3% MEPIVICAINE | dental lab equipments, dental supply, dental products, dental health products, dental supplies, dental supplies near me, dental supply companies, dental cleaning tools, dental tools for sale, dental cleaning, dental deep cleaning, dental cleaning near me, dental laboratory equipments, dental equipments manufacturers, dental equipment, dental tools

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  • 3% MEPIVICAINE | dental lab equipments, dental supply, dental products, dental health products, dental supplies, dental supplies near me, dental supply companies, dental cleaning tools, dental tools for sale, dental cleaning, dental deep cleaning, dental
  • 3% MEPIVICAINE | dental lab equipments, dental supply, dental products, dental health products, dental supplies, dental supplies near me, dental supply companies, dental cleaning tools, dental tools for sale, dental cleaning, dental deep cleaning, dental

3% MEPIVICAINE - PLAIN SKU:101-mp3

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$42.95

Availability: In stock

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Qty: 50/Bx

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MEPIVICAINE 3% - Plain Mepivacaine stabilizes the neuronal membrane and prevents the initiation and transmission of nerve impulses, thereby effecting local anesthesia. Mepivacaine is rapidly metabolized, with only a small percentage of the anesthetic (5 to 10 percent) being excreted unchanged in the urine. Mepivacaine because of its amide structure, is not detoxified by the circulating plasma esterases. The liver is the principal site of metabolism, with over 50 percent of the administered dose being excreted into the bile as metabolites. Most of the metabolized Mepivacaine is probably resorbed in the intestine and then excreted into the urine since only a small percentage is found in the feces. The principal route of excretion is via the kidney. Most of the anesthetic and its metabolites are eliminated within 30 hours. It has been shown that hydroxylation and N-demethylation, which are detoxification reactions, play important roles in the metabolism of the anesthetic. Three metabolites of Mepivacaine have been identified from adult humans: two phenols, which are excreted almost exclusively as their glucuronide conjugates, and the N-demethylated compound (2', 6' - pipecoloxylidide).

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