Cited by 76Hydrogels: synthesis, properties, applicationsPolymer Surface Interaction StudiesAdvanced Drug Delivery Systems

Heparin release from thermosensitive polymer coatings: in vivo studies

Open access
Gutowska, Anna, Bae, You Han, Jacobs, Harvey, Mohammad, Fazal, Mix, Donald, Feijen, Jan, Kim, Sung Wan·1995·Journal of Biomedical Materials Research

Abstract

Biomer/poly(N‐isopropylacrylamide)/[poly(NiPAAm)] thermosensitive polymer blends were prepared and their application as heparin‐releasing polymer coatings for the prevention of surface‐induced thrombosis was examined. The advantage of using poly(NiPAAm)‐based coatings as heparin‐releasing polymers is based of the unique temperature‐dependent swelling of these materials. At room temperature, i.e., below the lower critical solution temperature (LCST) of poly(NiPAAm), the Biomer/(poly(NiPAAm)) coatings are highly swollen. The high swelling enables fast loading of hydrophilic macromolecules (e.g., heparin) into the coating by a solutions sorption technique. At a body temperature, i.e., above the LCST of poly(NiPAAm) the coatings are in a deswollen state and the absorbed macromolecules may be slowly released from a dense coating via a diffusion controlled mechanism. Biomer/poly(NiPAAm)) coatings were obtained by blending and coprecipitation of the two linear polymers, Biomer and (poly(NiPAAm). The structure and water‐swelling properties of the coatings were examined. Significant differences in water swelling at room temperature (RT) and 37°C were observed as a result of the thermosensitivity of poly(NiPAAm). The surface structure of the coatings in dry and swollen states at RT and 37°C was examined by scanning electron microscopy. Heparin was loaded into the coatings via a solution sorption at room temperature. Kinetic studies of heparin loading demonstrated that maximum loading was obtained within 1 h. The in vitro (37°C) release profiles were characterized by a rapid initial release due to the squeezing effect of the collapsing polymer network, followed by a slower release phase controlled by heparin diffusion through the dense coating. The short‐term antithrombogenicity of intravenous polyurethane catheters coated with heparin‐releasing Biomer/poly(NiPAAm) thermosensitive coating was evaluated in a canine animal model. The results show that the heparin release from Biomer/poly(NiPAAm)‐coated surfaces resulted in a significant reduction of thrombus formation on test surfaces in contact with venous blood as compared to control surfaces. © 1995 John Wiley & Sons, Inc.

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Crossref · 10.1002/jbm.820290705

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Authors
Gutowska, A., Bae, Y. H., Jacobs, H., Mohammad, F., Mix, D., Feijen, J., & Kim, S. W.
Affiliations
University of Utah (US)
Corresponding author
Kim, Sung Wan
Venue
Journal of Biomedical Materials Research
Publisher
Wiley
Published
1995-07
Volume
29
Issue
7
Pages
811-821
ISSN
  • 0021-9304 (ISSN-L)
  • 1097-4636
OpenAlex
W1973859023
Cited by
76
References
36
Citations by year
2022: 1 · 2021: 2 · 2020: 1 · 2018: 4 · 2017: 4 · 2016: 3 · 2015: 4 · 2014: 2 · 2013: 1 · 2012: 3
FWCI
2.19
Type
journal article
Language
en
Open access
Locations
  • Journal of Biomedical Materials Research (publishedVersion)
  • PubMed (publishedVersion)
  • University of Twente Research Information (submittedVersion, other-oa)
Funders
  • National Institutes of Health (5r01hl017623-19)
  • National Heart, Lung, and Blood Institute (HL 17623-19)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Medicine › Hydrogels: synthesis, properties, applications
  • Physical Sciences › Materials Science › Surfaces, Coatings and Films › Polymer Surface Interaction Studies
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advanced Drug Delivery Systems
Keywords
heparin release, poly(N-isopropylacrylamide), Biomer, polyurethane catheters, antithrombogenicity, lower critical solution temperature, water swelling, controlled drug release, co-precipitation, intravenous catheters
MeSH terms
Acrylic Resins, Animals, Anticoagulants, Catheterization, Diffusion, Dogs, Heparin, Kinetics, Microscopy, Electron, Scanning, Polyurethanes, Solubility, Temperature, Thrombosis

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