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The effect of hepatic impairment on pharmacokinetics is well described and can be multifaceted, impacting not only the quantity and activity of hepatic enzymes [15,16,17], but also hepatic blood flow, protein binding, absorption, and renal elimination

Literature from Giampietri and co-authors [263], and, in a more meat analogue-oriented perspective, from Begho and Zhu [264], unveils that risk preference is an important determinant of food consumption for consumers

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These steps minimise copper coordination shifts and mechanical shear that drive aggregation, keeping the peptide in monomeric (single-molecule) form for optimal cellular uptake