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Iran J Pharm Res. 2013;12(1):147-54.

Comparative pharmacokinetics of levofloxacin in healthy volunteers and in patients suffering from typhoid Fever.

Iranian journal of pharmaceutical research : IJPR

Muhammad Usman, Muhammad Ashraf, Muhammad Imran Khokhar, Bilal Ashiq, Muhammad Irfan Masood, Shehryar Afzal, Ovais Omer, Mohsin Ali, M Imran Qadir

Affiliations

  1. Institute of Pharmaceutical Sciences, University of Veterinary and Animal Sciences, Lahore, Pakistan.

PMID: 24250583 PMCID: PMC3813201

Abstract

The aim of this study was to characterize the effect of typhoid fever on pharmacokinetic parameters of levofloxacin (LF) and compare the pharmacokinetic parameters of the said antibiotic in healthy human volunteers and patients with typhoid fever. Total of 12 subjects were divided into two groups "A" (healthy volunteers) and "B" (typhoid patients). Single oral dose of LF 500 mg was given and 5 mL of blood was collected from each subject at 0, 0.25, 0.5, 1, 2, 3, 6, 12, 24, 36 and 72 h. Plasma concentrations of LF were measured by HPLC. Pharmacokinetic parameters were calculated from plasma concentration-time data by using MW/PHARM pharmacological analysis. In healthy volunteers, the average pharmacokinetic parameters were as Cmax (6.79 μg/mL), Tmax (1.84 h), T(½) (10.03 h), Ka (2.23 h(-1)), AUC (110.09 μgh/mL), Vd (85.84 L), Cl (4.57 L/h) and in typhoid patients were Cmax (6.90 μg/mL), Tmax (1.82 h), T(½) (9.42 h), Ka (2.21 h(-1)), AUC (105.55 μgh/mL), Vd (64.31 L), Cl (4.75 L/h). The difference between pharmacokinetic parameters of LF in healthy human volunteers and typhoid patients was calculated by using unpaired t-test. As the p-value in case of all pharmacokinetic parameters was more than 0.05, the difference between pharmacokinetic parameters in both healthy human volunteers and typhoid patients was insignificant. It is concluded that there is no need to adjust the dose of LF in typhoid patients.

Keywords: HPLC; Levofloxacin; Pharmacokinetics; Typhoid fever; Volunteers

References

  1. Drugs. 1995;49 Suppl 2:211-4 - PubMed
  2. J Antimicrob Chemother. 1986 Nov;18 Suppl D:43-8 - PubMed
  3. J Pharm Biomed Anal. 1997 Mar;15(6):765-71 - PubMed
  4. Iran J Pharm Res. 2011 Summer;10(3):391-2 - PubMed
  5. Clin Pharmacokinet. 1997 Feb;32(2):101-19 - PubMed
  6. Antimicrob Agents Chemother. 2006 Jun;50(6):1937-45 - PubMed
  7. N Engl J Med. 2005 Sep 8;353(10):977-87 - PubMed
  8. Clin Infect Dis. 2003 Jul 1;37(1):75-81 - PubMed
  9. Antimicrob Agents Chemother. 1994 Apr;38(4):799-804 - PubMed
  10. Presse Med. 1991 Feb 23;20(7):291-3 - PubMed
  11. Ther Clin Risk Manag. 2008 Oct;4(5):843-53 - PubMed
  12. Int J Antimicrob Agents. 2007 Aug;30(2):162-8 - PubMed
  13. J Vet Pharmacol Ther. 2005 Aug;28(4):363-9 - PubMed
  14. Antimicrob Agents Chemother. 1986 Jan;29(1):7-12 - PubMed
  15. Antimicrob Agents Chemother. 1998 May;42(5):1098-104 - PubMed
  16. J Antimicrob Chemother. 1994 Sep;34(3):446-8 - PubMed
  17. Chest. 2007 Mar;131(3):796-802 - PubMed

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