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. 2023 Feb 28;296:122071. doi: 10.1016/j.biomaterials.2023.122071

Fig. 7.

Fig. 7

Co-loading of AZ and MPS to NVs ameliorates bacterial burden and inflammation-induced lung damage in a mouse lung infection model. (A) Animal protocol for evaluating the therapeutic effect of AZ-MPS-NVs in the lung infection. CFU of bacteria in blood (B) and in the lung (C). Leukocytes (D) and neutrophils (E) in BALF; (F) the lung permeability determined by total proteins in BALF. Cytokines in BALF (G) and in blood (H). Data presented as the mean ± SD, n = 3,4. *P < 0.05, **P < 0.01, and ***P < 0.001.