Drug intelligence / Profile preview

liposome bupivacaine (bupivacaine liposome) (Pacira BioSciences)

Development stage
Approved
Lead developer
Pacira BioSciences
Modality
Small Molecules, Lipid-based Nanoparticles → Nanoparticles → Drug Delivery Systems
Administration
Percutaneous, Parenteral
01

Overview

Liposome bupivacaine is an extended-release formulation of the amide-type local anesthetic bupivacaine, utilizing the DepoFoam multivesicular liposomal delivery technology. Developed by Pacira BioSciences, it is designed to provide prolonged postsurgical analgesia by slowly releasing bupivacaine over an extended period (up to 72 hours), thereby reducing the need for systemic opioids. The drug works by binding to the intracellular portion of voltage-gated sodium channels, blocking sodium influx and preventing the generation and conduction of nerve impulses. It is primarily administered via local infiltration, field blocks, or interscalene brachial plexus nerve blocks for various surgical procedures.

Brand names
Exparel
Other names
liposomal bupivacainebupivacaine liposome injectable suspensionliposome bupivacaine
02

Targets

SCN5A (Sodium channel protein type 5 subunit alpha)PTGER1 (Prostaglandin E Receptor 1)CaV (Voltage-gated calcium channel protein complex)Kir (Inward-rectifier potassium channels)NaV (Voltage-gated sodium channels)

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