“…Its widespread offline utilization is due to the purification capacity of intact proteins with mild chromatographic conditions to permit further additional sample preparation steps with minimal impact on the conformational structure. The type of analytes and samples investigated by SEC in recent studies included exosomal proteins in human plasma [30], plasma exosomal proteins of corneal epithelial injury [31], extracellular vesicles in cancer cells [32,33], foam of recombinant biosurfactant apolipoprotein [34], peptides in alcalase hydrolisated pollen [35], circulating microparticles proteins to identify preterm babies before the end of 35 weeks of gestation [36], extracellular vesicle in cord blood of preterm and term births [37], α-Glucosidase-inhibitory peptides in dry-cured ham [38], extracellular vesicle in blood plasma [39], proteins in endogenous membrane proteins [40], N-Glycoproteins and phosphoproteins in human urine [41], high-density lipoproteins from plasma [42], proteins in antivenoms [43] and venoms of snakes [44], artificially created immune complexes on human serum [45], labelled proteins of E. coli lysate [46], extracellular vesicles in serum [47], β-Type Hemocyanin in shrimps [48], and extracellular vesicles in PLB-985 neutrophil-like cells [49].…”