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Volumn 23, Issue 5, 2009, Pages 557-562

Highly sensitive method for the determination of ropinirole with a lower limit of quantitation of 3.45 pg/mL in human plasma by LC-ESI-MS/MS: Application to a clinical pharmacokinetic study

Author keywords

Human plasma; LC MS MS; Method validation; Pharmacokinetics; Ropinirole

Indexed keywords

LIQUID CHROMATOGRAPHY; MASS SPECTROMETRY; PHARMACOKINETICS; PLASMA (HUMAN); POSITIVE IONS;

EID: 67649643754     PISSN: 02693879     EISSN: 10990801     Source Type: Journal    
DOI: 10.1002/bmc.1144     Document Type: Article
Times cited : (18)

References (7)
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    • Matrix effect in bioanalysis of illicit drugs with LC-MS/MS: Influence of ionization type, sample preparation, and biofluid
    • Dams R, Huestis MA, Lambert WE and Murphy CM. Matrix effect in bioanalysis of illicit drugs with LC-MS/MS: influence of ionization type, sample preparation, and biofluid. Journal of American Society for Mass Spectrometry 2003; 14: 1290-1294.
    • (2003) Journal of American Society for Mass Spectrometry , vol.14 , pp. 1290-1294
    • Dams, R.1    Huestis, M.A.2    Lambert, W.E.3    Murphy, C.M.4
  • 4
    • 0033765997 scopus 로고    scopus 로고
    • Clinical pharmacokinetics of ropinirole
    • Kaye CM and Nicholls B. Clinical pharmacokinetics of ropinirole. Clinical Pharmacokinetics 2000; 39: 243-254.
    • (2000) Clinical Pharmacokinetics , vol.39 , pp. 243-254
    • Kaye, C.M.1    Nicholls, B.2
  • 5
    • 0033877002 scopus 로고    scopus 로고
    • Ropinirole: A review of its use in the management of Parkinson's disease
    • Matheson AJ and Spencer CM. Ropinirole: a review of its use in the management of Parkinson's disease. Drugs 2000; 60: 115-137.
    • (2000) Drugs , vol.60 , pp. 115-137
    • Matheson, A.J.1    Spencer, C.M.2
  • 6
    • 85161789697 scopus 로고    scopus 로고
    • US DHHS, FDA, CDER. Guidance for Industry: Bioanalytical Method Validation. US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research, Center for Veterinary Medicine, 2001. Available at: http://www/fda.gov/cder/ guidance/index.htm
    • US DHHS, FDA, CDER. Guidance for Industry: Bioanalytical Method Validation. US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research, Center for Veterinary Medicine, 2001. Available at: http://www/fda.gov/cder/ guidance/index.htm


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.