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Delivery of lipophilic porphyrin by liposome vehicles: preparation and photodynamic therapy activity against cancer cell lines.

Abstract
Porphyrin photosensitizers are mostly used components in photodynamic therapy (PDT). The poor solubility of porphyrins in aqueous medium is the problem to be solved for the in vivo applications. The delivery of photosensitizers to the tumor cells using liposome vehicles can help to overcome this problem. In this work, we have first functionalized the protoporphyrin IX with lipophilic oleylamine arms and encapsulated it into 1,2 dioleyl-sn-glycero-phosphatidylcholine (DOPC) liposomes. The appropriate sizes of liposomes are about 140 nm and have the characteristic Soret and Q band absorptions at 405 nm (Soret), 507 nm, 541 nm, 577 nm and 631 nm (Q bands), respectively. In the photodynamic activity studies, the liposomal porphyrins were irradiated with light (375 nm, 10 mW) in the presence of cancer cell lines, HeLa and AGS. We have found that both liposomal porphyrins and oleylamine conjugated porphyrins are much more effective than PpIX. This result can be attributed to the drug delivery characteristic of the liposomes which plays effective role in endocytosis. We also found that, in AGS cells, liposomal PpIX-Ole induced apoptosis more than HeLa cells under light conditions.
AuthorsEmine Temizel, Tugba Sagir, Esra Ayan, Sevim Isik, Ramazan Ozturk
JournalPhotodiagnosis and photodynamic therapy (Photodiagnosis Photodyn Ther) Vol. 11 Issue 4 Pg. 537-45 (Dec 2014) ISSN: 1873-1597 [Electronic] Netherlands
PMID25107838 (Publication Type: Journal Article)
CopyrightCopyright © 2014 Elsevier B.V. All rights reserved.
Chemical References
  • Liposomes
  • Photosensitizing Agents
  • Porphyrins
Topics
  • Cell Line, Tumor
  • Cell Survival (drug effects, radiation effects)
  • Drug Compounding (methods)
  • HeLa Cells
  • Humans
  • Liposomes (administration & dosage, chemical synthesis)
  • Neoplasms, Experimental (drug therapy, pathology)
  • Photochemotherapy (methods)
  • Photosensitizing Agents (administration & dosage, chemical synthesis)
  • Porphyrins (administration & dosage, chemistry)
  • Treatment Outcome

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