(–)-Cotinine, 1-hydroxypyrene, nicotine hydrogen bitartrate, sodium acetate, potassium cyanide, chloramine, barbituric acid, and β-glucuronidase/arylsulfatase were obtained from Sigma-Aldrich (St. Louis, MO, USA). Methanol was purchased from Merck (Darmstadt, Germany). All reagents used in this study were of analytical grade. The white-fleshed fruits of Prunus persica (L.) Batsch (Family Rosaceae; peaches) were purchased at the Kyeonggi Dong-Boo Fruit Agriculture Co. (Incheon, Korea), where a voucher specimen (PE20060801) has been deposited.
Nicotine hydrogen bitartrate
Manufactured by Merck Group
Sourced in United States
Nicotine hydrogen bitartrate is a salt compound used in laboratory settings. It serves as a chemical reagent and is commonly used as a precursor in the synthesis of various nicotine-based compounds. The core function of this product is to provide a consistent and reliable source of nicotine for research and development purposes.
Automatically generated - may contain errors
Lab products found in correlation
Potassium cyanide, by Merck Group (1 mentions)
Barbituric acid, by Merck Group (1 mentions)
1 hydroxypyrene, by Merck Group (1 mentions)
β glucuronidase arylsulfatase, by Merck Group (1 mentions)
Sodium acetate, by Merck Group (1 mentions)
Cotinine, by Merck Group (1 mentions)
Methanol, by Merck Group (1 mentions)
Gts 21, by Merck Group (1 mentions)
Dihydro β erythroidine hydrobromide dhβe, by Bio-Techne (1 mentions)
3 protocols using nicotine hydrogen bitartrate
1
Metabolic Profiling of Peach Extracts
2
Nicotine and Nicotinic Receptor Ligands
3
Nicotine-Induced Oxidative Stress Attenuation
Check if the same lab product or an alternative is used in the 5 most similar protocols
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Nicotine hydrogen bitartrate (Sigma Aldrich Co., St. Louis, Mo) was dissolved in 0.9% saline and neutralised to PH 7.2 with NaOH. The treatment was given at a dose of 2.5 mg/kg subcutaneously once daily for 5 days per week/18 weeks [11] . Selection of dose of nicotine was constructed on the previous studies and doses commonly used by other laboratories [11] and the selection of time schedule was based on that more than 20 days of nicotine injection leads to oxidative stress and tissue injury [38, 39] .
Red onion was used because of its reported high antioxidant potentials [32] . It was dressed and frozen (4°C). 100 mL of distilled water per 100 g of onion were added and crushed in a mixing machine. The resultant mixture was squeezed and filtered [32] . The onion extract was given orally once/day in a dose of 50 mg/kg [44] . This dose is nontoxic and has few ill effects [44] .
The NS oil was given at a daily dose of 0.1 g/kg orally. The dosage was chosen based on human NS oil consumption which is equal to 2 g/day; 0.1 g/kg/day was accepted as the corresponding dose in the rat [12] .
All chemicals were purchased from Cap Pharma Company, Egypt.
Red onion was used because of its reported high antioxidant potentials [32] . It was dressed and frozen (4°C). 100 mL of distilled water per 100 g of onion were added and crushed in a mixing machine. The resultant mixture was squeezed and filtered [32] . The onion extract was given orally once/day in a dose of 50 mg/kg [44] . This dose is nontoxic and has few ill effects [44] .
The NS oil was given at a daily dose of 0.1 g/kg orally. The dosage was chosen based on human NS oil consumption which is equal to 2 g/day; 0.1 g/kg/day was accepted as the corresponding dose in the rat [12] .
All chemicals were purchased from Cap Pharma Company, Egypt.
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