The particle in the spider's web: transport through biological hydrogels

Biological hydrogels such as mucus, extracellular matrix, biofilms, and the nuclear pore have diverse functions and compositions, but all act as selectively permeable barriers to the diffusion of particles. Each barrier has a crosslinked polymeric mesh that blocks penetration of large particles such...

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Bibliographic Details
Main Authors: Witten, Jacob (Author), Ribbeck, Katharina (Contributor), Witten, Jacob Julian Seid (Contributor)
Other Authors: Massachusetts Institute of Technology. Computational and Systems Biology Program (Contributor), Massachusetts Institute of Technology. Department of Biological Engineering (Contributor)
Format: Article
Language:English
Published: Royal Society of Chemistry (RSC), 2018-09-11T15:38:44Z.
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Online Access:Get fulltext
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100 1 0 |a Witten, Jacob  |e author 
100 1 0 |a Massachusetts Institute of Technology. Computational and Systems Biology Program  |e contributor 
100 1 0 |a Massachusetts Institute of Technology. Department of Biological Engineering  |e contributor 
100 1 0 |a Witten, Jacob Julian Seid  |e contributor 
100 1 0 |a Ribbeck, Katharina  |e contributor 
700 1 0 |a Ribbeck, Katharina  |e author 
700 1 0 |a Witten, Jacob Julian Seid  |e author 
245 0 0 |a The particle in the spider's web: transport through biological hydrogels 
260 |b Royal Society of Chemistry (RSC),   |c 2018-09-11T15:38:44Z. 
856 |z Get fulltext  |u http://hdl.handle.net/1721.1/117712 
520 |a Biological hydrogels such as mucus, extracellular matrix, biofilms, and the nuclear pore have diverse functions and compositions, but all act as selectively permeable barriers to the diffusion of particles. Each barrier has a crosslinked polymeric mesh that blocks penetration of large particles such as pathogens, nanotherapeutics, or macromolecules. These polymeric meshes also employ interactive filtering, in which affinity between solutes and the gel matrix controls permeability. Interactive filtering affects the transport of particles of all sizes including peptides, antibiotics, and nanoparticles and in many cases this filtering can be described in terms of the effects of charge and hydrophobicity. The concepts described in this review can guide strategies to exploit or overcome gel barriers, particularly for applications in diagnostics, pharmacology, biomaterials, and drug delivery. 
520 |a National Science Foundation (U.S.). Materials Research Science and Engineering Centers (Program) (DMR - 0819762) 
520 |a National Science Foundation (U.S.) (NSF R01 R01-EB017755) 
520 |a National Science Foundation (U.S.) (NSF Career PHY-1454673) 
520 |a National Science Foundation (U.S.). Graduate Research Fellowship Program (Grant 1122374) 
655 7 |a Article 
773 |t Nanoscale