Simultaneous quantification of cefuroxime and clindamycin in human lumbar anulus fibrosus, nucleus pulposus and serum via UPLC-MS/MS

J Chromatogr B Analyt Technol Biomed Life Sci. 2021 Feb 15:1165:122522. doi: 10.1016/j.jchromb.2021.122522. Epub 2021 Jan 18.

Abstract

Background: This study aimed to develop a sensitive, accurate method for simultaneously quantifying cefuroxime and clindamycin in human serum, lumbar anulus fibrosus and nucleus pulposus.

Methods: Cefuroxime and clindamycin were quantified using ultra high-performance liquid chromatography-electrospray ionization tandem mass spectrometry in multiple-reaction-monitoring mode on a triple-quadrupole AB Qtrap 5500 system in positive ion mode. Internal standards were D3-cefuroxime and D3,13C-clindamycin. Samples were pretreated by precipitating total protein.

Results: The method showed high sensitivity and good linearity over broad calibration ranges from 100 to 100 000 ng/mL for cefuroxime and 10 to 10 000 ng/mL for clindamycin in serum, and from 10 to 10 000 ng/mL for cefuroxime and 1 to 1 000 ng/mL for clindamycin in lumbar nucleus pulposus. In all sample types, correlation coefficients were greater than 0.99, intra- and inter-day precision (relative standard deviation) was less than 15%, and accuracy (relative error) was within 14% for both analytes. This method was effective at quantifying penetration of cefuroxime and clindamycin in patients undergoing oblique lumbar interbody fusion surgery.

Conclusions: A very sensitive, specific method for simultaneous detection of cefuroxime and clindamycin has been developed for human lumbar anulus fibrosus, nucleus pulposus and serum samples.

Keywords: Cefuroxime; Clindamycin; Human lumbar nucleus pulposus; Lumbar anulus fibrosus; Serum; UPLC-ESI-MS/MS.

MeSH terms

  • Annulus Fibrosus / chemistry*
  • Annulus Fibrosus / metabolism
  • Cefuroxime / analysis*
  • Cefuroxime / blood
  • Cefuroxime / pharmacokinetics
  • Chromatography, High Pressure Liquid / methods*
  • Clindamycin / analysis*
  • Clindamycin / blood
  • Clindamycin / pharmacokinetics
  • Humans
  • Linear Models
  • Lumbosacral Region
  • Nucleus Pulposus / chemistry*
  • Nucleus Pulposus / metabolism
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Tandem Mass Spectrometry / methods

Substances

  • Clindamycin
  • Cefuroxime