2014
DOI: 10.1039/c4fd00152d
|View full text |Cite
|
Sign up to set email alerts
|

Protein A-conjugated iron oxide nanoparticles for separation ofVibrio choleraefrom water samples

Abstract: Pathogen separation is of great significance for precise detection and prevention of disease outbreaks. For the first time, protein A conjugated with chitosan-coated iron oxide nanoparticles was prepared for pathogen separation at low concentrations from liquid samples. Vibrio cholerae O1 (VO1) bacteria were used for testing the effectiveness of this conjugate. Transmission electron microscopy (TEM) was used to confirm the presence of captured VO1. The results showed that, after binding with a specific antibod… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

1
12
0

Year Published

2015
2015
2023
2023

Publication Types

Select...
10

Relationship

1
9

Authors

Journals

citations
Cited by 21 publications
(13 citation statements)
references
References 46 publications
1
12
0
Order By: Relevance
“…The nanoparticle surface provides the stability for these nanoparticles as well as their functionality by which biological moieties (antibodies, peptides, drug encapsulation) may potentially be grafted. [19][20][21][22][23][24] For instance, many studies have recently explored their therapeutic potential to kill cancer cells by hyperthermia (heat induced after the application of an alternating magnetic field) and simultaneous triggered drug delivery [25][26][27] . Furthermore, when a biological moiety (e.g., antibody, peptide) is conjugated to the surface of the nanoparticles, the latter may be actively targeted towards cancer cells to minimise any secondary effects from medical treatment may have on neighbouring healthy cells.…”
Section: Introductionmentioning
confidence: 99%
“…The nanoparticle surface provides the stability for these nanoparticles as well as their functionality by which biological moieties (antibodies, peptides, drug encapsulation) may potentially be grafted. [19][20][21][22][23][24] For instance, many studies have recently explored their therapeutic potential to kill cancer cells by hyperthermia (heat induced after the application of an alternating magnetic field) and simultaneous triggered drug delivery [25][26][27] . Furthermore, when a biological moiety (e.g., antibody, peptide) is conjugated to the surface of the nanoparticles, the latter may be actively targeted towards cancer cells to minimise any secondary effects from medical treatment may have on neighbouring healthy cells.…”
Section: Introductionmentioning
confidence: 99%
“…Samples were prepared by pressing dried powders on a zero background silicon wafer. Field-dependent magnetisation, isothermal remanent magnetisation (IRM) and direct current demagnetisation (DCD) measurements of IONPs were carried out in a Quantum Design hybrid superconducting quantum interference device-vibrating sample magnetometer (SQUID-VSM) at 300 and 5 K, with applied fields up to 7 T. 57 Fe Mössbauer spectra were collected from freeze-dried samples mixed with boron nitride and measured in transmission mode in a commercial spectrometer (SEE Co Inc, USA) working in constant acceleration mode, calibrated relative to metallic α-Fe at room temperature (RT).…”
Section: Characterisation Of Citric-acid Coated Iron Oxide Nanoparticlesmentioning
confidence: 99%
“…Small molecules like folic acid [113,114,115] or aptamers [116,117,118] and bigger molecules as peptides [119,120], proteins [121], or antibodies [122] can bind to many cells receptors and are used as targeting agents. …”
Section: Main Grafted Moleculesmentioning
confidence: 99%