In vitro binding and partitioning of irinotecan (CPT-11) and its metabolite, SN-38, in human blood

Invest New Drugs. 2000 Feb;18(1):1-5. doi: 10.1023/a:1006379730137.

Abstract

The binding of CPT-11 and SN-38 to human plasma proteins was studied by ultrafiltration at 37 degrees C and pH 7.4. In plasma, CPT-11 was 66-60% bound in the range 100-4000 ng/ml and SN-38 was 94-96% bound in the range 50-200 ng/ml. At these concentrations the plasma binding of CPT-11 was slightly saturable, but the plasma binding of SN-38 was concentration-independent. Albumin was the main carrier of CPT-11 and SN-38 in plasma. In blood, the binding of CPT-11 was moderate (80%), mainly to plasma proteins (47%) and erythrocytes (33%). The binding of SN-38 was high (99%) and most of SN-38 in blood was located in blood cells (approximately 66%) The simulation of a grade 3 hematotoxicity (according to National Cancer Institute's Common Toxicity Criteria grading) on the SN-38 blood distribution yielded an increase in fu (free fraction of drug in plasma) from 1.05 to 2.08 and a decrease in C(Bl)/C(P) from 1.66 to 1.14 (both resulting from a decreased cell binding).

MeSH terms

  • Antineoplastic Agents, Phytogenic / blood
  • Antineoplastic Agents, Phytogenic / pharmacokinetics*
  • Blood Cell Count
  • Blood Cells / metabolism
  • Blood Platelets / metabolism
  • Blood Proteins / metabolism
  • Camptothecin / analogs & derivatives*
  • Camptothecin / blood
  • Camptothecin / pharmacokinetics
  • Humans
  • In Vitro Techniques
  • Irinotecan
  • Protein Binding
  • Ultrafiltration

Substances

  • Antineoplastic Agents, Phytogenic
  • Blood Proteins
  • Irinotecan
  • Camptothecin