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4 protocols using 1 hexadecyl trimethyl ammonium bromide

1

Synthesis and Characterization of Metal-Doped Silica Nanoparticles

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All chemicals were used without purification. The ammonium hydroxide solution (NH4OH in H2O, 30–33%), methanol (CH3OH, 99.99%), and tetraethyl orthosilicate (TEOS, 99.99%) were obtained from Sigma‐Aldrich (Saint Louis, MO, US). Ethanol (C2H5OH, 99.8%) was purchased from Thermo Fisher Chemical (Waltham, Massachusetts, US). (1‐Hexadecyl) trimethyl ammonium bromide (CTAB, 98%), zinc acetate (Zn(CH3COO)2, 99.98%), tin(II) chloride (99%), and chromium(III) nitrate nonahydrate (Cr(NO3)3·9H2O, 98.5%) were obtained from Alfa Aesar (Haverhill, MA,USA). Gallium oxide (Ga2O3, 99.99%) was procured from Gredmann. Nitric acid (HNO3, 69–70%) was from J. T. Baker (Phillipsburg, NJ, USA). The Keratinocyte Serum‐Free Growth (K‐SFM) and Roswell Park Memorial Institute (RPMI 1640) media were purchased from Thermo Fisher Scientific (Waltham, Massachusetts, US) for cell seeding. The Beas2B normal lung bronchus cells used K‐SFM medium, and A549 and CL1‐5 lung cancer cells were incubated in RPMI 1640 medium. The penicillin–streptomycin–glutamine (PSG) supplement for culture media was purchased from GIBCO (Waltham, MA, USA).
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2

Colorimetric Redox Reaction Assay

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Copper (II) chloride dehydrate (Riedel-de Haën, USA), Iron(II) chloride anhydrous(Alfa Aesar, USA), Hydrogen tetrachloroaurate(III) hydrate(Alfa Aesar, USA), (1-Hexadecyl) trimethylammonium bromide(Alfa Aesar, USA), Hydrazine hydrate(Acros Organics, USA), Poly(styrene-alt-maleic acid) sodium salt solution (PSMA)(Aldrich, USA), L-Ascorbic acid(Sigma-Aldrich, USA), Hydrogen peroxide solution(Sigma, USA), p-Toluenesulfonic Acid, 12% in Acetic Acid (TA) (Acros Organics, USA), N, N-Dimethyl-4-nitrosoaniline (RNO) (Alfa Aesar, USA).
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3

Characterization of Synthesized AuNPs

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Gold(iii) chloride hydrate (99.995%), cysteamine (∼95%), l-ascorbic acid (reagent grade), silver nitrate (99.9999%), sodium borohydrate (99%) and trisodium citrate dihydrate were purchased from Sigma Aldrich. (1-Hexadecyl)trimethylammonium bromide (98%) were purchased from Alfa Aesar.
To characterize the synthesized AuNPs, dynamic light scattering (Zetasizer Nano ZSP, Malvern Panalytical) was used to measure the zeta potential and hydrodynamic radius. UV-vis spectra were measured using a spectrophotometer (Biowave II, WPA) and a fluorometer plate reader (Infinite M200 PRO, Tecan). Images of the well plates were taken using a commercially available CCD camera (Lumix DC-TZ91, Panasonic).
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4

Synthesis of (CrMnFeNiCu)3O4 High-Entropy Oxide

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The HEO sample was synthesized using a surfactant‐assisted hydrothermal method.[18] Equimolar (1 mmol) Fe(NO3)3·9H2O (J. T. Baker, 99%), Ni(NO3)2·6H2O (Alfa Aesar, 98.5%), Mn(NO3)2·6H2O (Alfa Aesar, 98.5%), Cr(NO3)3·9H2O (Alfa Aesar, 98.5%), and Cu(NO3)2·2.5H2O (Alfa Aesar, 98%) were dissolved in 40 mL of deionized water, followed by the addition of 1.25 mmol (1‐hexadecyl)trimethylammonium bromide (Alfa Aesar, 98.5%) as a surfactant. 30 mmol urea (UniRegion Bio‐Tech, 99%) was then added with continuous stirring to form a homogenous solution. The solution was then transferred into a Teflon‐lined stainless steel autoclave for a hydrothermal reaction at 140 °C for 5 h. The precipitate was collected via centrifugation, repeatedly washed with deionized water and ethanol, and then dried at 60 °C in a vacuum oven for 12 h. The resulting material was annealed in air at 900 °C for 2 h to produce (CrMnFeNiCu)3O4 HEO powder.
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