4.5 Article

Magnetite Nanoparticle with Positively Charged Surface for Immobilization of Peptide Nucleic Acid and Deoxyribonucleic Acid

Journal

JOURNAL OF BIOMEDICAL NANOTECHNOLOGY
Volume 9, Issue 9, Pages 1509-1520

Publisher

AMER SCIENTIFIC PUBLISHERS
DOI: 10.1166/jbn.2013.1645

Keywords

Magnetite; Nanoparticle; DNA Sequence Analysis; PNA Probe; Surface Modification

Funding

  1. Thailand Research Fund (TRF) [RTA5280002]
  2. Royal Golden Jubilee [PHD/0325/2550]
  3. Center of Excellence for Innovation in Chemistry (PERCH-CIC), Commission on Higher Education, Ministry of Education

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We herein report the surface modification of magnetite nanoparticle (MNP) with the (co)polymer of poly(ethylene glycol) methyl ether methacrylate (PEGMA) and/or diethylamino ethyl methacrylate (DEAEMA) via atom transfer radical polymerization (ATRP) for use as anion exchanger solid support for detection of DNA sequence using peptide nucleic acid (PNA) probe. Molar ratio of the PEGMA:DEAEMA (co)polymer was systematically varied to tune the positive charges on the particle surface. Kinetic studies of the (co)polymerizations were investigated via (HNMR)-H-1 to disclose the relative reactivity of the (co)polymers in the reaction. Zeta potential of the (co)polymer-grafted MNP was analyzed by photo correlation spectroscopy (PCS). Transmission electron microscopy (TEM) and PCS indicated an improvement in the particle dispersibility in water upon quaternization of the DEAEMA entities grafted on the particle surface. From the preliminary results, these (co)polymer-grafted MNPs can be used as a nanosolid support to differentiate between full match and single-base mismatch DNA sequences using an acpcPNA probe. These novel cationic MNPs might be efficiently applicable for use as a magnetically guidable tool for detection of DNA sequences.

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