4.7 Article

Thermosensitive and biodegradable hydrogel encapsulating targeted nanoparticles for the sustained co-delivery of gemcitabine and paclitaxel to pancreatic cancer cells

Journal

INTERNATIONAL JOURNAL OF PHARMACEUTICS
Volume 593, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.ijpharm.2020.120139

Keywords

Targeted drug delivery; Sustained release; Liposomes; Targeting integrin alpha(5)beta(1); PR_b fibronectin-mimetic peptide

Funding

  1. Whiting School of Engineering of the Johns Hopkins University
  2. Whiting School of Engineering
  3. Krieger School of Arts Sciences

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The translated system enhances the delivery of gemcitabine and paclitaxel to pancreatic cancer, effectively killing cancer cells and inhibiting tumor growth with sustained release.
Pancreatic cancer represents a life threatening disease with rising mortality. Although the synergistic combination of gemcitabine and albumin-bound paclitaxel has proven to enhance the median survival rates as compared to gemcitabine alone, their systemic and repeated co-administration has been associated with serious toxic side effects and poor patient compliance. For this purpose, we designed a thermosensitive and biodegradable hydrogel encapsulating targeted nanoparticles for the local and sustained delivery of gemcitabine (GEM) and paclitaxel (PTX) to pancreatic cancer. GEM and PTX were loaded into PR_b-functionalized liposomes targeting integrin alpha(5)beta(1), which was shown to be overexpressed in pancreatic cancer. PR_b is a fibronectin-mimetic peptide that binds to alpha(5)beta(1) with high affinity and specificity. The PR_b liposomes were encapsulated into a poly (delta-valerolactone-co-D,L-lactide)-b-poly(ethylene glycol)-b-poly(8-valemlactone-co-D,L-lactide) (PVLA-PEG-PVLA) hydrogel and demonstrated sustained release of both drugs compared to PR_b-functionalized liposomes free in solution or free drugs in the hydrogel. Moreover, the hydrogel-nanoparticle system was proven to be very efficient towards killing monolayers of human pancreatic cancer cells (PANC-1), and showed a significant reduction in the growth pattern of PANC-1 tumor spheroids as compared to hydmgels encapsulating non-targeted liposomes with GEM/PTX or free drugs, after a one week treatment period. Our hybrid hydrogel-nanoparticle system is a promising platform for the local and sustained delivery of GEM/PTX to pancreatic cancer, with the goal of maximizing the therapeutic efficacy of this synergistic drug cocktail while potentially minimizing toxic side effects and eliminating the need for repeated co-administration.

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