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Pharmacokinetics of fluoroquinolones in critical care patients: A bio-analytical HPLC method for the simultaneous quantification of ofloxacin, ciprofloxacin and moxifloxacin in human plasma
Abstract
A high-performance liquid chromatographic (HPLC) method with fluorescence detection was developed and validated for the simultaneous quantification of ofloxacin, ciprofloxacin and moxifloxacin in human plasma. Sarafloxacin was used as internal standard. Chromatography was carried out using a Waters XBridge C(18) HPLC column and a gradient mobile phase consisting of CH(3)CN/MeOH/0.025M TBA.Cl/TFA (eluent A at 75/25/899/1 (v/v); eluent B at 150/50/799/1 (v/v); both at pH 3.5). Excitation/emission wavelengths were 279/442nm for ciprofloxacin and 290/500nm for ofloxacin, moxifloxacin and internal standard. Prior to chromatography, plasma samples were treated with acetonitrile for protein precipitation, followed by evaporation of the liquid layer and reconstitution in eluent A. The method was validated for the three fluoroquinolones over the clinically relevant concentration range from 0.02 to 7.50mug/ml. The method showed acceptable linearity with correlation coefficients, r(2)>0.995, as well as high precision (RSD% <7% in each case), accuracy (90.4-105.4%) and selectivity. The limit of quantification for the three fluoroquinolones was established at 0.02mug/ml. Ofloxacin, ciprofloxacin and moxifloxacin were extracted from plasma with a mean recovery of 95%, 86.4% and 94.2%, respectively. During validation, the concentration of the three fluoroquinolones was found to be stable after 3 freeze-thaw cycles and for at least 15h after extraction. This bio-analytical method was finally…
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These reported HPLC assays have extensive chromatographic run times.
“These assays have some disadvantages in terms of extensive chromatographic run times [9,11-13,15,16] a large consumption of non environmentally friendly solvents [11] or a large amount of sample [11,15,16].”
Several HPLC assays with ultraviolet detection for the determination of these drugs, alone or in combination, have been reported.
“Several HPLC assays with ultraviolet (UV) detection for the determination of these drugs, alone or in combination, have been reported [9-17].”
These reported HPLC assays require a large amount of sample.
“These assays have some disadvantages in terms of extensive chromatographic run times [9,11-13,15,16] a large consumption of non environmentally friendly solvents [11] or a large amount of sample [11,15,16].”
These reported HPLC assays consume large amounts of non environmentally friendly solvents.
“These assays have some disadvantages in terms of extensive chromatographic run times [9,11-13,15,16] a large consumption of non environmentally friendly solvents [11] or a large amount of sample [11,15,16].”
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Research works printed but not linked: 24
- Viale, 2003, J. Chemother., 15, 5, 10.1179/joc.2003.15.Supplement-2.5 · DOI
- Peyrani, 2008, Infect. Med., 25, 161
- Moran, 2006, Emerg. Med., 30, 377, 10.1016/j.jemermed.2005.07.009 · DOI
- Boucher, 2006, Crit. Care Clin., 22, 255, 10.1016/j.ccc.2006.02.011 · DOI
- Zagli, 2008, Fund. Clin. Pharmacol., 22, 493, 10.1111/j.1472-8206.2008.00623.x · DOI
- Soy, 2006, Curr. Opin. Crit. Care, 12, 477, 10.1097/01.ccx.0000244130.77365.c2 · DOI
- Laban-Djurdjevic, 2006, J. Chromatogr. B, 844, 104, 10.1016/j.jchromb.2006.07.001 · DOI
- Takacsnovak, 1995, J. Liquid Chromatogr., 18, 807, 10.1080/10826079508009274 · DOI
- Garcia, 1999, Biomed. Chromatogr., 13, 350, 10.1002/(SICI)1099-0801(199908)13:5<350::AID-BMC889>3.0.CO;2-C · DOI
- Idowu, 2004, J. Pharm. Biomed. Anal., 35, 143, 10.1016/j.jpba.2004.01.006 · DOI
- Sowinski, 2004, J. Clin. Pharm. Ther., 29, 381, 10.1111/j.1365-2710.2004.00575.x · DOI
- Imre, 2003, J. Pharm. Biomed. Anal., 33, 125, 10.1016/S0731-7085(03)00151-1 · DOI
- Zotou, 2002, J. Pharm. Biomed. Anal., 28, 559, 10.1016/S0731-7085(01)00689-6 · DOI
- Maya, 2001, J. Chromatogr. B, 755, 320, 10.1016/S0378-4347(01)00126-8 · DOI
- Ulu, 2007, J. Pharm. Biomed. Anal., 43, 320, 10.1016/j.jpba.2006.11.005 · DOI
- Lemoine, 2000, J. Chromatogr. B, 742, 247, 10.1016/S0378-4347(00)00166-3 · DOI
- Garcia, 2002, Chromatographia, 55, 431, 10.1007/BF02492272 · DOI
- Immanuel, 2001, J. Chromatogr. B, 760, 91, 10.1016/S0378-4347(01)00260-2 · DOI
- Macek, 1995, J. Chromatogr. B, 673, 316, 10.1016/0378-4347(95)00263-5 · DOI
- Samanidou, 2003, Anal. Bioanal. Chem., 375, 623, 10.1007/s00216-003-1749-9 · DOI
- Chan, 2006, Anal. Biochem., 353, 30, 10.1016/j.ab.2006.03.016 · DOI
- Liang, 2002, J. Chromatogr. B, 772, 53, 10.1016/S1570-0232(02)00046-6 · DOI
- Long, 1983, Anal. Chem., 55, 712A, 10.1021/ac00258a001 · DOI
- Montay, 1985, J. Chromatogr., 339, 214, 10.1016/S0378-4347(00)84647-2 · DOI
Cited by
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Ferrone, V., Cotellese, R., Carlucci, M., Di Marco, L., & Carlucci, G. (2018) · Journal of Pharmaceutical and Biomedical Analysis · doi:10.1016/j.jpba.2017.12.039 · Cited by 43
Metadata
- Authors
- De Smet, J., Boussery, K., Colpaert, K., De Sutter, P., De Paepe, P., Decruyenaere, J., & Van Bocxlaer, J.
- Affiliations
- Ghent University (BE)
- Ghent University Hospital (BE)
- Venue
- Journal of Chromatography B
- Publisher
- Elsevier BV
- Published
- 2009-04
- Volume
- 877
- Issue
- 10
- Pages
- 961-967
- ISSN
- 1570-0232 (ISSN-L)
- OpenAlex
- W1980041883
- Cited by
- 71
- References
- 0
- Citations by year
- 2026: 1 · 2025: 4 · 2024: 2 · 2023: 2 · 2022: 4 · 2021: 1 · 2020: 5 · 2019: 2 · 2018: 4 · 2017: 3 · 2016: 7 · 2015: 5 · 2014: 4 · 2013: 7 · 2012: 7
- FWCI
- 6.40
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Chromatography B (publishedVersion)
- PubMed (publishedVersion)
- Ghent University Academic Bibliography (Ghent University) (submittedVersion)
- Topics
- Physical Sciences › Chemistry › Analytical Chemistry › Analytical Methods in Pharmaceuticals
- Health Sciences › Medicine › Pharmacology (medical) › Antibiotics Pharmacokinetics and Efficacy
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Toxicology › Forensic Toxicology and Drug Analysis
- Keywords
- fluoroquinolones, ofloxacin, ciprofloxacin, moxifloxacin, pharmacokinetics, critically ill patients, simultaneous determination, human plasma, fluorescence detection, HPLC method validation
- MeSH terms
- Moxifloxacin, Aza Compounds, Chromatography, High Pressure Liquid, Ciprofloxacin, Humans, Quinolines, Ofloxacin, Fluoroquinolones
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