TY - JOUR
T1 - Diffusion of botulinum toxins
AU - Brodsky, Matthew A.
AU - Swope, David M.
AU - Grimes, David
N1 - Funding Information:
* To whom correspondence should be addressed. E-mail: brodskym@ohsu.edu Editor: Elan D. Louis, Columbia University, United States of America Received: December 3, 2011 Accepted: June 3, 2012 Published: August 6, 2012 Copyright: ’ 2012 Brodsky et al. This is an open-access article distributed under the terms of the Creative Commons Attribution–Noncommercial–No Derivatives License, which permits the user to copy, distribute, and transmit the work provided that the original author(s) and source are credited; that no commercial use is made of the work; and that the work is not altered or transformed. Funding: Funding for editorial support was provided by Merz Pharmaceuticals, LLC, Greensboro, NC. Financial Disclosures: Dr. Brodsky has served as an advisor to Merz Pharma, Ipsen, Allergan, Inc., UCB, and Teva. Dr. Swope has received grant/research support from Allergan, Inc., Teva, Synosia/Biotie, and St Jude Medical Center; has served as an advisor for Allergan, Inc., Ipsen, Merz Pharma, and Teva; and has received fellowship support from Merz. He also is a member of the speakers’ bureau for Allergan, Inc. and is affiliated with its Injection Training Center. Dr. Grimes has served as an advisor to Merz Pharma, Allergan, Novartis, and Teva; he has received grant/research support from NIH, Michael J. Fox Foundation, CIHR, Parkinson Research Consortium, Impax Pharmaceuticals, Merz Pharma, Allergan and Schering-Plough. Conflict of Interest: The authors report no conflict of interest.
Funding Information:
for editorial support was provided by Merz Pharmaceuticals, LLC, Greensboro, NC. Financial Disclosures: Dr. Brodsky has served as an advisor to Merz Pharma, Ipsen, Allergan, Inc., UCB, and Teva. Dr. Swope has received grant/research support from Allergan, Inc., Teva, Synosia/Biotie, and St Jude Medical Center; has served as an advisor for Allergan, Inc., Ipsen, Merz Pharma, and Teva; and has received fellowship support from Merz. He also is a member of the speakers’ bureau for Allergan, Inc. and is affiliated with its Injection Training Center. Dr. Grimes has served as an advisor to Merz Pharma, Allergan, Novartis, and Teva; he has received grant/research support from NIH, Michael J. Fox Foundation, CIHR, Parkinson Research Consortium, Impax Pharmaceuticals, Merz Pharma, Allergan and Schering-Plough.Editorial support, consisting of substantive editing, copy editing, and styling of the authors’ draft, as well as assistance with literature searches, was provided by Linnéa Elliott and Maria Vinall of The Curry Rockefeller Group, LLC, Tarrytown, NY.
Publisher Copyright:
© 2012 Brodsky et al.
PY - 2012
Y1 - 2012
N2 - Background: It is generally agreed that diffusion of botulinum toxin occurs, but the extent of the spread and its clinical importance are disputed. Many factors have been suggested to play a role but which have the most clinical relevance is a subject of much discussion. Methods: This review discusses the variables affecting diffusion, including protein composition and molecular size as well as injection factors (e.g., volume, dose, injection method). It also discusses data on diffusion from comparative studies in animal models and human clinical trials that illustrate differences between the available botulinum toxin products (onabotulinumtoxinA, abobotulinumtoxinA, incobotulinumtoxinA, and rimabotulinumtoxinB). Results: Neither molecular weight nor the presence of complexing proteins appears to affect diffusion; however, injection volume, concentration, and dose all play roles and are modifiable. Both animal and human studies show that botulinum toxin products are not interchangeable, and that some products are associated with greater diffusion and higher rates of diffusion-related adverse events than others. Discussion: Each of the botulinum toxins is a unique pharmacologic entity. A working knowledge of the different serotypes is essential to avoid unwanted diffusion-related adverse events. In addition, clinicians should be aware that the factors influencing diffusion may range from properties intrinsic to the drug to accurate muscle selection as well as dilution, volume, and dose injected.
AB - Background: It is generally agreed that diffusion of botulinum toxin occurs, but the extent of the spread and its clinical importance are disputed. Many factors have been suggested to play a role but which have the most clinical relevance is a subject of much discussion. Methods: This review discusses the variables affecting diffusion, including protein composition and molecular size as well as injection factors (e.g., volume, dose, injection method). It also discusses data on diffusion from comparative studies in animal models and human clinical trials that illustrate differences between the available botulinum toxin products (onabotulinumtoxinA, abobotulinumtoxinA, incobotulinumtoxinA, and rimabotulinumtoxinB). Results: Neither molecular weight nor the presence of complexing proteins appears to affect diffusion; however, injection volume, concentration, and dose all play roles and are modifiable. Both animal and human studies show that botulinum toxin products are not interchangeable, and that some products are associated with greater diffusion and higher rates of diffusion-related adverse events than others. Discussion: Each of the botulinum toxins is a unique pharmacologic entity. A working knowledge of the different serotypes is essential to avoid unwanted diffusion-related adverse events. In addition, clinicians should be aware that the factors influencing diffusion may range from properties intrinsic to the drug to accurate muscle selection as well as dilution, volume, and dose injected.
KW - Botulinum toxin
KW - Diffusion
KW - Injection technique
KW - Spread
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U2 - 10.5334/TOHM.120
DO - 10.5334/TOHM.120
M3 - Review article
AN - SCOPUS:85113193207
SN - 2160-8288
VL - 2
JO - Tremor and Other Hyperkinetic Movements
JF - Tremor and Other Hyperkinetic Movements
ER -