Enzyme-containing Michael-adduct-based coatings

Biomacromolecules. 2003 May-Jun;4(3):675-82. doi: 10.1021/bm034034l.

Abstract

A two-step method was developed to homogeneously insert carbonic anhydrase (CA, E.C. 4.2.1.1) into Michael-adduct-based coatings. CA was first covalently coupled to an N-vinylformamide-based water-soluble polymer. Unlike native CA, the resulting polymer/CA system could be dispersed within a film matrix. The enzyme-containing coating (ECC) hydrolyzes p-nitrophenyl propionate in buffered media at high rates retaining approximately 7% apparent activity. In comparison, other two-step techniques for the chemical coupling of CA to the coating surface were less efficient and led to coatings with significantly less activity. A three-step immobilization process coupling the enzyme to the surface of a partially hydrolyzed coating also raised retention of activity after coating synthesis. CA-ECC is stable under ambient conditions retaining 45% activity after 90 days of storage at room temperature.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Carbonic Anhydrases / chemistry*
  • Carbonic Anhydrases / metabolism
  • Coated Materials, Biocompatible / chemistry*
  • Coated Materials, Biocompatible / metabolism
  • DNA Adducts* / chemical synthesis
  • Drug Stability
  • Hot Temperature
  • Neurotensin / chemistry
  • Surface Properties

Substances

  • Coated Materials, Biocompatible
  • DNA Adducts
  • Neurotensin
  • Carbonic Anhydrases