Prolongation of sciatic nerve blockade by in situ cross-linked hyaluronic acid

Biomaterials. 2004 Aug;25(19):4797-804. doi: 10.1016/j.biomaterials.2003.12.012.

Abstract

Controlled release technology has been applied extensively in providing prolonged duration local anesthesia. Here we used modified hyaluronic acids (HAs; hydrazide and aldehyde) that cross-link upon mixing, as the vehicle for bupivacaine. We assessed the formulations' efficacy and biocompatibility in a rat model of sciatic nerve blockade. We found that 2% (w/v) cross-linked HA doubled the duration of block of 0.1%, 0.25%, and 0.5% (w/v) bupivacaine, without a statistically significant increase in myotoxicity. 1% (w/w) cross-linked HA also prolonged nerve block, but unmodified HA, and both modified HAs did not. HA itself was associated with a mild to moderate inflammatory response with macrophages and lymphocytes. Cross-linked HA is an effective and biocompatible vehicle for enhancing local anesthetic efficacy.

Publication types

  • Comparative Study
  • Evaluation Study
  • Research Support, U.S. Gov't, P.H.S.
  • Validation Study

MeSH terms

  • Animals
  • Bupivacaine / administration & dosage*
  • Bupivacaine / chemistry
  • Cross-Linking Reagents / chemistry*
  • Diffusion
  • Dose-Response Relationship, Drug
  • Hyaluronic Acid / adverse effects
  • Hyaluronic Acid / chemistry*
  • Hydrogels / adverse effects
  • Hydrogels / chemistry
  • Male
  • Materials Testing
  • Nerve Block / adverse effects
  • Nerve Block / methods*
  • Pharmaceutical Vehicles / chemistry*
  • Rats
  • Rats, Sprague-Dawley
  • Sciatic Nerve / drug effects*
  • Sciatic Nerve / pathology
  • Sciatic Nerve / physiology*

Substances

  • Cross-Linking Reagents
  • Hydrogels
  • Pharmaceutical Vehicles
  • Hyaluronic Acid
  • Bupivacaine