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49 protocols using quinine sulfate

1

ssDNA Aptamer Design for Sensing

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Sodium hydroxide, ethylenediamine, phosphate salt buffer, citric acid, (98%, suitable for fluorescence), and hydrogen tetrachloroaurate(III) hydrate were obtained from Merck (≥ 99%, Merck Co., Darmstadt, Germany). IL-6 and quinine sulfate were purchased from Sigma-Aldrich (Sigma-Aldrich Co., Saint Louis, Missouri, USA). Two sequences of single-strand DNA aptamers (Table 1) were designed based on the previous studies [28 (link)] and synthesized by DynaBio and Tacapo Zist Company (Iran). The reagents and chemicals were applied as received with no purification.

The sequences of the ssDNA aptamer

Sample nameSequence (5′-3′)
1SH-CTTCCAACGCTCGTATTGTCAGTCTTTAGT-3′
2SH-(CH2)6-TGGTGGATGGCGCAGTCGGCGACAA-3′
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2

Synthesis and Characterization of Novel Photosensitizers

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The known phenothiazine and anthracene compounds like C5-PTZ, C5-PTZA, and ANTCN were synthesized using reported procedures.15,16 (link)C5-PTZCN, C5-PTZDCA, and ANTDCA are the compounds that were newly synthesized. Their structures were verified by FT-IR, LCMS (Liquid Chromatography Mass Spectrometry)/HRMS (High-Resolution Mass Spectrometry), and 1H and 13C NMR data (see ESI; pages (3–6) and Fig. (S11–S16)). PTZ, ANT, ANTA, and BSA were procured from Alfa-Aesar and Sigma Aldrich. They were taken into use as received. BSA protein concentration was kept constant at 5 μM for all measurements. HEPES buffer was bought from SRL, India. H2SO4 and NaOH were procured from SDFCL, India, and SRL, India, respectively. Quinine sulfate was obtained from Sigma Aldrich. Spectral grade tetrabutylammonium perchlorate (TBAP) and MeCN were purchased from TCI, India.
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3

Anticancer Potential of Terminalia Chebula

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Terminalia Chebula fruits were collected from Tamil Nadu, India. Aqueous ammonia (NH4OH, 25%) was purchased from Sigma-Aldrich, Republic of Korea. Phosphate-buffered saline (PBS), N-(2-hydroxyethyl)piperazine-N’-(2-ethane sulfonic acid) (HEPES), p-formaldehyde, quinine sulfate, and dimethyl sulfoxide (DMSO) were purchased from Sigma-Aldrich, Seoul, Republic of Korea. 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) was purchased from Generay Biotech, Shanghai, China. HCT-116 human colon cancer cells were purchased from ATCC, CCL-247, Manassas, VA, USA. All the chemicals were used as purchased, and distilled water was used throughout this study.
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4

Alkaloid and Phenolic Compound Analysis

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Water, LC–MS-grade methanol, and eluent-additive LC–MS ultra-ammonium formate (NH4HCO2) were purchased from Fluka Analytical (St. Louis, MO, USA).
Alkaloid standards such as chelidonine (purity ≥ 95%), sanguinarine (purity ≥ 90%), chelerythrine (purity ≥ 90%), and berberine (purity ≥ 95%) were purchased from Extrasynthese (France). Coptisine (purity ≥ 98%), p-coumaric acid, tannic acid, salicylic acid, chlorogenic acid, vanillic acid, trans-caffeic acid, vanillin, rosmarinic acid, quinine sulfate, and quercetin were purchased from Sigma (St. Louis, MO, USA).
Water was deionized and purified by ULTRAPURE Millipore Direct-QVR 3UV-R (Merck, Darmstadt, Germany).
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5

Vancomycin Assay and Purification

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Vancomycin (Assay 99.9%) pure powder was obtained as a gift from Egy pharma (Nasr City, Cairo, Egypt). Aconitic acid, 4-dimethylaminobenzaldehyde, phosphoric acid, acetic acid, boric acid, sodium hydroxide, cobalt chloride, and quinine sulfate were purchased from Sigma Aldrich (Steinheim, Germany). All chemicals and reagents were of analytical reagent grade and were used as received without further purification. Double distilled water was purified using a Milli-Q Plus Water Purification System (Millipore, Billerica, MA, USA).
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6

Cytotoxicity Evaluation of Pharmaceutical Compounds

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Glycine and quinine sulfate (98%, suitable for fluorescence) were purchased from Sigma (New York, NY, USA). Iodixanol was purchased from Hengrui Pharmaceutical Co., Ltd (Lianyungang, Jiangsu, People’s Republic of China). 3-(4,5-Dimethyl-thiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium (MTS) was purchased from Promega (CellTiter Aqueous One Solution cell proliferation Assay kit, Madison, WI, USA). NaH2PO4, Na2HPO4, and H2SO4 were obtained from Guangfu Fine Chemical Research Institute (Nankai, Tianjin, People’s Republic of China). Fetal bovine serum and Dulbecco’s Minimum Essential Medium (DMEM) were purchased from Invitrogen China Limited (Shanghai, People’s Republic of China). All chemicals were of analytical grade and were used without further purification.
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7

Characterization of Oil Palm EFBs

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CMC of oil palm empty fruit bunches (EFBs) were purchased from Waris Nove Company, Malaysia. Polyethylene glycol (M.W. 400) and quinine sulfate were obtained from Sigma-Aldrich (USA). Deionized water (DI) was used throughout all the experiments. All the chemicals used were of analytical grade and used as received without further modification.
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8

Antioxidant Evaluation of CND Purification

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Citric acid (CA), boric acid (BA), ethylenediamine
(EDA), phosphoric acid (PA), quinine sulfate (QS), sulfuric acid (SA),
2,2-diphenyl-1-picrylhydrazyl (DPPH), and methanol were purchased
from Sigma-Aldrich Chemie GmbH (Munich, Germany) and were used as
received. All aqueous solutions were prepared using fresh deionized
water. Dialysis bags were purchased from Sigma-Aldrich Chemie GmbH
(Munich, Germany) and used for CND purification.
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9

Lignans Purification and Characterization

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d-(+)-glucose, d-(−)-fructose, and quinine sulfate were purchased from Sigma-Aldrich (Saint-Quentin-Fallavier, France). Ultrapure water (Milli-Q purification system, Millipore, France) and HPLC grade solvent (acetonitrile, ethanol, ethyl acetate, n-heptane, methanol, and propan-2-ol; VWR International, Pessac, France) were used for sample preparation and lignan purification. acetonitrile (ACN) and water used for chromatographic separation were LC-MS grade and were purchased from Fisher Chemical (Illkirch, France). Lignans were isolated as previously described by Marchal et al. [26 (link)].
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10

Fluorescent Probe Characterization for Analytical Applications

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All three fluorophores were commercially available and purchased from Sigma Aldrich. fluorescein for fluorescence, free acid (46955 SIGMA), quinine sulfate, United States Pharmacopeia (USP) reference standard (1597005 USP), and GFP from jellyfish Aequorea victoria, recombinant expressed in E. coli (11814524001 ROCHE). The structural formulas of fluorescein and quinine sulfate are shown in Fig. 1. GFP is composed of 238 amino acid residues, and its structural formula is not shown here (see [37 (link)] for more information about the structure and composition of GFP). Ethanol and methanol of spectrophotometric grade, as well as 1 M sulfuric acid (H2SO4) were used as solvents for fluorescein, while quinine sulfate was only dissolved in H2SO4. The GFP was purchased and used in a solution form of 1 mg/ml in 5 mM Tris-HCl, 5 mM EDTA, pH 8.0. fluorescein and quinine sulfate were prepared in concentrations of 10− 3 M, 10− 4 M and 10− 5 M for all solvents. Samples were prepared by placing a droplet onto a microscope slide and covered by a 0.17 mm thick glass. All measurements were performed in room temperature (20C).

The structural formulas of fluorescein (a) and quinine sulfate (b) (from Sigma Aldrich product catalogue)

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