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bupivacaine(intraperitoneally)

Ain Shams University · FDA-approved active Small molecule

Bupivacaine blocks sodium channels in nerve cell membranes, preventing the initiation and propagation of action potentials to produce local anesthesia.

Bupivacaine blocks sodium channels in nerve cell membranes, preventing the initiation and propagation of action potentials to produce local anesthesia. Used for Local anesthesia and analgesia for intra-abdominal procedures via intraperitoneal administration.

At a glance

Generic namebupivacaine(intraperitoneally)
SponsorAin Shams University
Drug classLocal anesthetic (amide class)
TargetVoltage-gated sodium channels
ModalitySmall molecule
Therapeutic areaAnesthesia / Pain Management
PhaseFDA-approved

Mechanism of action

As a long-acting amide local anesthetic, bupivacaine reversibly inhibits sodium influx through voltage-gated sodium channels in nerve fibers, thereby stabilizing the neuronal membrane and preventing depolarization. When administered intraperitoneally, it anesthetizes visceral nerves and peritoneal tissues to reduce pain during or after abdominal procedures. The intraperitoneally route allows direct contact with peritoneal surfaces and visceral innervation.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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