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Liposome targeting to tumors using vitamin and growth factor receptors.

Abstract
Liposome-encapsulated anticancer drugs reveal their potential for increased therapeutic efficacy and decreased nonspecific toxicities due to their ability to enhance the delivery of chemotherapeutic agents to solid tumors. Advances in liposome technology have resulted in the development of ligand-targeted liposomes capable of selectively increasing the efficacy of carried agents against receptor-bearing tumor cells. Receptors for vitamins and growth factors have become attractive targets for ligand-directed liposomal therapies due to their high expression levels on various forms of cancer and their ability to internalize after binding to the liposomes conjugated to receptors' natural ligands (vitamins) or synthetic agonists (receptor-specific antibodies and synthetic peptides). This chapter summarizes various strategies and advances in targeting liposomes to vitamin and growth factor receptors in vitro and in vivo with special emphasis on two extensively studied liposome-targeting systems utilizing folate receptor and HER2/neu growth factor receptor.
AuthorsD C Drummond, K Hong, J W Park, C C Benz, D B Kirpotin
JournalVitamins and hormones (Vitam Horm) Vol. 60 Pg. 285-332 ( 2000) ISSN: 0083-6729 [Print] United States
PMID11037627 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S., Review)
Chemical References
  • Antineoplastic Agents
  • Carrier Proteins
  • Folate Receptors, GPI-Anchored
  • Ligands
  • Liposomes
  • Receptors, Cell Surface
  • Receptors, Growth Factor
  • Vitamins
  • Folic Acid
Topics
  • Antineoplastic Agents (administration & dosage, therapeutic use)
  • Carrier Proteins (metabolism)
  • Drug Delivery Systems (methods)
  • Folate Receptors, GPI-Anchored
  • Folic Acid (metabolism)
  • Humans
  • In Vitro Techniques
  • Ligands
  • Liposomes
  • Microscopy, Confocal
  • Neoplasms (drug therapy)
  • Receptors, Cell Surface
  • Receptors, Growth Factor (metabolism)
  • Vitamins (metabolism)

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