Hindawi Publishing Corporation
Journal of Nanomaterials
Volume 2014, Article ID 978284, 7 pages
http://dx.doi.org/10.1155/2014/978284
Research Article
Development of Antibody-Coated Magnetite Nanoparticles for
Biomarker Immobilization
Christian Chapa Gonzalez,
1
Carlos A. Martínez Pérez,
1
Alejandro Martínez Martínez,
1
Imelda Olivas Armendáriz,
1
Oscar Zavala Tapia,
1
and Perla E. García-Casillas
1,2
1
Universidad Aut´ onoma de Ciudad Ju´ arez, Avenida del Charro 610 Norte, Colonia Partido Romero, 32315 Ciudad Ju´ arez, CHIH,
Mexico
2
Universidad Aut´ onoma de Ciudad Ju´ arez, Instituto de Ingenier´ ıa y Tecnolog´ ıa, Avenida del Charro 610 Norte, Colonia Partido
Romero, 32315, Ciudad Ju´ arez, CHIH, Mexico
Correspondence should be addressed to Perla E. Garc´ ıa-Casillas; perlaelviagarcia@yahoo.com
Received 2 September 2013; Accepted 21 January 2014
Academic Editor: Chih-Hung Hsiao
Copyright © 2014 Christian Chapa Gonzalez et al. his is an open access article distributed under the Creative Commons
Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is
properly cited.
Magnetic nanoparticles (MNPs) have great potential in biomedical applications because of their magnetic response ofers the
possibility to direct them to speciic areas and target biological entities. Magnetic separation of biomolecules is one of the most
important applications of MNPs because their versatility in detecting cancer biomarkers. However, the efectiveness of this method
depends on many factors, including the type of functionalization onto MNPs. herefore, in this study, magnetite nanoparticles have
been developed in order to separate the 5
-nucleotidase enzyme (5eNT). he 5eNT is used as a bio-indicator for diagnosing diseases
such as hepatic ischaemia, liver tumor, and hepatotoxic drugs damage. Magnetic nanoparticles were covered in a core/shell type with
silica, aminosilane, and a double shell of silica-aminosilane. A ScFv (fragment antibody) and anti-CD73 antibody were attached to
the coated nanoparticles in order to separate the enzyme. he magnetic separation of this enzyme with fragment antibody was found
to be 28% higher than anti-CD73 antibody and the enzyme adsorption was improved with the double shell due to the increased
length of the polymeric chain. Magnetite nanoparticles with a double shell (silica-aminosilane) were also found to be more sensitive
than magnetite with a single shell in the detection of biomarkers.
1. Introduction
1
Nanomedicine is generally deined as the biomedical appli-
cation of nanotechnology. Nanomagnetism is at the forefront
of the nanosciences as magnetic nanomaterials are the most
promising materials used in the clinical diagnosis and in
various therapeutic applications [1, 2]. Magnetic particles
have special features that make them viable for biomedical
applications [3]. heir particle size can be controlled in
the nanometric scale and they can be functionalized with
biocompatible molecules to interact with biological entities.
Many researchers have been focusing on the nanoscale
because magnetic nanoparticles contain a simple magnetic
domain and show a superparamagnetic behavior at room
temperature, which means that the magnetization is close
to zero in the absence of a magnetic ield, but when an
external magnetic ield is applied, the magnetic moments are
aligned with the ield [4]. his kind of magnetic response
is highly desired in biomedical applications because these
materials ofer the possibility of being manipulated to a
speciic body area and target biological entities through
an external stimulus. his ability of magnetic nanoparticles
has allowed them to be used for labeling and manipulating
biomolecules as drugs and genes [5–8]. Drug delivery is the
most studied application of the magnetic nanoparticles in
order to develop a new therapeutic method that increases
the efectiveness of anticancer drug [9]. Magnetic drug
targeting (MDT) has also been used to improve localized
drug delivery to interstitial tumor targets. MDT involves
attaching an antibody to the nanoparticles surface in order
to get an antibody-antigen coupling ensuring an eicient
and controlled drug release [10]. In order to improve the