In this work, a novel optical fiber sensor system for ultra-low perfluorooctanoic acid (PFOA) detection in aqueous solutions is proposed. It is based on the connection, in series, of two different plastic optical fiber (POF) platforms: the first is a chemical chip realized by using a D-shaped POF with microholes filled with a specific molecularly imprinted polymer (MIP); the second is a typical surface plasmon resonance (SPR) sensor based on a D-shaped POF. In particular, the MIP-based chemical chip was used to launch the light inside the SPR–POF chip to change the SPR phenomenon by exploiting the PFOA–MIP interaction in the microholes. At first, experimental results were performed in water to demonstrate the applicability of the proposed sensing approach for measuring PFOA (or C8) in a concentration range of 1 ppt to 750 ppt, obtaining an ultra-low limit of detection (LOD) equal to about 0.81 ppt. Then, experimental results were carried out in simulated seawater to implement a complex matrix. The obtained results denoted a slight matrix effect, paving the way for the applicability of the proposed chemical sensing mechanism in several aqueous solutions.

In this work, a novel optical–chemical sensor for the detection of per- and polyfluorinated substances (PFASs) in a real scenario is presented. The proposed sensing approach exploits the multimode characteristics of plastic optical fibers (POFs) to achieve unconventional sensors via surface plasmon resonance (SPR) phenomena. The sensor is realized by the coupling of an SPR-POF platform with a novel chemical chip based on different polymeric nanolayers over the core of a D-shaped POF, one made up of an optical adhesive and one of a molecularly imprinted polymer (MIP) for PFAS. The chemical chip is used to launch the light into the SPR D-shaped POF platform, so the interaction between the analyte and the MIP’s sites can be used to modulate the propagated light in the POFs and the SPR phenomena. Selectivity tests and dose–response curves by standard PFOA water solutions were carried out to characterize the detection range sensor response, obtaining a wide PFAS response range, from 1 ppt to 1000 ppt. Then, tests performed on river water samples collected from the Bormida river paved the way for the applicability of the proposed approach to a real scenario.

Cortisol is a clinically validated stress biomarker that takes part in many physiological and psychological functions related to the body’s response to stress factors. In particular, it has emerged as a pivotal tool for understanding stress levels and overall well-being. Usually, in clinics, cortisol levels are monitored in blood or urine, but significant changes are also registered in sweat and saliva. In this work, a surface plasmon resonance probe based on a D-shaped plastic optical fiber was functionalized with a glucocorticoid receptor exploited as a highly efficient bioreceptor specific to cortisol. The developed plastic optical fiber biosensor was tested for cortisol detection in buffer and artificial saliva. The biosensor response showed very good selectivity towards other hormones and a detection limit of about 59 fM and 96 fM in phosphate saline buffer and artificial saliva, respectively. The obtained detection limit, with a rapid detection time (about 5 min) and a low-cost sensor system, paved the way for determining the cortisol concentration in saliva samples without any extraction process or sample pretreatment via a point-of-care test.

Interleukins are involved in several diseases and cancers, and their detection and monitoring are of great interest. Their low abundance and short half-lives suggest the need to develop rapid, specific, and highly sensitive detection platforms, easily integrable in point-of-care (POC) systems. Among the other interleukins, interleukin IL-17A is associated with inflammations, neurodegenerative diseases, and cancers, and no biosensors have been previously reported for its detection. In this work, for the detection of IL-17A, a highly sensitive nanoplasmonic sensor based on natural nanostructures like pollen shells, covered by a gold film and a bio-receptor layer, is presented. Hybrid plasmonic modes are exploited to reach high sensitivity without using costly techniques to fabricate periodic nanostructures, such as electron beam lithography. A transparent amino-modified glass substrate is functionalized with carboxylic activated pollen via carbodiimide chemistry. Then, the pollen-based nanostructures are covered by a gold film and derivatized by an immuno-layer specific to IL-17A recognition. The developed IL-17A biosensor is monitored via a simple, small-sized, and low-cost experimental setup, demonstrating high selectivity, a fast response time of about five minutes, and sensitivity with a limit of detection in the ag/mL concentration range. The biosensor allows for the detection of IL-17A in complex solutions thanks to the possibility of high dilution, an advantageous aspect to POC systems.

Molecularly imprinted polymers (MIPs) can be combined with optical fibers (OFs) to create various sensor configurations, yielding low-cost and highly sensitive extrinsic and intrinsic sensors. In this work, an MIP-based extrinsic optical fiber sensor is obtained by two silica OFs connected via an optical waveguide using an MIP as a core of micrometer size (micro OF-MIP-OF sensor). The proposed sensing approach can be used only with MIP receptors and implements an intensity-based sensor configuration. MIPs present several advantages over bio-receptors and can be exploited to realize novel sensing methods. The MIP used in this work is specifically designed for 2-furaldehyde (2-FAL) detection, and the experimental results demonstrate that the micro-probe performs well in terms of sensitivity and selectivity, with capabilities applicable to several application fields. In particular, a nanomolar detection range, from 1.5 nM to 150 nM, has been achieved. Moreover, the results are comparable to or better than those of other previously proposed MIP optical fiber sensors for 2-FAL, which employ more complex sensing principles or fabrication steps.

A successful immunosensor is characterized by a proper antibody immobilization and orientation in order to enhance the antigen recognition. In this work, a thorough characterization of the antibody functionalized gold surface is performed to set up the best conditions to implement in an optical platform for the detection of Brucella sp. Two different strategies are evaluated, based on a random immobilization and on an oriented one: a direct antibody immobilization on carboxylic mixed polyethylene (PEG) self-assembled monolayer (SAM) or only carboxylic PEG SAM interface is compared to an oriented immobilization on a layer of protein G on the same PEG SAM interfaces. X-ray Photoelectron Spectroscopy (XPS), Time of Flight Secondary Ion Mass Spectrometry (ToF-SIMS) and contact angle (CA) are used to chemically characterize the gold functionalized surface and ToF-SIMS is also used to confirm the right antibody orientation. Optical characterization is applied to monitor the functionalization steps and fluorescence measurements are used to set up the proper experimental conditions and also to detect Brucella bacteria on the surface. Best results are obtained with a 10 ng/μl incubation solution of antibody immobilized, in an oriented way, on a mixed PEG SAM interface.