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The linker-doxorubicin (DOX) conjugate can be conjugated (a) to a peptide prior to the assembly of the peptide onto the quantum dot (QD) surface or (b) directly to a QD-capping ligand, such as dihydrolipoic acid (DHLA). EDC—N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride.
