• Title of article

    Intact collagen and atelocollagen sponges: Characterization and ESEM observation

  • Author/Authors

    Ruozi، نويسنده , , Barbara and Tosi، نويسنده , , Giovanni and Leo، نويسنده , , Eliana and Parma، نويسنده , , Bruna and Vismara، نويسنده , , Susanna and Forni، نويسنده , , Flavio and Vandelli، نويسنده , , Maria Angela، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2007
  • Pages
    9
  • From page
    802
  • To page
    810
  • Abstract
    In this study we have investigated the chemical–physical and morphological properties of intact and atelocollagen sponges used for tissue engineering. The porous sponges were prepared by lyophilization and their physico-chemical characteristics (water binding capacity, denaturing temperature, amino group content) were investigated. Considering the importance of the “in vivo” interactions between these sponges and the tissue, our attention was addressed (a) to clarify the relationships between the morphology and the amount of water absorbed and (b) to evaluate the influence of pepsin-alkaline treatment on the reorganization of the atelocollagen fibres. Conventional scanning electron microscopy (SEM) and environmental scanning electron microscopy (ESEM) were employed to study the morphology and wetting behaviour of the intact and atelocollagen sponges. The observations by SEM indicated remarkable differences both in the structure and dimension of the pores between intact and atelocollagen sponges. At the data are related to a different water binding capacity. However, the ESEM observations, achieved by changing the relative humidity in the operative chamber, demonstrated that the water adsorbed can be removed with major difficulty from atelocollagen sponges than from intact ones.
  • Keywords
    Collagen , Swelling , Environmental Scanning Electron Microscopy (ESEM) , microstructure
  • Journal title
    Materials Science and Engineering C
  • Serial Year
    2007
  • Journal title
    Materials Science and Engineering C
  • Record number

    2096617