Drug intelligence / Profile preview

liposomal bupivacaine + bupivacaine

Development stage
Phase 4
Lead developer
Pacira BioSciences
Modality
Small Molecules, Nanoparticles → Drug Delivery Systems
Administration
Local Infiltration, Nerve Block, Perineural Injection, Intra-articular Injection
01

Overview

This is a combination of two local anesthetic formulations—liposomal bupivacaine and conventional bupivacaine (bupivacaine hydrochloride). Liposomal bupivacaine is an extended-release formulation in which the active drug is encapsulated within multivesicular liposomes, allowing for prolonged release and sustained analgesic effect at the site of administration. Conventional bupivacaine provides rapid onset but shorter duration of action. The combination aims to provide both immediate and extended postoperative pain control by leveraging the fast onset of conventional bupivacaine with the prolonged effect of liposomal bupivacaine. Both act as sodium channel blockers, inhibiting nerve impulse transmission to produce local or regional anesthesia or analgesia, primarily used in surgical settings for postsurgical pain management[1][4][6][9].

Brand names
Exparel (for bupivacaine liposome)
Other names
bupivacaine liposomebupivacaine liposomal suspensionbupivacaine
02

Targets

KATP channel (ATP-sensitive potassium channel)SCN2A (Voltage-gated sodium channel protein type 2 subunit alpha)SCN5A (Sodium channel protein type 5 subunit alpha)SCN9A (Sodium channel protein type 9 subunit alpha)SCN1A (Voltage-gated sodium channel protein type 1 subunit alpha)

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