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Based on the encouraging data from this cohort of patients, the optimal dosing, timing of up-titration, and ideal start time in patient disease stage warrant further study in a prospective manner." As noted above, the FDA approved S/V for humans in 2015 to reduce the risk of cardiac death in patients with chronic heart failure

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Among these, the in vivo immunotoxicity caused by nanoparticles mainly includes blood immunotoxicity, tissue inflammation, and immune organ damage

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