“…As demonstrated in previous studies [ 70 , 71 , 72 ], DCDR analysis showed detection sensitivity superior to conventional Raman for small biological molecules, such as acetylsalicylic acid, riboflavin, and contaminants [ 73 , 74 ], down to a detection limit of 10 −8 M. It also proved to be an important tool for membrane-interaction studies, such as the liposome–porphyrin complex [ 75 ], for the quantitative determination of creatinine in urine [ 76 ], and for colorectal cancer detection in blood plasma [ 77 ]. The advantages of DCDR analysis include the use of dried, preconcentrated samples, a small sample volume, no interference from solvents, and the capability to segregate any existing impurities [ 76 ].…”