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The antitumor activity of PNA modified vinblastine cationic liposomes on Lewis lung tumor cells: In vitro and in vivo evaluation.

Abstract
Non-small cell lung cancer (NSCLC) is one of the frequently-occurring disease in the world, and the treatment effects are usually unsatisfactory. Vinblastine is an anti-microtubule drug in clinic. In this study, a nanostructured liposome was designed and prepared for treating NSCLC. In the liposomes, peanut agglutinin (PNA) was modified on the liposomal surface, 3-(N-(N',N'-dimethylaminoethane)carbamoyl) cholesterol was used as cationic materials, and vinblastine was encapsulated in the aqueous core of liposomes, respectively. The PNA modified vinblastine cationic liposomes were approximately 100 nm in size with a positive potential. In vitro results showed that the targeting liposomes could significantly enhance cellular uptake, selectively accumulate in LLT cells, and dramatically initiate apoptosis via activating pro-apoptotic proteins and apoptotic enzymes, thus leading to the strongest antitumor efficacy to LLT cells. In vivo results demonstrated that the targeting liposomes could display a prolonged circulation time in the blood, accumulate more drug in tumor location, and induce most of tumor cells apoptosis. As a result, a robust overall antitumor efficacy in tumor-bearing mice was observed subsequently. In conclusion, the chemotherapy using the PNA modified vinblastine cationic liposomes could provide a potential strategy for treating non-small cell lung cancer.
AuthorsXue-Tao Li, Mei-Li He, Zhi-Yan Zhou, Ying Jiang, Lan Cheng
JournalInternational journal of pharmaceutics (Int J Pharm) Vol. 487 Issue 1-2 Pg. 223-33 (Jun 20 2015) ISSN: 1873-3476 [Electronic] Netherlands
PMID25895716 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2015 Elsevier B.V. All rights reserved.
Chemical References
  • Antineoplastic Agents, Phytogenic
  • Apoptosis Regulatory Proteins
  • Coumarins
  • Liposomes
  • Peanut Agglutinin
  • Vinblastine
Topics
  • Animals
  • Antineoplastic Agents, Phytogenic (administration & dosage, pharmacology)
  • Apoptosis Regulatory Proteins (metabolism)
  • Carcinoma, Lewis Lung (drug therapy)
  • Carcinoma, Non-Small-Cell Lung (drug therapy)
  • Cell Line, Tumor
  • Coumarins (chemistry)
  • Drug Compounding
  • Liposomes
  • Mice
  • Mice, Inbred C57BL
  • Nanoparticles
  • Particle Size
  • Peanut Agglutinin (pharmacology)
  • Vinblastine (administration & dosage, pharmacology)
  • Xenograft Model Antitumor Assays

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