4.5 Article

Poly-allylamine hydrochloride and fucoidan-based self-assembled polyelectrolyte complex nanoparticles for cancer therapeutics

Journal

JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A
Volume 107, Issue 2, Pages 339-347

Publisher

WILEY
DOI: 10.1002/jbm.a.36526

Keywords

fucoidan; drug delivery; self-assembly; antitumor; biocompatibility

Funding

  1. Subsidized Project for Postgraduates' Innovative Fund in Scientific Research of Huaqiao University
  2. Science Research Foundation of National Health and Family Planning Commission of PRC & United Fujian Provincial Health and Education Project for Tacking the Key Research [WKJ2016-2-22]
  3. Natural Science Foundation of China [31570974]
  4. National Marine Economic Innovation and Development Project

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Herein, we fabricated the novel drug delivery system based on the self-assembly of two polyelectrolytes, poly-allylamine hydrochloride (PAH) and fucoidan, as the polycation and polyanion, respectively, under mild conditions for cancer therapeutics. Furthermore, the designed polyelectrolyte complex nanoparticles as well as the methotrexate (MTX) disodium salt-loaded composites were systematically characterized using various techniques. The MTX loading in the nanoparticles was confirmed by zeta potential values that changed from -36.2 +/- 2.2 to -28.3 +/- 3.1 mV at a loading amount of 13.3 +/- 1.2%. Furthermore, the obtained eventual particle sizes of nanoparticles were various with different concentrations and ratios of polyelectrolytes. The particle size also has increased from 130 +/- 2.6 to 162.9 +/- 2.3 nm after loading MTX. The drug release investigations in vitro at a pH value of 6.0 (acid environment) showed that the release of MTX was sustained in the conditions provided. Finally, we investigated the anticancer efficacy of MTX-loaded nanoparticles on MCF-7 cells and HeLa cells and the satisfactory results were obtained. Together, these self-assembled PAH/fucoidan nanoparticles with sustained drug release property will become the promising delivery system for cancer therapeutics. (c) 2018 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 107A: 339-347, 2019.

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