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282 protocols using acetaminophen

1

Acetaminophen Hepatotoxicity in Ex Vivo Perfusion

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Control livers were run for 24 h (n = 5). Acetaminophen-treated livers (n = 6) received doses of Acetaminophen (Sigma-Aldrich Canada, Oakville, ON, Canada) dissolved directly into the perfusate, starting 1 h after beginning perfusion. Acetaminophen was dosed at 30-min intervals up to 12 h, with the dose titrated to avoid excessive methemoglobinemia. Acetaminophen-treated livers were intended to run for 24 h, but were stopped early as necessitated by perfusion parameters and circuit volume. These livers similarly received additives necessary to maintain physiological blood gas parameters. Since we were unable to achieve sufficient toxicity without causing methemoglobinemia, further perfusions were discontinued, which lead to unequal numbers between groups. An additional experimental group treated with carbon tetrachloride (CCl4; Sigma-Aldrich Canada, Oakville, ON, Canada) as the hepatotoxic agent was also attempted, but discontinued after two perfusions, due to circuit and perfusate incompatibility.
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2

Murine CAR Activation and Hepatotoxicity

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Murine CAR agonist 1,4-bis (2-[3,5-dichloropyridyloxy]) benzene (TCPOBOP), referred here as TC, was obtained from Sigma, St. Louis, MO, USA. TC was first dissolved in 100% ethanol at a concentration of 4 mg/ml, followed by dilution in corn oil and stirred overnight to make a final concentration of 2 mg/ml. Thirty-six hours after a single intraperitoneal injection with corn oil or 3 mg/kg TC, WT mice were sacrificed to collect livers. For acetaminophen treatments, WT and DKO mice were fasted overnight, followed by a single intraperitoneal injection with 0.9% saline or 300 mg/kg acetaminophen (Sigma). Another cohort of control and DKO mice were also treated with androstanol (100 mg/kg) 1 h after acetaminophen injection. The mice were then sacrificed to collect liver and blood serum after 1, 6, and 24 h. A 0-h time point was used as controls. WT and DKO mice were injected intraperitoneally once with either 250 mg/kg zoxazolamine (Sigma) alone, or with 100 mg/kg androstanol (Sigma) 3 days before zoxazolamine treatment to inhibit CAR activity. Immediately after zoxazolamine injection, the mice were placed on their backs. The time taken by the mice to regain the righting reflex and start walking was recorded as the paralysis time.
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3

Acetaminophen-Enriched Ensure Plus Meal

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Ensure Plus (Abbott Labs, USA; Per 8 oz [237 mL] bottle consists of total fat [11 g], cholesterol [0.01 g], total carbohydrates [51 g containing 1 g dietary fiber and 22 g sugar), protein [13 g] and various vitamins plus minerals) was used for the MMTT as previously reported34 . Acetaminophen (Sigma-Aldrich, USA) was slowly added to Ensure Plus solution (4 mg/mL) and continuously stirred for 6 h. The prepared meal solution containing Acetaminophen was kept at room temperature (22 °C) and protected from light until being used within 24 h. The meal solution was continuously mixed with a magnetic stir-bar at least 30 min before dosing.
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4

Synthesis of Transition-Metal-Substituted Barium Ferrite Nanomaterials

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The chemicals BaCl2.2H2O, CoCl2.2H2O, and CuCl2.6H2O (reagent grade RG) were purchased from Merck, FeCl3 was bought from Sigma Aldrich, >98% purity citric acid and C6H8O7 from Merck, RG grade propylene glycol (C3H8O2) and glycerin (C3H8O3) were from Merck. NH4OH (RG grade) and acetaminophen (Analytical grade AG) were used as received from Merck. The AG-grade PBS solution (supporting electrolyte) (0.1-M KH2PO4) was purchased from Merck, and the pH was adjusted using 0.1-M KOH (AG grade, Merck) and H3PO4 from Sigma Aldrich at a ratio of 1:1. The solutions were prepared using distilled water. The citrate sol gel method was utilized for the synthesis of the transition-metal-substituted barium ferrite nanomaterials, which were characterized using XRD, SEM, Fourier-transform infrared, and Raman analysis techniques [20 (link)].
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5

Electrochemical Detection of Illicit Drugs

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All chemicals used in this study were of analytical grade and were used as received from the manufacturer without further purification. All solutions used were prepared with ultrapure water (18.2 MΩ, Millipore Simplicity). Cocaine, methamphetamine, MDMA, MMC, PVP where purchased from Cayman Chemicals, while, acetaminophen, benzocaine, K2HPO4, KH2PO4, KCl, H2PtCl6, HCl, HAuCl4, H2SO4, [Fe(CN)6]4-/3-, NaOH, Tween 20 were purchased from Merck. Phosphate buffer saline (PBS) solution of 0.1 M with 0.1 M KCl was used as the supporting electrolyte and it was prepared with K2HPO4 and KH2PO4, adjusted to the mentioned values of pH with either NaOH or HCl.
The electrochemical experiments were performed using an AUTOLAB PGSTAT 302N (EcoChemie, Netherlands) equipped with the associated NOVA 1.10 software. All the SPEs with a silver pseudo reference, a carbon counter electrode and with different working electrodes: graphite-based, graphite-based modified with GPH and MWCNTs, were provided by Metrohm (Spain). The data analysis and the creation of figures were performed using the Origin 8.5 software (OriginLab, United States). For a better visualization, all the SWV voltammograms presented here were baseline-corrected using the moving average filter included in the NOVA 1.10 software (window size 1), without affecting the results.
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6

Electrochemical Analysis of Cephalosporin Antibiotics

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All reagents were of analytical grade and were used as received. All solutions were prepared with ultrapure water (18.2 MΩ, Millipore Simplicity). Cefalexin monohydrate, ceftriaxone sodium salt, cefadroxil monohydrate, cefotaxime sodium salt, cefaclor monohydrate, cefuroxime sodium salt, ceftazidime pentahydrate were provided by Antibiotice SA (Iași, Romania).
Ampicillin trihydrate, monosodium Hexaammineruthenium(III) chloride ([Ru(NH3)6]Cl3), 1,1′-Ferrocenedimethanol, HCl, Na2HPO4, NaH2PO4, NaCl, I3AA were purchased from Merck; K4[Fe(CN)6], K3[Fe(CN)6] and disodium phosphate, sodium dodecyl sulfate and methanol from Sigma-Aldrich (St. Louis, MO, USA), phosphoric acid, acetaminophen and ascorbic acid were purchased from Merck (Whitehouse Station, NJ, USA).
Capsules containing 500 mg cefalexin (Cefalexina Atb® (Antibiotice SA)) and Someș River water collected near Cluj-Napoca, Romania were used for real samples analysis.
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7

Quantifying Oxidative Stress Biomarkers

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Some materials were purchased from Sigma Chemical Co (St Louis, MO, USA), including acetaminophen, (5, 5′-dithiols-(2-nitrobenzoic acid)) (DTNB) and ethylenediaminetetraacetic acid (EDTA). And also remaining components tested were standard laboratory materials, provided primarily from Merck (Germany), including trichloroacetic acid (TCA), 2, 4-dinitrophenylhydrazine (DNPH), guanidine hydrochloride and 2,4,6-tris (2-pyridyl) -s-triazine (TPTZ). It should be noted that all chemicals and reagents used in the experiment, had analytical grade.
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8

Electrochemical Analysis of Pharmaceuticals

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All chemicals used were of analytical grade and used as received without any further purification. All solutions were prepared with deionised water of resistivity not less than 18.2 MΩ cm from a Milli-Q Integral 3 system from Millipore UK (Watford, UK). Hexaamineruthenium (III) chloride (RuHex, 98%), castor oil, potassium ferricyanide (99%), potassium ferrocyanide (98.5–102%), sodium hydroxide (>98%), potassium chloride (99.0–100.5%), acetaminophen (≥99.0%), and phosphate-buffered saline (PBS) tablets were purchased from Merck (Gillingham, UK). (R)-Phenylephrine hydrochloride was purchased from TCI Chemicals (Zwijndrecht, Belgium). Carbon black (Super P®, >99+%) was purchased from Fisher Scientific (Loughborough, UK). Multi-walled carbon nanotubes (MWCNT, 10–30 μm length, 10–20 nm outer diameter) were purchased from Cheap Tubes (VT, USA). Recycled poly(lactic acid) (rPLA) was purchased from Gianeco (Turin, Italy). Commercial conductive PLA/carbon black filament (1.75 mm, ProtoPasta, Vancouver, Canada) was purchased from Farnell (Leeds, UK). Recycled non-conductive PLA filament was produced in-house, as shown previously [28 (link)]. Real samples of pharmaceuticals Max Strength Cold & Flu Capsules (Optipharma), Max Strength Cold & Flue Relief powder (Sainsbury’s), and Cold & Flu Powder (Beechams) were obtained from local convenience stores.
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9

Evaluating Hepatoprotective Agents: A Protocol

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Taurine (2-amino-ethane sulfonic acid) was obtained from Acros (New Jersey, USA). Acetaminophen, thioacetamide, trichloroacetic acid (TCA), 5,5′-dithionitrobenzoic acid (DTNB), thiobarbituric acid (TBA), sodium citrate, sodium hypochlorite solution (5%), ammonium chloride, nicotinamide adenine dinucleotide phosphate (NADPH), phenol, sodium nitroprusside dihydrate, ethylenediamine tetra-acetic acid (EDTA), 4-nitrophenol, phosphoric acid, 2‐amino‐2-hydroxymethyl-propane-1,3-diol-hydrochloride (Tris–HCl), were obtained from Merck (Darmstadt, Germany). Kits for evaluating biomarkers of liver injury, including ALT, LDH, AST, ALP and bilirubin, were obtained from Pars Azmun® (Tehran, Iran). All salts used for preparing buffer solutions were of analytical grade and obtained from Merck (Darmstadt, Germany).
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10

Shungite Electrodes for Electroanalysis

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Standard solutions of heavy metals (1000 mg L−1 Bi3+, Pb2+, Cd2+ and Zn2+) suitable for atomic-absorption spectrometry, ≥99.0% acetaminophen, 99.9% dopamine hydrochloride, sodium dodecyl sulfate, sodium decyl sulfate, sodium octyl sulfate, cetylpyridinium chloride (CPC), polyvinyl chloride (PVC) and tetrahydrofuran (THF) from Merck (Darmstadt, Germany) were used to demonstrate electroanalytical usefulness of shungite electrodes. Sodium hydroxide, 98.5% boric acid, 85% phosphoric acid, glacial acetic acid, di-sodium hydrogen phosphate 12-hydrate, 98.5% sodium dihydrogen phosphate dihydrate and 99% sodium acetate anhydrous from Lach-Ner s.r.o. (Neratovice, Czech Republic) were chosen for preparation of Britton–Robinson buffer (BRB) of 0.1 mol L−1, phosphate buffer (PB) of pH 7 and acetate buffer (AcB) of pH 4.5. All these working solutions were prepared using deionized water with resistivity of 18.3 MΩ cm, which was obtained from the Millipore Milli-Q®® purification unit from Merck (Darmstadt, Germany).
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