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BIOLOGICAL INFO
Solubility:
DMSO: 65mg/mL; H2O: 23mg/mL; EtOH: 65mg/mL
Application(s):
Sodium channel blocker
Form:
HCl salt
REVIEW A local anaesthetic drug belonging to the amino amide group. Bupivacaine binds to the intracellular portion of sodium channels and blocks sodium influx into nerve cells, which prevents depolarization.
REFERENCES
[1]
Partownavid P, Umar S, Li J, Rahman S, Eghbali M (2012). Fatty-acid oxidation and calcium homeostasis are involved in the rescue of bupivacaine-induced cardiotoxicity by lipid emulsion in rats. Crit Care Med. 40(8):2431-7. PMID 22647409.
[2]
Gurney MA, Rysnik M, Comerford EJ, Cripps PJ, Iff I (2012). Intra-articular morphine, bupivacaine or no treatment for postoperative analgesia following unilateral elbow joint arthroscopy. J Small Anim Pract. 53(7):387-92. PMID 22712686.
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All batches backed with full quality assurance.
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All products are for research and development use only, not for any other uses, and must be handled by technically-qualified persons.
These products are explicitly not intended to be used in foods and/or cosmetics and/or drugs (human and veterinary) and/or consumer products and/or biocides and/or pesticides of any kind unless explicitly stated otherwise.
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