Drug intelligence / Profile preview

articaine + triamcinolone

Development stage
Preclinical
Lead developer
Irkutsk State Medical University
Modality
Small Molecules
Administration
Percutaneous
01

Overview

Articaine + triamcinolone is a combination drug regimen consisting of the amide local anesthetic articaine and the synthetic corticosteroid triamcinolone (administered as triamcinolone acetonide). It is being investigated by Irkutsk State Medical University for the treatment of refractory pudendal neuralgia. The combination is administered as a single ultrasound-guided transperineal pudendal nerve block. Articaine acts by reversibly binding to and blocking voltage-gated sodium channels, thereby inhibiting sodium influx and preventing nerve impulse conduction to provide local anesthesia. Triamcinolone acetonide acts as a glucocorticoid receptor agonist, reducing perineural inflammation and edema. This synergistic combination aims to provide both immediate pain relief and long-term reduction of inflammatory pain in patients with pudendal neuralgia who are refractory to conservative therapy.

Other names
articaine and triamcinolonearticaine hydrochloride + triamcinolone acetonidearticaine hydrochloride and triamcinolone acetonidetriamcinolone + articainetriamcinolone and articaine
02

Targets

GR (Glucocorticoid receptor)NaV alpha (Voltage-gated sodium channel alpha subunit family)

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