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    Rights statement: This is the author’s version of a work that was accepted for publication in International Journal of Pharmaceutics. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in International Journal of Pharmaceutics, 535, 1-2, 2018 DOI: 10.1016/j.ijpharm.2017.11.043

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Anti-Adherent Biomaterials for Prevention of Catheter Biofouling

Research output: Contribution to journalJournal articlepeer-review

Published

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Anti-Adherent Biomaterials for Prevention of Catheter Biofouling. / McCoy, Colin; Irwin, Nicola J.; Donnelly, Louise; Jones, David; Hardy, John George; Carson, Louise.

In: International Journal of Pharmaceutics, Vol. 535, No. 1-2, 15.01.2018, p. 420-427.

Research output: Contribution to journalJournal articlepeer-review

Harvard

McCoy, C, Irwin, NJ, Donnelly, L, Jones, D, Hardy, JG & Carson, L 2018, 'Anti-Adherent Biomaterials for Prevention of Catheter Biofouling', International Journal of Pharmaceutics, vol. 535, no. 1-2, pp. 420-427. https://doi.org/10.1016/j.ijpharm.2017.11.043

APA

McCoy, C., Irwin, N. J., Donnelly, L., Jones, D., Hardy, J. G., & Carson, L. (2018). Anti-Adherent Biomaterials for Prevention of Catheter Biofouling. International Journal of Pharmaceutics, 535(1-2), 420-427. https://doi.org/10.1016/j.ijpharm.2017.11.043

Vancouver

McCoy C, Irwin NJ, Donnelly L, Jones D, Hardy JG, Carson L. Anti-Adherent Biomaterials for Prevention of Catheter Biofouling. International Journal of Pharmaceutics. 2018 Jan 15;535(1-2):420-427. https://doi.org/10.1016/j.ijpharm.2017.11.043

Author

McCoy, Colin ; Irwin, Nicola J. ; Donnelly, Louise ; Jones, David ; Hardy, John George ; Carson, Louise. / Anti-Adherent Biomaterials for Prevention of Catheter Biofouling. In: International Journal of Pharmaceutics. 2018 ; Vol. 535, No. 1-2. pp. 420-427.

Bibtex

@article{63ac00b62f684ccfa94b6f07106fbcdb,
title = "Anti-Adherent Biomaterials for Prevention of Catheter Biofouling",
abstract = "Medical device-associated infections present a leading global healthcare challenge, and effective strategies to prevent infections are urgently required. Herein, we present an innovative anti-adherent hydrogel copolymer as a candidate catheter coating with complementary hydrophobic drug-carrying and eluting capacities. The amphiphilic block copolymer, Poloxamer 188, was chemically-derivatized with methacryloyl moieties and copolymerized with the hydrogel monomer, 2-hydroxyethyl methacrylate. Performance of the synthesized copolymers was evaluated in terms of equilibrium swelling, surface water wettability, mechanical integrity, resistance to encrustation and bacterial adherence, and ability to control release of the loaded fluoroquinolone antibiotic, ofloxacin. The developed matrices were able to provide significant protection from fouling, with observed reductions of over 90% in both adherence of the common urinary pathogen Escherichia coli and encrusting crystalline deposits of calcium and magnesium salts relative to the commonly employed hydrogel, poly (hydroxyethyl methacrylate). Additionally, the release kinetics of a loaded hydrophobic drug could be readily tuned through facile manipulation of polymer composition. This combinatorial approach shows significant promise in the development of suitable systems for prevention of catheter-associated infections.",
keywords = "drug delivery, Biofouling, Catheter, medical device, materials science, biomedical engineering, pharmacy",
author = "Colin McCoy and Irwin, {Nicola J.} and Louise Donnelly and David Jones and Hardy, {John George} and Louise Carson",
note = "This is the author{\textquoteright}s version of a work that was accepted for publication in International Journal of Pharmaceutics. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in International Journal of Pharmaceutics, 535, 1-2, 2018 DOI: 10.1016/j.ijpharm.2017.11.043",
year = "2018",
month = jan,
day = "15",
doi = "10.1016/j.ijpharm.2017.11.043",
language = "English",
volume = "535",
pages = "420--427",
journal = "International Journal of Pharmaceutics",
issn = "0378-5173",
publisher = "Elsevier",
number = "1-2",

}

RIS

TY - JOUR

T1 - Anti-Adherent Biomaterials for Prevention of Catheter Biofouling

AU - McCoy, Colin

AU - Irwin, Nicola J.

AU - Donnelly, Louise

AU - Jones, David

AU - Hardy, John George

AU - Carson, Louise

N1 - This is the author’s version of a work that was accepted for publication in International Journal of Pharmaceutics. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in International Journal of Pharmaceutics, 535, 1-2, 2018 DOI: 10.1016/j.ijpharm.2017.11.043

PY - 2018/1/15

Y1 - 2018/1/15

N2 - Medical device-associated infections present a leading global healthcare challenge, and effective strategies to prevent infections are urgently required. Herein, we present an innovative anti-adherent hydrogel copolymer as a candidate catheter coating with complementary hydrophobic drug-carrying and eluting capacities. The amphiphilic block copolymer, Poloxamer 188, was chemically-derivatized with methacryloyl moieties and copolymerized with the hydrogel monomer, 2-hydroxyethyl methacrylate. Performance of the synthesized copolymers was evaluated in terms of equilibrium swelling, surface water wettability, mechanical integrity, resistance to encrustation and bacterial adherence, and ability to control release of the loaded fluoroquinolone antibiotic, ofloxacin. The developed matrices were able to provide significant protection from fouling, with observed reductions of over 90% in both adherence of the common urinary pathogen Escherichia coli and encrusting crystalline deposits of calcium and magnesium salts relative to the commonly employed hydrogel, poly (hydroxyethyl methacrylate). Additionally, the release kinetics of a loaded hydrophobic drug could be readily tuned through facile manipulation of polymer composition. This combinatorial approach shows significant promise in the development of suitable systems for prevention of catheter-associated infections.

AB - Medical device-associated infections present a leading global healthcare challenge, and effective strategies to prevent infections are urgently required. Herein, we present an innovative anti-adherent hydrogel copolymer as a candidate catheter coating with complementary hydrophobic drug-carrying and eluting capacities. The amphiphilic block copolymer, Poloxamer 188, was chemically-derivatized with methacryloyl moieties and copolymerized with the hydrogel monomer, 2-hydroxyethyl methacrylate. Performance of the synthesized copolymers was evaluated in terms of equilibrium swelling, surface water wettability, mechanical integrity, resistance to encrustation and bacterial adherence, and ability to control release of the loaded fluoroquinolone antibiotic, ofloxacin. The developed matrices were able to provide significant protection from fouling, with observed reductions of over 90% in both adherence of the common urinary pathogen Escherichia coli and encrusting crystalline deposits of calcium and magnesium salts relative to the commonly employed hydrogel, poly (hydroxyethyl methacrylate). Additionally, the release kinetics of a loaded hydrophobic drug could be readily tuned through facile manipulation of polymer composition. This combinatorial approach shows significant promise in the development of suitable systems for prevention of catheter-associated infections.

KW - drug delivery

KW - Biofouling

KW - Catheter

KW - medical device

KW - materials science

KW - biomedical engineering

KW - pharmacy

U2 - 10.1016/j.ijpharm.2017.11.043

DO - 10.1016/j.ijpharm.2017.11.043

M3 - Journal article

VL - 535

SP - 420

EP - 427

JO - International Journal of Pharmaceutics

JF - International Journal of Pharmaceutics

SN - 0378-5173

IS - 1-2

ER -