Toxicogenomic analysis of a sustained release local anesthetic delivery system

Iris Shichor, Noam Shomron, Michael W. Lawlor, Seul A. Bae, Janet Zoldan, Robert Langer, Daniel S. Kohane*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

Concerns over neurotoxicity have impeded the development of sustained release formulations providing prolonged duration local anesthesia (PDLA) from a single injection, for which there is an urgent clinical need. Here, we have used toxicogenomics to investigate whether nerve injury occurred during week-long continuous sciatic nerve blockade by microspheres containing bupivacaine, tetrodotoxin, and dexamethasone (TBD). Animals treated with amitriptyline solution (our positive control for local anesthetic-associated nerve injury) developed irreversible nerve blockade, had severely abnormal nerve histology, and the expression of hundreds of genes was altered in the dorsal root ganglia at 4 and 7 days after injection. In marked contrast, TBD-treated nerves reverted to normal function, were normal histologically and there were changes in the expression of a small number of genes. Toxicogenomic studies have great potential in delineating patterns of gene expression associated with specific patterns of tissue injury (e.g. amitriptyline neurotoxicity), and in identifying related changes in gene expression upon exposure to a drug, biomaterial, or drug delivery system.

Original languageEnglish
Pages (from-to)3586-3593
Number of pages8
JournalBiomaterials
Volume33
Issue number13
DOIs
StatePublished - May 2012

Funding

FundersFunder number
National Institutes of Health
National Institute of General Medical SciencesR01GM073626

    Keywords

    • Biocompatibility
    • Drug delivery
    • Nerve injury
    • Neurotoxicity
    • Prolonged duration local anesthesia
    • Toxicogenomics

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