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Addition of GSH led to significant increase in the FRET ratio that reached to the saturation at 50 min of incubation (Fig

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Finally, emerging evidence indicates that chitosan-based carriers (l-serinemodified chitosan) can exploit kidney injury molecule-1 (KIM1), a phosphatidylserine receptor markedly upregulated on the apical membrane of injured proximal tubular epithelial cells [90], to achieve active, injury-selective drug delivery [91]

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