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Oral administration demonstrates activity in gastrointestinal conditions despite lower systemic bioavailability, as direct mucosal exposure may contribute to therapeutic effects
doi: 10.3389/fpls.2011.00045 Received 02 August 2011 Accepted 16 August 2011 Published 05 September 2011 Volume 2 - 2011 Edited by Ikuro Abe, The University of Tokyo, Japan Reviewed by Ikuro Abe, The University of Tokyo, Japan
Polymer solution contained 300 L PEGDA (d = 1.1 g/mL, Sigma), 600 L PBS, 5 L eosin Y
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