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. Author manuscript; available in PMC: 2019 Feb 1.
Published in final edited form as: Biomaterials. 2017 Nov 21;155:217–235. doi: 10.1016/j.biomaterials.2017.11.025

Fig. 4.

Fig. 4

(a) Schematic illustration of SPN12 preparation by nanoprecipitation and ClO sensing. (b) Fluorescence performance of SPN12 in the presence of different concentrations of ClO. (c) Fluorescence spectra of SPN12 in the presence of various ROS and biologically relevant analytes. (d) In vivo imaging of exogenous ClO using SPN12. Representative ratiometric (pseudocolor) image of mouse with the subcutaneous implantation of SPN12 (left) and SPN12 + ClO (right). (e) In vivo imaging of endogenous ClO production from the peritoneal cavity of the mice with SPN12 during an LPS-mediated inflammatory response. Representative ratiometric images (pseudocolor) of mice intraperitoneally treated with saline (left) and LPS (right), followed by an intraperitoneal injection of SPN12 at 4 h later. Fluorescence images were acquired 30 min after the injection of SPN12 with a 465 nm excitation filter and 540 nm (green channel) and 680 nm (red channel) emission filters. Ratiometric images were obtained by pixel-by-pixel calculation using ImageJ software. Reprinted with permission from Ref. [87], copyright 2017, American Chemical Society.