Drug intelligence / Profile preview

nalbuphine + ropivacaine + lidocaine

Development stage
Unknown
Lead developer
Zunyi Medical University Affiliated Hospital
Modality
Small Molecules
Administration
Epidural
01

Overview

This combination drug is an analgesic cocktail administered via thoracic epidural anesthesia (TEA) for the management of severe acute pancreatitis (SAP). Developed and studied by the Affiliated Hospital of Zunyi Medical University, the formulation combines nalbuphine, a mixed opioid agonist-antagonist, with the local anesthetics ropivacaine and lidocaine. Nalbuphine acts as an agonist at kappa-opioid receptors and an antagonist at mu-opioid receptors, providing potent analgesia while minimizing common opioid side effects like respiratory depression and pruritus. Ropivacaine and lidocaine function as sodium channel blockers to inhibit nerve conduction. In the context of SAP, this combination is intended not only for pain relief but also to improve pancreatic microcirculation and mitigate the systemic inflammatory response by inhibiting sympathetic nerve activity through epidural blockade.

Other names
nalbuphine + ropivacaine + lidocaine mixturenalbuphine-ropivacaine-lidocaine cocktailnalbuphine + ropivacaine + lidocaine solution
02

Targets

NaV (Voltage-gated sodium channels)KOR (Kappa opioid receptor)MOR (Mu opioid receptor)

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