Safety Evaluation of EXPAREL (DepoFoam Bupivacaine) Administered by Repeated Subcutaneous Injection in Rabbits and Dogs: Species Comparison

Author:

Richard Brigitte M.1,Rickert Douglas E.2,Newton Paul E.3,Ott Laura R.3,Haan Dean3,Brubaker Abram N.3,Cole Phaedra I.3,Ross Paul E.3,Rebelatto Marlon C.3,Nelson Keith G.3

Affiliation:

1. Department of Toxicology, Clinical Research & Drug Safety Assessment, Pacira Pharmaceuticals Inc., San Diego, CA 92121, USA

2. Pharmacokinetics, Mill Ridge Road, Raleigh, NC 27613, USA

3. Toxicology Division, MPI Research Laboratories, North Main Street, Mattawan, MI 49071, USA

Abstract

EXPAREL (bupivacaine extended-release liposome injection), DepoFoam bupivacaine, is in development for prolonged postsurgical analgesia. Repeat-dose toxicity studies were conducted in rabbits and dogs to compare the potential local and systemic toxicities of EXPAREL and bupivacaine HCl (Bsol), and the reversibility of any effects. Dogs tolerated much larger doses than rabbits. EXPAREL-related minimal-to-moderate granulomatous inflammation was noted at the injection sites. In recovery animals, the granulomatous inflammation was observed less frequently and was characterized by an increased number of multinucleated giant cells. These effects were considered a normal response to liposomes and nonadverse. Rabbits are more sensitive than dogs. In rabbits, convulsions were noted with EXPAREL and more frequently with Bsol; a NOAEL was not identified. In dogs, EXPAREL was well tolerated (NOAEL > 30 mg/kg/dose). The cumulative exposure of EXPAREL in these studies is well in excess of the proposed maximum single-dose exposure that is intended in humans.

Publisher

Hindawi Limited

Subject

Automotive Engineering

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