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To further validate the multivalent interactions of D-CuP, SPR analysis was performed to quantify its binding ability to p53 and HDAC7 in comparison with M-CuP
Lyophilized forms maintain stability for 12-18 months at proper temperatures
Focus on bioavailability by choosing liposomal formats
Good middle-ground option between CagriSema and cag + reta
Current clinical-trial and FDA materials provide additional topical, compounding, and regulatory context [9] [10] [11] [12]
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