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Autor(en) / Beteiligte
Titel
Guidable Thermophoretic Janus Micromotors Containing Gold Nanocolorifiers for Infrared Laser Assisted Tissue Welding
Ist Teil von
  • Advanced science, 2016-12, Vol.3 (12), p.1600206-n/a
Ort / Verlag
Germany: John Wiley & Sons, Inc
Erscheinungsjahr
2016
Link zum Volltext
Quelle
Wiley Online Library - AutoHoldings Journals
Beschreibungen/Notizen
  • Current wound sealing systems such as nanoparticle‐based gluing of tissues allow almost immediate wound sealing. The assistance of a laser beam allows the wound sealing with higher controllability due to the collagen fiber melting which is defined by loss of tertiary protein structure and restoration upon cooling. Usually one employs dyes to paint onto the wound, if water absorption bands are absent. In case of strong bleeding or internal wounds such applications are not feasible due to low welding depth in case of water absorption bands, dyes washing off, or the dyes becoming diluted within the wound. One possible solution of these drawbacks is to use autonomously movable particles composing of biocompatible gold and magnetite nanoparticles and biocompatible polyelectrolyte complexes. In this paper a proof of principle study is presented on the utilization of thermophoretic Janus particles and capsules employed as dyes for infrared laser‐assisted tissue welding. This approach proves to be efficient in sealing the wound on the mouse in vivo. The temperature measurement of single particle level proves successful photothermal heating, while the mechanical characterizations of welded liver, skin, and meat confirm mechanical restoration of the welded biological samples. Guidable autonomous moving Janus particles and capsules employed as dyes for infrared laser tissue welding may be useful candidates to prevent a dye wash off from bleeding sites. This study introduces such particles and their use in tissue welding on meat samples and mouse models. Temperature measurements prove photothermal particle heating.
Sprache
Englisch
Identifikatoren
ISSN: 2198-3844
eISSN: 2198-3844
DOI: 10.1002/advs.201600206
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5157175

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