کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5434634 | 1509150 | 2017 | 10 صفحه PDF | دانلود رایگان |
- Soy protein isolate was hydrolyzed by compound enzymes to prepare nanoparticles.
- Nanoparticles are spherical like and very stable in various conditions.
- Cellular uptake and cytotoxicity were investigated in monolayer cell model.
- 3-D multicellular spheroids were using to evaluate nanoparticles' effect.
- Antitumor effect of these nanoparticles was measured using H22 tumor-bearing mice.
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 200Â 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.
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Journal: Materials Science and Engineering: C - Volume 71, 1 February 2017, Pages 298-307