Combination of HPLC "inverted chirality columns approach" and MS/MS detection for extreme enantiomeric excess determination even in absence of reference samples. Application to camptothecin derivatives

Anal Chem. 2007 Aug 1;79(15):6013-9. doi: 10.1021/ac070776j. Epub 2007 Jun 29.

Abstract

An original, extremely sensitive and selective HPLC-MS/MS technique for the identification and determination of the minor enantiomer in nonracemic mixtures, even when only one enantiomer is available as reference, is described. The method is based on the so-called "inverted chirality columns approach" (ICCA) and consists of the use of chiral stationary phases (CSPs) available in both enantiomeric forms: in fact, inversion of the elution order for a pair of enantiomers is observed in response to the change in column chirality. This offers two key advantages: first, it is possible to demonstrate the potential enantioselectivity of the system by generating a virtual racemate, and second, it permits the choosing of the right column chirality for trace determination. Combination with MS/MS detection affords high specificity allowing not only high sensitivity (down to 0.0025% of the minor enantiomer) but also unequivocal peak identification in complex mixtures. Applications to semisynthetic derivatives of camptothecin, endowed with antitumor activity, are reported. Moreover, applicability of ICCA is not limited to this class of molecules but generates universal support. Its use might also be extended to other classes of compounds by using other CSPs, available in both enantiomeric forms.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Camptothecin / analogs & derivatives
  • Camptothecin / analysis*
  • Chromatography, High Pressure Liquid / methods*
  • Circular Dichroism / methods
  • Mass Spectrometry / methods*
  • Sensitivity and Specificity
  • Spectrophotometry, Ultraviolet / methods
  • Stereoisomerism

Substances

  • Camptothecin