Abstract
Plasmonic bio/chemical sensing based on optical fibers combined with molecularly imprinted nanoparticles (nanoMIPs), which are polymeric receptors prepared by a template-assisted synthesis, has been demonstrated as a powerful method to attain ultra-low detection limits, particularly when exploiting soft nanoMIPs, which are known to deform upon analyte binding. This work presents the development of a surface plasmon resonance (SPR) sensor in silica light-diffusing fibers (LDFs) functionalized with a specific nanoMIP receptor, entailed for the recognition of the protein human serum transferrin (HTR). Despite their great versatility, to date only SPR-LFDs functionalized with antibodies have been reported. Here, the innovative combination of an SPR-LFD platform and nanoMIPs led to the development of a sensor with an ultra-low limit of detection (LOD), equal to about 4 fM, and selective for its target analyte HTR. It is worth noting that the SPR-LDF-nanoMIP sensor was mounted within a specially designed 3D-printed holder yielding a measurement cell suitable for a rapid and reliable setup, and easy for the scaling up of the measurements. Moreover, the fabrication process to realize the SPR platform is minimal, requiring only a metal deposition step.

Abstract
Nanoparticles create localized surface plasmonic resonances (LSPR) with lower surrounding refractive index (SRI) sensitivities than their propagating SPR counterpart, originated in thin films. Historically, LSPR SRI sensitivities enhancements were achieved through spectral analysis methods that focus on unique spectral features. Herein, a study using that methodology was applied on SPR devices resulting in an increased sensitivity to SRI. It was found that by applying the inflection point method on optical fiber SPR sensors resulted in both sensitivity and resolution increments up to 44 and 35 %, respectively, in the SRI range from 1.3333 to 1.4150. Thus, successfully improving sensing capabilities of SPR based optical fiber sensors. © 2022, Universidade do Porto - Faculdade de Engenharia. All rights reserved.

Abstract
Relative humidity is an important parameter in controlled environments and is typically monitored using low-cost electrochemical sensors with low resolution and accuracy. This kind of sensors cannot not be implemented in harsh or explosive environments (as in pyrotechnic facilities) due to electrical discharges, or in marine structures where the oxidation of the sensing probe materials changes the sensing response). In these cases, fiber optic sensors can provide solutions due to their intrinsic properties, such as immunity to electromagnetic interference and resistance in harsh environments. This work presents preliminary results regarding the steps of the fabrication of Long-Period Fiber Gratings, the coating processes with a thin layer of poly(ethylene glycol) (PEG) and its sensing performance to relative humidity, displaying a from 60 to 100%sensitivity of 0.6 nm/%RH in the range of 80 to 100%RH. © 2022, Universidade do Porto - Faculdade de Engenharia. All rights reserved.

Abstract
Fiber optic-based refractometers is a thoroughly researched field, with many different configurations being used. However, most designs require external calibration using substances of known refractive index (RI) and their fabrication process might be impractical and time consuming, creating the need for a quick and accurate method of measuring RI of different substances. A simple method for simultaneous measurement in real-time of RI and thickness of polymer thin films is presented, allowing dynamic measurements in the presence of changing environmental parameters, such as temperature or humidity. This method, which does not require previous calibration, is based on an inline Fabry-Perot (FP) cavity, created by dipping the tip of a cleaved optical fiber (OF) in a polymer solution. The procedure consists of using the equations of the low finesse FP interferometers to directly extract information from the structure created, such as RI and cavity length, by working in the spectral window from 1500 to 1600nm. The method was validated by creating FP cavities with liquids of known RI, for which a typical precision of 3 x 10(-3) was achieved, along with errors lower than 0.6% and 1% for RI and cavity length determination, respectively, The procedure was then used to monitor three different curing processes, namely the temperature curing of Sylgard (TM) 184, the UV curing of Norland Optical Adhesives (TM) 65 and the mixing and curing of Ceys (TM) Araldite epoxy glue. Both RI and cavity length were compared to reference values, showing excellent agreement with the experimental results for a method that does not require external calibration.

Abstract
A new sensing platform based on long-period fiber gratings (LPFGs) for direct, fast, and selective detection of human immunoglobulin G (IgG; Mw = 150 KDa) was developed and characterized. The transducer's high selectivity is based on the specific interaction of a molecularly imprinted polymer (MIPs) design for IgG detection. The sensing scheme is based on differential refractometric measurements, including a correction system based on a non-imprinted polymer (NIP)-coated LPFG, allowing reliable and more sensitive measurements, improving the rejection of false positives in around 30%. The molecular imprinted binding sites were performed on the surface of a LPFG with a sensitivity of about 130 nm/RIU and a FOM of 16 RIU-1. The low-cost and easy to build device was tested in a working range from 1 to 100 nmol/L, revealing a limit of detection (LOD) and a sensitivity of 0.25 nmol/L (0.037 mu g/mL) and 0.057 nm.L/nmol, respectively. The sensor also successfully differentiates the target analyte from the other abundant elements that are present in the human blood plasma.

Abstract
A strategy for the detection of H2O2 as a milk adulterant using a single shot membrane sensor, is presented. Direct quantitative evaluation of H2O2 in raw, skimmed, semi-skimmed and whole milk was carried out based on a chemiluminescence reaction with luminol. For H2O2 water solutions a linear response was attained from 0.0001% to 0.007 %w/w, with a limit of detection of 3x10(-5) %w/w. A coefficient of determination, R-2, greater than 0.97 was achieved, with a relative standard deviation (RSD) not exceeding 10%. In the analyzed milk samples, the lowest H2O2 concentration detected was 0.001% w/w for raw and for skim milk and 0.002%w/w for, semi-skimmed and whole milk. The presented method is original, sensitive, rapid, and cost-effective. Due to the achieved sensitivity the method has great potential to be used for H2O2 detection in diverse areas, such as environmental monitoring and food quality.