A Review on
Gold Nanoparticles
R.B. Saudagar1*, Kanchan T. Mandlik2
1Department of Pharmaceutical Chemistry, R.G. Sapkal
College of Pharmacy Anjenari, Nasik, Maharashtra,
India.
2Department of Quality Assurance Techniques, R.G. Sapkal
College of Pharmacy Anjenari, Nasik, Maharashtra,
India.
*Corresponding Author E-mail: mandlikkanchan24@gmail.com
ABSTRACT:
This review is focused essentially on the types and
applications of gold nanoparticles in the field of
medicine and targeted drug delivery. Nanotechnology has become one of the most
interesting and advanced areas of research in this field. Among nanoparticles, gold nanoparticles
demonstrate special advantages in this field due to their unique properties,
small size and high surface area-to-volume ratio. These particles have been
widely used in various biomedical applications and drug delivery systems due to
their inert nature, stability, high dispersity, non-cytotoxicity and biocompatibility. Gold nanoparticles
can be functionalized with protein, peptides and nucleic acid. So these have a
great application not only in bio sensing drugs but also in drug, gene and
protein delivery.
KEY WORDS: Gold Nanoparticle, Nanotechnology, Advantages,
applications.
INTRODUCTION:
Nanoparticles are defined as particulate dispersions or solid particles with a size
in the range of 10-1000nm. The drug is dissolved, entrapped, encapsulated or
attached to a nanoparticle matrix. Depending upon the method of preparation, nanoparticles, nanospheres or nanocapsules can be obtained. Nanocapsules
are systems in which the drug is confined to a cavity surrounded by a unique
polymer membrane, while nanospheres are matrix
systems in which the drug is physically and uniformly dispersed. In recent
years, biodegradable polymeric nanoparticles,
particularly those coated with hydrophilic polymer such as poly (ethylene
glycol) (PEG) known as long-circulating particles, have been used as potential
drug delivery devices because of their ability to circulate for a prolonged
period time target a particular organ, as carriers of DNA in gene therapy, and
their ability to deliver proteins, peptides and genes. 1-4
The major goals in designing nanoparticles as
a delivery system are to control particle size, surface properties and release
of pharmacologically active agents in order to achieve the site-specific action
of the drug at the therapeutically optimal rate and dose regimen. Though liposomes have been used as potential carriers with unique
advantages including protecting drugs from degradation, targeting to site of
action and reduction toxicity or side effects, their applications are limited
due to inherent problems such as low encapsulation efficiency, rapid leakage of
water-soluble drug in the presence of blood components and poor storage
stability. On the other hand, polymeric nanoparticles
offer some specific advantages over liposomes. For
instance, they help to increase the stability of drugs/proteins and possess
useful controlled release properties.5, 6
Drug delivery systems based on nanoparticles
have proved to be a great route for targeting malignant brain tumors where the
conventional therapy is not as much effective. Enhanced permeability and
retention (EPR) is the unique property of nanoparticles
to accumulate and interact with the tumor cells 7 Platelets plays a
vital role in the development of cardiovascular diseases so the antiplatelet agents are considered as the necessary
components for the curing such diseases. Therefore, the interaction of nanoparticles and the vascular pathway becomes an essential
part of the management and prevention of cardiovascular disease. Among all
metallic nanoparticles the gold nanoparticles
proved to be the safest and much less toxic agents for drug delivery and for hyperthermic agents for the cancer treatment. 8
Nanotechnology induced advance approaches in the field of biomedical
sciences specially related to the cancer therapy and for diagnostic
applications regarding efficient drug delivery and reduced side effects as
compared to the conventional drugs, which have been used for cancer treatment.
Main properties of nanoparticles to be an effective
drug delivery agent includes monodispersity, lack of cytotoxicity and simple mechanism of interaction with
desired ligands. One the basis of these characteristics many nanoparticles have been synthesized and used in cancer
treatment, drug delivery systems and imaging such as dendrimers,
quantum dots, polymer gels, gold nanoparticles, ZnO, or Fe2O3 9. Various chemical and physical
methods have been adapted for the synthesis of nanoparticles
which are quite expensive and the chemicals used are harmful to the
environment. To overcome these problems green synthesis is emerging field of
research of current era. Inorganic nanoparticles have
particular application in molecular imaging as contrast agent such as magnetic
resonance imaging (MRI), positron emission tomography (PET), computed
tomography (CT), ultrasound and optical imaging. 10
Gold
Nanoparticle:
Properties of gold nanoparticles are
different from its bulk form because bulk gold is yellow solid and it is inert
in nature while gold nanoparticles are wine red
solution and are reported to be anti-oxidant. Inter particle interactions and
assembly of gold nanoparticles networks play key role
in the determination of properties of these nanoparticles
11. Gold nanoparticles exhibit various
sizes ranging from 1 nm to 8 μm and they also
exhibit different shapes such as spherical, sub-octahedral, octahedral,
decahedral, icosahedral multiple twined, multiple
twined, irregular shape, tetrahedral, nanotriangles, nanoprisms, hexagonal platelets and nanorods.
(Figure 1).
Figure 1: Various shapes of gold nanoparticles
Among all these shapes triangular shaped nanoparticles
show attractive optical properties as compared to the spherical shaped nanoparticles. Using of single active substance from plant
extract in the synthesis of gold nanoparticles is an
important bio synthesis technique to purify gold nanoparticles
and to investigate about their medical uses. Gold nanoparticles
have been widely used in the field of radiation medicine as radiation enhancer.12
Those also provide therapeutic enhancement in
radiation therapy due to the efficient and targeted drug delivery to the tumor
site. Gold nanoparticles have various applications as
platform nanomaterials for biomolecular
ultrasensitive detection, killing cancer cells by hyperthermal
treatment, labeling for cells and proteins and delivering therapeutic agents
within cells.
Fluorescent nanoparticles or nanoprobes based on gold nanoparticles
have good biocompatibility for molecular imaging of many enzymes and
metabolites which is necessary for cellular functions in cancer. Gold nanorods have gained much attention in recently few past
years due to their specific optical and chemical property and hence used for
biological applications. 13
Advantages of Gold Nanoparticle:
Gold nanoparticles mediated drug delivery
systems have many advantages over other nanocarriers
as well as to conventional drugs. Gold nanoparticles
have been widely used as a cancer antigen and in tumor therapies.14 Some advantages are listed here;
(i) Gold nanoparticles
have unique optical [16], physical and chemical properties due to their size
and shape.9
(ii) Gold nanoparticles have high surface
area which provide dense drug loading; 15
(iii) These particles are biocompatible [1] and are readily available
for conjugation with small biomolecules such as
proteins, enzymes, carboxylic acid, DNA, and amino acids. 16
(iv)Gold nanoparticles have controlled dispersity.17
(v) Due to small size and uniform dispersion they can easily reach to
the targeted site with blood
Flow.18
(vi) They
are non-cytotoxic to the normal cells. 19
(vii) Gold nanoparticles are easily
synthesized by various methods. 20
Types of gold nanoparticles 21
Gold nanorods
Gold nanoshells
Gold nanocages
Gold nanosphere
Gold Nanorods:
These are synthesized by template method. These are prepared by
electrochemical deposition of gold within the pores of nanoporous
polycarbonate template membranes. Goldnanorods
diameter is according to the diameter of pore of the template membrane
Gold Nanoshells:
Surface plasmon resonance peaks (ranging from
visible to near I.R. region) is used for the designing and fabrication of gold nanoshells. The core of gold nanoshells
is made up of silica and outer surface is made up of gold. Gold controls the
thickness of the shell.
Gold Nanocage:
Through galvanic replacement reaction between
truncated silver nanocubes and aqueous. HAuCl gold nanocage is synthesized.
Gold Nanospheres:
These are synthesized by reduction
of an aqueous HAuCl4 by using citrate as reducing agent. Through
citrate /gold ratio the size of nanospheres can be controlled . By two phase ratio the size of nanospheres can be affected by thiol/gold molar ratios.
APPLICATIONS:
·
Old Nanoparticles for the Delivery of Protein, Peptides and
Nucleic acid:
These can be employed as a carrier
for delivery of peptides, proteins and nucleic acid like DNA due to their
tunable size.22 Gold nanoparticles are
functionalized with cationic4° ammonium group, can bind DNA plasmid through
helectrostatic interactions and protect DNA from enzymatic
digestion. Gold nanoparticles can work as a carrier
for peptides and proteins, have reported that the cationic tetra alkyl ammonium
functionalized GNP’s recognise the cell
surfacereceptor.23
Gold nanoparticles
act as a carrier of insulin. Chitosan coated gold nanoparticles easily adsorb insulinon
their surface and the transmucosal delivery of insulinis enhanced.24
·
Photo Physical
Property of GNPs for Delivery of Drug:
GNPs cause local heating when
irradiated with light in 800 to 1200 nm. They cause the photo thermal destruction
of tumours. GNPs are doped into the shells of
capsules containing the drug. When the light irradiated on it then the shells
rupture and the drug release25
·
In vivo Targeting Using Gold Nanoparticles:
It can
bedone by using two approaches26
Active Targeting:
It depends on the recognition of ligands
on the gold nanoparticles surface by cell surface
receptors. 27
Passive Targeting:
It depends on the extravasations of vectors through leaky blood vessels
in unhealthy tissue.28
·
Gold nanoparticles are used for identifying the different
classes of bacteria. At present time identification of bacteria is done by
expensive machine. So GNPs are used for identification of different bacterial
classes that will be beneficial for cancer diagnosis29
REFERENCES:
1.
Langer R. Biomaterials in Drug Delivery and Tissue Engineering: One
Laboratory's Experience. Acc Chem Res 2000; 33:
94-101.
2.
Bhadra D, Bhadra S, Jain P, Jain
NK. Pegnology: a review of PEG-ylated
systems. Pharmazie 2002; 57: 5-29.
3.
Kommareddy S, Tiwari SB, Amiji MM. Long-circulating polymeric nanovectors
for tumor-selective gene delivery. Technol Cancer Res
Treat 2005; 4: 615- 25.
4.
Lee M, Kim SW. Polyethylene glycol-conjugated copolymers for plasmid
DNA delivery. Pharm Res 2005; 22: 1-10.
5.
Vila A, Sanchez A, Tobio M, Calvo P, Alonso MJ. Design of biodegradable particles for
protein delivery. J Control Release 2002; 78: 15-24.
6.
Mu L, Feng SS. A novel controlled release
formulation for the anticancer drug paclitaxel (Taxol(R)): PLGA nanoparticles
containing vitamin E TPGS. J Control Release 2003; 86: 33-48.
7.
Hartono D, Hody,
Yang KL, Yung LY. The effect of cholesterol on protein-coated gold nanoparticle
binding to liquid crystal-supported models of cell membranes. Biomater 2010; 31: 3008-3015.
8.
Lukianova-Hleb
EY, Wagner DS, Brenner MK, Lapotko DO. Cell-specific transmembrane injection of molecular cargo with gold
nanoparticle-generated transient plasmonicnano bubbles.
Biomater 2012; 33: 5441-5450.
9.
Mishra
A, Tripathy SK, Yun S-I.
Fungus mediated synthesis of gold nanoparticles and
their conjugation with genomic DNA isolated from Escherichia coli and Staphylococcus
aureus. Process Biochem
2012; 47: 701-711.
10. Etame AB, Smith CA, Chan WC, Rutka
JT. Design and potential application of PEGylated
gold nanoparticles with size-dependent permeation
through brain microvasculature. Nanomed: Nanotechnol Biol Med 2011; 7:
992-1000.
11. Deb
S, Patra HK, Lahiri P, Dasgupta AK, Chakrabarti K, Chaudhuri U. Multistability in
platelets and their response to gold nanoparticles. Nanomed: Nanotechnol Biol Med 2011; 7: 376-384.
12. Ganeshkumar M, Sastry TP, Sathish Kumar M, Dinesh MG, Kannappan S, Suguna L. Sun light
mediated synthesis of gold nanoparticles as carrier
for 6- mercaptopurine: Preparation, characterization
and toxicity studies in zebrafish embryo model. Mater
Res Bull 2012; 47: 2113-2119.
13. Pal
R, Panigrahi S, Bhattacharyya D, Chakraborti
AS. Characterization of citrate capped gold nanoparticle quercetin
complex: Experimental and quantum chemical approach. J MolStruct
2013; 1046: 153-163.
14. Guo Q, Guo Q, Yuan J, Zeng J. Biosynthesis of gold nanoparticles
using a kind of flavonol: Dihydromyricetin.
Colloids and Surfaces A: Physicochemical and Engineering Aspects 2014; 441:
127-132.
15. Chithrani DB, Dunne M, Stewart J, Allen C, Jaffray DA. Cellular uptake and transport of gold nanoparticles incorporated in a liposomal carrier. Nanomed: Nanotechnol Biol Med 2010; 6: 161-169.
16. Di
Guglielmo C, Lopez DR, De Lapuente
J, Mallafre JM, Suarez MB. Embryotoxicity
of cobalt ferrite and gold nanoparticles: a first in
vitro approach. Reproduct Toxicol
2010; 30: 271-276.
17. Tedesco
S, Doyle H, Blasco J, Redmond G, Sheehan D. Oxidative
stress and toxicity of gold nanoparticles in Mytilusedulis. Aquatic Toxicol
2010; 100: 178-186.
18. Kojima
C, Umeda Y, Harada A, Kono
K. Preparation of -infrared light absorbing gold nanoparticles
using polyethylene glycol-attached dendrimers.
Colloid Surfac B, Biointerfac
2010; 81: 648-651.
19. Lee
K, Lee H, Bae KH, Park TG. Heparin immobilized gold nanoparticles for targeted detection and apoptotic death of
metastatic cancer cells. Biomater 2010; 31: 6530-6536.
20. Gao W, Xu K, Ji L, Tang B. Effect of gold nanoparticles
on glutathione depletion-induced hydrogen peroxide generation and apoptosis in
HL7702 cells. Toxicol Lett
2011; 205: 86-95.
21. Cai, W., T. Gao, H. Hong and J. Sun, 2008. Chem.
Application of gold nanoparticles in cancer nanotechnology.
Nanotechnology, Science and Applications 1: 17,32
22. Fan, J., S.W. Chen and Y. Gao, 2003. Coating gold nanoparticles with peptide molecules via a peptide elongation
approach, Colloids Surf, B Bio Interfaces, 28: 199-207.
23. Ducan, B., K. Chaekyu
and V.M. Rotello, 2010.Gold nanoparticle platforms as
drug and biomolecule delivery systems, Journal of
Controlled Release, 148: 122-127.
24. Verma, A., J.M. Simard, J.W.E. Worrall and V.M. Rotello,
2004. Tunable reactivation of nanoparticle-inhibited beta-galactosidase
by glutathione at intracellular concentrations. J. Am. Chem. Soc, 126:
13987-13991.
25. Bhumkar, D.R., H.M. Joshi, M. Sastry and V.B. Pokharkar, 2007. Chitosan reduced gold nanoparticles
as novel carriers for transmucosal delivery of
insulin, Pharm. Res., 24: 1415-1426.
26. Angelatos, A.S., B. Radt and F. Caruso, 2005.Light-responsive
polyelectrolyte/gold nanoparticles microcapsules, J.
Phys. Chem., 109: 3071-3076.
27. Brannon-Peppas,
L. and J.O. Blanchette, 2004.Nanoparticle and
targeted systems for cancer therapy, Adv. Drug Delivery Review,56: 1649-1659.
28. Brigger, I., C. Dubernet
and P. Couvreur, 2002.Nanoparticles in cancer therapy
and diagnosis, Adv. Drug Delivery Review, 54: 631-651.
29. Baban, D. and L.W. Seymour, 1998.
Control of tumourvascular Permeability, Adv. Drug Deliv. Rev.,34: 109-119.
Received on 23.01.2016 Accepted
on 15.02.2016
© Asian Pharma Press All
Right Reserved
Asian J. Pharm. Res. 6(1): January -March, 2016; Page 45-48
DOI: 10.5958/2231-5691.2016.00008.3