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Conclusions Complexes (1,2) are expected to be isostructural due to similarity of the N.N-chelating ligands used, but due to the difference in supramolecular architectures no similar unit cells were observed

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Herein, Au nanoparticles (AuNPs), mesoporous silica nanoparticles (MSN), cationic ligand (triphenylphosphine (TPP)), doxorubicin (DOX), and carbon nanodots (CDs) were utilized to fabricate mitochondrial targeting drug delivery system (denoted as CDs(DOX)@MSN-TPP@AuNPs)

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