Green synthesis of gold nanoparticles and their anticancer activity
© Springer-Verlag Wien 2013
Received: 21 March 2013
Accepted: 5 May 2013
Published: 5 June 2013
As the nano revolution unfolds, it is imperative to integrate nanoscience and medicine. The secret gleaned from nature have led to the generation of biogenic technologies for the fabrication of advanced nanomaterials. Present investigation discloses the gold nanoparticles biosynthesizing capability of the flower of pharmacologically important tree Couroupita guianensis. Rapid, cost-effective, one-step process of synthesis has been achieved. Newly genre gold nanoparticles were characterized by involving UV–vis spectroscopy, FTIR, XRD, SEM, and TEM analysis. Interestingly, as a result of extensive screening on the application of newly synthesized gold nanoparticles their anticancer potential has been discovered using MTT assay, DNA fragmentation, apoptosis by DAPI staining, and comet assay for DNA damage.
KeywordsCouroupita guianensis Gold nanoparticles Anticancer DNA fragmentation
Metal nanoparticles are of great importance due to their high surface area and a high fraction of surface atoms. The scientific and technological significance of metal nanoparticles has made them the subject of intensive research, given their special chemical and physical properties. In particular, gold nanoparticles are employed in many fields: biosensing (Mirkin et al. 1996), catalysis (Sen et al. 2012), electronics (Rao and Cheetham 2001), enzyme electrodes (Crumbliss et al. 1992), super conductors (Sun and Xia 2002), and cancer therapy (EI-Sayed et al. 2006) among others.
Presently, biological nanoscience has drawn increasing attention due to its avant-garde nature and the efficacy of produced nanoparticles in industrial, biomedical, and electronic applications such as catalyst (Hashmi and Hutchings 2006), cancer detection (Huang et al. 2007b), and bioimaging (Wu et al. 2006). Among the loads of metal nanoparticles, gold nanoparticles have an especially wide application in DNA recognition, heredity medicine, and nano-catalysis. It has been pointed out that the divergent capabilities of these nanoparticles are controlled by their size (Alivisatos 1996; Jin et al. 2001; Aizpurua et al. 2003).
Numerous methodologies are developed to synthesize noble metal nanoparticles of particular shape and size depending on specific requirements. Biosynthesis of nanoparticles has an emerging highlight of the intersection of nanotechnology and biotechnology which has received increased attention to a growing need to develop environmentally benign technologies in material syntheses. Biomolecules as reductants are found to have significant advantage over chemical reductants due to their non biocompatible nature (Huang et al. 2007a).
In the present cram, a simple biosynthetic method using flower extract of Couroupita guianensis is addressed herein for synthesizing gold nanoparticles. The newly synthesized gold nanoparticles were characterized by employing standard technologies. The plant C. guianensis, commonly known as cannon ball tree, has innumerable medicinal applications including antibiotic, antiseptic, anti-inflammatory activity (Geetha et al. 2004). Indeed, it is expected that gold nanoparticles synthesized using the flower of the tree C. guianensis might have medicinal properties. Accordingly, efforts are made to identify the newly generated gold nanoparticles’ medicinal value. As a result, their antileukemic cancer activity has been explored. Cancer is the leading cause of death worldwide after cardiovascular diseases (Garrett and Workman 1999). Leukemia is a major type of cancer affecting a significant segment of the population, especially children. In fact, leukemia is the most frequent childhood cancer, with 26 % of all cases, and 30 % mortality (Canadian Cancer Society 2005). Clinical trials in identifying new agents and treatment modalities has been studied and achieved. However, current treatments have many limitations related to their side effects and the development of acquired drug resistance (Robert and Jarry 2003). Thus, the new therapeutic agents needed should be more active and produce fewer side effects and they also should act through a mechanism different from that of cytotoxic agents already used.
2 Materials and methods
2.1 Preparation of flower extract
Fresh flowers of C. guianensis were collected, washed thoroughly with double distilled water, air dried, and powdered. About 1 g of powdered flower was transferred into a 100-mL beaker containing 50 mL double distilled water and mixed well. The extract obtained was filtered through Whatmann no. 1 filter paper and the filtrate was collected in a separate flask.
2.2 Synthesis of gold nanoparticles using plant extract
One hundred milliliter solution of 1 mM chloroauric acid at concentration of 10−3 M was prepared by dissolving in double distilled water. Different reaction concentrations of C. guianensis extract and HAuCl4 solution (1:9, 2:8, 3:7, 4:6, and 5:5) were subjected, respectively. The reduction of gold ions to gold nanoparticles was completed within 5 min. The pale yellow color solution turns to ruby red color indicating the formation of gold nanoparticles. The reduction of metal ions was continuously monitored by visual inspection as well as by measuring with UV–visible spectrometer in the wavelength range 300–800 nm.
2.3 Characterization of gold nanoparticles
UV–visible spectrum was recorded as a function of the reaction time on a Techomp (UV 2300) double beam spectrophotometer.
For FTIR measurements, the newly synthesized gold nanoparticles were centrifuged at 8,000 rpm for 10 min and the resulting suspension was redispersed in distilled water. The purified pellets were dried and smirk with KBr pellets and analyzed by Thermo Nicolet Quator instrument in the diffuse reflectance mode operating at a resolution of 4 cm−1.
XRD measurements of the C. guianensis-synthesized gold nanoparticles solution drop coated on to glass substrates was done on a Siefert X-ray diffractometer, operated at a voltage of 40 kV and tube current of 30 mA with Cu-Kα radiation. Surface morphology of newly formed gold nanoparticles was determined using scanning electron microscope (FEI Quanta 200 SEM).
For TEM studies, newly synthesized gold nanoparticles were prepared by placing a drop of nanoparticle solution on carbon-coated copper grids and allowing water to evaporate. TEM measurements were performed on JEOL 3010 UHR TEM equipped with a Gatan Imaging Filter.
2.3.1 Assessment of cell morphology
HL-60 cells were cultured in 24-well plates and incubated at 37 °C for 24 h before each well were individually treated with 0, 60, 90, 120, 150, and 180 μg/mL gold nanoparticles for 48 h. Determination of cell morphology was made using a phase contrast microscope (Lu et al. 2010).
2.3.2 DAPI staining for apoptosis
Cells in 12-well plates were treated with or without 0, 80, 120, 180, and 200 μg/mL gold nanoparticles for 48 h. Cells were then stained by using 4,6-diamidino-2-phenylindole dihydrochloride (DAPI) (Chen et al. 2009a).
2.3.3 Comet assay for DNA damage
Cells in 96-well plates were treated with or without 0, 60, 90, 120, 150, and 180 μg/mL gold nanoparticles for 48 h. Cells were then harvested and DNA damage was determined with the Comet assay (Chen et al. 2009b).
2.3.4 DNA gel electrophoresis for DNA fragmentation
Cells in six-well plates were incubated with 0 and 150 μg/mL gold nanoparticles 48 h. Cells were harvested by centrifugation and DNA was isolated before DNA fragmentation was determined by DNA gel electrophoresis (Lu et al. 2010).
2.3.5 Effect of gold nanoparticles on cytotoxicity
HL-60 cells were obtained from the NCCS, Pune, India, and grown in RPMI1640 medium and supplemented with a 2 mg mL−1 sodium bicarbonate, 4.5 mg mL−1 glucose, 100 μg mL−1 streptomycin sulfate, 40 μg mL−1 gentamycin, 100 U mL−1 penicillin as well as 10 % heat-inactivated fetal calf serum. An environment of humidified air containing 5 % CO2 was maintained at 37 °C. Peripheral blood mononuclear cells (PBMC) were obtained from healthy donors and cultured as described. Effects of gold nanoparticles on the proliferation of cells was determined by MTT [3-(4, 5-dimethyl thiazoyl-2-yl)-(2,5-diphenyltetrazolium bromide)] assay. Briefly, the cells were suspended at 3 × 105 Cell mL−1. The cells were placed in 96-well microtiter plates (200 μl well−1) and incubated at 37 °C in a CO2 incubator in the presence of the gold nanoparticles. After 5 days, cell viability was measured by MTT assay, from which cytotoxic concentration (CC50) was calculated (Premnathan et al. 1996).
3 Results and discussion
There are reports on the plant-mediated synthesis of gold nanoparticles. Ghoreshi and co-workers (2011) reported on the synthesis of gold nanoparticles using the flower extract of Rosa damascene. Studies also demonstrate that the flavanoids and polyphenols of the flower are responsible for the formation of quasi-spherical nanoparticles. Philip (2010) demonstrated Hibiscus rosa sinensis-mediated synthesis of gold nanoparticles and it has been reported that carboxylic group of malic acid may be the active principle for the reduction and capping of gold nanoparticles. Cinnamomum zeylanicum-mediated synthesis of gold nanoparticles have been reported and possibly the amines of proteins bound the newly formed nanoparticles (Smitha et al. 2009). It has been illustrated that flavanoids of the plant Syzygium aromaticum found to have the property of synthesizing irregular-shaped nanoparticles (Deshpande et al. 2010). Pioneering works on nanoparticles synthesis using plant extracts have been carried out by Sastry and co-workers using geranium leaves, neem, Aloe vera, and lemon grass are extensively studied (Ankamwar et al. 2005; Shankar et al. 2004; Chandran et al. 2006; Shankar et al. 2005). Singaravelu and co-workers (Singaravelu et al. 2007, Govindaraju et al. 2008, Khaleel et al. 2010) reported on the biological synthesis of gold and silver nanoparticles using Sargassum wightii, Spirulina platensis, Psidium guajava as green chemistry approach.
Despite the widespread use of gold nanoparticles, there are only few studies to determine the cytotoxic effects of biologically synthesized gold nanoparticles, particularly in the context of apoptosis. MTT assay was used to appraise the effect of gold nanoparticles on proliferation of HL-60 cells. This is the first study to evaluate C. guianensis-based gold nanoparticles’ cytotoxicity against cancer cell lines. Thus we hypothesize that cell killing could be the possible mechanism induced by the cytotoxic effect of biosynthesized gold nanoparticles.
Nanotechnology has attracted a great interest in recent years due to its expected impact on many areas such as energy, medicine, and electronics. The development of new materials with nanometer size including nanoparticles, nanotubes, nanowires, etc., is the major activity. Among all, nanoparticles with the unique properties in chemistry, optics, electronics, and magnetics have led to an increasing interest in their synthesis.
Much of the existing research in the development of anticancer therapeutics from the plants has been focused on investigating the molecular mechanism by which an agent induces cytotoxicity and apoptosis in cancer cells. This study provides valuable insight in developing nanotherapeutics against dreadful cancer.
Investigation suggests that ethnopharmacological approach on the production of gold nanoparticles will greatly facilitate on the creation of an important symbiosis between nanoscience and medical science.
The results addressed herein disclose anticancer activity of gold nanoparticles synthesized using aqueous flower extract of C. guianensis. It is reasonable to infer that the pharmacological properties of C. guianensis provide the anticancer activity of newly formed gold nanoparticles. Interestingly, it has been demonstrated that the functionalization of gold nanoparticles as anticancer nanomaterial has been achieved without doping of molecules.
G.S and R.G thank the INSPIRE—Department of Science and Technology, New Delhi, for financial assistance.
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