Assessment of light stability of drugs in blood and plasma

Bioanalysis. 2016 Oct;8(19):2007-21. doi: 10.4155/bio-2016-0109. Epub 2016 Sep 9.

Abstract

Aim: A procedure was developed for the assessment of photochemical stability of drugs in blood and plasma under standardized conditions. The procedure avoids a variable outcome of photochemical stability experiments and tests relevant worst case conditions so that unnecessary light protection is avoided. Results/methodology: Blood and plasma were spiked with a mixture of drugs and incubated in a Suntest CPS(+), in the laboratory on the bench and near the window on a sunny summer day. The results were compared.

Discussion/conclusion: No protection from light, limited protection from light and full protection from light are advised for drugs that are stable in plasma in the Suntest CPS(+) at 250 W/m(2) for at least 30 min, for 5-30 min and for <5 min, respectively.

Keywords: LC–MS/MS; bioanalysis; blood; method validation; photochemical degradation; plasma.

MeSH terms

  • Chromatography, High Pressure Liquid
  • Drug Stability*
  • Humans
  • Light*
  • Pharmaceutical Preparations / blood*
  • Pharmaceutical Preparations / radiation effects*
  • Photolysis / radiation effects
  • Tandem Mass Spectrometry
  • Ultraviolet Rays

Substances

  • Pharmaceutical Preparations