Skip to main content

Part of the book series: Methodological Surveys in Biochemistry and Analysis ((MSBA,volume 18 A))

Abstract

AI* agents in biological fluids are commonly analyzed chromatographically, maybe by GC but usually by HPLC — typically RP — with UV detection (sometimes fluorescence or EC). HPLC is also convenient in percutaneous absorption studies on AI agents in gels and creams. Solvent extraction is often not necessary if the drug concentration, e.g. in plasma, is relatively high: precipitation of plasma proteins is often sufficient, provided that a pre-column is used.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 129.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 169.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 169.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Abbreviations

AI:

anti-inflammatory

EC:

electrochemical

Fa:

fluocinolone acetonide

i.s.:

internal standard

r:

correlation coefficient

RP:

reversed phase

SDS:

sodium dodecyl sulphate

References

  1. Rance, M.J., Jordan, B.J. & Nichols, J.D. (1975) J. Pharm. Pharmacol. 27, 425–429.

    Article  CAS  Google Scholar 

  2. Moffat, A.C., Jackson, J.V., Moss, M.S. & Widdop, B., eds. (1986) Clarke’s Isolation and Identification of Drugs, 2nd edn., The Pharmaceutical Press, London.

    Google Scholar 

  3. McElnay, J.C. & Nicol, A.C. (1984) Int. J. Pharm. 19, 89–96.

    Article  CAS  Google Scholar 

  4. McElnay, J.C, Taggart, A.J., Kerr, B. & Passmore, P. (1986) Int. J. Pharm. 33, 195–199.

    Article  CAS  Google Scholar 

  5. Skellern, G.G. & Salole, E.G. (1975) J. Chromatog. 114, 483–485.

    Article  CAS  Google Scholar 

  6. Shaffer, J.A., Williams, S.E., Turnberg, L.A., Houston, J.B. & Rowland, M. (1983) Gut 24, 182–186.

    Article  CAS  Google Scholar 

  7. Olivesi, A. (1985) Therapie 40, 5–7.

    CAS  Google Scholar 

  8. Hayes, M., Alam, A.F., Bruckner, F.E., Doherty, S.M., Myles, A., English, J., Marks, V. & Chakraborty, J. (1983) Annals Rheum. Dis. 42, 151–154.

    Article  CAS  Google Scholar 

  9. McCann, J.P., McElnay, J.C., Nicholls, D.P., Scott, M.G. & Stanford, CF. (1987) Br. J. Clin. Pharmacol. 23, 652P.

    Google Scholar 

  10. Delargy, H. (1981) Ph.D. Thesis, Dept. of Pharmacy, The Queen’s University of Belfast.

    Google Scholar 

  11. Rose, J.Q. & Jusko, W.J. (1979) J. Chromatog. 162, 273–280.

    CAS  Google Scholar 

  12. McElnay, J.C., Mukhtar, H.A., D’Arcy, P.F. & Temple, D.T. (1982) J. Trop. Med. Hyg. 85, 153–158 (& see 159-163).

    CAS  Google Scholar 

  13. Yahya, A.M., McElnay, J.C. & D’Arcy, P.F. (1985) Int. J. Pharm. 25, 217–223.

    Article  CAS  Google Scholar 

  14. Yahya, A.M., McElnay, J.C. & D’Arcy, P.F. (1986) Int. J. Pharm. 34, 137–143.

    Article  CAS  Google Scholar 

  15. McElnay, J.C, Sidahmed, A.M., D’Arcy, P.F. & McQuade, R.D. (1985) Int. J. Pharm. 26, 267–274.

    Article  CAS  Google Scholar 

  16. Bergqvist, Y. & Olin, A. (1982) Acta Pharmaceutica Suecica 19, 161–174.

    CAS  Google Scholar 

  17. Alvan, G., Ekman, L. & Lindstrom, B. (1982) J. Chromatog. 229, 241–247.

    CAS  Google Scholar 

  18. Staiger, M.A., Nguyen-Dinh, P. & Churchill, F.C. (1981) J. Chromatog. 225, 139–149.

    CAS  Google Scholar 

  19. Anderson, K. & Larsson, H. (1974) Arzneim.-Forsch./Drug Res. 24, 1686–1688.

    Google Scholar 

  20. Giacalone, E. & Valzelli, L. (1966) Med. Pharmacol. Exp. 16, 102–106.

    Google Scholar 

  21. Catanesse, B., Lagana, A., Marino, A., Picollo, R. & Rotatori, M. (1986) Pharmacol. Res. Comm. 18, 385–403.

    Article  Google Scholar 

  22. Benson, H.A.E. & McElnay, J.C. (1987) J. Chromatog. 394, 395–399.

    CAS  Google Scholar 

  23. Skauen, D.M. & Zentner, G.M. (1984) Int. J. Pharm. 20, 234–235.

    Article  Google Scholar 

  24. McElnay, J.C., Kennedy, T.A. & Harland, R. (1987) Int. J. Pharm. 40, 105–110.

    Article  CAS  Google Scholar 

  25. Giese, R.W. (1983) Clin. Chem. 29, 1331–1343.

    CAS  Google Scholar 

  26. Drayer, D.E. (1984) in Proceedings of the Second World Conference on Clinical Pharmacology and Therapeutics (Lemberger, L. & Reidenberg, M., eds.), Am. Soc. for Pharmacology & Experimental Therapeutics, Bethesda, MD., pp. 809–819.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1988 Springer Science+Business Media New York

About this chapter

Cite this chapter

McElnay, J.C. (1988). HPLC Analysis of Anti-Inflammatory Agents (Non-Steroidal and Steroidal). In: Reid, E., Robinson, J.D., Wilson, I.D. (eds) Bioanalysis of Drugs and Metabolites, Especially Anti-Inflammatory and Cardiovascular. Methodological Surveys in Biochemistry and Analysis, vol 18 A. Springer, Boston, MA. https://doi.org/10.1007/978-1-4757-9424-3_11

Download citation

  • DOI: https://doi.org/10.1007/978-1-4757-9424-3_11

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4757-9426-7

  • Online ISBN: 978-1-4757-9424-3

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics