Drug intelligence / Profile preview

ropivacaine + poloxamer 407

Development stage
Unknown
Lead developer
Innocoll Technologies
Modality
Small Molecules, Hydrogel Systems → Drug Delivery Systems
Administration
Infiltration, Local Application
01

Overview

Ropivacaine + poloxamer 407 is a sustained-release, thermosensitive hydrogel formulation of the local anesthetic ropivacaine. It utilizes poloxamer 407, a biocompatible triblock copolymer that exhibits reverse thermal gelation, remaining a liquid at room temperature and transitioning into a semi-solid gel at physiological temperatures. This characteristic allows the formulation to be injected or applied as a liquid into surgical sites, where it forms a drug reservoir that slowly releases ropivacaine over an extended period (typically up to 72 hours). The primary indication is the management of postoperative pain, aiming to provide long-lasting local analgesia and reduce the requirement for systemic opioids. The formulation was notably investigated in clinical trials by Innocoll for applications such as hemorrhoidectomy, though development has primarily focused on the related collagen-based sponge formulation, Xaracoll.

Other names
Ropivacaine-Poloxamer 407 GelRopivacaine-Poloxamer407 GelRopivacaine-Poloxamer-407 GelSustained-release ropivacaine gelRopivacaine thermosensitive hydrogel
02

Targets

SCN1A (Voltage-gated sodium channel protein type 1 subunit alpha)SCN2A (Voltage-gated sodium channel protein type 2 subunit alpha)SCN3A (Sodium channel protein type 3 subunit alpha)SCN4A (Voltage-gated sodium channel protein type 4 subunit alpha)SCN5A (Sodium channel protein type 5 subunit alpha)SCN8A (NaV1.6)SCN9A (Sodium channel protein type 9 subunit alpha)

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