2157-7439-3-133
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Research Article Open Access
Nanomedicine & NanotechnologyAbdelhalim et al., J Nanomed Nanotechol 2012, 3:3
http://dx.doi.org/10.4172/2157-7439.1000133
Volume 3 Issue 3 1000133J Nanomed Nanotechol
ISSN:2157-7439 JNMNT an open access journal
Keywords: Gold nanoparticles; particle size; absorbance;fluorescence; spectroscopy
Introduction
One particularly exciting field o research involves the use o GNPsin the detection and treatment o cancer cells [1]. Current methods ocancer diagnosis and treatment are costly and can be very harmul tothe body. GNPs, however, offer an inexpensive route to targeting onlycancerous cells, leaving healthy cells untouched [2].
Te very small size o nanoparticles (
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Citation:Abdelhalim MAK, Mady MM, Ghannam MM (2012) Physical Properties of Different Gold Nanoparticles: Ultraviolet-Visible and Fluorescence
Measurements. J Nanomed Nanotechol 3:133. doi:10.4172/2157-7439.1000133
Page 2 of 5
Volume 3 Issue 3 1000133J Nanomed Nanotechol
ISSN:2157-7439 JNMNT an open access journal
surace Plasmon band o GNPs has been widely investigated, studieson the photoluminescence rom GNPs are scarce [21].
Te properties o NPs give them high potential or use in variousmedical applications, particularly in diagnostics and therapy. In thisstudy we would like to shed the light on the physical properties oGNPs because these effects have not been documented beore. TeUltraviolet-Visible and fluorescence properties o non-unctionalizedGNPs have not thus ar been comprehensively documented. Here weocus our attention in the absorption and fluorescence spectra o GNPsolutions as a unction o particle size and concentration. We also useransmission Electron Microscopy (EM) to evaluate the morphologyand exact size o the GNPs.
Materials and Methods
GNP size determination
GNPs with nominal sizes o 10, 20 and 50 nm were purchased(Products MKN-Au-010; MKN-Au-020; MKN-Au-050, MK ImpexCorp, Canada) and used in this study. Te GNPs were dissolved inaqueous solution to give a concentration 0.01%. Te mean sizes,morphology and good particle size distribution or these GNPs wereevaluated rom the EM images. Te images indicate that the particlesare homogeneous in both shape and size. Te high electron densitieso the GNPs make EM as an effective way o characterizing theirmorphology and size.
UV-Visible and fluorescence spectroscopy
UVvisible characterization o solutions o 10, 20 and 50 nmGNPs at concentrations rom 0.210-3110-2% was perormed usinga UV-Visible spectrophotometer (UV-1601 PC, Shimadzu, Japan; H14
grating (UV through shortwave NIR with optical resolution o 0.4nm)). Te absorbance measurements were made over the wavelengthrange o 250-700 nm using 1 cm path length quartz cuvettes, whichwere cleaned beore each use by sonicating them or 5 min in deionizedwater and then rinsing with deionized water. Te pH values o allsolutions remained at 6.3.
Fluorescence characterization o the GNP solutions was perormedusing a FluoroMax-2 JOBAN YVON-SPEX, Instruments S.A., Inc.,France. Te fluorescence measurements were also made over thewavelength range o 250-700 nm.
Results and Discussion
Size and morphology of gold nanoparticles
Te 10 and 20 nm GNPs show spherical morphology while the50 nm GNPs show hexagonal morphology. All GNPs show narrowparticle size distribution and good dispersion in the solution. Te meansizes or these GNPs were calculated rom the EM images. Mean sizeor 10 nm GNPs was 9.45 1.33 nm, 20 nm GNPs was 20.18 1.80 nmand 50 nm GNPs was 50.73 3.58 nm (Figure 1).
UV-Visible spectroscopy
Figure 2 shows the UVVisible absorption spectra o 10, 20 and 50nm GNPs; the maximum in the Au absorbance intensity varies around517 nm.
Te optical properties such as absorption maxima and absorption
intensity are particle size dependent. An intense absorption peak at 517nm is generally attributed to the surace plasmon excitation o smallspherical gold particles.
10 20 50
0
10
20
30
40
50
60
MeanSize(nm)
Gold nanoparticles Size (nm)
Figure1: The size of different gold nanoparticles (n = 7).
200 300 400 500 600 700 800
-0.05
0.00
0.05
0.10
0.15
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0.30
0.35
0.40
Abso
rbance
Wavelength (nm)
GNPs sizes: 10, 20 and 50 nmS10nmC2.5S20nmC2.5S50nmC2.5
Figure2:The UVVisible absorption spectra of 10, 20 and 50 nm GNPs.
0 10 20 30 40 50 60
0.040
0.048
0.056
0.064
0.072
0.080
517
524
532
ExtinctionCoefficient
Size (nm)
Ext.Coeff
Figure3: The variation in the extinction coefcient with GNPs size.
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Citation:Abdelhalim MAK, Mady MM, Ghannam MM (2012) Physical Properties of Different Gold Nanoparticles: Ultraviolet-Visible and Fluorescence
Measurements. J Nanomed Nanotechol 3:133. doi:10.4172/2157-7439.1000133
Page 3 of 5
Volume 3 Issue 3 1000133J Nanomed Nanotechol
ISSN:2157-7439 JNMNT an open access journal
Figure 3 shows the variation in the extinction coefficient withGNPs size. When the GNP size changed rom 10 nm to 50 nm, themaximum extinction o Surace Plasmon Band (SPB) shifed rom
517 nm to 532 nm in the visible region which may be attributed tothe surace plasmon oscillation o ree electrons. Te surace plasmonresonance o the gold particles is red shifed with increase in particlesize in accordance with Mie theory [22].
Figure 4shows the variation in the absorbance o 10, 20 and 50 nmGNPs with concentration (0.210-3110-2%). At a constant GNP size,the absorbance was ound to be proportional to the concentration ogold. Tis is not surprising, since the increased number o nanoparticlesalso provides increased surace or surace plasmon resonance.
Te optical properties o gold are due to 5d (valence) and 6sp(conduction) electrons. Te outermost d and s electrons o theconstituent atoms must be treated together leading to six bands: five othem are airly flat, lying a ew eV below the Fermi level, and are usuallydenoted as d bands; the sixth one, which is almost ree-electron like isknown as the conduction band or sp band [23].
Single photon luminescence rom gold has been described [23,24]as a three-step process as ollows: (i) excitation o electrons rom theoccupied d to the sp band which is above the Fermi level to generateelectronhole pairs, (ii) scattering o electrons and holes on thepicosecond time scale with partial energy transer to the phonon latticeand (iii) recombination o an electron rom an occupied sp band withthe hole resulting in photon emission.
Fluorescence spectroscopy
Te fluorescence spectra o 10, 20 and 50 nm GNP solutionsmeasured with an excitation wavelength o 308 nm are displayed inFigure 5. Te centre o the photoluminescence (PL) band appears at423 nm. An increase in fluorescence intensity with increasing GNP sizewas observed. Te incident light at 308 nm will lead to excitation o thesurace plasmon coherent electronic motion as well as the d electrons.Te applied concentration or each particle size was included in able1.
At a fixed GNP size o 10 nm, the intensity o the emission bandincreased with increasing GNP concentration, and the trend wasconsistent with the changes corresponding to surace plasmon band oGNPs (Figure 6). Tese results indicate that the fluorescence emissionband intensity and the absorption band o GNPs were concentrationand particle size dependent.
When quantitative analysis was perormed on the fluorescencespectra, the fluorescent intensity was increased linearly as theconcentration goes higher with correlation coefficient R2 = 0.995.
Te results o this study are o high significance to the field onanotechnology or these reasons: Advances in nanotechnology haveidentified promising candidates or many biological and biomedicalapplications. Since the properties o NPs differ rom that o theirbulk materials, they are being increasingly exploited or medicalapplications. Nanoparticles (NPs) have potentially caused adverseeffects on organ, tissue, cellular, subcellular and protein levels due totheir unusual physicochemical properties [25-30].
Abdelhalim and Jarrar [26-29], 2011 and 2012 have reported thatintraperitoneal administration o different sizes o GNPs inducedtoxicity in several organs such as liver, heart, kidneys and lungs thatbecame unable to deal with the accumulated residues resulting rommetabolic and structural disturbances caused by these NPs. Tese
alterations were size-dependent with smaller ones (10 nm GNPs)induced the most effects and related to time exposure o GNPs [25-30].
Te appearance o hepatocytes cytoplasmic degeneration and
0 2 4 6 8 10
0.0
0.2
0.4
0.6
0.8
1.0
Absorbance(au)
Concentraton x10-3%
size 10 nm: absorption band at 517 nmsize 20 nm: absorption band at 524 nmsize 50 nm: absorption band at 532 nm
Figure4: The variation in the absorbance of 10, 20 and 50 nm GNPs withconcentration.
350 400 450 500 550
0
500000
1000000
1500000
2000000
2500000
3000000
3500000
Counts
Wavelength (nm)
Fluorescence
Excitation at 308 nm
10 nm GNPs
20 nm GNPs
50 nm GNPs
Figure5: The uorescence spectra of GNP solutions measured with an
excitation wavelength of 308 nm.
350 400 450 500 550
0
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120
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160
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220
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Fluo
rescence
Intensity
Wavelength (nm)
FluorescenceGNPs 10 nm
Conc. 0.5 x 10-3%
Conc. 0.8 x 10-3%
Conc. 1.0 x 10-3%
Conc. 2.5 x 10-3%
Conc. 10 x 10-3%
Figure6: The emission uorescence peak intensity for GNP of size 10nm atdifferent concentrations.
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Citation:Abdelhalim MAK, Mady MM, Ghannam MM (2012) Physical Properties of Different Gold Nanoparticles: Ultraviolet-Visible and Fluorescence
Measurements. J Nanomed Nanotechol 3:133. doi:10.4172/2157-7439.1000133
Page 4 of 5
Volume 3 Issue 3 1000133J Nanomed Nanotechol
ISSN:2157-7439 JNMNT an open access journal
nuclear destruction may suggest that GNPs interact with proteins andenzymes o the hepatic tissue interering with the antioxidant deencemechanism and leading to Reactive Oxygen Species (ROS) generationwhich in turn may induce stress in the hepatocytes to undergo atrophyand necrosis. One possible way o avoiding significant toxicity is to coatthe GNPs with biocompatible polymers. Now-a-days other experimentsto effectively demonstrate and avoid the possible side effects o GNPsin the in vivostudies are taken in consideration and conducted [26,29].
Conclusions
Te aim o the present study was to investigate the absorption andfluorescence spectra or 10, 20 and 50 nm GNPs at concentrations rom0.210-3to 110-2%.
Te high electron density and homogeneity o GNPs make themhighly conspicuous under the EM.
Te maximum absorption o SPB shifed rom 517 nm to 532nm, when the GNPs size changed rom 10 nm to 50 nm which mightbe attributed to the surace plasmon oscillation o the ree electrons.At a constant GNP size, the absorbance was proportional to theconcentration o gold. Te fluorescence emission band o the GNPs
varied with GNP size and concentration. Te fluorescence emissionband intensity increased with increasing GNP size and concentration.
Tis study demonstrates that the absorption and fluorescencespectra or different GNP sizes were size and concentration-dependent.
Further experiments using absorbance and fluorescence spectra arerequired to be perormed afer the administration o GNPs throughdifferent routes in rats in vivo.
Acknowledgements
The authors are very grateful to NPST. This research was nancially supported
by the National Science and Technology Innovation Plan (NSTIP), Research No.
08-ADV206-02 and Research No. 09-NAN670-02,College of Science, King Saud
University, Saudi Arabia.
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Product type Product # MKN-Au-010 Gold
nanoparticles in aqueous solution
Product # MKN-Au-020 Gold
nanoparticles in aqueous solution
Product # MKN-Au-050 Gold
nanoparticles in aqueous solution
Number of particles/mL 5.7 x 1012
particles/mL 7.0 x 1011
particles/mL 4.5 x 1010particles/mL
Concentration Concentration: 0.01% Au Concentration: 0.01% Au Concentration: 0.01% Au
Size Size: 10 nm Size: 20 nm Size: 50 nm
Table1: The applied concentration for each particle size.
http://dx.doi.org/10.4172/2157-7439.1000133http://www.sciencedirect.com/science/article/pii/S138917230670620Xhttp://www.sciencedirect.com/science/article/pii/S138917230670620Xhttp://jap.aip.org/resource/1/japiau/v103/i7/p074301_s1?isAuthorized=nohttp://jap.aip.org/resource/1/japiau/v103/i7/p074301_s1?isAuthorized=nohttp://jap.aip.org/resource/1/japiau/v103/i7/p074301_s1?isAuthorized=nohttp://www.ncbi.nlm.nih.gov/pubmed/15923216http://www.ncbi.nlm.nih.gov/pubmed/15826019http://www.ncbi.nlm.nih.gov/pubmed/15826019http://www.nanoarchive.org/4849/http://www.nanoarchive.org/4849/http://www.nanoarchive.org/4849/http://www.nanoarchive.org/4849/http://pubs.acs.org/doi/abs/10.1021/cr00016a002http://pubs.acs.org/doi/abs/10.1021/cr00016a002http://pubs.acs.org/doi/abs/10.1021/jp0257449http://pubs.acs.org/doi/abs/10.1021/jp0257449http://pubs.acs.org/doi/abs/10.1021/jp0257449http://pubs.acs.org/doi/abs/10.1021/jp0209289http://pubs.acs.org/doi/abs/10.1021/jp0209289http://www.its.caltech.edu/~mankei/ee150sp03/Shipway_nanoparticle_arrays_chemphyschem_2000.pdfhttp://www.its.caltech.edu/~mankei/ee150sp03/Shipway_nanoparticle_arrays_chemphyschem_2000.pdfhttp://pubs.acs.org/doi/abs/10.1021/la010566ghttp://pubs.acs.org/doi/abs/10.1021/la010566ghttp://pubs.acs.org/doi/abs/10.1021/la010566ghttp://pubs.acs.org/doi/abs/10.1021/la010566ghttp://www.ncbi.nlm.nih.gov/pubmed/8757129http://www.ncbi.nlm.nih.gov/pubmed/8757129http://www.ncbi.nlm.nih.gov/pubmed/8757129http://www.ncbi.nlm.nih.gov/pubmed/15475384http://www.ncbi.nlm.nih.gov/pubmed/15475384http://www.ncbi.nlm.nih.gov/pubmed/15475384http://www.ncbi.nlm.nih.gov/pubmed/18157524http://www.ncbi.nlm.nih.gov/pubmed/18157524http://www.ncbi.nlm.nih.gov/pubmed/18157524http://www.ncbi.nlm.nih.gov/pubmed/16709623http://www.ncbi.nlm.nih.gov/pubmed/16709623http://www.ncbi.nlm.nih.gov/pubmed/15780707http://www.ncbi.nlm.nih.gov/pubmed/15780707http://www.ncbi.nlm.nih.gov/pubmed/15780707http://www.ncbi.nlm.nih.gov/pubmed/18762845http://www.ncbi.nlm.nih.gov/pubmed/18762845http://www.ncbi.nlm.nih.gov/pubmed/17890442http://www.ncbi.nlm.nih.gov/pubmed/17890442http://www.sciencedirect.com/science/article/pii/S1748013207700166http://www.sciencedirect.com/science/article/pii/S1748013207700166http://www.ncbi.nlm.nih.gov/pubmed/17084659http://www.ncbi.nlm.nih.gov/pubmed/17084659http://www.ncbi.nlm.nih.gov/pubmed/17084659http://www.ncbi.nlm.nih.gov/pubmed/19546942http://www.ncbi.nlm.nih.gov/pubmed/19546942http://www.ncbi.nlm.nih.gov/pubmed/19546942http://www.ncbi.nlm.nih.gov/pubmed/16239346http://www.ncbi.nlm.nih.gov/pubmed/16239346http://www.ncbi.nlm.nih.gov/pubmed/16239346http://www.ncbi.nlm.nih.gov/pubmed/16239346http://www.ncbi.nlm.nih.gov/pubmed/16239346http://www.ncbi.nlm.nih.gov/pubmed/16239346http://www.omicsonline.org/1948-5956/JCST-04-046.pdfhttp://www.omicsonline.org/1948-5956/JCST-04-046.pdfhttp://www.omicsonline.org/1948-5956/JCST-04-046.pdfhttp://www.omicsonline.org/1948-5956/JCST-04-046.pdfhttp://www.ncbi.nlm.nih.gov/pubmed/21819574http://www.ncbi.nlm.nih.gov/pubmed/21819574http://www.ncbi.nlm.nih.gov/pubmed/21819574http://www.ncbi.nlm.nih.gov/pubmed/21859444http://www.ncbi.nlm.nih.gov/pubmed/21859444http://www.ncbi.nlm.nih.gov/pubmed/21859444http://www.ncbi.nlm.nih.gov/pubmed/21936889http://www.ncbi.nlm.nih.gov/pubmed/21936889http://www.ncbi.nlm.nih.gov/pubmed/21936889http://www.ncbi.nlm.nih.gov/pubmed/21936889http://www.ncbi.nlm.nih.gov/pubmed/21936889http://www.ncbi.nlm.nih.gov/pubmed/21936889http://www.ncbi.nlm.nih.gov/pubmed/21859444http://www.ncbi.nlm.nih.gov/pubmed/21859444http://www.ncbi.nlm.nih.gov/pubmed/21859444http://www.ncbi.nlm.nih.gov/pubmed/21819574http://www.ncbi.nlm.nih.gov/pubmed/21819574http://www.ncbi.nlm.nih.gov/pubmed/21819574http://www.omicsonline.org/1948-5956/JCST-04-046.pdfhttp://www.omicsonline.org/1948-5956/JCST-04-046.pdfhttp://www.omicsonline.org/1948-5956/JCST-04-046.pdfhttp://www.omicsonline.org/1948-5956/JCST-04-046.pdfhttp://www.ncbi.nlm.nih.gov/pubmed/16239346http://www.ncbi.nlm.nih.gov/pubmed/16239346http://www.ncbi.nlm.nih.gov/pubmed/16239346http://www.ncbi.nlm.nih.gov/pubmed/19546942http://www.ncbi.nlm.nih.gov/pubmed/19546942http://www.ncbi.nlm.nih.gov/pubmed/19546942http://www.ncbi.nlm.nih.gov/pubmed/17084659http://www.ncbi.nlm.nih.gov/pubmed/17084659http://www.ncbi.nlm.nih.gov/pubmed/17084659http://www.sciencedirect.com/science/article/pii/S1748013207700166http://www.sciencedirect.com/science/article/pii/S1748013207700166http://www.ncbi.nlm.nih.gov/pubmed/17890442http://www.ncbi.nlm.nih.gov/pubmed/17890442http://www.ncbi.nlm.nih.gov/pubmed/18762845http://www.ncbi.nlm.nih.gov/pubmed/18762845http://www.ncbi.nlm.nih.gov/pubmed/15780707http://www.ncbi.nlm.nih.gov/pubmed/15780707http://www.ncbi.nlm.nih.gov/pubmed/15780707http://www.ncbi.nlm.nih.gov/pubmed/16709623http://www.ncbi.nlm.nih.gov/pubmed/16709623http://www.ncbi.nlm.nih.gov/pubmed/18157524http://www.ncbi.nlm.nih.gov/pubmed/18157524http://www.ncbi.nlm.nih.gov/pubmed/18157524http://www.ncbi.nlm.nih.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Citation:Abdelhalim MAK, Mady MM, Ghannam MM (2012) Physical Properties of Different Gold Nanoparticles: Ultraviolet-Visible and Fluorescence
Measurements. J Nanomed Nanotechol 3:133. doi:10.4172/2157-7439.1000133
Page 5 of 5
Volume 3 Issue 3 1000133J Nanomed Nanotechol
ISSN:2157-7439 JNMNT an open access journal
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29.Abdelhalim MA, Jarrar BM (2011) Gold nanoparticles induced cloudy swelling
to hydropic degeneration, cytoplasmic hyaline vacuolation, polymorphism,
binucleation, karyopyknosis, karyolysis, karyorrhexis and necrosis in the liver.
Lipids Health Dis 10: 166.
30.Abdelhalim MA (2011) Exposure to gold nanoparticles produces cardiac tissue
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