Determination of bis(tributyltin) oxide by GC-MS with on-line hydride derivatization: application to drug substance analysis

Citation
Tp. O'Brien et al., Determination of bis(tributyltin) oxide by GC-MS with on-line hydride derivatization: application to drug substance analysis, J PHARM B, 19(3-4), 1999, pp. 327-333
Citations number
24
Categorie Soggetti
Chemistry & Analysis
Journal title
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS
ISSN journal
07317085 → ACNP
Volume
19
Issue
3-4
Year of publication
1999
Pages
327 - 333
Database
ISI
SICI code
0731-7085(199903)19:3-4<327:DOBOBG>2.0.ZU;2-Q
Abstract
We report the determination of residual bis(tributyltin) oxide in a drug su bstance by GC-MS after extraction and on-line conversion to tributyltin hyd ride. Gas chromatography was performed using a 15 m x 0.25 mm i.d. DB-5 HT column with a temperature program from 100 to 160 degrees C at 15 degrees C min(-1). A mass range of 165-185 amu was monitored with the MS detector. H ydride generation is performed by placing a small amount of solid sodium bo rohydride in the injection port of a gas chromatograph and injecting sample s and standards through this material. Conversion to tributyltin hydride is shown to be quantitative and linear for levels of bis(tributyltin) oxide b etween 1 and 100 ppm in the drug substance. The use of GC-MS provides sensi tive and selective detection of tin containing species and the tin isotope pattern allows for confirmation of the presence of tin in chromatographic p eaks. Recovery at 6 ppm was 89% with an injection precision of 6%. The limi t of detection for bis(tributyltin) oxide in drug substance is I ppm. (C) 1 999 Elsevier Science B.V. All rights reserved.