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Development and validation of rapid LC-MS with electrospray ionization for the quantification of pramipexole in human plasma

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A rapid, accurate and precise LC-MS method is described for the quantitative determination of pramipexole in human plasma matrix using ropinirole as internal standard. Pramipexole and ropinirole were extracted from plasma by liquid-liquid extraction technique. The method was validated over the concentration range of 100-2514 pg/mL. The method was found to have acceptable accuracy, precision, linearity and selectivity. The mean extraction recovery from spiked plasma samples was in the range of 79.415-87.00 %. The intra-day accuracy of the assay ranged from 98.924 to 112.236 % and intra-day precision ranged from 3.489 to 6.756 %. Inter-day accuracy and precision results for quality control samples ranged between 100.340 and 107.443% of nominal and precision is observed to be 3.970-5.714 %. The pramipexole was found to be stable after several stability studies. The proposed method yielded a quick, simple and reliable protocol for estimating pramipexole concentrations in human plasma.
Słowa kluczowe
Rocznik
Tom
Strony
1--15
Opis fizyczny
Bibliogr. 11 poz., rys., tab.
Twórcy
autor
  • Department of Pharmaceutical Biotechnology, Vishnu Institute of Pharmaceutical Education and Research, Narsapur, Andhra Pradesh – 502313, India
autor
  • University College of Pharmaceutical Sciences, Acharya Nagarjuna University, Guntur, Andhra Pradesh – 522510, India
  • Department of Biotechnology, Jagarlamudi Kuppuswamy Choudary College, Guntur, Andhra Pradesh – 522006, India
Bibliografia
  • [1] Dooley M., Markham A., Drugs & Aging. 12 (1998) 495-514.
  • [2] Hoerger T.J., Bala M.V., Rowland C., Greer M., Chrischilles E.A., Holloway R.G., PharmacoEeconomics. 14 (1998) 541-557.
  • [3] Bennett J.P. Jr., Piercey M.F., J. Neurol. Sci. 163 (1999) 25-31.
  • [4] Courtney I.J., Jeremy G., Am. Fam. Physician. 75 (2007) 1239-1240.
  • [5] Inoue Y., Kuroda K., Hirata K., Uchimura N., Kagimura T., Shimizu T., Neuropsychobiology 63 (2011) 35-42.
  • [6] Lau Y.L., Glenn D.H., Nita I., J. Chromatogr B: Biomed. Sci. Appl. 683 (1996) 217-223.
  • [7] Lau Y.L., Jeffrey M.S., Glenn D.H., Rasmy T., Nita I., J. Chromatogr B: Biomed. Sci. Appl. 683 (1996) 209-216.
  • [8] Nirogi R.V., Kandikere V., Shrivastava W., Mudigonda K., Maurya S., Ajjala D., Biomed. Chromatogr. 21 (2007) 1151-1158.
  • [9] Bharathi D.V., Hotha K.K., Sagar P.V., Kumar S.S., Naidu A., Mullangi R., Biomed. Chromatogr. 23 (2009) 212-220.
  • [10] Uma G., Manimala M., Vasudevan M., Karpagam S., Deecarman., Int. J. Pharma. Sci. Let. 2 (2012) 10-11.
  • [11] Guidance for Industry: Bioanalytical Method Validation, U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), Center for Biologics Evaluation and Research (CBER), May 2001.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-23d8d837-08be-4966-9a43-e1a1499c8c67
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