Literature DB >> 28732161

Elegant pH-Responsive Nanovehicle for Drug Delivery Based on Triazine Dendrimer Modified Magnetic Nanoparticles.

Amir Landarani-Isfahani1, Majid Moghadam1, Shima Mohammadi2, Maryam Royvaran2, Naimeh Moshtael-Arani3, Saghar Rezaei1, Shahram Tangestaninejad1, Valiollah Mirkhani1, Iraj Mohammadpoor-Baltork1.   

Abstract

Owing to properties of magnetic nanoparticles and elegant three-dimensional macromolecule architectural features, dendrimeric structures have been investigated as nanoscale drug delivery systems. In this work, a novel magnetic nanocarrier, generation two (G2) triazine dendrimer modified Fe3O4@SiO2 magnetic nanoparticles (MNP-G2), was designed, fabricated, and characterized by Fourier transform infrared (FT-IR), thermal gravimetric analysis (TGA), vibrating sample magnetometer (VSM), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), and dynamic light scattering (DLS). The prepared MNP-G2 nanosystem offers a new formulation that combines the unique properties of MNPs and triazine dendrimer as a biocompatible material for biomedical applications. To demonstrate the potential of MNP-G2, the nanoparticles were loaded with methotrexate (MTX), a proven chemotherapy drug. The MTX-loaded MNP-G2 (MNP-G2/MTX) exhibited a high drug-loading capacity of MTX and the excellent ability for controlled drug release. The cytotoxicity of MNP-G2/MTX using an 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide based assay and MCF-7, HeLa, and Caov-4 cell lines revealed that MNP-G2/MTX was more active against the tumor cells than the free drug in a mildly acidic environment. The results of hemolysis, hemagglutination, and coagulation assays confirmed the good blood safety of MNP-G2/MTX. Moreover, the cell uptake and intracellular distribution of MNP-G2/MTX were studied by flow cytometry analysis and confocal laser scanning microscopy (CLSM). This research suggests that MNP-G2/MTX with good biocompatibility and degradability can be selected as an ideal and effective drug carrier in targeted biomedicine studies especially anticancer applications.

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Year:  2017        PMID: 28732161     DOI: 10.1021/acs.langmuir.7b00742

Source DB:  PubMed          Journal:  Langmuir        ISSN: 0743-7463            Impact factor:   3.882


  4 in total

Review 1.  Overcoming Hurdles in Nanoparticle Clinical Translation: The Influence of Experimental Design and Surface Modification.

Authors:  Jacob W Shreffler; Jessica E Pullan; Kaitlin M Dailey; Sanku Mallik; Amanda E Brooks
Journal:  Int J Mol Sci       Date:  2019-11-30       Impact factor: 5.923

2.  Modification of Magnetite Nanoparticles with Triazine-Based Dendrons and Their Application as Drug-Transporting Systems.

Authors:  Mateusz Pawlaczyk; Grzegorz Schroeder
Journal:  Int J Mol Sci       Date:  2021-10-21       Impact factor: 5.923

Review 3.  Fe₃O₄ Nanoparticles in Targeted Drug/Gene Delivery Systems.

Authors:  Lazhen Shen; Bei Li; Yongsheng Qiao
Journal:  Materials (Basel)       Date:  2018-02-23       Impact factor: 3.623

4.  Aminopropylimidazole as an Advantageous Coating in the Synthesis of Functionalized Magnetite Nanoparticles.

Authors:  Alexandrina Nan; Iolanda-Veronica Ganea; Sergiu Macavei; Rodica Turcu
Journal:  Nanomaterials (Basel)       Date:  2021-12-02       Impact factor: 5.076

  4 in total

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