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Once the autophagosome has formed around its target, a lysosome can merge with it, delivering its degradative enzymes to the enclosed, pathogenic cargo

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Studien deuten darauf hin, dass die krpereigene Glutathion-Produktion ab dem 40

Particle size is a critical determinant of biodistribution: nanoparticles exceeding approximately 100 nm are readily captured by the mononuclear phagocyte system (MPS) in the liver and spleen, significantly limiting renal access [54]

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