• Title of article

    Probing microbubble targeting with atomic force microscopy

  • Author/Authors

    Sboros، نويسنده , , V. and Glynos، نويسنده , , E. and Ross، نويسنده , , J.A. and Moran، نويسنده , , C.M. and Pye، نويسنده , , S.D. and Butler، نويسنده , , M. and McDicken، نويسنده , , W.N. and Brown، نويسنده , , S.B. and Koutsos، نويسنده , , V.، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2010
  • Pages
    6
  • From page
    12
  • To page
    17
  • Abstract
    Microbubble science is expanding beyond ultrasound imaging applications to biological targeting and drug/gene delivery. The characteristics of molecular targeting should be tested by a measurement system that can assess targeting efficacy and strength. Atomic force microscopy (AFM) is capable of piconewton force resolution, and is reported to measure the strength of single hydrogen bonds. An in-house targeted microbubble modified using the biotin–avidin chemistry and the CD31 antibody was used to probe cultures of Sk-Hep1 hepatic endothelial cells. We report that the targeted microbubbles provide a single distribution of adhesion forces with a median of 93 pN. This interaction is assigned to the CD31 antibody–antigen unbinding event. Information on the distances between the interaction forces was obtained and could be important for future microbubble fabrication. In conclusion, the capability of single microbubbles to target cell lines was shown to be feasible with AFM.
  • Keywords
    Targeted microbubbles , Microbubble adhesion , Atomic Force Microscope , Microbubble-cell avidity , CD31 , PECAM
  • Journal title
    Colloids and Surfaces B Biointerfaces
  • Serial Year
    2010
  • Journal title
    Colloids and Surfaces B Biointerfaces
  • Record number

    1971711