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In infarcted heart tissue, the nanoparticle achieves a 23.1-fold higher puerarin concentration versus free drug, 2.2-fold versus non-targeted PUE-SLN, and 1.3-fold versus PEGylated nanoparticles without RGD
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α-lipoic acid protects against microcystin-LR induced hepatotoxicity through regeneration of glutathione via activation of Nrf2
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