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Determination of Propylene Glycol in Low Volume Plasma and Urine Samples of Neonates by LC with Photodiode Array Detection

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Abstract

In order to enhance the sensitivity and to develop a method suitable for quantification of propylene glycol (PG) in low volume neonate plasma and urine samples, several steps in earlier described high performance liquid chromatographic methods were optimised. Chromatographic separation on a reversed-phase column and ultraviolet detection resulted in cleaner chromatograms without interfering compounds. Linearity of the standard curves was validated in the concentration range 0.25–50 mg L−1. The lower limit of quantification was 20 times lower than in earlier described methods. Presented method was suitable for quantification of PG concentrations in low volume neonate plasma (15–46 mg L−1) and urine samples (20–175 mg L−1) enabling us to document very low renal versus non-renal contribution of PG clearance in neonates.

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References

  1. U.S. Food and Drug Administration (2001) Fed Regist 66:28526

  2. Arbour R, Esparis B (2000) Chest 118:545–546

    Article  CAS  Google Scholar 

  3. Reynolds HN, Teiken P, Regan ME, Habashi NM, Cottingham C, McCunn M, Scalea TM (2000) Crit Care Med 28:1631–1634

    Article  CAS  Google Scholar 

  4. Laine GA, Hamid-Hossain SM, Solis RT, Adams SC (1995) Ann Pharmacother 29:1110–1114

    CAS  Google Scholar 

  5. Wilson KC, Reardon C, Theodore AC, Farber HW (2005) Chest 128:1674–1681

    Article  CAS  Google Scholar 

  6. Arroliga AC, Shehab N, McCarthy K, Gonzales JP (2004) Crit Care Med 32:1709–1714

    Article  CAS  Google Scholar 

  7. Glasgow AM, Boeckx RL, Miller MK, MacDonald MG, August GP, Goodman SI (1983) Pediatrics 72:353–355

    CAS  Google Scholar 

  8. Nelsen JL, Haas CE, Habtemariam B, Kaufman DC, Partridge A, Welle S, Forrest A (2008) J Intensive Care Med 23:184–194

    Article  Google Scholar 

  9. American Academy of Pediatrics (1997) Pediatrics 99:268–278

    Google Scholar 

  10. Chicella M, Jansen P, Parthiban A, Marlowe KF, Bencsath FA, Krueger KP, Boerth R (2002) Crit Care Med 30:2752–2756

    Article  CAS  Google Scholar 

  11. Allegaert K, Vanhaesebrouk S, Kulo A, Cosaert K, Verbesselt R, Debeer A, de Hoon J (2010) Arch Dis Child 95:1054–1058

    Google Scholar 

  12. Nahata MC (2009) Arch Dis Child Fetal Neonatal Ed 94:392–393

    Article  Google Scholar 

  13. Whittaker A, Currie AE, Turner MA, Field DJ, Mulla H, Pandya HC (2009) Arch Dis Child Fetal Neonatal Ed 94:236–240

    Article  Google Scholar 

  14. Allegaert K, Verbesselt R, Naulaers G, van den Anker JN, Rayyan M, Debeer A, de Hoon J (2008) Acta Clin Belg 63:16–24

    CAS  Google Scholar 

  15. Yu DK, Sawchuk RJ (1983) Clin Chem 29:2088–2090

    CAS  Google Scholar 

  16. Houzé P, Chaussard J, Harry P, Pays M (1993) J Chromatogr 619:251–257

    Article  Google Scholar 

  17. Ferrala NF, Ghanayem BI, Nomeir AA (1994) J Chromatogr B 660:291–296

    Article  CAS  Google Scholar 

  18. Zhu J, Feng YL, Aikawa B (2004) J Environ Monit 6:881–887

    Article  CAS  Google Scholar 

  19. Gao S, Wilson DM, Edinboro LE, McGuire GM, Williams SGP, Karnes HT (2003) J Liq Chromatogr Relat Technol 26:3413–3431

    Article  CAS  Google Scholar 

  20. Sinjewel A, Swart EL, Lingeman H, Wilhelm AJ (2007) Chromatographia 66:103–105

    Article  CAS  Google Scholar 

  21. Zhou T, Zhang H, Duan G (2007) J Sep Sci 30:2620–2627

    Article  CAS  Google Scholar 

  22. Isakau H, Robert M, Shingel KI (2009) J Pharm Biomed Anal 49:594–600

    Article  CAS  Google Scholar 

  23. Gupta RN, Eng F, Gupta ML (1982) Clin Chem 28:32–33

    CAS  Google Scholar 

  24. Allegaert K, Anderson BJ, Naulaers G, de Hoon J, Verbesselt R, Debeer A, Devlieger H, Tibboel D (2004) Eur J Clin Pharmacol 60:191–197

    Article  CAS  Google Scholar 

  25. 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 Veterinary Medicine (CVM), BP (2001) http://www.fda.gov/cvm

  26. Shah VP, Midha KK, Findlay JW, Hill HM, Hulse JD, McGilveray IJ, McKay G, Miller KJ, Patnaik RN, Powell ML, Tonelli A, Viswanathan CT, Yacobi A (2000) Pharm Res 17:1551–1557

    Article  CAS  Google Scholar 

  27. Rosing H, Man WY, Doyle E, Bult A, Beijnen JH (2000) J Liq Chromatogr Relat Technol 23:329–354

    Article  CAS  Google Scholar 

  28. Vollmer PA, Harty DC, Erickson NB, Balhon AC, Dean RA (1996) J Chromatogr B Biomed Appl 685:370–374

    Article  CAS  Google Scholar 

  29. Speth PA, Vree TB, Neilen NF, de Mulder PH, Newell DR, Gore ME, de Pauw BE (1987) Ther Drug Monit 9:255–258

    Article  CAS  Google Scholar 

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Acknowledgments

The clinical research of Karel Allegaert is supported by the Fund for Scientific Research, Flanders (Belgium) (F.W.O. Vlaanderen) by a Fundamental Clinical Investigatorship (1800209 N), and of Aida Kulo by a JoinEU-SEE scholarship (2009–2010). We would like to thank Sonia Demarsin for her technical assistance.

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Correspondence to Aida Kulo.

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Kulo, A., Allegaert, K., de Hoon, J. et al. Determination of Propylene Glycol in Low Volume Plasma and Urine Samples of Neonates by LC with Photodiode Array Detection. Chromatographia 73, 463–470 (2011). https://doi.org/10.1007/s10337-011-1923-8

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  • DOI: https://doi.org/10.1007/s10337-011-1923-8

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