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Synergistic interaction of paclitaxel and curcumin with cyclodextrin polymer complexation in human cancer cells.

Abstract
The use of cytotoxic chemotherapic agents is the most common method for the treatment of metastatic cancers. Poor water solubility and low efficiency of chemotherapic agents are among the major hurdles of effective chemotherapy treatments. Curcumin and paclitaxel are well-known chemotherapic agents with poor water solubility and undesired side effects. In this study, a novel drug nanocarrier system was formulated by encapsulating curcumin and paclitaxel in poly(β-cyclodextrin triazine) (PCDT) for the therapy of four cancer models; ovarian, lung, prostate, and breast cancer. Cell viability and colony formation assays revealed enhanced curcumin cytotoxicity upon complexation. Annexin V apoptotic studies showed that the PCDT complexation improved curcumin induced apoptosis in human ovarian cancer cell lines A2780 and SKOV-3, human nonsmall cell lung carcinoma cell line H1299, and human prostate cancer line DU-145, while no significant effect was observed with paclitaxel/PCDT complexation. The bioactivity of combining curcumin and paclitaxel was also investigated. A synergism was found between curcumin and paclitaxel, particularly when complexed with PCDT on A2780, SKOV-3, and H1299 cancer cell lines.
AuthorsAli O Boztas, Ozgur Karakuzu, Gabriela Galante, Zafer Ugur, Fatih Kocabas, Cengiz Z Altuntas, A Ozgur Yazaydin
JournalMolecular pharmaceutics (Mol Pharm) Vol. 10 Issue 7 Pg. 2676-83 (Jul 01 2013) ISSN: 1543-8392 [Electronic] United States
PMID23730903 (Publication Type: Journal Article)
Chemical References
  • Cyclodextrins
  • cyclodextrin polymer
  • Cellulose
  • Curcumin
  • Paclitaxel
Topics
  • Apoptosis (drug effects)
  • Cell Line, Tumor
  • Cell Survival (drug effects)
  • Cellulose (chemistry)
  • Curcumin (chemistry, pharmacology)
  • Cyclodextrins (chemistry)
  • Drug Synergism
  • Flow Cytometry
  • Humans
  • Paclitaxel (chemistry, pharmacology)
  • Spectroscopy, Fourier Transform Infrared

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