Ecologically evaluated and FDA-validated HPTLC method for assay of pregabalin and tramadol in human biological fluids

Biomed Chromatogr. 2021 Apr;35(4):e5023. doi: 10.1002/bmc.5023. Epub 2020 Dec 6.

Abstract

The introduced research presents a novel in vivo quantitative method for assay of mixtures of pregabalin and tramadol as a common combinations approved for treatment of neuropathic pain. Green analytical chemistry is a recently emerging science concerned with control of the use of chemicals harmful to the environment in various analytical methods. Consequently, a green high-performance thin layer chromatography (HPTLC) method was achieved for determination of the mixture in human plasma and urine satisfying both analytical and environmental standards. The separation was achieved on HPTLC sheets using a separating mixture of ethanol-ethyl acetate-acetone-ammonia solution (8:2:1:0.05, by volume) as a mobile phase. The sheets were dried in air then scanned at two wavelengths. For tramadol, 220 nm was chosen; however, pregabalin is an unconjugated drug, so its determination was a challenge. Hence for pregabalin, the plates were sprayed with ethanolic solution of ninhydrin (3%, w/v), to obtain a conjugated complex, which could be assessed at 550 nm. Furthermore, the developed method fulfilled the US Food and Drug Administration validation guidelines, and proved to be useful in therapeutic drug monitoring of this combination. The Eco-scale assessment protocol was implemented to determine the greenness profile of the applied method.

Keywords: FDA guidelines; HPTLC; analytical Eco-scale; pregabalin; tramadol.

MeSH terms

  • Chromatography, High Pressure Liquid / methods*
  • Chromatography, Thin Layer / methods*
  • Humans
  • Limit of Detection
  • Linear Models
  • Pregabalin* / blood
  • Pregabalin* / urine
  • Reproducibility of Results
  • Tramadol* / blood
  • Tramadol* / urine

Substances

  • Tramadol
  • Pregabalin