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. 2016 Nov 11;7:13437. doi: 10.1038/ncomms13437

Figure 2. PCBAA surface modification enabling SERS detection in undiluted human blood plasma.

Figure 2

(a) SERS spectra acquired with the unmodified SERS optofluidic system. From top to bottom, spectra shown were recorded after flowing undiluted plasma, PBS and plasma spiked with 1 μM R6G each for 10 min. (b) SERS spectra acquired with the pCBAA-modified SERS optofluidic system. From top to bottom, spectra shown were recorded after flowing PBS, undiluted plasma and plasma containing 1 μM R6G each for 10 min, along with the subtracted spectrum from the last two. λex=785 nm, Plaser=1 mW and t=30 s with three accumulations. (c) Monitoring plasma protein adsorption and detecting R6G in plasma with the unmodified and pCBAA-modified SERS optofluidic system. Peak intensity of the amide I at 1,649 cm−1 for protein and the C–C stretching at 1,508 cm−1 for R6G were recorded as a function of time as PBS, plasma, PBS and R6G-spiked plasma were flowed sequentially. (d) Typical SPR sensorgram of protein adsorption from undiluted plasma on a bare gold and pCBAA-modified gold surface, showing protein adsorption of 452 and 0.3 ng cm−2, respectively.