{"title":"Determination of clenbuterol and salbutamol in urine by capillary gas chromatography with capillary columns of 100 microns.","authors":"J A García Regueiro, B Pérez, G Casademont","doi":"10.1016/0021-9673(93)87012-b","DOIUrl":null,"url":null,"abstract":"<p><p>A method to determine clenbuterol and salbutamol in calf urine is described. Two independent extraction procedures using Extrelut (clenbuterol) and octadecylsilica (salbutamol) were used; the extracts obtained were mixed and purified over a cyanopropyl minicolumn. Trimethylsilyl derivatives were prepared and analysed by GC-MS in selected-ion monitoring mode using a fused-silica open tubular capillary column, 10 m x 100 microns coated with 5% phenylmethylsilicone. Splitless injection was optimized to achieve low percentage residual standard deviation of absolute areas. The best conditions were: injection volume 0.5 microliter, column head pressure 22 p.s.i. (1 p.s.i. = 6894.76 Pa), inlet temperature 250 degrees C and glass liner volume 250 microliters. The recoveries of the complete procedure were in the range 50-60% for both compounds.</p>","PeriodicalId":15508,"journal":{"name":"Journal of chromatography","volume":"655 1","pages":"73-6"},"PeriodicalIF":0.0000,"publicationDate":"1993-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0021-9673(93)87012-b","citationCount":"21","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of chromatography","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/0021-9673(93)87012-b","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 21
Abstract
A method to determine clenbuterol and salbutamol in calf urine is described. Two independent extraction procedures using Extrelut (clenbuterol) and octadecylsilica (salbutamol) were used; the extracts obtained were mixed and purified over a cyanopropyl minicolumn. Trimethylsilyl derivatives were prepared and analysed by GC-MS in selected-ion monitoring mode using a fused-silica open tubular capillary column, 10 m x 100 microns coated with 5% phenylmethylsilicone. Splitless injection was optimized to achieve low percentage residual standard deviation of absolute areas. The best conditions were: injection volume 0.5 microliter, column head pressure 22 p.s.i. (1 p.s.i. = 6894.76 Pa), inlet temperature 250 degrees C and glass liner volume 250 microliters. The recoveries of the complete procedure were in the range 50-60% for both compounds.