Integrin-targeted nano-sized polymeric systems for paclitaxel conjugation: a comparative study

Anat Eldar-Boock, Rachel Blau, Claudia Ryppa, Hemda Baabur-Cohen, Ariel Many, María Jesús Vicent, Felix Kratz, Joaquin Sanchis*, Ronit Satchi-Fainaro

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review


The generation of rationally designed polymer therapeutics via the conjugation of low molecular weight anti-cancer drugs to water-soluble polymeric nanocarriers aims to improve the therapeutic index. Here, we focus on applying polymer therapeutics to target two cell compartments simultaneously–tumour cells and angiogenic endothelial cells. Comparing different polymeric backbones carrying the same therapeutic agent and targeting moiety may shed light on any correlation between the choice of polymer and the anti-cancer activity of the conjugate. Here, we compared three paclitaxel (PTX)-bound conjugates with poly-l-glutamic acid (PGA, 4.9 mol%), 2-hydroxypropylmethacrylamide (HPMA, 1.2 mol%) copolymer, or polyethyleneglycol (PEG, 1:1 conjugate). PGA and HPMA copolymers are multivalent polymers that allow the conjugation of multiple compounds within the same polymer backbone, while PEG is a bivalent commercially available Food and Drug Administration (FDA)-approved polymer. We further conjugated PGA–PTX and PEG–PTX with the integrin αvβ3-targeting moiety RGD (5.5 mol% and 1:1 conjugate, respectively). We based our selection on the overexpression of integrin αvβ3 on angiogenic endothelial cells and several types of cancer cells. Our findings suggest that the polymer structure has major effect on the conjugate's activity on different tumour compartments. A multivalent PGA–PTX–E-[c(RGDfK)2] conjugate displayed a stronger inhibitory effect on the endothelial compartment, showing a 50% inhibition of the migration of human umbilical vein endothelial cell cells, while a PTX–PEG–E-[c(RGDfK)2] conjugate possessed enhanced anti-cancer activity on MDA-MB-231 tumour cells (IC50 = 20 nM versus IC50 300 nM for the PGA conjugate).

Original languageEnglish
Pages (from-to)829-844
Number of pages16
JournalJournal of Drug Targeting
Issue number9-10
StatePublished - 26 Nov 2017


  • Angiogenesis
  • HPMA copolymer
  • Integrin
  • PEG
  • PGA
  • RGD
  • paclitaxel
  • polymer therapeutics


Dive into the research topics of 'Integrin-targeted nano-sized polymeric systems for paclitaxel conjugation: a comparative study'. Together they form a unique fingerprint.

Cite this