Abstract
G A A b st ra ct s higher than the mean intensity values for squamous (t=3.1, p<0.01) and gastric mucosa (t= 3.0, p<0.01). There was no statistically significant difference in the mean intensity values between squamous and gastric mucosa (t=0.4, p=0.71). Conclusions: We demonstrate selective binding of the novel fluorescence-labeled SNF peptide to Barrett's dysplasia over mucosal surface areas on the centimeter scale. These results are promising as a future means to target dysplasia in Barrett's esophagus on fluorescence endoscopy.
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