Liposomes as potential masking agents in sport doping. Part 2: Detection of liposome-entrapped haemoglobin by flow cytofluorimetry

Drug Test Anal. 2017 Feb;9(2):208-215. doi: 10.1002/dta.1956. Epub 2016 Feb 23.

Abstract

This work presents an analytical procedure for the identification and characterization of liposome-entrapped haemoglobins, based on flow cytofluorimetry. Flow cytofluorimetric detection is carried out following labelling by two distinct fluorescent reagents, an anti-haemoglobin antibody, fluorescein isothiocyanate conjugated, and an anti-poly(ethylene glycol) antibody, streptavidin-phycoerythrin conjugated. This experimental strategy allows the detection of liposome-entrapped haemoglobins in aqueous media, including plasma; the efficacy of the proposed approach has been verified on whole blood samples added with the liposomal formulation (ex-vivo). Additionally, the proposed technique allows the characterization of several key parameters in the study of liposomal haemoglobins, including, for instance (1) the determination of the degree of haemoglobin entrapment by liposomes; (2) the poly(ethylene glycol) insertion efficiency; and (3) the evaluation of liposome-entrapped haemoglobins stability following storage at 4 °C, allowing to follow both the process of haemoglobin loss from liposomes and the liposome degradation. The procedure is proposed for the detection and characterization of liposome-entrapped haemoglobin formulations to control their misuse in sport, but is also suggested for further applications in biological and clinical laboratory investigations. Copyright © 2016 John Wiley & Sons, Ltd.

Keywords: blood doping; flow cytofluorimetry; haemoglobin-based oxygen carriers; liposome-entrapped haemoglobin; liposomes; poly(ethylene glycol).

MeSH terms

  • Blood Substitutes / administration & dosage
  • Blood Substitutes / analysis*
  • Doping in Sports
  • Flow Cytometry
  • Hemoglobins / administration & dosage
  • Hemoglobins / analysis*
  • Humans
  • Liposomes / analysis*
  • Liposomes / blood
  • Particle Size
  • Polyethylene Glycols / analysis*
  • Protein Stability

Substances

  • Blood Substitutes
  • Hemoglobins
  • Liposomes
  • Polyethylene Glycols