Literature DB >> 23537340

Ziconotide: a clinical update and pharmacologic review.

Jason E Pope1, Timothy R Deer.   

Abstract

INTRODUCTION: Ziconotide is an N-type calcium channel antagonist to treat chronic pain that is delivered intrathecally. It is the only intrathecal, FDA-approved, non-opioid analgesic and is recommended as first-line therapy. Despite these advantages, a small therapeutic window limits ziconotide's clinical utility, with adverse event (AE) challenges that include, but are not limited to, dizziness, nausea, and somulence. AREAS COVERED: Pharmacokinetics, pharmacodynamics, efficacy, safety, trialing, and chronic infusion after searching EMBASE, PubMed, and Cochrane Database of Systemic Reviews were used to search published literature from 1966 to January 1, 2013 to identify studies related to the intrathecal delivery of ziconotide. EXPERT OPINION: Ziconotide is a safe and effective strategy to treat chronic pain, although limitations remain, including a small therapeutic window. Low starting doses and slow incremental increases and long titration intervals may improve tolerability. AEs may be mitigated by also employing combination therapy, although further study is needed. Concomitant use of ziconotide and morphine is an option when considering use of FDA-labeled intrathecal drugs in those resistant to monotherapy.

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Year:  2013        PMID: 23537340     DOI: 10.1517/14656566.2013.784269

Source DB:  PubMed          Journal:  Expert Opin Pharmacother        ISSN: 1465-6566            Impact factor:   3.889


  38 in total

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Journal:  Toxins (Basel)       Date:  2017-03-16       Impact factor: 4.546

Review 4.  Peptidomimetic therapeutics: scientific approaches and opportunities.

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Review 5.  Structure and function of μ-conotoxins, peptide-based sodium channel blockers with analgesic activity.

Authors:  Brad R Green; Grzegorz Bulaj; Raymond S Norton
Journal:  Future Med Chem       Date:  2014-10       Impact factor: 3.808

6.  Inhibition of human N- and T-type calcium channels by an ortho-phenoxyanilide derivative, MONIRO-1.

Authors:  Jeffrey R McArthur; Leonid Motin; Ellen C Gleeson; Sandro Spiller; Richard J Lewis; Peter J Duggan; Kellie L Tuck; David J Adams
Journal:  Br J Pharmacol       Date:  2017-07-21       Impact factor: 8.739

Review 7.  Nociceptin/Orphanin FQ Receptor Structure, Signaling, Ligands, Functions, and Interactions with Opioid Systems.

Authors:  Lawrence Toll; Michael R Bruchas; Girolamo Calo'; Brian M Cox; Nurulain T Zaveri
Journal:  Pharmacol Rev       Date:  2016-03-08       Impact factor: 25.468

Review 8.  Why do we study animal toxins?

Authors:  Yun Zhang
Journal:  Dongwuxue Yanjiu       Date:  2015-07-18

9.  In Silico Target Prediction of Overexpressed microRNAs from LPS-Challenged Zebrafish (Danio rerio) Treated with the Novel Anti-Inflammatory Peptide TnP.

Authors:  Geonildo R Disner; Maria A P Falcão; Carla Lima; Monica Lopes-Ferreira
Journal:  Int J Mol Sci       Date:  2021-07-01       Impact factor: 5.923

10.  Venom duct origins of prey capture and defensive conotoxins in piscivorous Conus striatus.

Authors:  Ai-Hua Jin; Brett Hamilton; Subash K Rai; S W A Himaya; Paul Alewood; Richard J Lewis
Journal:  Sci Rep       Date:  2021-06-24       Impact factor: 4.996

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