Determination of free vancomycin, ceftriaxone, cefazolin and ertapenem in plasma by ultrafiltration: impact of experimental conditions.

Ultrafiltration is a rapid and convenient method to determine the free concentrations of drugs. In the present work, we aimed to develop an ultrafiltration method which is appropriate for routine determination of the free fraction of vancomycin and highly protein bound beta-lactams such as ertapenem, ceftriaxone and cefazolin in plasma from intensive care unit patients. Different filter types and experimental conditions (molecular weight cut-off, centrifugal force and time, pH, temperature) were evaluated and found to have influence on the result. In the final protocol, serum or plasma was buffered to pH 7.4-7.5, ultrafiltered at 1000×g at 37°C for 20min using Nanosep Omega 10K filters and subsequently analysed for the antibiotics by RP-HPLC with UV detection. The data from our investigation suggest to aim physiological conditions, i.e. 37°C and pH 7.4, and low to moderate relative centrifugal forces in order to get reliable results. With regard to the chromatographic separation, modulation of the pH in the range of 2.5-7.0 allows to determine several beta-lactams isocratically and/or to avoid interferences by co-administered drugs.

[1]  Martin Brunner,et al.  Impaired target site penetration of &bgr; -lactams may account for therapeutic failure in patients with septic shock , 2001, Critical care medicine.

[2]  Masao Kobayashi,et al.  High-performance liquid chromatography with ultraviolet detection for real-time therapeutic drug monitoring of meropenem in plasma. , 2007, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

[3]  W. Stigelman,et al.  Goodman and Gilman's the Pharmacological Basis of Therapeutics , 1986 .

[4]  J. Rello,et al.  Flucloxacillin dosing in critically ill patients with hypoalbuminaemia: special emphasis on unbound pharmacokinetics. , 2010, The Journal of antimicrobial chemotherapy.

[5]  Jingwei Shao,et al.  Compilation of 222 drugs' plasma protein binding data and guidance for study designs. , 2012, Drug discovery today.

[6]  W. Vetter,et al.  Isolation of 6,9,12,15-Hexadecatetraenoic Fatty Acid (16:4n-1) Methyl Ester from Transesterified Fish Oil by HSCCC , 2011, Chromatographia.

[7]  N. Williams,et al.  A mass balance approach for calculation of recovery and binding enables the use of ultrafiltration as a rapid method for measurement of plasma protein binding for even highly lipophilic compounds. , 2013, Journal of pharmaceutical and biomedical analysis.

[8]  K. Korzekwa,et al.  Impact of pH on plasma protein binding in equilibrium dialysis. , 2008, Molecular pharmaceutics.

[9]  Stephan Schmidt,et al.  Effect of Protein Binding on the Pharmacological Activity of Highly Bound Antibiotics , 2008, Antimicrobial Agents and Chemotherapy.

[10]  D. Musson,et al.  Assay methodology for the quantitation of unbound ertapenem, a new carbapenem antibiotic, in human plasma. , 2003, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

[11]  T. Bjornsson,et al.  The artifactual nature of heparin‐induced drug protein‐binding alterations , 1981, Clinical pharmacology and therapeutics.

[12]  J. Roberts,et al.  A method for determining the free (unbound) concentration of ten beta-lactam antibiotics in human plasma using high performance liquid chromatography with ultraviolet detection. , 2012, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

[13]  J. Roberts,et al.  The Clinical Relevance of Plasma Protein Binding Changes , 2012, Clinical Pharmacokinetics.

[14]  G. McMillin,et al.  Effect of Ultrafiltrate Volume on Determination of Free Phenytoin Concentration , 2005, Therapeutic drug monitoring.

[15]  J. Roberts,et al.  Analysis of 12 beta-lactam antibiotics in human plasma by HPLC with ultraviolet detection. , 2010, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

[16]  V. Samanidou,et al.  Chromatographic analysis of penicillins in pharmaceutical formulations and biological fluids. , 2006, Journal of separation science.

[17]  C. Michelet,et al.  Simultaneous Determination of 12 β-Lactam Antibiotics in Human Plasma by High-Performance Liquid Chromatography with UV Detection: Application to Therapeutic Drug Monitoring , 2011, Antimicrobial Agents and Chemotherapy.

[18]  O. Brørs,et al.  pH lability in serum during equilibrium dialysis. , 1985, British journal of clinical pharmacology.

[19]  C. Jarry,et al.  Determination of third-generation cephalosporins by high-performance liquid chromatography in connection with pharmacokinetic studies. , 1998, Journal of chromatography. A.

[20]  Rachel F. Eyler,et al.  Pharmacokinetics of Ertapenem in Critically Ill Patients Receiving Continuous Venovenous Hemodialysis or Hemodiafiltration , 2013, Antimicrobial Agents and Chemotherapy.

[21]  A. Lorenzo,et al.  Effects of pressure on the plasma binding of digoxin and ouabain in an ultrafiltration apparatus. , 1973, Biochemical pharmacology.

[22]  A. Fura,et al.  Shift in pH of biological fluids during storage and processing: effect on bioanalysis. , 2003, Journal of pharmaceutical and biomedical analysis.

[23]  N. D. Kim,et al.  Factors influencing the protein binding of vancomycin , 1991, Biopharmaceutics & drug disposition.

[24]  R. White,et al.  Comparative Stability of Cephalothin and Cefazolin in Buffer or Human Serum , 1977, Antimicrobial Agents and Chemotherapy.

[25]  D. Breilh,et al.  Diffusion of ertapenem into bone and synovial tissues. , 2007, The Journal of antimicrobial chemotherapy.

[26]  Carsten Gnewuch,et al.  Clearance of vancomycin during continuous infusion in Intensive Care Unit patients: correlation with measured and estimated creatinine clearance and serum cystatin C. , 2010, International journal of antimicrobial agents.

[27]  H. Ushikoshi,et al.  Simultaneous determination of eight β-lactam antibiotics in human serum by liquid chromatography-tandem mass spectrometry. , 2011, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

[28]  Yi Wang,et al.  Population pharmacokinetics of piperacillin/tazobactam in neonates and young infants , 2013, European Journal of Clinical Pharmacology.

[29]  S. Wicha,et al.  Unbound fraction of vancomycin in intensive care unit patients , 2014, Journal of clinical pharmacology.

[30]  A. Marzo,et al.  Chromatography as an analytical tool for selected antibiotic classes: a reappraisal addressed to pharmacokinetic applications. , 1998, Journal of chromatography. A.

[31]  S. Bauer,et al.  Therapeutic Drug Monitoring of Piperacillin-Tazobactam Using Spent Dialysate Effluent in Patients Receiving Continuous Venovenous Hemodialysis , 2010, Antimicrobial Agents and Chemotherapy.

[32]  A. Pesce,et al.  Free drug concentrations are constant in serial fractions of plasma ultrafiltrate. , 1982, Clinical chemistry.

[33]  K. Brown,et al.  Ultrafiltration in serum protein binding determinations. , 1981, Journal of pharmaceutical sciences.