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Variations in nanomaterial size, surface charge, or functionalization can critically alter pharmacokinetics and therapeutic outcomes, making standardization a pressing bottleneck

The number of sessions varies based on individual skin concerns, treatment goals, and the chosen treatment plan

Dipeptidyl boronic acid inhibitors (e.g., bortezomib, MG-132, and MG-262) potently inhibit both the 26S proteasome and LONP1 proteolytic activity [45, 53, 176]