4.3 Article

Folic acid-modified soy protein nanoparticles for enhanced targeting and inhibitory

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.msec.2016.10.018

Keywords

Soy protein; Nanoparticles; Drug delivery; Folic acid; Antitumor

Funding

  1. National Natural Science Foundation of China [21174054, 21004030, 51503001]
  2. Natural Science Foundation of Anhui Province of China [1408085MB26]
  3. Research Foundation for Key Program of Education Department of Anhui Province of China [KJ2016A030]
  4. Doctor Research Foundation of Anhui University [J10113190075]
  5. Academic and Technology Introduction Project of Anhui University [AU02303203]

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Soy protein isolate (SPI) was hydrolyzed by compound enzymes to give water soluble low molecular soy protein (SP). SP and folic acid (FA) modified SP was polymerized with N-3-acrylamidophenylboronic acid (APBA) monomer in aqueous solution to give SP nanoparticles (SP NPs) and FA modified nanoparticles (FA-SP NPs), respectively. These NPs display excellent stability in different conditions, and have a uniform spherical shape with a diameter around of 200 nm. Doxorubicin (DOX) was then successfully loaded into SP and FA-SP NPs with a desirable loading content of 13.33% and 16.01%, respectively. The cellular uptake and cytotoxicity of DOX-loaded SP NPs and FA-SP NPs were investigated using the two-dimensional (2D) monolayer cell model and three-dimensional (3D) multicellular spheroids (MCs). In vivo, tumor accumulation and growth inhibitory were then examined using H22 tumor-bearing mice. All these results demonstrated that conjugation of FA can efficiently enhance SP-based NPs' tumor accumulation and antitumor effect (C) 2016 Elsevier B.V. All rights reserved.

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