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10 units = 250 mcg each

This strategic design allows researchers to fully engage the GIP pathway for enhanced metabolic effects while minimizing the dose-limiting gastrointestinal tolerability issues common with high-dose GLP-1 agonism, making it uniquely valuable for studying synergistic incretin mechanisms

Overall, the in vitro results of the 13 studies on melanoma cells revealed the potential of nanotechnology-mediated drug delivery systems for the treatment of melanoma (Table 6)

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