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. Author manuscript; available in PMC: 2019 May 14.
Published in final edited form as: Anal Chem. 2019 Feb 6;91(4):3110–3117. doi: 10.1021/acs.analchem.8b05709

Figure 2.

Figure 2.

Molecular platform of 9’-phenyl-3’-hydroxyfluorone-, rosamine-, and rosol-based fluorescent dyes, their analogues having a pendant benzene moiety with a charged 2-carboxylate group (-COO-), each respective initial pKa value, and the off-on fluorescence intensity-pH profile of the molecular platforms having a 3’- amino-6’-hydroxyxanthene-based scaffold and the maximum contrast level they would afford upon use toward visualizing tumor- draining lymphatics. A) The presence of the charged 2-carboxylate group imparts an increased pKa value to their respective underlying xanthene core-based scaffold. B) The off-on fluorescence intensity- pH profiles of a generic rosol (X) and rhodol (Z) dye with a pKa value of ~4.8 and ~6.3, respectively, and a proposed rosol dye (Y) designed with a pKa value of 5.8–6.0. The dashed red lines circumscribe the pH level range that a fluorescent molecular dye having a pKa value within them would afford optimal contrast upon use in lymphatic mapping applications. The circle identifies the pKa value. C) Only the proposed rosol dye (Y) designed to have a pKa value of 5.8–6.0 would afford a steady maximal response and optimal contrast. A solid or striped intensity ratio bar indicates that the dye would be either pH-insensitive or pH-sensitive when within tumor-draining lymphatic pH levels (pH 6.8–7.4), respectively.