 2–200 µg mL–1 (0.1–10 % IPA present in the drug product). LOD and LOQ were 0.1 and 2 µg mL–1, respectively. Accuracy at low (2 µg mL–1) and high (200 µg mL–1) IPA concentrations of the calibration curve was 103.3–113.3 and 98.9–102.2 % of the nominal value, resp. The validated method was precise, as indicated by the RSD value of less than 2 % at three concentration levels of the calibration curve. The method reported here was utilized to determine accurately and precisely the IPA content in in-house formulations and commercial products. In summary, IPA determination by HS-GC provides an indirect measure of WS crystallinity in the drug product. Nevertheless, it should be confirmed by another analytical method since IPA from the drug substance is not distinguishable from IPA that may be present outside the drug crystals in a dosage form when prepared by wet granulation with IPA.

Ključne riječi

warfarin crystallinity; isopropanol; headspace-gas chromatography

Hrčak ID:

192735

URI

https://hrcak.srce.hr/192735

Datum izdavanja:

31.3.2018.

Posjeta: 3.847 *