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Efficacy of dual-functional liposomes containing paclitaxel for treatment of lung cancer.

Abstract
This study was mainly focused on the development of a dual-ligand liposomal delivery system for targeting the delivery of paclitaxel (PTX) to lung cancer. The specific ligand peptide HAIYPRH (T7) and the cationic cell-penetrating peptide TAT were connected with phospholipid via a polyethylene glycol (PEG) spacer to prepare the dual-ligand liposomes (T7/TAT-LP-PTX). Physicochemical characterizations of T7/TAT-LP-PTX, such as particle size, ΞΆ potential, morphology, encapsulation efficiency, and in vitro PTX release, were also evaluated. In the cellular uptake study, the T7/TAT-LP endocytosed by the A549 cells was 2.26-, 3.48- and 8.56-fold higher than TAT-LP, T7-LP and LP, respectively. The IC50 values of TAT-LP-PTX, T7-LP-PTX and LP-PTX were much higher than those of T7/TAT-LP-PTX, respectively. The homing specificity of T7/TAT-LP was evaluated on the tumor spheroids, which revealed that T7/TAT-LP was more efficaciously internalized in tumor cells than TAT-LP, T7-LP and LP, respectively. Compared to LP, TAT-LP and T7-LP, T7/TAT-LP showed the strongest cell uptake property, and the highest accumulation ability in tumor spheroids in vitro. In the in vivo study, the T7/TAT-LP-PTX exhibited the best inhibitory effect of tumor growth for A549-bearing mice. Collectively, these results suggested that T7/TAT-LP-PTX is a promising drug delivery system for the treatment of lung cancer.
AuthorsRong-Hua Wang, Hong-Mei Cao, Zhi-Ju Tian, Bo Jin, Qing Wang, Hong Ma, Jing Wu
JournalOncology reports (Oncol Rep) Vol. 33 Issue 2 Pg. 783-91 (Feb 2015) ISSN: 1791-2431 [Electronic] Greece
PMID25482610 (Publication Type: Journal Article, Retracted Publication)
Chemical References
  • Cell-Penetrating Peptides
  • Liposomes
  • Polyethylene Glycols
  • Paclitaxel
Topics
  • Animals
  • Cell Line, Tumor
  • Cell-Penetrating Peptides (chemistry)
  • Drug Delivery Systems
  • Humans
  • Liposomes (administration & dosage, chemistry)
  • Lung Neoplasms (drug therapy)
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Paclitaxel (administration & dosage, pharmacokinetics)
  • Particle Size
  • Polyethylene Glycols (chemistry)
  • Signal Transduction (drug effects)
  • Xenograft Model Antitumor Assays

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