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3 protocols using mepivacaine

1

Antioxidant Activity of Amide Local Anesthetics

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The amide local anesthetics (mepivacaine, lidocaine, bupivacaine, and dibucaine, Fig. 1) were purchased from Sigma-Aldrich (St. Louis, MO). tert-Butyl hydroperoxide and 2,2-diphenyl-1-picrylhydrazyl (DPPH) were purchased from Sigma-Aldrich. 5,5-Dimethyl-1-pyrroline-N-oxide (DMPO), N-methyl-3-(1-methyl-2-hydroxy-2-nitrosohydrazino)-1-propanamine (NOC7), and 2-(4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl 3-oxide (carboxy-PTIO) were purchased from Dojindo (Kumamoto, Japan). 2-(5,5-Dimethyl-2-oxo-2λ5-[1,3,2]dioxaphosphinan-2-yl)-2-methyl-3,4-dihydro-2H-pyrrole 1-oxide (CYPMPO) was purchased from Mikuni Pharmaceutical Industrial (Osaka, Japan). Sodium ascorbate, dimethyl sulfoxide, and hydrogen peroxide were purchased from Wako Pure Chemical Industries (Osaka, Japan). 2,2'-Azobis (2-amidinopropane) dihydrochloride (AAPH), Acid Red 94, and 4-hydroxy-2,2,6,6-tetramethylpiperidine (4-OH TEMP) were purchased from Tokyo Chemical Industry (Tokyo, Japan). Other reagents used were of the highest commercially available quality.
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2

Antioxidant and Cytoprotective Compounds

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Lidocaine, mepivacaine, bupivacaine, NAC, and (±)-6-Hydroxy-2,5,7,8-tetramethylchromane-2-carboxylic acid (Trolox) were obtained from Sigma-Aldrich (St. Louis, MO, USA), teprenone (geranylgeranylacetone, GGA) was obtained from Wako Pure Chemical Industries (Osaka, Japan), and recombinant human TRX (rhTRX) was obtained from Oriental Yeast Co., Ltd. (Tokyo, Japan). GGA and Trolox were dissolved in absolute ethanol, while bupivacaine and NAC were dissolved in H2O, and rhTRX was dissolved in citric acid. Rotenone, oligomycin and antimycin A were obtained from Abcam, Inc. (Cambridge, MA, USA).
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3

Mepivacaine Quantification in Plasma

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All solutions were prepared using reagent grade chemicals and double distilled water. Mepivacaine standard solution (2830.0 μg mL -1 , 1.0 × 10 -2 mol L -1 ) was prepared daily by dissolving 0.2830 g of Mepivacaine hydrochloride (Sigma-Aldrich, Germany) in water in a 100.0-mL volumetric flask. Operational solutions were prepared by appropriate dilution of the stock solution when used. Standard solution of Ru(phen) 3 2+ (0.01 mol L -1 ) was prepared by dissolving 0.3640 g of dichlorotris(1,10-phenanthroline)ruthenium(II) hydrate (Sigma-Aldrich, Germany) in water in a 50.0 mL volumetric flask. In order to prepare each one of Ce(IV) solutions with concentrations between 1.0 × 10 -3 and 2.0 × 10 -2 mol L -1 , the calculated amount of ceric ammonium nitrate (Riedel-de Haën, Germany) was dissolved in appropriate volume of H 2 SO 4 solution (1.0 mol L -1 ) and then, the solution was further diluted with distilled water in a 100.0-mL volumetric flask. Final concentration of H 2 SO 4 in the Ce(IV) solutions was between 0.03 and 0.20 mol L -1 . Methanol was purchased from Caledon, Canada. The plasma was obtained from patients not exposed to any drug for at least 72 h (blank plasma) and was kindly supplied by health centre of Gorgan, Iran. Mepivacaine injections were purchased from local drugstores.
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