Drug intelligence / Profile preview

bupivacaine + fentanyl (Mansoura University)

Development stage
Unknown
Lead developer
Mansoura University
Modality
Small Molecules
Administration
Epidural
01

Overview

This specific epidural analgesia regimen, utilized in clinical research at Mansoura University, consists of a combination of the amide-type local anesthetic bupivacaine (0.125%) and the synthetic opioid fentanyl (2 μg/ml). It is administered via continuous epidural infusion at a rate of 8-15 ml/hr to provide pain relief during normal labor. Bupivacaine acts by binding to the intracellular portion of voltage-gated sodium channels, blocking sodium influx and inhibiting the propagation of action potentials in nerve fibers. Fentanyl complements this by acting as a potent agonist at mu-opioid receptors in the central nervous system, particularly within the substantia gelatinosa of the spinal cord, thereby modulating pain transmission and providing regional analgesia.

Other names
Epidural analgesiaBupivacaine-fentanyl epiduralContinuous epidural analgesia
02

Targets

SCN2A (Voltage-gated sodium channel protein type 2 subunit alpha)MOR (Mu opioid receptor)

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