Liposomal chemotherapeutics

Future Oncol. 2013 Dec;9(12):1849-59. doi: 10.2217/fon.13.146.

Abstract

Currently, six liposomal chemotherapeutics have received clinical approval and many more are in clinical trials or undergoing preclinical evaluation. Liposomes exhibit low toxicity and improve the biopharmaceutical features and therapeutic index of drugs, thereby increasing efficacy and reducing side effects. In this review we discuss the advantages of using liposomes for the delivery of chemotherapeutics. Gemcitabine and paclitaxel have been chosen as examples to illustrate how the performance of a metabolically unstable or poorly water-soluble drug can be greatly improved by liposomal incorporation. We look at the beneficial effects of liposomes in a variety of solid and blood-borne tumors, including thyroid cancer, pancreatic cancer, breast cancer and multiple myeloma.

Publication types

  • Review

MeSH terms

  • Breast Neoplasms / drug therapy
  • Breast Neoplasms / pathology
  • Deoxycytidine / administration & dosage
  • Deoxycytidine / analogs & derivatives*
  • Doxorubicin / administration & dosage*
  • Drug Delivery Systems / adverse effects
  • Female
  • Gemcitabine
  • Humans
  • Liposomes / adverse effects
  • Liposomes / therapeutic use*
  • Multiple Myeloma / drug therapy
  • Multiple Myeloma / pathology
  • Paclitaxel / administration & dosage*
  • Pancreatic Neoplasms / drug therapy
  • Pancreatic Neoplasms / pathology
  • Thyroid Neoplasms / drug therapy
  • Thyroid Neoplasms / pathology

Substances

  • Liposomes
  • Deoxycytidine
  • Doxorubicin
  • Paclitaxel
  • Gemcitabine