Journal of Materials Science and Chemical Engineering
Vol.04 No.02(2016), Article ID:63390,10 pages

Silver and Gold Nanoparticles Embedded in Potato Starch Gel Films

Karen Khachatryan, Gohar Khachatryan, Maciej Fiedorowicz

Department of Chemistry and Physics, Agricultural University, Cracow, Poland

Copyright © 2016 by authors and Scientific Research Publishing Inc.

This work is licensed under the Creative Commons Attribution International License (CC BY).

Received 26 November 2015; accepted 1 February 2016; published 6 February 2016


Facile and environmentally friendly method of the preparation of silver and gold nanoparticles embedded in potato starch matrix (Sp) was developed. UVVIS spectroscopy, transmission electron microscopy (TEM) and Fourier transform infrared (FTIR) spectra confirmed formation of ball shaped Ag and Au nanoparticles situated within the polysaccharide template. EDS spectra confirm presence of silver and gold nanocrystals in the obtained composites. Differential scanning calorimetry (DSC) showed that Sp/Au composite started to decompose earlier. The decomposition is slower and two-step, in contrast to Sp and Sp/Ag. NanoAg accelerates carbonization. Molecular weights of polysaccharide chains of the matrix were estimated with the size exclusion chromatography coupled with multiangle laser light scattering and refractometric detectors (HPSEC-MALLS- RI). Formation of nanosilver containing composites led to partial depolymerisation of polysaccharides from the amylose fraction. In the case of nanogold we observed depolymerisation of polysaccharide chains from both fractions.


Nanocomposites, Polysaccharide Foils, Potato Starch Matrix, Potato Starch Template, Metal Nanoparticles

1. Introduction

For a wide spectrum of amazing properties metal nanoparticles received much attention in a variety of areas including physics, chemistry, materials science, and biomedical science [1] . They are frequently used either in form of diluted solutions ready for application in form of sprays or ready to use suspensions, for instance, in glass or cosmetics. Their distribution on solid surfaces such as cloths is another possibility [2] -[6] .

There are some arguments rationalizing this study. As all nanoparticles, also metal nanoparticles readily undergo aggregation loosing their unique properties. Their disaggregation presents a task. Suspending these nanoparticles in starch foils would stabilize these nanoparticles from aggregation [7] . Since the matrix for these nanoparticles is biodegradable there should be a chance for controlled prolonged distribution of minute but significant concentration of nanoparticles suitable for their application as bactericidals [3] -[5] [8] -[10] , fungicides [11] and catalysts [12] -[16] . For their provenience polysaccharides received attention as biodegradable environmentally benign materials of numerous applications, for instance, as packaging foils, encapsulating material, wound dressing and nanometal carriers [17] -[24] . Unfortunately, foils of plain starch appear too sensitive to microorganisms. Suspended metal nanoparticles might extend the period of safe application of the foils. Polysaccharides and their derivatives in which metal nanoparticles have been embedded usually contained functional groups providing anchoring the nanoparticles in the matrix and/or acting as reductors for metal cations, for instance, chitosan and its derivatives [18] [22] [23] , heparin [19] , glycosylamino glycans [20] , starch dialdehyde [7] , beta- chitin [21] , hydroxymethylpropyl cellulose [17] . When polysaccharides did not contain such groups and did not dispose with sufficiently strong reducing properties, additional complexing agents such as thiolate, boronic acid, had been applied [24] .

There is in a literature a growing concern about harm for the contact of organisms with nanoobjects. Nanoparticles are shown to affect the immunological system of living organisms [25] -[27] . For that sake opinion is presented that distribution of nanoparticles to the environment should be limited and taken under control. Recycling of materials containing nanoparticles, especially metal nanopowders and some quantum dots, is one of possible solutions in line with these suggestions. Suspending nanoparticles in biodegradable polysaccharide matrices would facilitate recycling of nanoparticles [28] -[31] .

This paper presents preparation and characteristics of potato starch foils with embedded silver and gold nanoparticles generated from AgNO3 and HAuCl4, reduced with NaBH4. Potato starch is the sole native starch containing phosphate groups in its amylopectin component [10] . Such groups carrying negative charge when ionized can play a role of anchor for generated nanoparticles.

2. Materials and Methods

2.1. Materials

Potato starch (amylose: amylopectin ratio = 26%:74%; moisture content: 12% and phosphorus content: 550 ppm) was purchased from Pepees SA, Łomża, Poland. AgNO3 (99.99%), HAuCl4 (≥99.9%, trace metals basis) and NaBH4 (99.99% trace metals basis) was purchased from Sigma-Aldrich.

2.2. Synthesis of Metal Nanoparticles―Potato Starch (PS) Composites

Potato starch (Sp), (5 g) was suspended in distilled water (95 mL). Resulted suspension was maintained on continuous agitation at 90˚C for 2 h to produce a gel. Silver (PS/Ag) and gold (Sp/Au) nanocrystals were generated by addition to the starch gel either AgNO3 solution (1 mL 0.05 M/dm3) or HAuCl4 solution (0.4 mL, 0.03 M/dm3), respectively, 30 min stirring this mixture followed by stepwise admixing NaBH4 aqueous solution (1 mL, 0.05 M/dm3). The reaction mixtures were agitated at the same temperature for 1 h, then cooled and applied to a clean, smooth, defatted either Teflon or glass surface and left for drying in the air. The dry foils were stored in closed container.

2.3. UV-VIS Absorption Spectrophotometry

The UVVIS absorption spectra of, Sp Sp/nanoAg and Sp/nanoAu composites were recorded using a Shimadzu 2101 scanning spectrophotometer in the range of 200 - 700 nm using 10 mL, 10 cm thick quartz cells. Nanocomposite foils were dissolved in distilled water at 35˚C - 40˚C to obtain solutions containing 0.001g/L.

2.4. FTIR-ATR Spectrophotometry

The FTIR-ATR spectrum of the composites was recorded in the range of 500 − 4000 cm−1 at resolution of 4 cm−1 using a MATTSON 3000 FT-IR (Madison, Wisconsin, USA) spectrophotometer. That instrument was equipped with a 30SPEC 30 Degree Reflectance adapter fitted with the MIRacle ATR accessory from PIKE Technologies Inc., Madison, Wisconsin, USA.

2.5. Scanning and Transmission Electron Microscopy (SEM and TEM)

Analyses of sizes and morphologies of the as-prepared nanoparticles were studied using a high resolution JEOL 7550 scanning electron microscope equipped with Energy dispersion X-ray spectroscopy (EDS) analyzer for local chemical analysis. Samples for TEM and SEM microscopies were prepared after drop-coating 10 μL of the sample on a carbon-coated copper grid (PELCO®). Because the material was sufficiently conducting, the gold sputtering of the samples was dispensable.

2.6. High Performance Size Exclusion Chromatography (HPSEC- MALLS-RI)

Values of absolute molecular weight (Mw) and radii of gyration (RG) of polysaccharide molecules from starch (Sp) and silver (Sp/Ag) and gold (Sp/Au) were measured by means of high pressure size exclusion chromatography coupled with multiangle laser light scattering and refractometric index detectors (HPSEC-MALLS- RI).

The high performance size exclusion chromatography (HPSEC) system for determination of average molecular weight and radii of gyration consisted of a pump (Shimadzu 10AC, Tokyo, Japan), an injection valve (model 7021, Rheodyne, Palo Alto, CA, USA), a guard column TSK PWH (Tosoh Corporation, Tokyo, Japan), and two connected size exclusion columns TSKgel GMPWXL (300 × 7.8 mm , Tosoh Corporation, Tokyo, Japan) and TSKgel 2500 PWXL (300 × 7.8 mm , Tosoh Corporation, Tokyo, Japan). A multiangle laser light scattering detector (MALLS) operating in chromatographic mode using a He−Ne laser light source (630.0 nm) (Dawn-DSP-F, Wyatt Technology, Santa Barbara, CA, USA) and a differential refractive index detector (L-7490, Merck, Darmstadt, Germany) were connected to the columns. The columns were maintained at 30˚C. The mobile phase ( 0.15 M NaNO3 with 0.02% sodium azide) was filtered through 0.2 and 0.1 microm cellulose acetate filters ( Whatman , England ). The flow rate of the mobile phase and the sample injection volume were 0.4 mL/min and 500 microL respectively. The output voltage of refractive index (RI) and light scattering (LS) at 18 angles was used for calculation of the weight-average molecular weight (Mw) and radius of gyration (Rg) using Astra 4.73.04 software (Wyatt Technology, Santa Barbara, CA, USA).

Sp and nanocomposite samples (100 mg) moistened with water (10 mL) were suspended in dimethylsulfoxide (DMSO, 90 mL) then boiled for 12 h on agitation. Resulting solutions were filtered by 0.8 mm cellulose acetate filters ( Whatman , England ) and immediately injected on chromatography column.

2.7. Thermogravimetric Analysis (TG)

For ~5 mg solid samples, the thermogravimetric analyses (TG) coupled with mass spectrometer (MS-TG/DTG/ SDTA) were performed in Mettler-Toledo 851e apparatus in 150 μl corundum crucibles, closed by a lid with a hole, under flow of argon (80 mL/min), within temperature range 30˚C - 800˚C with heating rate of 10˚C/min. The simultaneous analysis of evolved gas (EGA) was performed during the experiments by joined on-line quadruple mass spectrometer (QMS) (Thermostar Balzers).

2.8. Differential Scanning Calorimetry

The differential scanning calorimetry (DSC) experiments for the ~10 mg samples were performed in Mettler- Toledo 821e calorimeter equipped with an intracooler Haake in 40 microL aluminum crucibles under constant flow of argon (80 mL/min) within temperature range 25˚C - 400˚C.

2.9. α-Amylolysis

α-Amylase from porcine pancreas (EC.,Merck, Darmstadt, Germany) was reconstituted in 20 mM phosphate buffer (pH 6.5 - 7.0) containing 2 mM NaCl and 0.25 mM CaCl2 to obtain a stock solution with an enzyme activity of 250 units/mL. Nanocomposites were precisely weighed into Erlenmeyer flasks and suspended in the phosphate buffer (38 mL). Aliquots of the enzyme stock solution (2 mL) were added to achieve a 1 mg/mL final concentration of amylopectin and a final enzyme activity of 12.5 units/mg substrate. The Erlenmeyer flasks were incubated at 37˚C. The amount of maltose was determined by the 3,5−dinitrosalicylic acid method [32] . The extent of amylopectin amylolysis was calculated as the ratio of the amounts of hydrolysed amylopectin and total dry substrate.

3. Results and Discussion

The UVVIS absorption spectra of potato starch and Sp/Ag and Sp/Au nanocomposites are presented Figure 1. Formation of strong absorption band centered at 410 and 580 nm in the case of Sp/Ag Sp/Au foils, respectively clearly suggest formation of Ag and Au nanoparticles embedded in starch matrix.

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Typical TEM images of silver (A) and gold (B) nanoparticles embedded in the starch matrix are displayed on Figure 2.

Spherical Ag and Au nanocrystals are well separated in starch matrix and particle size distribution ranges between 10 and 20 nm for both silver and gold nanostructures. EDS spectra of nanocomposites (Figure 3) fully confirm formation of silver and gold nanocrystals.

Morphology of polysaccharide matrix of Sp/Au and Sp/Ag composites distinguish from one another. The Sp/Au sample seems to be amorphous whereas polysaccharide chains of Sp/Ag composites form organized semicrystalline structures. Such differences in the matrix structures could be explained by substantial acid-catalyzed degradation of polysaccharide molecules in the presence of HAuCl4.

Mw and RG of starch polysaccharide molecules for native starch (Sp) and silver (Sp/Ag) and gold (Sp/Au) nanocomposites, respectively, are presented in Table 1.

These results fit explanation of the differences between TEM images of Sp/Ag and Sp/Au. The whole chromatogram was, based on patterns, arbitrarily divided into two regions attributed to amylopectin (Fraction I) and amylose (Fraction 2) fractions, respectively. Under reaction condition, during formation of nanosilver in the starch matrix diminishing of Mw of amylose molecules was observed together with rise of the Mw of polysaccharide chains from amylopectin fraction as compared to native starch. Such effect indicates that formation of silver nanocrystals induced degradation of amylose chains. In the next step small chains from the amylose degradation add to the amylopectin chains. Formation of gold nanocrystals is associated with strong degradation of polysaccharide chains of both, amylose and amylopectin fraction. However, it is clear that amylopectin chains were more prone to degradation, up to complete depolymerization. Such effect, could explain great differences in morphology between Sp/Ag and Sp/Au nanocomposites observed on SEM images (Figure 2). FTIR spectra of potato starch (Sp) as well as Sp/Ag and Sp/Au composites are shown in Figure 4. In the fingerprint region, the spectra of potato starch and starch silver and gold nanocomposites have similar profiles with peaks at 1150, 1050 and 930 cm−1 which could be attributed to the C-O bond stretching vibrations [33] .

Figure 1. UVVIS spectra of potato starch (Sp), Sp/Ag and Sp/Au composites.

Figure 2. TEM images of Sp/Ag (a) and Sp/Au (b) composites.

Another characteristic band occurred on Sp and Sp/Ag spectra at 1652 cm−1. This peak originates from tightly bound water present in starch [34] . In the spectra of Sp/Au nanocomposite besides the absorption at 1652 cm−1, a additional broad peak centered at 1600 cm−1 could be seen. The latter reflects presence of water more loosely bound within more disrupted polysaccharide matrix of Sp/Au.

The pattern of the thermal decomposition (TG) of Sp and Sp/Ag (Figure 5) closely resemble one another. A slightly higher water content of in the latter sample resulted from a certain loosening the starch structure on processing starch towards the composite.

The theromogram of Sp/Au confirms essential degradation of the polysaccharide in that composite. Because

Figure 3. EDS spectra of Sp/Ag (a) and Sp/Au (b) composites.

Table 1. Absolute molecular weight of the original starch fractions and their changes after generation of nanoAg (Sp/Ag) and nanoAu crystals inside starch gel (Rg, radius of gyration).

Figure 4. The FTIR spectra of Sp, Sp/Ag and Sp/Au composites.

of the degradation, it contained less humidity, only slightly more than unprocessed starch. Because of the deeper interference into the native structure also stabilizing intermolecular hydrogen bonds partly ceased and due to depolymerization the structure became more non-uniform. The composite started to decompose by approximately 100˚C earlier, the decomposition is slower, and in contrast to Sp and Sp/Ag two-step. Also the high- temperature decomposition pattern of Sp and Sp/Ag are essentially different. NanoAg accelerates carbonization. In Sp/Ag it is completed at around 340˚C and further heating caused burning the carbonizate out leaving at 600˚C approximately 20% residue. The decomposition pattern of Sp/Au in this temperature range resembled decomposition of plain Sp. At 600˚C both samples left approximately 30% residue. It pointed to the presence of silver oxide on thermolyzed Sp/Ag which promoted deeper burning out the carbonizate.

DSC thermograms registered for and Sp/Ag and Sp/Au nanocomposites together with the thermogram of Sp are displayed on Figure 6.

Figure 5. TG analysis of Sp, Sp/Ag and Sp/Au.

Figure 6. DSC thermograms of Sp, Sp/Ag and Sp/Au composites.

The shapes of the thermograms taken for starch and Sp/Au composite, consisting roughly of one endothermic and one exothermic peak, are similar to some extent. In both cases exothermic peak centered at 310˚C for Sp and 320˚C for Sp/Au could be attributed to decomposition of the polymer. Temperature of endothermic transition for Sp/Au nanocomposite (220˚C) is much lower than temperature of such transition recorded for starch indicating disintegration of polysaccharide matrix during nanogold formation. DSC thermogram patterns observed for Sp/Ag differs greatly from thermograms of starch and starch silver nanocomposite. Two exothermic peaks one at 200˚C and second at 330˚C could be observed indicating that silver nanocrystals formation leads to the more ordered orientation of polysaccharide chains as compared with starch and Sp/Au composite. Thermal properties of starch and starch silver (Sp/Ag) and gold (Sp/Au) nanocomposites are in good agreement with results of molecular weight measurements of polysaccharide chains constituting starch nanometals composites.

Silver and gold nanoparticles embedded in the potato starch foil very efficiently inhibit these foils against several hydrolases. Results of these studies will be published separately.

4. Conclusions

Silver and gold nanoparticles were successfully formed in potato starch matrix. Polysaccharide matrix makes nanometals stable and prevents from aggregation.

1) Potato starch is suitable matrix for silver and gold nanoparticles.

2) When HAuCl4 is applied as a source for nanoparticles, generation of the nanoparticles is accompanied by acid-catalyzed depolymerization of gelatinized starch.

3) Foils can be drawn from gelatinized starch suspensions of silver and gold nanoparticles in the manner avoiding agglomeration of suspended nanoparticles.

Cite this paper

KarenKhachatryan,GoharKhachatryan,MaciejFiedorowicz, (2016) Silver and Gold Nanoparticles Embedded in Potato Starch Gel Films. Journal of Materials Science and Chemical Engineering,04,22-31. doi: 10.4236/msce.2016.42003


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