Shell-sheddable and charge switchable magnetic nanoparticle as pH-sensitive nanocarrier for targeted drug delivery applications

被引:3
|
作者
Aram, Elham [1 ,3 ]
Sadeghi-Abandansari, Hamid [2 ,3 ,8 ]
Radmanesh, Fatemeh [4 ]
Khorasani, Hamid Reza [3 ,5 ]
Nowroozi, Mohammad Reza [4 ]
Hassanpour, Ali [6 ]
Baharvand, Hossein [5 ,7 ]
Sabour, Davood [3 ,5 ,8 ]
机构
[1] Golestan Univ, Fac Engn, Dept Polymer Engn, Gorgan, Iran
[2] ACECR, Royan Inst Stem Cell Biol & Technol, Cell Sci Res Ctr, Dept Cell Engn, Tehran, Iran
[3] ACECR, Royan Inst Stem Cell Biol & Technol, Cell Sci Res Ctr, Dept Canc Med, Babol, Iran
[4] Univ Tehran Med Sci, Urooncol Res Ctr, Tehran, Iran
[5] ACECR, Royan Inst Stem Cell Biol & Technol, Cell Sci Res Ctr, Dept Stem Cells & Dev Biol, Tehran, Iran
[6] Univ Leeds, Sch Chem & Proc Engn, Leeds, England
[7] Univ Sci & Culture, Sch Basic Sci & Adv Technol Biol, Dept Dev Biol, Tehran, Iran
[8] ACECR, Royan Inst Stem Cell Biol & Technol, Cell Sci Res Ctr, Dept Canc Med, Babol 4713818981, Iran
关键词
curcumin; magnetic nanoparticle; prostate cancer; shell-sheddable; targeted delivery; PEGYLATION; RELEASE; STARCH;
D O I
10.1002/pat.6366
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A pH-sensitive shell-sheddable magnetic nanocarrier was prepared based on Fe3O4@SiO2 nanoparticles coated with polyethyleneimine (PEI) and polyethyleneglycol (PEG). The PEI was coated on Fe3O4@SiO2 nanoparticles through an electrostatic attraction and the PEG chains were connected to the PEI via pH-sensitive benzoic-imine bonds. The synthesized products and final nanocarrier were characterized with FT-IR, H-1 NMR, dynamic light scattering (DLS), zeta-potential, TEM, and vibrating-sample magnetometer (VSM). The PEI, as a middle layer, was used to load the curcumin (an anticancer drug) via van der Waals interactions and the shedding of PEG as a hydrophilic corona at the tumor pH (acidic) could induce the release of the drug. The curcumin loading content was found to be similar to 15% and curcumin-loaded magnetic nanoparticles (C-LMNs) showed more triggered release at the tumor pH (5.6) than physiological pH (7.4). In comparison to pure magnetic nanoparticles (MNs), the C-LMNs showed more cytotoxicity to human prostate cancer cell (PC-3) and also resulted in an increased rate of late apoptotic/necrotic PC-3 cells, assessed by flow cytometry analysis. In conclusion, the C-LMN as pH- and magnetic responsive nanocarrier showed good potential for targeted curcumin delivery in therapy of prostate cancer.
引用
收藏
页数:11
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