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. Author manuscript; available in PMC: 2020 Apr 21.
Published in final edited form as: ACS Appl Mater Interfaces. 2018 Nov 13;10(47):40378–40387. doi: 10.1021/acsami.8b08254

Figure 2.

Figure 2.

A) and B) GPC signals of Nap-Dex (blue), dextran (black) and Nap-Dex incubated with 10 mM H2O2 (green). Samples were incubated for 24 hours before the measurement in 80 v% DMF and 20 v% aqueous solutions. C) Nap-Dex solution with/without 10 mM H2O2. Nap-Dex was dissolved in 50 v% DMSO and 50 v% H O and incubated for 3 hours at 37 ° Polymer concentration was 10 mg/ml and H2O2 concentration was adjusted to 0 mM or 10 mM. D) Turbidity change of the Nap-Dex solution measured by UV-Vis spectrometer. Nap-Dex solution (2 mg/ml in 50 v% DMSO and 50 v% aqueous) was incubated at 37 °C and the absorption at 750 nm was monitored by incubation time. E) LC-MS comparison between released molecules from Nap-Dex by H2O2 and pure naproxen. The Nap-Dex solution incubated with 10 mM H2O2 was filtrated using ultracentrifugal filtration and filtrated molecules were injected into LC-MS. F) Naproxen release from Nap-Dex by H2O2. The naproxen signal in LC-MS was monitored by incubation time. The release amount was calculated based on a calibration curve.