ABSTRACT
A cheap, compact, and simply prepared all-fiber bidirectional optical modulator based on the Pockels effect of water and the band population effect was first, to the best of our knowledge, proposed and demonstrated. The transparent conductive oxide indium-tin-oxide (ITO) was coated on the surface of a nonadiabatic microfiber and first used as a modulating electrode on the microfiber. The device was realized by just submerging the microfiber in water. With supplying an electric field perpendicular to the interface between the microfiber and water, the refractive index was modulated in the electric double layer near the tapered region of the microfiber, under the Pockels effect of water. Subsequently, the interference spectrum was modulated. Meanwhile, the intensity of the light was modulated due to the band population effect in the space-charge layer. In this Letter, the proposed all-fiber optical modulator can realize simultaneous bidirectional modulation of the phase and intensity of output light. Experimentally, the maximum phase shift and the extinction ratio were 4.38 nm and 4.87 dB at 1550 nm, respectively. Significantly, the work used the Pockels effect of water and the band population effect to realize an all-fiber optical modulator, showing great potential in the optical phase modulators, optical switches, and electric field sensors.
ABSTRACT
In this Letter, we propose a microstructured in-fiber optofluidic surface-enhanced Raman spectroscopy (SERS) sensor for the initial inspection of uremia through the detection of unlabeled urea and creatinine. As a natural microfluidic device, microstructured hollow fiber has a special structure inside. Through chemical bonds, the SERS substrate can be modified and grown on the surface of the suspended core. Here, the silver nanoparticles (Ag NPs) are embedded on the poly diallyl dimethyl ammonium chloride-modified graphene oxide sheet to achieve the self-assembled SERS substrate. The reduced distance between Ag NPs can increase the strong hot spots that generate enhanced Raman signals. Therefore, it can effectively detect the Raman signal of unlabeled trace uremic toxin analytes (urea, creatinine) inside the optical fiber. The results show that under simulated biophysical conditions, the limit detection (LOD) for urea is 10-4M and the linearity is good, especially at the clinical conventional concentration range (2.5-6.5×10-3M). In addition, the online Raman detection of creatinine aqueous solution LOD is 10-6M, which also has good linearity. Significantly, this Letter provides a microstructured optofluidic in-fiber Raman sensor for the preliminary detection of uremia, which will have good development prospects in the field of clinical biomedicine.
Subject(s)
Limit of Detection , Optical Fibers , Spectrum Analysis, Raman/instrumentation , Toxins, Biological/metabolism , Uremia/metabolismABSTRACT
In this paper, we present a microstructured optofluidic in-fiber Raman sensor for the detection of quinolone antibiotic residue in a water environment based on Ag surface-enhanced Raman scattering (SERS) substrate grown on the surface of the suspended core of micro-hollow optical fiber (MHF). Here, MHF has a special structure with a suspended core and a microchannel inside, which can become a natural in-fiber optofluidic device. Meanwhile, the self-assembled Ag SERS substrate can be grown on the suspended core's surface through chemical bonds, forming a microstructured optofluidic device with a Raman enhancement effect. Therefore, it can effectively detect the Raman signal of unlabeled trace quinolone antibiotic residue (ciprofloxacin and norfloxacin) inside the optical fiber. The results show that the ciprofloxacin and norfloxacin detection limits (LOD) are 10-10M and 10-11M, respectively. Compared with the maximum residue limit (3.01×10-7mol/L) stipulated by the European Union, the results are much lower, and an ideal quantitative relationship can be obtained within the detection range. Significantly, this study provides an in-fiber microstructured optofluidic Raman sensor for the label-free detection of quinolone antibiotic residue, which will have good development prospects in the field of antibiotic water pollution environmental detection.
Subject(s)
Drug Residues/analysis , Metal Nanoparticles , Optical Fibers , Quinolones/analysis , Spectrum Analysis, Raman/instrumentation , Water Pollutants, Chemical/analysis , Anti-Bacterial Agents/analysis , Ciprofloxacin/analysis , Europe , Metal Nanoparticles/ultrastructure , Microscopy, Electron, Scanning , Norfloxacin/analysis , Reference Values , SilverABSTRACT
All-fiber modulators and switches have drawn great interest in the photonics domain, and they are applied in viable photonic and optoelectronic devices. In this work, with the assistance of an agarose membrane, aspherical gold nanoparticles are embedded on the surface of the microfiber treated with the piranha solution. An all-fiber Mach-Zehnder interferometer was used to realize a low-cost, low-loss, and conveniently prepared all-fiber phase modulator. By taking advantage of the local surface plasmon resonance effect of gold nanoparticles embedded in the agarose membrane, under the excitation of near-infrared region light, the gold nanoparticles were excited to change the effective refractive index of one arm of the Mach-Zehnder interferometer. A maximum phase shift of â¼6π at 1550 nm was obtained from the device. In addition, an all-optical switch was achieved with a rising edge time of 47 ms and falling edge time of 14 ms. The proposed all-fiber modulator and switch based on the local surface plasmon resonance effect of gold nanoparticles embedded in agarose membrane will provide great potential in all-optical fiber systems.
ABSTRACT
Arsenic contamination of drinking water is a global concern. Standard laboratory methods that are commonly used for arsenic detection in water, such as atomic absorption spectroscopy and mass spectroscopy, are not suitable for mass monitoring purposes. Autonomous microfluidic detection systems combined with a suitable colorimetric reagent could provide an alternative to standard methods. Moreover, microfluidic detection systems would enable rapid and cost efficient in situ monitoring of water sources without the requirement of laborious sampling. The aim of this study is to optimize a colorimetric method based on leucomalachite green dye for integration into a microfluidic detection system. The colorimetric method is based on the reaction of arsenic (III) with potassium iodate in acid medium to liberate iodine, which oxidizes leucomalachite green to malachite green. A rapid colour development was observed after the addition of the dye. Beer's law was obeyed in the range between 0.07â»3 µg mL-1. The detection limit and quantitation limit were found to be 0.19 and 0.64 µg mL-1, respectively.
Subject(s)
Arsenic/analysis , Colorimetry , Rosaniline Dyes , Water Pollutants, Chemical/analysis , Water/analysis , Water/chemistry , Colorimetry/methods , Hydrogen-Ion Concentration , Indicators and Reagents , Rosaniline Dyes/chemistry , Sensitivity and Specificity , TemperatureABSTRACT
In this paper, we propose a self-assembled graphene oxide (GO)/Ag NPs SERS Raman sensor based on a novel type of optofluidic MHF as a point-of-care testing (POCT) device. This device is used to diagnose jaundice and its related diseases through on-line detection of free bilirubin content in human serum. This optofluidic Raman sensor is composed of a microstructured hollow fiber (MHF) with a microstructured channel and a suspended core, which allows the sample solution to flow in the channel while interacting with the strong evanescent field on the suspended core. Here, the suspended core was modified by a GO/Ag NPs SERS substrate. When the sample flows through the channel, and interacts with the strong evanescent field generated by the suspended core, the on-line SERS signal is generated and can be coupled back to the suspended core to be detected. In addition, both the electrostatic interaction and interference between GO/Ag NPs with the target enriched bilirubin. The results show that the detection concentration range of bilirubin aqueous, bilirubin in albumin and bilirubin in human blood are all in the range of 2 µM-100 µM, and all have a good linear response. The limit of detection reaches the order of 10-6 M. This rapid, sensitive and label-free SERS Raman sensor of free bilirubin in blood can detect excessive levels of bilirubin in the actual blood environment of the human body, providing a broad prospect for clinically accurate diagnosis of jaundice and related diseases.
Subject(s)
Jaundice , Metal Nanoparticles , Bilirubin , Graphite , Humans , Silver , Spectrum Analysis, RamanABSTRACT
Chromium contamination of drinking water has become a global problem due to its extensive use in industry. The most commonly used methods for chromium detection in water are laboratory-based methods, such as atomic absorption spectroscopy and mass spectroscopy. Although these methods are highly selective and sensitive, they require expensive maintenance and highly trained staff. Therefore, there is a growing demand for cost effective and portable detection methods that would meet the demand for mass monitoring. Microfluidic detection systems based on optical detection have great potential for onsite monitoring applications. Furthermore, their small size enables rapid sample throughput and minimises both reagent consumption and waste generation. In contrast to standard laboratory methods, there is also no requirement for sample transport and storage. The aim of this study is to optimise a colorimetric method based on 1,5-diphenylcarbazide dye for incorporation into a microfluidic detection system. Rapid colour development was observed after the addition of the dye and samples were measured at 543 nm. Beer's law was obeyed in the range between 0.03-3 mg·L-1. The detection limit and quantitation limit were found to be 0.023 and 0.076 mg·L-1, respectively.