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. 2020 Feb 10;11(3):1316–1326. doi: 10.1364/BOE.379518

Fig. 5.

Fig. 5.

(a) Spectral response of the fabricated end-capped sensor at different stages of the immunoassay: functionalization with antigenic lipids and immersion in Pre-immune and Hype-immune sera. The dashed and the continuous lines represent the first and last acquired interference pattern, respectively. (b) Wavelength shift (Δλ) during detection of antigen-antibody binding on PDMS. Curves A, B and C show the performance of untreated (i.e., without the lipid antigen) sensors during incubation in PBS (T=37 °C) (A), control (PS) (B) and specific antibody-containing Hyper-immune (HS) (C) sera from lipid-immunized rabbits (1:400(μL/μL)). Curves D and E were obtained with functionalized sensors immersed in PS (D) and HS (E) sera (see text for details). The shadows on the curves represent the standard deviation from triplicate measurements.