| CPC A61B 17/0057 (2013.01) [A61L 24/0031 (2013.01); A61L 24/02 (2013.01); A61L 24/04 (2013.01); B29C 70/766 (2013.01); C08L 71/02 (2013.01); A61B 2017/00495 (2013.01); A61B 2017/00526 (2013.01); A61B 2017/00561 (2013.01); A61B 2017/0065 (2013.01); A61B 2017/00654 (2013.01); A61B 2017/00672 (2013.01); A61B 2017/00871 (2013.01); A61B 2017/00884 (2013.01); A61B 2017/00889 (2013.01); A61B 2017/00893 (2013.01); A61B 2017/00898 (2013.01); A61B 2017/00951 (2013.01); A61B 2017/22067 (2013.01); A61B 2017/22069 (2013.01); A61B 90/90 (2016.02)] | 37 Claims |
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1. A sealant for sealing a puncture through tissue, comprising:
an elongate first section extending from a proximal end to a distal end, and a cross-section sized for delivery into a puncture through tissue; and
a second section fused to and extending from the distal end of the first section, the second section comprising PEG-precursors comprising PEG-ester and PEG-amine precursors in an equivalent ratio of active group sites of PEG-ester/PEG-amine of at least about one-to-one (1:1), at least some of the precursors remaining in an unreactive state until exposed to an aqueous physiological environment, whereupon the precursors undergo in-situ cross-linking with one another to provide adhesion to tissue adjacent the puncture.
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