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. Author manuscript; available in PMC: 2016 Oct 1.
Published in final edited form as: Biomaterials. 2015 Jul 17;67:183–193. doi: 10.1016/j.biomaterials.2015.07.033

Figure 4.

Figure 4

(A) The loading efficiency and particle size of TDP-A/DCMs versus the amount of drug added at initial loading. The final concentration of the polymers was kept at 20 mg/mL. Representative DLS size distribution (B) and TEM image (C) of TDP-A/DCMs (TDP-A loading was 1 mg/mL; TEM scale bar: 50 nm). (D) Cumulative drug release profile of TDP-A/DCMs in PBS or GSH (10 mM) when compared to that of free TDP-A dissolved in cyclodextrin or DMSO. Values reported are the mean diameter ± SD for triplicate samples.