Biofabrication of silver nanoparticles from various plant extracts: blessing to nanotechnology

ABSTRACT

Nanotechnology is influencing life in many ways. Researchers are developing their interest in biofabrication of silver nanoparticles because of its excellent properties and boundless utilisation in almost every branch of science. Plant extract is used to synthesise silver nanoparticles and reduce silver ion, and act as capping and reducing agent. The phyto-chemicals and metabolites present in the extract help in biogenic reduction of silver ion, forming non-toxic nanoparticles. This review focuses on the green synthesis of nanoparticles from various plants and their parts as an easy and eco-friendly approach.     

Nanocomposite polyester fabrics with in situ generated silver nanoparticles using tamarind leaf extract reducing agent

Using tamarind leaf extract as a reducing agent and various concentrated aq?AgNO₃ solutions as source, the silver nanoparticles (AgNPs) were in situ generated in polyester fabrics. The nanocomposite polyester fabrics were characterized by scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction and antibacterial tests. The size of the generated AgNPs varied between 50 and 120?nm. The X-ray analysis indicated the generation of both AgNPs and AgO nanoparticles in the nanocomposite fabrics. The nanocomposite polyester fabrics exhibited excellent antibacterial activity against both the Gram negative and Gram positive bacteria and hence can be considered for making antibacterial textiles.     

Synthesis of silver nanoparticles in mesoporous high-aluminum aluminosilicate matrices

A new method for the synthesis of Ag/Al_xSi_1–x O_2–0.5x nanocomposite materials was proposed. The method is based on the use of charged mesoporous aluminosilicate matrices as nanoreactors. The porous structure of the matrices was characterized by ²⁷Al NMR spectroscopy and nitrogen capillary sorption at 77 K. An increase in the aluminum loading destroys the matrix structure and decreases the specific surface area. The resulting aluminosilicates were used as matrices for the synthesis of silver nanoparticles. The nanocomposites were examined by transmission electron microscopy and chemical analysis to estimate the silver percentage in specimens. Silver nanowires (20% Ag) are formed in the low-aluminum (<10 mol.%) matrices, whereas an increase in the aluminum percentage affords both nanowires and spherical particles 3–10 nm in size and decreases the total amount of silver in the nanocomposite.__________Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 2391–2393, November, 2004.     

以葡聚糖-乙二胺聚合物为载体制备纳米银

以葡聚糖-乙二胺聚合物为载体制备纳米银.首先合成葡聚糖-乙二胺聚合物,并用紫外光谱红外光谱对聚合物进行表征;该聚合物与硝酸银反应生成葡聚糖-乙二胺聚合物-银配合物,再通过化学还原或光化学还原法使配合物中的银离子转变成单质银纳米粒,以透射电子显微镜激光纳米测定仪对制备的纳米银进行测定.结果表明制备出了粒径为23.1nm的纳米单质银.以葡聚糖-乙二胺聚合物为载体制备纳米银的方法是可行的.     

Chemical interactions between silver nanoparticles and thiols: a comparison of mercaptohexanol against cysteine

The interaction between citrate capped silver nanoparticles and two different thiols, mercaptohexanol(MH) and cysteine, was investigated. The thiols interacted with silver nanoparticles in a significantly contrasting manner. With MH, a sparingly soluble silver(I) thiolate complex AgSRm(Rm = –(CH2)6OH) was formed on the silver nanoparticle surface. Cyclic voltammograms and UV-vis spectra were used to infer that the AgSRm complex on the nanoparticle surface undergoes a phase transition to give a mixture of AgSRm and Ag2S-like complexes. In contrast, when silver nanoparticles were exposed to cysteine, the citrate capping agent on the silver nanoparticles was replaced by cysteine to give cysteine capped nanoparticles. As cysteine capped nanoparticles form, the electrochemical data displayed a decrease in oxidative peak charge but the UV-vis spectra showed a constant signal. Therefore, cysteine capped nanoparticles were suggested to have either inactivated the silver surface or else promoted detachment from the electrode surface.     

Antibiotic glass slide coated with silver nanoparticles and its antimicrobial capabilities

Silver nanoparticles were covalently coated on a glass surface by overnight exposure of the glass substrate to nanoparticle solutions, using 3‐aminopropyltriethoxysilane (APTES) as a coupling agent. Washing and air‐drying yield a uniformly coated glass substrate, which can be used as a material capable of killing harmful microorganisms in food industry. Nanoparticles are stable on the glass surface and are not washed away by water; they even remain on the glass surface under short‐term ultrasonic irradiation. The morphology of silver nanoparticles on the glass substrate was characterized by scanning electron microscope (SEM). The existence of Ag nanoparticles on the substrate was also confirmed by ultraviolet‐visible (UV–Vis) spectroscopy. Fourier transform infrared (FT‐IR) measurement shows that the connection is based on covalent bonds between silver nanoparticle surface/APTES molecules. Combining the effects of low cost and effectiveness in prohibiting the growth of Escherichia coli, such materials are expected to be used as antibacterial coatings, which may have large potential applications in food industry. Copyright © 2008 John Wiley & Sons, Ltd.     

Lectin sensitized anisotropic silver nanoparticles for detection of some bacteria

A method of bacteria detection by sensitized anisotropic silver nanoparticles is presented. Anisotropic silver nanoparticles with two bands of surface plasmon resonance (SPR) are prepared and sensitized with potato lectin. These nanoparticles are able to detect three bacterial species: Escherichia coli, Bacillus subtilis and Staphylococcus aureus. The interaction of these bacteria with such nanoparticles induces drastic changes in optical spectra of nanoparticles that are correlated with bacteria titer. The maximal sensitivity is observed for S. aureus (up to 1.5 × 10⁴ mL⁻¹).     

Biofunctionalized silver and gold nanoparticles as potential curative agents

In this study, the bark of an important medicinal plant, Indigofera aspalathoides is utilized as a bioreductant for the synthesis of silver nanoparticles (AgNPs) and gold nanoparticles (AuNPs). The formation of nanoparticles was monitored, and the reaction parameters were optimized by UV–Vis spectroscopy. The attachment of biocomponents as stabilizer was proved employing Fourier‐transform infrared (FT‐IR) studies. Through transmission electron microscopy (TEM), the morphology was found to be predominantly spherical and a mixture of triangle and hexagon in the case of AgNPs and AuNPs, respectively. The crystallite size of AgNPs and AuNPs was affirmed through X‐ray diffraction (XRD) studies using Sherrer formula as 22.03 and 47.70 nm, respectively. DPPH method was adopted to analyse the free‐radical quenching ability, and the AgNPs, AuNPs and extract showed inhibition of 76%, 89% and 59% at a concentration of 200 μg ml^?1, and the corresponding IC₅₀ values were 86.49, 55.20 and 149.19 μg ml^?1. The binding of nanoparticles to calf‐thymus DNA (CT‐DNA) was through groove and the high binding constants (8.49 × 10⁶ M^?1 and 2.34 × 10⁷ M^?1 for AgNPs and AuNPs) point out the potential of these nanoparticles as curative drugs. The MTT assay showed that AgNPs were 100% toxic, and the low IC₅₀ value suggests that this can be used in the medicinal field as a safe drug.     

三角形纳米银颗粒的制备及其热稳定性的研究

具有独特的光学和化学性质的纳米三角形银纳米颗粒在光电、催化和生物传感器等领域中有广泛的应用.提供一种简单的方法制备三角银纳米颗粒,对其进行表征研究,且详细讨论了其热力学稳定性.     

天然松香用于制备球型纳米银的研究

以AgNO3为原料,利用天然松香中的还原性物质枞酸还原银氨络离子得到银纳米颗粒,利用油酸等与纳米颗粒的相互作用在表面形成一层保护层来防止纳米颗粒的聚集。并用UV-vis、TEM和XRD对其进行检测和表征。通过控制反应条件,可制得粒度分布较均匀、结晶性能良好的银纳米颗粒。     

Tryptophan-based peptides to synthesize gold and silver nanoparticles: a mechanistic and kinetic study

Synthetic oligopeptides with a tryptophan residue at the C-terminus have been used for the synthesis of gold and silver nanoparticles at pH 11. The tryptophan residue in the peptides is responsible for the reduction of metal ions to the respective metals, possibly through electron transfer. A mechanistic pathway has been proposed to explain the reductive properties of the tryptophan moiety of the peptide based on some spectroscopic techniques, such as UV-visible and fluorescence spectroscopy. This study reveals that some of the peptide molecules are converted to its corresponding ditryptophan, kynurenine form and some cross-linked products, all of which are highly fluorescent species. The resultant peptide-functionalized metal nanoparticles have also been characterized by UV-visible spectroscopy, transmission electron microscopy, and Fourier transform IR spectroscopy and thermogravimatric analysis.     

Synthesis and optical properties of silver nanoparticles and arrays.

This Minireview systematically examines optical properties of silver nanoparticles as a function of size. Extinction, scattering, and absorption cross-sections and distance dependence of the local electromagnetic field, as well as the quadrupolar coupling of 2D assemblies of such particles are experimentally measured for a wide range of particle sizes. Such measurements were possible because of the development of a novel synthetic method for the size-controlled synthesis of chemically clean, highly crystalline silver nanoparticles of narrow size distribution. The method and its unique advantages are compared to other methods for synthesis of metal nanoparticles. Synthesis and properties of nanocomposite materials using these and other nanoparticles are also described. Important highlights in the history of the field of metal nanoparticles as well as an examination of the basic principles of plasmon resonances are included.     

Paramagnetic behaviour of silver nanoparticles generated by decomposition of silver oxalate

Silver oxalate Ag₂C₂O₄, was already proposed for soldering applications, due to the formation when it is decomposed by a heat treatment, of highly sinterable silver nanoparticles. When slowly decomposed at low temperature (125 °C), the oxalate leads however to silver nanoparticles isolated from each other. As soon as these nanoparticles are formed, the magnetic susceptibility at room temperature increases from −3.14 10⁻⁷ emu.Oe⁻¹.g⁻¹ (silver oxalate) up to −1.92 10⁻⁷ emu.Oe⁻¹.g⁻¹ (metallic silver). At the end of the oxalate decomposition, the conventional diamagnetic behaviour of bulk silver, is observed from room temperature to 80 K. A diamagnetic-paramagnetic transition is however revealed below 80 K leading at 2 K, to silver nanoparticles with a positive magnetic susceptibility. This original behaviour, compared to the one of bulk silver, can be ascribed to the nanometric size of the metallic particles.     

Synthesis of aza-crown ether-modified silver nanoparticles as colorimetric sensors for Ba2+

In this paper, we have demonstrated a facile strategy of preparing aza-crown ether (ACE)-modified silver nanoparticles (Ag NPs) by an efficient nano-conjugate technology named dithiocarbamate. This is the first report of using ACE to modify Ag NPs. ACE-modified Ag NPs have a good recognition of Ba²⁺, with the detection limit of 10^? 8 mol/l. It is reasonable to believe that Ba²⁺ induced the self-assembly of Ag NPs by the formation of the sandwich structure with ACE.

     

Pulsed laser excitation of phosphate stabilised silver nanoparticles

Laser flash photolysis studies were carried out on two types of silver nanoparticles prepared byγ-radiolysis of Ag⁺ solutions in the presence of polyphosphate as the stabiliser. Type I silver nanoparticles displayed a surface plasmon band at 390 nm. Type II silver nanoparticles showed a 390 nm surface plasmon band with a shoulder at 550 nm. On photoexcitation in the surface plasmon band region, using 35 picosecond laser pulses at 355 nm and 532 nm, the type II solutions showed transient bleaching and absorption signals in the 450–900 nm region, which did not decay appreciably up to 5 nanoseconds. These transient changes were found to get annealed in the intervalt where 5 ns<t< 100 ns. Extended photolysis of the nanoparticle solutions with repetitive laser pulses resulted in a decrease in the values of the average particle size which were measured by employing the dynamic light scattering technique.     

Biosynthesis and characterization of Dillenia indica-mediated silver nanoparticles and their biological activity

Dillenia indica L. is a traditional medicinal plant well known for its ability to cure various human diseases. In the current study, silver nanoparticles have been synthesized by simple and eco-friendly method using Dillenia indica extract. The green synthesized nanoparticles were characterized by Fourier transform infrared (FTIR), UV–visible spectroscopy, Atomic force microscopy (AFM), High-resolution transmission electron microscopy (HR-TEM), Zeta Potential and Size Distribution. UV–visible and FTIR spectra, AFM, HR-TEM and Zeta Potential readings and size distribution conformed that the synthesized silver particles were in the size of nano. The green synthesized silver nanoparticles were subjected for antibacterial activity against Gram-positive bacteria Enterococcus faecalis and Gram-negative bacteria Escherichia coli by agar well diffusion method. The synthesized AgNPs exhibited significant inhibition of 27 and 16 mm against the test bacteria at 0.25 mg/ml. Further the antibacterial activity was confirmed by live and dead cell assay by fluorescence microscopy and morphological changes of bacteria were studied by Scanning electron microscope (SEM). The study recommends that the synthesized silver nanoparticles using Dillenia indica extract have potential application in inhibition of bacteria owing to their potent antibacterial activity.