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Conclusion Cu(II)-binding affinities for three major blood copper proteins: human serum albumin, ceruloplasmin and alpha-2-macroglobulin, were studied through their competition with a set of low-molecular weight Cu(II)-binding reference ligands (DTPA, EDTA, NTA, His) by using an unified LC-ICP MS-based approach

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To facilitate regulatory approval and clinical adoption, future research should focus on standardized formulation strategies, robust pharmacokinetic profiling (including C_max, AUC, and tissue distribution), long-term reproductive safety studies, and carefully planned randomized controlled trials comparing nanoformulations with both free phytochemicals and standard-of-care therapies