Recent development in nanomaterials fabricated paper-based colorimetric and fluorescent sensors: A review

The paper-based sensing devices have drawn a broad interest in analytical chemistry for colorimetric and fluorescent-based analysis of biological, environmental, clinical, and food samples. It is due to the simple, rapid, biodegradable, user-friendly, less expensive, and low waste generation into the environment. Here, the recent development of paper-based sensors fabricated with different noble metal nanoparticles (NPs) and semiconductor and carbon quantum dots (QDs) is demonstrated to analyze several chemical substances from various samples. User-friendly and portable recording devices such as digital cameras, smartphones, scanners, etc. along with color detecting softwares are employed to measure the color intensity of nanomaterials fabricated paper devices after the deposition of a sample solution containing various chemical substances. The advantages and disadvantages of incorporating nanomaterials in the paper substrate (direct deposition, inkjet printing, screen printing and wax printing) are illustrated. The mechanism for colorimetric, fluorescence, phosphorescence, and chemiluminescence sensing using noble metal NPs (Ag, Cu, and Au), semiconductors, and carbon QDs for the determination of metal ions, anions, pesticides, biomolecules, and other toxic chemical substances are discussed. Thus, this review article would be highly useful for scientists and researchers to design colorimetric sensors to monitor chemical toxicants in clinical, environment, foods, and many other related samples.     

Lipopolysaccharide identification with functionalized polydiacetylene liposome sensors

The outer membrane of Gram negative bacteria contains lipopolysaccharides, which are glycolipids with carbohydrate sequences that are unique for each bacterial species and serotype. In this communication, we report a method for identifying LPS from different bacteria using an electronic tongue approach. Two functionalized polydiacetylene liposomes were used as colorimetric sensors for detecting various types of LPS. These liposomes were assayed under four different experimental conditions to generate a data set of eight colorimetric responses. This data set constitutes a unique fingerprint for each analyte and permits identification of each LPS type.     

Fabrication of paper-based microfluidic sensors by printing

A novel method for the fabrication of paper-based microfluidic diagnostic devices is reported; it consists of selectively hydrophobizing paper using cellulose reactive hydrophobization agents. The hydrophilic–hydrophobic contrast of patterns so created has excellent ability to control capillary penetration of aqueous liquids in paper channels. Incorporating this idea with digital ink jet printing techniques, a new fabrication method of paper-based microfluidic devices is established. Ink jet printing can deliver biomolecules and indicator reagents with precision into the microfluidic patterns to form bio-chemical sensing zones within the device. This method thus allows the complete sensor, i.e. channel patterns and the detecting chemistries, to be fabricated only by two printing steps. This fabrication method can be scaled up and adapted to use high speed, high volume and low cost commercial printing technology. Sensors can be fabricated for specific tests, or they can be made as general devices to perform on-demand quantitative analytical tasks by incorporating the required detection chemistries for the required tasks.     

Use of multiple colorimetric indicators for paper-based microfluidic devices

We report here the use of multiple indicators for a single analyte for paper-based microfluidic devices (μPAD) in an effort to improve the ability to visually discriminate between analyte concentrations. In existing μPADs, a single dye system is used for the measurement of a single analyte. In our approach, devices are designed to simultaneously quantify analytes using multiple indicators for each analyte improving the accuracy of the assay. The use of multiple indicators for a single analyte allows for different indicator colors to be generated at different analyte concentration ranges as well as increasing the ability to better visually discriminate colors. The principle of our devices is based on the oxidation of indicators by hydrogen peroxide produced by oxidase enzymes specific for each analyte. Each indicator reacts at different peroxide concentrations and therefore analyte concentrations, giving an extended range of operation. To demonstrate the utility of our approach, the mixture of 4-aminoantipyrine and 3,5-dichloro-2-hydroxy-benzenesulfonic acid, o-dianisidine dihydrochloride, potassium iodide, acid black, and acid yellow were chosen as the indicators for simultaneous semi-quantitative measurement of glucose, lactate, and uric acid on a μPAD. Our approach was successfully applied to quantify glucose (0.5-20 mM), lactate (1-25 mM), and uric acid (0.1-7 mM) in clinically relevant ranges. The determination of glucose, lactate, and uric acid in control serum and urine samples was also performed to demonstrate the applicability of this device for biological sample analysis. Finally results for the multi-indicator and single indicator system were compared using untrained readers to demonstrate the improvements in accuracy achieved with the new system.     

Visible colorimetric fluoride ion sensors

[structure: see text] Five new urea derivative naphthalene compounds were synthesized by a reaction of 1,8-diaminonaphthalene and the corresponding isocyanates and showed a distinct color change only when treated with fluoride ions.     

Vesicular polydiacetylene sensor for colorimetric signaling of bacterial pore-forming toxin

A vesicle-based polydiacetylene biosensor for colorimetric detection of bacterial pore-forming toxin streptolysin O (SLO) is reported. The sensor was constructed with three lipid constituents: glycine-terminated diacetylene lipid Gly-PCDA, cell membrane-mimicking component PC-DIYNE, and cholesterol (CHO), which serves as the bait molecule. UV irradiation led to photopolymerization of the diacetylene lipids that gave the material a blue appearance. Incubation of the vesicles with SLO from Streptococcus pyrogenes turned the vesicle solution red, and the color change was found to be correlated to SLO concentration. The optimal sensing performance was found with vesicles consisting of 71% Gly-PCDA, 25% CHO, and 4% PC-DIYNE, and a correlation relationship was obtained for 20 HU to 500 HU/mL, or 100 pM to 6.3 nM of SLO toxin. Transmission electron microscopy and dynamic light scattering was used for further characterization of the vesicular assemblies. Transmembrane pores (holes) with diameter around 30 nm were observed on the vesicle membranes, in particular on the peripheral of the membrane structures, suggesting pore formation by SLO toxin provides the driving force for the color change of the functional vesicles.     

Plastic colorimetric film sensors for gaseous ammonia

The preparation and characterization of three different plastic thin-film colorimetric sensors for gaseous ammonia is described. In the film sensors, the neutral form of a pH-sensitive dye (Bromophenol Blue, Bromocresol Green or Chlorophenol Red) was encapsulated in a plastic medium, either poly(vinyl butyral) or ethylcellulose plasticized with tributyl phosphate. Each of these film optodes gave a reproducible and reversible response towards gaseous ammonia. The sensitivity of the film sensors towards ammonia was found to be strongly dependent upon the pK _a of the encapsulated dye. Thus, the film with Chlorophenol Red (pK _a = 6.25), proved to be very insensitive (operating range: 0.29% < %NH₃ < 100%), whereas the film with Bromophenol Blue (pK _a = 4.1), was much more sensitive (operating range: 0.0003% < %NH₃ < 0.11%). The sensitivity of a plastic film sensor decreased markedly with increasing operating temperature and the 90% response (15–38 s) and recovery (820-127 s) times were slow and activation-controlled.     

Progress in patterned paper sizing for fabrication of paper-based microfluidic sensors

In this paper, we report the progress in using paper sizing chemistry to fabricate patterned paper for chemical and biological sensing applications. Patterned paper sizing uses paper sizing agents to selectively hydrophobize certain area of a sheet. The hydrophilic-hydrophobic contrast of the pattern so created has an excellent ability to control capillary penetration of aqueous liquids in channels of the pattern. Incorporating this idea with digital ink jet printing technique, a new fabrication method of paper-based microfluidic devices is established. Ink jet printing can deliver biomolecules and chemicals with precision into the microfluidic patterns to form biological/chemical sensing sites within the patterns, forming the complete sensing devices. This study shows the potential of combining paper sizing chemistry and ink jet printing to produce paper-based sensors at low cost and at commercial volume.     

Size effect of polydiacetylene vesicles functionalized with glycolipids on their colorimetric detection ability

In this paper, the size effect of the polydiacetylene vesicles functionalized with glycolipids on their colorimetric detection ability has been studied. Polydiacetylene vesicles in which were incorporated glycolipids acted as a model system for the affinochromatic property. Visible color changes from blue to red could be observed to the naked eye owing to Con A binding to the sugar moiety and be detected quantitatively by the visible absorption spectrum. In the experiment, small and uniform vesicles were obtained after extrusion through membranes with different pore sizes. The morphology and mean size distribution of the extruded vesicles were studied by transmission electron microscopy (TEM) and dynamic light scattering (DLS), respectively. Our work shows that the smaller the vesicles are, the stronger is the effect, making the detection of Con A easier. The results may apply to the sensitivity enhancement of polydiacetylene biosensors for the recognition of other biomolecules.     

双原色发光比色氧传感器

简单、快速进行氧检测的方法一直是人们研究的热点.在众多检测氧的方法中,发光比色法由于简单和可直读的特性受到人们的广泛关注.本文将简单地介绍近几年国内外基于双原色发光比色氧传感器的研究进展,并展望其研究前景.     

Combining gold nanoparticle-based headspace single-drop microextraction and a paper-based colorimetric assay for selenium determination

Analytical and Bioanalytical Chemistry - A novel method combining headspace single-drop microextraction with a paper-based colorimetric assay was developed. Headspace single-drop microextraction...     

Urea and thiourea based efficient colorimetric sensors for oxyanions

Urea and thiourea based receptors 1 and 2 bind H₂PO₄⁻, OH⁻, CH₃CO₂⁻, and PhCO₂⁻ ions in an acetonitrile/DMSO (9:1, v/v) medium. Binding of these anions causes an appreciable change in the visible region of the spectrum, which can be detected by the naked eye. The affinity constant for H₂PO₄⁻ is higher by about an order of magnitude as compared to the other oxyanions mentioned above. Ab initio calculations predicted tweezer-like binding modes for receptors 1 and 2 with these anions and a higher affinity toward H₂PO₄⁻ was predicted in acetonitrile.     

Novel fused-LEDs devices as optical sensors for colorimetric analysis

The development of a novel, low power optical sensing platform based on light emitting diodes (LEDs) is described. The sensor is constructed from a pair of LEDs fused together at an angle where one LED functions as the light source and the other LED is reverse biased to function as a light detector. Sensor function is based on the level of light received by the detector diode, which varies with the reflectance of the interface between the device and its environment, or the chemochromic membrane that covers the device. A simple microprocessor circuit is used to measure the time taken for the photon-induced current to discharge the detector LED from an initial 5 V (logic 1) to 1.7 V (logic zero). This sensing device has been successfully used for colour and colour-based pH measurements and offers extremely high sensitivity, enabling detection down to the sub micro molar level of dyes.     

State-of-the-art molecular imprinted colorimetric sensors and their on-site inspecting applications

Molecular imprinted colorimetric sensors can realize visual semi-quantitative analysis without the use of any equipment. With the advantages of low cost, fast response, ease of handling, and excellent recognition ability, the molecular imprinted colorimetric sensor shows great application potential in the field of sample rapid assay. Molecular imprinted colorimetric sensors can be prepared in various forms to meet the needs of different sample determination, such as film, hydrogel, strip, and adsorption coating. In this review, the preparation methods for various types of molecularly imprinted colorimetric sensors are systematically introduced. Their applications in the field of on-site biological sample detection, drug detection, disease treatment, chiral substance detection and separation, environmental analysis, and food safety detection are introduced. The limitations encountered in the practical application are presented, and the future development directions prospect.     

Tunable, colorimetric DNA-based pH sensors mediated by A-motif formation

A colorimetric pH sensor has been developed based on GNP aggregation mediated by A-motif formation under acidic conditions. The pH response of the sensor can be tuned in the range of pH 2-5.5 by changing the length and the sequence of the A-motif forming poly dA tracts.     

Use of a mobile phone for potentiostatic control with low cost paper-based microfluidic sensors

By exploiting its ability to play sounds, a mobile phone with suitable software installed can serve the basic functions of a potentiostat in controlling an applied potential to oxidise ECL-active molecules, while the resultant photonic signal is monitored using the camera in video mode. In combination with paper microfluidic sensors this opens significant new possibilities for low-cost, instrument-free sensing.     

Carbohydrate-based fluorometric and colorimetric sensors for Cu2+ ion recognition

The development of optical sensors using carbohydrates for selective detection of copper in water and living system has been an active research area in the past few years because of widespread applications and biological importance of copper. Introduction of carbohydrate to design the sensors is an attractive field of research because of its chiral entities with hydroxyl groups and oxygen atoms, controlled ring-flipping capability, abundance, and biocompatibility. This minireview focuses on the reported carbohydrate-based fluorescent and colorimetric sensors for Cu²⁺ detection and is organized according to their structural categories such as triazole-linked, imine-linked, and non–triazole-/imine-linked carbohydrate–based sensors. To the best of our knowledge, this is the first review article focused on carbohydrate-based Cu²⁺ sensors.     

A colorimetric and fluorescent chemosensor for detection of Hg2+ using counterion exchange of cationic polydiacetylene

In this study, a colorimetric and fluorescent chemosensor for mercury ions (Hg²⁺) was developed. Cationic polydiacetylene (PDA) vesicles with a quaternary ammonium cation and iodide as a counterion show a blue-to-red color transition; the color change is accompanied by a fluorescence enhancement in selective response to Hg²⁺ ions because of a perturbation of the ene–yne conjugated backbone induced by counterion exchange. It allows for selective detection of Hg²⁺ with the naked eye and the sensor is used to determine Hg²⁺ concentrations in tap water samples.     

Alkynyl ruthenium colorimetric sensors: optimizing the selectivity toward fluoride anion

We report on the synthesis of alkynyl ruthenium colorimetric sensors whose receptors are constituted by thiazolidinedione, rhodanine, or barbituric heads as recognition centers for anions. As modifications in the charge density at these recognition centers affect the whole molecule, through the alkynyl ligand acting as a communicating wire, the effects of hydrogen-bonding interactions with the anions were observed with the naked eye and monitored by UV-vis absorption spectrometry. The selectivity of the sensors was improved through electronic modifications of the alkynyl ruthenium subunit: the higher the electron density at the receptor head, the higher the selectivity is. TD-DFT calculations rationalize the long-range electronic communication as a main characteristic of the alkynyl ruthenium species and as a key to improve the selectivity of alkynyl ruthenium-based sensors toward anions.