Literature DB >> 16464557

Simultaneous determination of formic acid and formaldehyde in pharmaceutical excipients using headspace GC/MS.

Mary-Anne del Barrio1, Jack Hu, Pengzu Zhou, Nina Cauchon.   

Abstract

Formic acid and its esters, as well as formaldehyde, are trace impurities that are often present in pharmaceutical excipients. These trace impurities can potentially react with amino and/or hydroxyl groups in drugs to form significant levels of degradants. To select the appropriate excipients for a stable formulation, a gas chromatography/mass spectrometry (GC/MS) method was developed and validated for the rapid screening of trace amounts of residual formic acid, its esters and formaldehyde in pharmaceutical excipients. Samples were dissolved or dispersed in acidified ethanol to convert formic acid and formaldehyde to ethyl formate and diethoxymethane, respectively. Identification was conducted using a GC/MS system under scan mode and quantified using a selected ion monitoring (SIM) mode. Evaluation of the mass spectra of ethyl formate and diethoxymethane in the samples indicated that the method is specific. The limits of quantitation of the method were 0.5 ppm for formic acid and 0.2 ppm for formaldehyde. The precision of the method was demonstrated by the acceptable R.S.D. (<or=10%) over a linear range of 0.5-10,000 ppm. The accuracy of the method was within 80-120% over the linearity range. The amounts of formic acid and formaldehyde in commonly used pharmaceutical excipients is reported.

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Year:  2006        PMID: 16464557     DOI: 10.1016/j.jpba.2005.12.033

Source DB:  PubMed          Journal:  J Pharm Biomed Anal        ISSN: 0731-7085            Impact factor:   3.935


  13 in total

Review 1.  Reactive impurities in excipients: profiling, identification and mitigation of drug-excipient incompatibility.

Authors:  Yongmei Wu; Jaquan Levons; Ajit S Narang; Krishnaswamy Raghavan; Venkatramana M Rao
Journal:  AAPS PharmSciTech       Date:  2011-09-27       Impact factor: 3.246

Review 2.  Impact of excipient interactions on solid dosage form stability.

Authors:  Ajit S Narang; Divyakant Desai; Sherif Badawy
Journal:  Pharm Res       Date:  2012-06-16       Impact factor: 4.200

3.  Stability of benzocaine formulated in commercial oral disintegrating tablet platforms.

Authors:  Melanie Köllmer; Carmen Popescu; Prashanth Manda; Leon Zhou; Richard A Gemeinhart
Journal:  AAPS PharmSciTech       Date:  2013-08-30       Impact factor: 3.246

Review 4.  Metabolomic signature of brain cancer.

Authors:  Renu Pandey; Laura Caflisch; Alessia Lodi; Andrew J Brenner; Stefano Tiziani
Journal:  Mol Carcinog       Date:  2017-07-17       Impact factor: 4.784

5.  Surface acidity and solid-state compatibility of excipients with an acid-sensitive API: case study of atorvastatin calcium.

Authors:  Ramprakash Govindarajan; Margaret Landis; Bruno Hancock; Larry A Gatlin; Raj Suryanarayanan; Evgenyi Y Shalaev
Journal:  AAPS PharmSciTech       Date:  2014-10-16       Impact factor: 3.246

6.  Isotopomer enrichment assay for very short chain fatty acids and its metabolic applications.

Authors:  Kristyen Tomcik; Rafael A Ibarra; Sushabhan Sadhukhan; Yong Han; Gregory P Tochtrop; Guo-Fang Zhang
Journal:  Anal Biochem       Date:  2010-11-26       Impact factor: 3.365

Review 7.  Oxidative Stability in Lipid Formulations: a Review of the Mechanisms, Drivers, and Inhibitors of Oxidation.

Authors:  Jasmine Musakhanian; Jean-David Rodier; Masumi Dave
Journal:  AAPS PharmSciTech       Date:  2022-05-20       Impact factor: 3.246

8.  Comparative toxicity of C60 aggregates toward mammalian cells: role of tetrahydrofuran (THF) decomposition.

Authors:  Michael Kovochich; Benjamin Espinasse; Melanie Auffan; Ernest M Hotze; Lauren Wessel; Tian Xia; Andre E Nel; Mark R Wiesner
Journal:  Environ Sci Technol       Date:  2009-08-15       Impact factor: 9.028

9.  Simultaneous measurement of formic acid, methanol and ethanol in vitreous and blood samples of postmortem by headspace GC-FID.

Authors:  Hamideh Ghorbani; Alireza Nezami; Behjat Sheikholeslami; Arya Hedjazi; Mahnaz Ahmadimanesh
Journal:  J Occup Med Toxicol       Date:  2018-01-08       Impact factor: 2.646

10.  Risk evaluation of impurities in topical excipients: The acetol case.

Authors:  Jente Boonen; Lieselotte Veryser; Lien Taevernier; Nathalie Roche; Kathelijne Peremans; Christian Burvenich; Bart De Spiegeleer
Journal:  J Pharm Anal       Date:  2014-01-08
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