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19 protocols using phthalic acid

1

Mushroom Tyrosinase Inhibition Assay

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Mushroom tyrosinase (EC 1.14.18.1), alpha-melanocyte stimulating hormone (α-MSH), 3-isobutyl-1-methylxanthine (IBMX), l-tyrosine, l-3,4-dihydroxyphenylalanine (l-DOPA), dimethyl sulfoxide (DMSO), kojic acid, phthalic acid, and trans-cinnamic acid were purchased from Sigma-Aldrich (St. Louis, MO, USA). Dulbecco’s modified Eagle’s medium (DMEM), fetal bovine serum (FBS), streptomycin, and amphotericin were purchased from WELGENE Inc. (Gyeongsan-si, South Korea). All other reagents were purchased from Sigma-Aldrich.
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2

Electrochemical Characterization of Pharmaceutical Compounds

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Copper(II) Carbonate Basic (>95%), Potassium Hydrogen Phthalate (>99.95%), Phthalic Acid (>98%), Sodium Hydroxide (>99.5%), D-Glucose, Paracetamol, Dopamine Hydrochloride (all—European Pharmacopoeia (EP) Reference Standard), PBS buffer, Nafion (5 wt% solution) and Ammonia (32% aqueous solution) were purchased from Sigma-Aldrich Ltd. (Darmstadt, Germany), Sodium Hydrogen Phthalate (> 99%) was supplied by Advanced Technology & Industrial Co., Ltd. (Hong Kong, China). All the reagents were used without further purification.
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3

Purification and Characterization of Organic Compounds

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All deionized water was obtained from a Milli-Q2 system and exhibited a specific resistance of at least 18 MΩ cm. Methanol (99.8%) and 1-pentanol (≥99%) were obtained from Sigma-Aldrich (Milwaukee, WI), as were tetraoctylammonium bromide (TOABr) (98%), tetraoctylammonium chloride (TOACl) (≥97%), menthol (99%), and decanoic acid (98%). All were employed without further purification. Concentrated hydrochloric acid (Optima™ grade), acetone (Optima™ grade), 1-propanol (HPLC grade), 1-butanol (HPLC grade), and hexane (HPLC grade), were purchased from Fisher Scientific (Pittsburgh, PA), while standard (0.100 N) sodium hydroxide solution was obtained from Ricca Chemical Company (Batesville, IN). Ethanol (≥99.5%) was purchased from Decon Labs Inc. (King of Prussia, PA). For liquid scintillation counting (LSC), Ultima Gold™ (Perkin Elmer Corp., Waltham, MA) LS cocktail was employed.
With the exception of phenol (Moravek Biochemicals, Brea, CA) and toluene (American Radiolabeled Chemicals, St. Louis, MO), all 14C-labeled reagents (aniline, benzoic acid, chlorobenzene, phthalic acid, p-toluic acid, and salicylic acid) were obtained from Sigma-Aldrich.
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4

Seed Germination and Phytochemical Analysis of Watermelon Varieties

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Waste onion bulbs were obtained from local growers and supermarkets. The seeds of diploid (Riverside) and triploid (Maxima) watermelon varieties obtained from Origene Seeds Ltd., Giv’aat Brener, Israel. Abscisic acid (ABA), 2,2-diphenyl-1-picrylhydrazyl (DPPH), gibberellic acid (GA), jasmonic acid (JA), potassium permanganate (KMnO4), salicylic acid (SA), zeatin (ZA), and phenolic acids (4-hydroxy-benzoic acid, caffeic acid, phthalic acid, protocatechuic acid, and trans-cinnamic acid) were procured from Sigma Aldrich (St. Louis, MO, USA). 12-oxo phytodienoic acid (OPDA) purchased from Cayman Chemical, Ann Arbor, MI, USA. 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid (ABTS) was obtained from Chem-Impex Int’l. Inc. (Bensenville, IL, USA).
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5

Luria-Bertani Broth (LB) Preparation

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Chemicals for the Luria-Bertani Broth (LB) culture medium were obtained from Difco (Lawrence, Kansas, USA). (NH4)2SO4, KH2PO4, CaCl2•7H2O, MgSO4•7H2O, Na2HPO4 and FeSO4•7H2O, BaP, pyrene, anthracene, phenanthrene, naphthalene, phthalic acid, salicylic acid, catechol; palmitic, oleic and stearic acids, were purchased from Sigma-Aldrich (St. Louis, MO, USA). Luria-Bertani Broth (LB) was purchased from Difco (Lawrence, Kansas, USA). All the chemicals were of analytical grades.
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6

GC-MS Analysis of Phenolic Compounds

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Methanol (MeOH), chloroform (CHCl3), n-hexane, and acetonitrile were obtained from Merck (Darmstadt, Germany). Methoxyamine hydrochloride, N-methyl-N-(trimethylsilyl) trifluoroacetamide (MSTFA), pyridine, normal alkane standards (C7–C30), isopentanol, ribitol, and standards of phenolic compounds (including apigenin, isorhamnetin, naringenin, hyperoside, luteolin, quercetin, quercitrin, myricetin, caffeic acid, ferulic acid, chlorogenic acid, p-coumaric acid, protocatechuic acid, resveratrol, and phthalic acid) were supplied by Sigma-Aldrich (St. Louis, Missouri, USA).
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7

Phthalate and Alcohol Compound Preparation

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Benzyl butyl phthalate (BBP), monobenzyl phthalate (MBzP), mono-n-butyl phthalate (MBP), benzyl alcohol, 1-butanol, benzaldehyde, butanal, benzoic acid (BA), butyric acid, phthalic acid (PA), protocatechuic acid (PCA), and other phthalate diesters were purchased from Sigma-Aldrich GmbH (Germany). Catechol was purchased from Merck (Germany). Methanol, chloroform, and ethyl acetate, both analytical and HPLC grade, were purchased from Merck (India). All other chemicals and reagents used in this study were of analytical grade and used without further purification.
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8

Phthalic Acid-Triethylenediamine Hexahydrate Nanoparticles

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Phthalic acid and triethylenediamine hexahydrate were obtained from Sigma–Aldrich and used as received. All reagents were used as received without further purification. Deionized water was used throughout the experiment. Fourier transform infrared spectroscopy (FT-IR) was performed on an FT-IR Nicolet 380 spectrometer. Transmission electron microscopy (TEM) observations were performed on Tecnai G2 F20 S-TWIN. Fluorescence emission spectra were obtained using a FluoroMax-4 Spectrofluorophotometer (HORIBA JobinYvon) at 298 K. The time-resolved fluorospectroscopy was performed using an FLS 920 spectrometer. HeLa cells lines were purchased from Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences.
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9

Leachate characterization and analysis

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Leachate was prepared using DEP (>98%), phthalic acid (>98%), phthalic anhydride (>99%), 4-hydroxy phthalic acid (>98%) (Sigma Aldrich, USA), potassium hydrogen phthalate (KHP), glucose (C6H12O6), ammonium sulfate ((NH4)2SO4), ammonium chloride (NH4Cl), copper sulfate (CuSO4), lead nitrate (Pb(NO3)2), nickel sulfate (NiSO4), potassium dichromate (K2Cr2O7), manganese sulfate (MnSO4), zinc sulfate (ZnSO4), propionic acid (C3H6O2), pentanoic acid (C5H10O2), and hexanoic acid (C6H12O2) (Holland Moran, Israel). Analytical grade H2O2 (30% w/w) was obtained from Merck Chemicals (USA). Stock solutions were prepared by dissolving each compound in deionized water (Direct-Q3 UV System, Millipore, France). COD test kits with a measuring range of 0 to 15,000 mg/L O2 were purchased from Lavibond (England), and were based on the dichromate method and determination in a Hach spectrophotometer. The UV absorbance coefficients of the samples with different H2O2 concentrations were measured using a UV-visible spectrophotometer (Varian, Cary 100BIO, Australia). Spectra were collected in quartz cuvettes using a wavelength range of 200–800 nm.
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10

Tyrosinase-Inhibitory Assay Protocol

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Mushroom tyrosinase (EC 1.14.18.1), α-melanocyte-stimulating hormone (α-MSH), 3-isobutyl-1-methylxanthine (IBMX), l-tyrosine, l-3,4-dihydroxyphenylalanine (l-DOPA), dimethyl sulfoxide (DMSO), kojic acid, phthalic acid and trans-cinnamic acid were acquired from Sigma-Aldrich (St. Louis, MO, USA). Dulbecco’s modified Eagle’s medium (DMEM), fetal bovine serum (FBS), penicillin-streptomycin, 0.25% trypsin-ethylenediaminetetraacetic acid (EDTA) and amphotericin were purchased from WELGENE Inc. (Gyeongsan-si, South Korea). All other reagents were purchased from Sigma-Aldrich. All other chemicals and solvents were purchased from Merck (Frnakfurt Str., Darmstadt, Germany), Fluka (St. Louis, Mo, USA) and Sigma-Aldrich unless otherwise stated.
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