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Circulating plasma biomolecules encompass the vast collection of proteins, lipids, metabolites, and signaling molecules found within the blood plasma (Source [1], [4]). This heterogeneous group includes major proteins such as albumin, which regulates oncotic pressure, and fibrinogen, which is essential for blood coagulation (Source [3], [7]). These biomolecules play critical roles in physiological processes including nutrient transport, immune defense, and systemic communication (Source [4], [8]). In clinical medicine, they serve as vital biomarkers for diagnosing and monitoring diseases like myocardial infarction, diabetes, and systemic inflammation (Source [3], [6]). While not a single therapeutic target, individual components within this category are frequently targeted by drugs to treat conditions ranging from hemophilia to hyperlipidemia (Source [5], [7]). For example, anticoagulants target specific clotting factors, while statins modulate lipoprotein levels (Source [4]). Furthermore, the interaction of these molecules with therapeutic agents, particularly nanoparticles, can significantly alter drug pharmacokinetics and biodistribution (Source [2]). Research into the plasma proteome and metabolome continues to identify novel specific targets for precision medicine (Source [5], [6]).
Therapeutic strategies involve the replacement of deficient plasma proteins, the inhibition of specific circulating enzymes or factors, and the modulation of lipid transport particles to treat systemic diseases (Source [4], [5], [7]).
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