A simplified method for the measurement of urinary free cortisol using LC-MS/MS.
| dc.contributor.author | Wear, Joanne E | |
| dc.contributor.author | Owen, Laura J | |
| dc.contributor.author | Duxbury, Katherine | |
| dc.contributor.author | Keevil, Brian G | |
| dc.date.accessioned | 2009-06-11T13:12:56Z | |
| dc.date.available | 2009-06-11T13:12:56Z | |
| dc.date.issued | 2007-10-15 | |
| dc.identifier.citation | A simplified method for the measurement of urinary free cortisol using LC-MS/MS. 2007, 858 (1-2):27-31 J. Chromatogr. B | en |
| dc.identifier.issn | 1570-0232 | |
| dc.identifier.pmid | 17698425 | |
| dc.identifier.doi | 10.1016/j.jchromb.2007.08.001 | |
| dc.identifier.uri | http://hdl.handle.net/10541/70194 | |
| dc.description.abstract | The measurement of 24 h urinary free cortisol is used in the investigation of patients with symptoms of hypercortisolism. Many different methods have been published for the measurement of cortisol, but most of these methods involve cumbersome pre-extraction of the cortisol prior to analysis. We have developed a method using in-well protein precipitation which serves to clean up the sample without requiring lengthy sample preparation. A Shimadzu SIL-HT autosampler was used to inject 50 microL of extract onto a Phenomemex Gemini C18 guard column attached to a Waters Xbridge C18 column. The eluant was introduced directly into a Waters Quattro Micro tandem mass spectrometer. The method was found to be linear up to 3448 nmol/L with a lower limit of detection of 5.3 nmol/L. Precision and accuracy were acceptable, and no interference was noted from compounds such as prednisolone or fenofibrate. This assay was compared to a previously published method, which uses solid phase extraction prior to LC-MS/MS analysis. We have developed a simplified, robust assay for the quantitation of urinary free cortisol that will increase the throughput of the assay and avoid the use of neurotoxic solvents such as dichloromethane. | |
| dc.language.iso | en | en |
| dc.subject.mesh | Chromatography, Liquid | |
| dc.subject.mesh | Humans | |
| dc.subject.mesh | Hydrocortisone | |
| dc.subject.mesh | Reproducibility of Results | |
| dc.subject.mesh | Tandem Mass Spectrometry | |
| dc.title | A simplified method for the measurement of urinary free cortisol using LC-MS/MS. | en |
| dc.type | Article | en |
| dc.contributor.department | Department of Clinical Biochemistry, Wythenshawe Hospital, Southmoor Road, Wythenshawe, Manchester M23 9LT, United Kingdom. Joanne.wear@nhs.net | en |
| dc.identifier.journal | Journal of Chromatography. B | en |
| html.description.abstract | The measurement of 24 h urinary free cortisol is used in the investigation of patients with symptoms of hypercortisolism. Many different methods have been published for the measurement of cortisol, but most of these methods involve cumbersome pre-extraction of the cortisol prior to analysis. We have developed a method using in-well protein precipitation which serves to clean up the sample without requiring lengthy sample preparation. A Shimadzu SIL-HT autosampler was used to inject 50 microL of extract onto a Phenomemex Gemini C18 guard column attached to a Waters Xbridge C18 column. The eluant was introduced directly into a Waters Quattro Micro tandem mass spectrometer. The method was found to be linear up to 3448 nmol/L with a lower limit of detection of 5.3 nmol/L. Precision and accuracy were acceptable, and no interference was noted from compounds such as prednisolone or fenofibrate. This assay was compared to a previously published method, which uses solid phase extraction prior to LC-MS/MS analysis. We have developed a simplified, robust assay for the quantitation of urinary free cortisol that will increase the throughput of the assay and avoid the use of neurotoxic solvents such as dichloromethane. |