“…As illustrated in the in vitro studies above, encapsulated MB permits not only sufficient light-stimulated generation of 1 O 2 , but also adequate diffusion out of the matrix to cause damage to the tumor cells. Furthermore, based on recent successful in vivo work with the similar polyacrylamide-based NPs, using the less efficient photofrin [17][18][19][20], rather than MB, as the PDT agent, we expect the MB-containing polyacrylamide NPs to be equally or more efficient in in vivo targeted treatment of glioma. Fluorescence emission at 680 nm vs time (after subtraction of photobleaching for both curves): (A) 3 mg/mL MB-containing NPs and (B) 1 μg/mL MB, respectively, when mixed in PBS (pH 7.2) with 0.45 μmol NADH and 0.05 mg diaphorase.…”