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. Author manuscript; available in PMC: 2022 Jul 14.
Published in final edited form as: Adv Healthc Mater. 2021 Mar 18;10(9):e2001941. doi: 10.1002/adhm.202001941

Figure 8.

Figure 8.

In vivo BMP-2 release from ROS-sensitive PTK-BAA and conventional PBAE-coated implants in rat calvarial defects. As quantified from (A) fluorescence imaging of Cy7-labeled BMP-2, growth factor delivery from the PTK-coated scaffolds (B) exhibits a lower initial bolus discharge and is significantly extended compared against PBAE films. Importantly though, over 95% of the PTK film’s drug payload is released over a three-week time course. (C) Quantification of half-life values for the respective release profiles (displayed as a 95% confidence interval) further demonstrates a nearly three-fold increase in drug retention for PTK-BAA coatings. N=3 animals per treatment, *p<0.05.