Cited by 126Hydrogels: synthesis, properties, applicationsNanoparticle-Based Drug DeliveryAdvanced Materials and Mechanics

Mechanoresponsive materials for drug delivery: Harnessing forces for controlled release

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Wang, Julia, Kaplan, Jonah A., Colson, Yolonda L., Grinstaff, Mark W.·2017·Advanced Drug Delivery Reviews

Abstract

Mechanically-activated delivery systems harness existing physiological and/or externally-applied forces to provide spatiotemporal control over the release of active agents. Current strategies to deliver therapeutic proteins and drugs use three types of mechanical stimuli: compression, tension, and shear. Based on the intended application, each stimulus requires specific material selection, in terms of substrate composition and size (e.g., macrostructured materials and nanomaterials), for optimal in vitro and in vivo performance. For example, compressive systems typically utilize hydrogels or elastomeric substrates that respond to and withstand cyclic compressive loading, whereas, tension-responsive systems use composites to compartmentalize payloads. Finally, shear-activated systems are based on nanoassemblies or microaggregates that respond to physiological or externally-applied shear stresses. In order to provide a comprehensive assessment of current research on mechanoresponsive drug delivery, the mechanical stimuli intrinsically present in the human body are first discussed, along with the mechanical forces typically applied during medical device interventions, followed by in-depth descriptions of compression, tension, and shear-mediated drug delivery devices. We conclude by summarizing the progress of current research aimed at integrating mechanoresponsive elements within these devices, identifying additional clinical opportunities for mechanically-activated systems, and discussing future prospects.

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Crossref · 10.1016/j.addr.2016.11.001

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  • Shear stress-sensitive liposomes and polymeric nanoparticles can release anti-inflammatory or antifibrotic agents specifically at sites with elevated hemodynamic shear stress, enabling localized drug release triggered by mechanical forces.

    “For example, shear stresssensitive liposomes and polymeric nanoparticles can release antiinflammatory or antifibrotic agents specifically at sites with elevated hemodynamic shear stress, enabling localized drug release triggered by mechanical forces (153, 154).”

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References 158 · Cited by 126

Research works printed but not linked: 2

  1. [126]Volodkin D Skirtach A Möhwald H Bioactive Surfaces 2011 Heidelberg Springer, Berlin
  2. [153]Xiao L Zhu J Londono DJ Pochan DJ Jia X Mechano-Responsive Hydrogels Crosslinked by Block Copolymer Micelles Soft Matter 2012 8 10233 10237 23024698 PMC3459338

Authors
Wang, J., Kaplan, J. A., Colson, Y. L., & Grinstaff, M. W.
Affiliations
  • Boston University (US)
  • Brigham and Women's Hospital (US)
Corresponding author
Grinstaff, Mark W.
Venue
Advanced Drug Delivery Reviews
Publisher
Elsevier BV
Published
2017-01
Volume
108
Pages
68-82
ISSN
0169-409X (ISSN-L)
OpenAlex
W2550312623
Cited by
126
References
158
Citations by year
2026: 16 · 2025: 15 · 2024: 8 · 2023: 11 · 2022: 19 · 2021: 9 · 2020: 18 · 2019: 12 · 2018: 10 · 2017: 8
FWCI
0.64
Type
journal article
Language
en
Open access
Locations
  • Advanced Drug Delivery Reviews (acceptedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • Wallace H. Coulter Foundation
  • National Institutes of Health (T32EB006359)
  • National Science Foundation (DMR-1507081, DGE-1247312)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Medicine › Hydrogels: synthesis, properties, applications
  • Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
  • Physical Sciences › Engineering › Mechanical Engineering › Advanced Materials and Mechanics
Keywords
mechanoresponsive materials, controlled release, hydrogels, elastomeric substrates, nanomaterials, spatiotemporal drug release
MeSH terms
Animals, Delayed-Action Preparations, Humans, Stress, Mechanical, Drug Delivery Systems, Hydrogels, Nanostructures

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