A 2-layer approach towards optical sensing of acetylcholine and detection of an acetylcholinesterase inhibitor using photonic crystal sensor technology.
A nanoengineered
interface fabricated by self-assembly enables
the online determination of vitamin B12 via a simple luminescence
readout in serum without any pretreatment. The interplay of Tm3+-doped NaYF4 nanoparticles (UCNPs) and a gold
nanotriangle array prepared by nanosphere lithography on a glass slide
is responsible for an efficient NIR to UV upconversion. Hot spots
of the gold assembly generate local electromagnetic-field enhancement,
favoring the four-photon upconversion process at the low-power excitation
of approximately 13 W·cm–2. An improvement
by about 6 times of the intensity for the emission peaking at 345
nm is achieved. The nanoengineered interface has been applied in a
proof-of-concept sensor for vitamin B12 in serum, which is known as
a marker for the risk of cancer; Alzheimer disease; or, during pregnancy,
neurological abnormalities in newborn babies. Vitamin B12 can be detected
in serum down to 3.0 nmol·L–1 by a simple intensity-based
optical readout, consuming only 200 μL of a sample, which qualifies
as easy miniaturization for point-of-care diagnostics. Additionally,
this label-free approach can be used for long-term monitoring because
of the high photostability of the upconversion nanoparticles.
Nanoparticles are ubiquitously used for signal enhancement in (bio)sensors, but their true possible performance is typically hampered by non-specific binding. A better understanding of the nature and the prevention of non-specific binding through surface engineering of the particles and sensor surfaces is needed to intelligently design (bio)sensors and potentially avoid bulk blocking methods. Hence, two types of liposomes were used as model for signal-enhancing nanoparticles. Their surface was engineered to bear negative surface charge. One type was synthesized with additional 6 mol% -COOH groups. Their interaction with four typical chemically modified sensor surfaces was then mechanistically characterized by surface plasmon resonance (SPR) spectroscopy. It was shown that the non-specific binding can be described with Langmuir isotherms providing quantitative information of dissociation constants and surface loading with especially high correlation coefficients (>0.97) for all the studied sensor surfaces modified with hydrophilic alkane thiols. By tailoring the sensor surface chemistry, non-specific binding was significantly minimized. Here, carboxyl- or methyl-terminated surfaces performed best. In fact, the pairing of -COOH groups on the sensor surface with -COOH groups on the liposomes almost completely eliminated non-specific binding, resulting in a SPR signal change of only 1 mRIU (refractive index unit) at 100 μM phospholipid concentration. Surprisingly though, -OH groups on the surface, which are also commonly used in sensing applications, did not lead to decreased adsorption, but caused significant signal changes (4 mRIU at 100 μM phospholipid) due to non-specific binding. Overall, the mechanistic studies presented here demonstrate that by careful design of the nanoparticle surface and by choosing sensor surfaces with terminal -CH3 or -COOH groups, improved sensing (micro)systems with very low non-specific adsorption can be obtained.
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