Optical Sensors 2013 2013
DOI: 10.1117/12.2016510
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Nanoliter-scale, regenerable ion sensor: sensing with surface functionalized microstructured optical fiber

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Cited by 5 publications
(5 citation statements)
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“…Each fiber was precleaned and hydroxylated by immersion in nitric acid followed by piranha solution and then functionalized with alternating layers of poly(allylamine hydrochloride) (PAH), poly(acrylic acid) (PAA) and further PAH 26 for the exposed core fiber and APTES for the suspended core fiber. 27 The SP2maltose-liposomes were then coupled onto to the surfacebound free amines using standard coupling conditions 27 (HATU/DIPEA; Supporting Information) to give the functionalized exposed core and suspended core sensors. The ability of the exposed core fiber-based sensor to bind and detect Zn 2+ was studied using the optical set up depicted in Figure 5.…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…Each fiber was precleaned and hydroxylated by immersion in nitric acid followed by piranha solution and then functionalized with alternating layers of poly(allylamine hydrochloride) (PAH), poly(acrylic acid) (PAA) and further PAH 26 for the exposed core fiber and APTES for the suspended core fiber. 27 The SP2maltose-liposomes were then coupled onto to the surfacebound free amines using standard coupling conditions 27 (HATU/DIPEA; Supporting Information) to give the functionalized exposed core and suspended core sensors. The ability of the exposed core fiber-based sensor to bind and detect Zn 2+ was studied using the optical set up depicted in Figure 5.…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…Details on the synthesis of SHL are reported in the synthesis section of the Supplemental Information. In brief, the Li 1 sensor was prepared from 1-aza-15-crown-5 and 1-(2-hydroxyethyl)-2,3,3-trimethyl-3H-indol-1ium to give SHL with an overall yield of 20% using a modification to existing methodology (Heng et al, 2013;Stubing et al, 2016).…”
Section: Resultsmentioning
confidence: 99%
“…Benzylic bromide ( 2 ) was prepared by reaction of the N -substituted benzylaldehyde with paraformaldehyde in the presence of HBr. Reaction of these halides with bis(2-pyridylmethyl) amine gave 3 , respectively, which was reacted with 4 , 39 with final purification by normal-phase chromatography, giving the desired sensor 5 , as detailed in the Supporting Information section. 1 H, 13 C NMR spectra for sensor 5 can be found in the Supporting Information section.…”
Section: Resultsmentioning
confidence: 99%
“…Compound 4 (Scheme 1) was prepared as previously described. 39 1 H and 13 C NMR spectra were recorded on a Varian 500 MHz and Varian Inova 600 MHz instruments in the indicated solvents. Chemical shifts are reported in ppm (δ).…”
Section: ■ Conclusionmentioning
confidence: 99%