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225 protocols using haucl4

1

Synthesis and Characterization of Gold Nanoparticles

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Chloroauric acid (HAuCl4) was purchased from Sigma-Aldrich Chemicals. A stock solution of HAuCl4 was prepared by dissolving 1.0 g HAuCl4 in 100 mL ultrapure water (18.2 MΩ cm−1) from a Millipore water purification system. Sodium citrate and hydrochloric acid were purchased from Sinopharm Chemical Reagent Co. Ltd. Purified DNA sequences were purchased from Sangon Biotechnology Co. Ltd (Shanghai, China) and schematically shown in Table 1. Standard liquid elemental mercury (1 mg mL−1) was purchased from Aladdin Industrial Corporation. Unless otherwise noted, all reagent grade chemicals were used directly without further purification.
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2

Citrate-Mediated Gold Nanoparticle Synthesis

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The synthesis of nanoparticles was carried out using the Turkevich-Frens
citrate reduction method.39 (link)−42 (link) In a conical flask, 2.43 mL of 0.83% HAuCl4 (99.995%, Sigma-Aldrich) was diluted with 200 mL of distilled water
(Milli-Q, 19 MΩ). The resulting solution was heated under vigorous
stirring until boiling. Immediately, 1.5 mL of 1% citric acid (≥99.5%,
Sigma-Aldrich) was added to the solution of HAuCl4. After
a few seconds, the solution changed from a pale-yellow color to transparent,
then black, and finally maroon. The suspension of nanoparticles was
stirred for another 20 min and then allowed to cool overnight at room
temperature. The obtained nanoparticle suspensions were stored away
from light sources for the duration of the experiments, remaining
stable throughout the process.
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3

Seed-Mediated Synthesis of Plasmonic Gold Nanorods

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AuNR-760 (LSPR wavelength ~760 nm) was prepared by a seed-mediated method.64 (link),65 (link) Au seed was synthesized by adding 0.6 ml of ice-cold NaBH4 solution (10 mM) (Sigma-Aldrich, 71321) into a solution containing 0.25 ml HAuCl4 (10 mM) (Sigma-Aldrich, 520918) and 9.75 ml CTAB (0.1 M) (Sigma-Aldrich, H5882) under vigorous stirring at room temperature for 10 min. The colour of the solution changed from yellow to brown indicating the formation of Au seed. For the synthesis of AuNR, the growth solution was prepared by the sequential addition of aqueous HAuCl4 (0.01 M, 2 ml), CTAB (0.1 M, 38 ml), AgNO3 (0.01 M, 0.5 ml, Sigma-Aldrich, 204390), HCI (1M, 0.8 ml, Sigma-Aldrich, H9892) and ascorbic acid (0.1 M, 0.22ml, Sigma-Aldrich, A92902) followed by gentle inversion to homogenize the solution. The AgNO3 and HCI volume ratio may vary to obtain the right wavelength. Subsequently, 5 μl of the seed solution was added into the growth solution and left undisturbed in the dark for 24 hours. AuNR solution was centrifuged at 7000 rpm for 40 minutes to remove the supernatant and the AuNR was re-dispersed into nanopure water to achieve a final peak extinction ~2.0. For AuNR-647 (LSPR wavelength ~647 nm), the growth solution contained HAuCl4 (0.01 M, 2 ml), CTAB (0.1M, 38 ml), AgNO3 (0.01 M, 0.2 ml, this value may vary), and ascorbic acid (0.1 M, 0.32ml).
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4

Synthesis and Functionalization of Gold Nanorods

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PEG-GNRs were prepared from cetyltrimethylammonium bromide (CTAB)-stabilized GNRs by exchanging CTAB with mPEG-thiol. The CTAB-stabilized GNRs with an aspect ratio of 4 were synthesized using a seed-mediated growth approach, as previously reported.24 Briefly, 5 mL of 0.5 mM HAuCl4 (Sigma, St. Louis, USA) and 5 mL of 0.2 M CTAB (Sigma) solutions were prepared and mixed. Then, 600 μL of ice-cold 0.01 M NaBH4 (Sigma) solution was added to the mixture and sonicated for 4 min at 28 °C, after which the seed solution was allowed to stand at room temperature for 2 h. Growth solution was prepared by sequentially adding 5 mL of 0.001 M HAuCl4, 250 μL of 0.004 M AgNO3 (Sigma) and 70 μL of 0.0788 M ascorbic acid (Sigma) to 5 mL of 0.2 M CTAB solution. After gentle mixing, 12 μL of seed solution was mixed with growth solution at room temperature to initiate growth. When the longitudinal absorption peak reached ~800-820 nm, GNRs were centrifuged at 12,000 rpm for 15 min. The supernatant was discarded, and GNRs were re-suspended in distilled water. CTAB was exchanged with mPEG-thiol (2 kDa; Laysan Bio, Arab, USA) by adding 20 mg of mPEG-thiol to 10 mL of 3 optical density (O.D.). 25 (link) GNRs were vortexed vigorously for 1 h, after which unincorporated mPEG-thiol was removed by centrifuging three times at 10,000 rpm for 10 min each.
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5

Synthesis of Spherical Gold Nanoparticles

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The synthesis of spherical Au NPs was performed following the Turkevich–Frens procedure with some modifications [20 (link)]. Briefly, 15 mg of tetrachloroauric (III) acid (HAuCl4, Sigma-Aldrich, Dorset, UK) was dissolved in MilliQ water to obtain a solution having a concentration of 0.25 mM. Then, 150 mL of a HAuCl4 solution was moved to a reaction flask and heated at 100 °C until boiling under stirring and reflux. Later, 0.1 M of a sodium citrate (10 mL) aqueous solution was quickly added and a change in a color reaction was observed, which became red wine colored. After cooling to room temperature, the reaction product was stored in the dark in a refrigerated room. Subsequently, the solution was transferred into polypropylene tubes and centrifuged at 7500 rpm for about 45 min followed by a washing step using water.
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6

Synthesis of Citrate-Stabilized Gold Nanoparticles

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Example 2

All glassware used for AuNPs synthesis are cleaned in NOCHROMIX solution (Godax Laboratories, Inc., Cabin John, Md.) and then aqua regia (3 parts HCL+1 part HNO3) according to standard lab procedure. The synthesis of citrate-stabilized gold nanoparticle (AuNP) was based on a modification of Turkevich method. (Enustum et al., 1963, J. Am. Chem. Soc. 85(21):3317-3328). Briefly, 100 mL solution of 1 mM HAuCl4 (Sigma-Aldrich, St. Louis, Mo.) was boiled with stirring until bubbles formation and having a uniform temperature. Heating was kept for a further 25 minutes. Then, 10 mL of preheated trisodium citrate (38.8 mM, Sigma-Aldrich, St. Louis, Mo.) was added to the boiling HAuCl4 solution quickly. The solution turned to colorless for a moment, followed by violet to dark ruby red. The solution was heated for a further five minutes before cooling to room temperature. The solution was stored in the dark in a flask covered with foil. The sizes of AuNPs were characterized to be 32±3 nm using transmission electron microscopy (TECHNAI T12, FEI, Hillsboro, Oreg.).

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7

Synthesis of Chitosan and Sodium Citrate Capped Gold Nanoparticles

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The Turkevich method, previously described in [19 (link)], was used to synthetize the CH-AuNPs and SC-AuNPs. For the CH-AuNP synthesis, we prepared an acid solution of chitosan (CH, 2% w/w in acetic acid 0.4 M) by dissolving CH (medium molecular weight, 300,000 g/mol, with 75–85% of deacetylation) in 2 mM hydrochloroauric acid solution (HAuCl4), then we homogenized the solution on a magnetic plate at room temperature for 15 min at 80–90 rpm until it changed to the color of red wine [18 (link)]. For the SC-AuNP synthesis, sodium citrate and HAuCl4 were purchased from Sigma-Aldrich, sodium citrate was dissolved in distilled water to obtain a 1% solution, the 1 mM HAuCl4 solution was mixed with sodium citrate and placed in a water bath for 15 min at 100 °C ± 2 °C, to a ratio of 1:1 (HAuCl4/sodium citrate) volume/volume, until it changed to the color of red wine. Finally, the synthesis was allowed to settle at room temperature, and was stored for later use. The CH-AuNPs and SC-AuNPs were diluted 1:1 in RPMI 1640 medium (GIBCO® by Life Technologies). The concentrations were determined based on precursor salt (HACl4) concentration (μM) involved in AuNPs synthesis.
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8

Seed-Mediated Synthesis of Gold Nanorods

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GNRs were synthesized using the seed-mediated growth approach.25 (link),26 (link) In the first step, a seed solution was prepared to reduce 250 µL of HAuCl4 (Sigma Chemical Co., St. Louis, Mo, USA) in 9.75 mL of cetyltrimethylammonium bromide 0.1 M (CTAB) and cold-prepared sodium borohydride (600 µL, 0.01 M) (Sigma Chemical Co., St. Louis, Mo, USA). Seeds were kept at 27 °C for two hours before use. Then, 55 µL of ascorbic acid 0.1 M (Sigma Chemical Co., St. Louis, MO, USA) were added to a growth solution containing 75 µL of AgNO3 0.01 M (Sigma Chemical Co., St. Louis, MO, USA), 9.5 mL of CTAB 0.1 M, and 500 µL of HAuCl4 0.01 M. Next, 250 µL of HCl 0.1 M and finally, 12 µL of the previously prepared seed solution were added. The solution was incubated for 10 minutes at 27 °C before centrifugation at 5900 g for 15 min. The supernatant was then removed, and the pellet was resuspended in Milli-Q water. Vis-NIR absorption spectra were recorded at room temperature using a Perkin Elmer Lambda 25 spectrophotometer. GNRs obtained from synthesis (GNR-CTAB) were observed using a scanning electron microscope with an electronic transmission module (STEM) FEI Inspect F50. The specimens for electron microscopy observation were prepared by dropping GNRs on Formvar carbon-coated copper microgrids (Ted Pella, Inc. Redding, CA, USA), and letting them dry.
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9

Synthesis of Spherical Gold Nanoparticles

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The synthesis of spherical Au NPs was performed following the Turkevich–Frens procedure with some modifications [20 (link)]. Briefly, 15 mg of tetrachloroauric (III) acid (HAuCl4, Sigma-Aldrich, Dorset, UK) was dissolved in MilliQ water to obtain a solution having a concentration of 0.25 mM. Then, 150 mL of a HAuCl4 solution was moved to a reaction flask and heated at 100 °C until boiling under stirring and reflux. Later, 0.1 M of a sodium citrate (10 mL) aqueous solution was quickly added and a change in a color reaction was observed, which became red wine colored. After cooling to room temperature, the reaction product was stored in the dark in a refrigerated room. Subsequently, the solution was transferred into polypropylene tubes and centrifuged at 7500 rpm for about 45 min followed by a washing step using water.
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10

Biosynthesis of Gold Nanoparticles

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Fusarium oxysporum (PTCC 238-21-3) was cultured in sterile Sabouraud dextrose broth (SDB, Merck, Germany) at 27 °C, 150 rpm, for 3 days. The fungal culture medium was centrifuged (5000 rpm for 10 min), and 50g of the mycelia was weighed and incubated in ddH2O at 27 °C, 150 rpm, for 3 days. The fungal suspension was centrifuged (5000 rpm for 10 min), then 150 μl of 1 M HAuCl4 (Sigma Aldrich, USA) solution was added to 150 ml of the achieved supernatant to obtain 1 mmol final concentration of HAuCl4 solution. GNPs production was done by incubating the solution at 35 °C, 220 rpm, for 1 day. The control flask containing 150 ml of ddH2O with 150 μl of 1 molar HAuCl4 was incubated under the above condition (Pourali et al. 2017 (link)).
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