4.5 Article

Synthesis, Characterization and Drug Release of Biocompatible/Biodegradable Non-toxic Poly(urethane urea)s Based on Poly(epsilon-caprolactone)s and Lysine-Based Diisocyanate

Journal

JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION
Volume 21, Issue 11, Pages 1483-1502

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1163/092050609X12518804794785

Keywords

Polyurethane ureas; lysine-based diisocyante; mechanical properties; in vitro drug release; cell adhesion

Funding

  1. MEXT, Japan
  2. Japan Society for Promotion of Science (JSPS)

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Segmented poly( urethane urea)s (SPUUs) based on aliphatic diisocyanato (2,6-diisocyanato methyl caproate (lysine-based diisocyanate, LDI)), poly(epsilon-caprolactone diol)s (PCLs) with molecular weights 530, 1250 and 2000, and 1,4-butanediamine were synthesized in absence of catalyst. The resulting SPUUs, with different soft segment length, were characterized by suitable analytical techniques. The synthesized SPUUs had high molecular weights, low glass-transition temperatures (<=-15 degrees C) and high elongation-at-break. The degradation of SPUUs in alkaline solution and in vitro drug release of sulfamethoxazole in pH 7.4 buffer were investigated. In addition, the degradation behavior of PCL1250-based SPUU was investigated by exposing to a buffer solution and biochemical oxygen demand (BOD) tests in an activated sludge. The drug release data was analyzed by an empirical equation ((M-t/M-infinity) = kt(n)). Finally, NIH3T3 fibroblasts have been used for cell-adhesion studies on these materials to investigate the biocompatibility. The synthesized SPUUs combine physical and bioresponsive and biodegradable properties that might be employed in wound dressing, drug delivery and tissue-engineering applications. (C) Koninklijke Brill NV, Leiden, 2010

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