| Literature DB >> 34803553 |
Adithya Sridhar1, Ashish Kapoor2, Ponnusamy Senthil Kumar3, Muthamilselvi Ponnuchamy2, Balasubramanian Sivasamy4, Dai-Viet Nguyen Vo5.
Abstract
The advent of microfluidic systems has led to significant developments in lab-on-a-chip devices integrating several functions onto a single platform. Over the years, these miniature devices have become a promising tool for faster analytical testing, displaying high precision and efficiency. Nonetheless, most microfluidic systems are not commercially available. Research is actually undergoing on the application of these devices in environmental, food, biomedical, and healthcare industries. The lab-on-a-chip industry is predicted to grow annually by 20%. Here, we review the use of lab-on-a-chip devices in the food sector. We present fabrication technologies and materials to developing lab-on-a-chip devices. We compare electrochemical, optical, colorimetric, chemiluminescence and biological methods for the detection of pathogens and microorganisms. We emphasize emulsion processing, food formulation, nutraceutical development due to their promising characteristics. Last, smart packaging technologies like radio frequency identification and indicators are highlighted because they allow better product identification and traceability.Entities:
Keywords: Analysis; Detection; Food packaging; Food processing; Food safety; Lab-on-a-chip; Microfluidics
Year: 2021 PMID: 34803553 PMCID: PMC8590809 DOI: 10.1007/s10311-021-01342-4
Source DB: PubMed Journal: Environ Chem Lett ISSN: 1610-3653 Impact factor: 13.615
Fig. 1Bibliometric analysis using Scopus and Dimensions for evaluating growth trends in the last two decades (2000–2020). Bibliometrics serves as an efficient tool for analyzing research trends in various scientific disciplines based on multiple criterions
Fig. 2Summary of country-wise analysis for the research contribution according to bibliometric data extracted from a Scopus and b Dimensions. The input data showed significant contributions made by the USA, China, and Korea for both the databases
Fig. 3Possible future themes using keyword cluster analysis of the bibliometric data extracted from Scopus using VOSviewer software. Keyword cluster analysis is conducted to visualize the research hotspots and transitions in the last two decades
Fig. 4Characteristics of traditionally used techniques and lab-on-a-chip technology. Lab-on-a-chip technology comprises of miniature devices incorporating multiple laboratory functions on a single platform. These devices find applications in diverse areas such as precise fluid delivery, intensified processing, and analytical studies
Lab-on-a-chip device fabrication techniques and food-related applications
| Fabrication technique | Features | Process limitation | Food-related applications | Reference |
|---|---|---|---|---|
| Photolithography | Utilizes a photoresist to fabricate the microfluidic device. In the presence of an ultraviolet lamp, the mask is prepared using an inkjet printer or can even be hand-drawn. Post-exposure, the photoresist is removed using the solvent, leaving a photoresist barrier pattern. Detection is then done by adding appropriate reagents | Laborious. High precision instruments. Cleanroom facilities. Time-consuming. Costly | Agarose-biodegradable and compatible substrate which can be used for dual applications (in energy storage as a flexible biodegradable battery) | Verma et al. ( |
| Plotting | Used to create flow channels and sensing areas on substrates. Polydimethylsiloxane is generally used as a substrate for plotting. After curing, bending or folding can be done without destruction. The plotting is done in a continuous fashion (line drawing method) | Suitable mainly in research laboratories. Less resolution. Difficult to dispense the liquid in some cases | Proteins-detection and sensing | Li et al. ( |
| Inkjet printing | Printing method for fabrication of microfluidic devices requiring low temperature and minimal resources for its operation. A unique feature of this technology is that the whole process gets completed within one cycle and relies completely on the inkjet printing equipment. High volumes of final product can be manufactured | Sensing material cannot be inkjet printed. Other techniques like casting need to be used for completion. Rheological conditions of inks like viscosity and surface tension need to be carefully followed | Water and oxygen sensing through additive inkjet printing-food packaging, pharmaceutical, and biomedical applications | Moya et al. ( |
| Volatile compounds, glucose, protein-analytical chemistry | Yamada et al. ( | |||
| Laser printing | This type of printing is generally a combination of laser printing and laminating process. The laser deposits the material layer by layer on transparent sheets with white regions representing microfluidic channels. Printing is followed by laminating process which seals the microfluidic channels | Distance between the two channels could sometimes be an issue | Proteins, glucose-healthcare industry (testing kits for people living in rural regions who have limited access to hospitals and clinics) | Oliverira ( |
| Food dyes | Gharaghani et al. ( | |||
| Finely ground pork-food safety and consumer health | Xia et al. ( | |||
| Wax screen printing | The wax printing process can be explained in the following steps: first, the wax is printed on the surface of the material using the paper screen-printing method. This is followed by the melting of wax onto the paper to form hydrophobic barriers. The process is feasible as the wax is of low cost and can be purchased easily | The patterned mesh is necessary for prototyping. This technique can sometimes require a heating step bringing questions about energy efficiency | Emulsions in food processing | Sher et al. ( |
| Plasma oxidation | Fabricating material is generally baked in an oven for about 100 °C for 45 min to cure the solution. The flexible patterns are then made on the baked fabricated material. The technology is generally used for making functional components like control switches, microreactors, or microfilters | Over-etching may take place sometimes due to excess baking | Ara h1 allergen detection in peanut and wheat | Weng et al. ( |
Substrates used for performing lab-on-a-chip studies in food samples
| Substrate | Concept used | Food material | Results | Reference |
|---|---|---|---|---|
| Polydimethylsiloxane | Gel electrophoresis | Ovalbumin-Texas red dye protein | The analyte enrichment gave detection limits of 250 pM with an increase in temperature to 30 °C. The involvement of temperature showed an increase of 30% in a single run | Peli Thanthri et al. ( |
| Glass fiber paper | Surface-enhanced Raman scattering and ELISA method | Fish samples | Concentration range of Malachite green residue in fish: 1 × 10–7 mol/L to 1 × 10–5 mol/L. Limit of detection: 5 × 10–10 mol/L. The technique proved better than the ELISA method showing responses within 1 h | Deng et al. ( |
| Polyethersulfone and glass fiber | Recombinase polymerase amplification method | Milk | Detection of | Ahn et al. ( |
| Paper layer containing carbon ink | Microfluidic sensing tongue | Orange juice and Cola beverage | One-step sampling design with a linear chip range measuring concentrations between 0.5 and 15 mM provided excellent precision for noting glucose levels | Amor-Gutiérrez et al. ( |
| Paper | Real-time Polymerase chain reaction test | Drinking water and milk | Three-dimensional book-shaped paper device for pathogen identification done based on sensitivity and specificity. DNA recovery rate: 25 ng/µL. Paper extraction recovery rate: 60–70% | He et al. ( |
| Polystyrene | Different T-junction geometries | Water–oil–water emulsion with an oil phase containing polystyrene | The value of flowrate at the second junction provides the most effective parameter for controlling the inner diameter, outer diameter, and thickness of the shell | Viza and Harding ( |
| Regenerated silk | Transfer printing process | Banana-film packaging | 30% water permeability reduction observed after applying on food sample post-fabrication. The shelf life of perishable food increased by 7 days | Valentini et al. ( |
| Chitosan | Electrochemical deposition | Active bacteria | The fabricated device showed its potential for the on-site detection of viable food pathogens. Can be used for detecting pathogens during the fermentation process | Li et al. ( |
| Chitosan reinforced with cellulose | ELISA | Using this special biopolymer membrane, the technique improved by: 17%—when kept in Tryptic soy broth and 24%—when kept in 0.5% dextrose broth. No cross-reaction was observed | Etty et al. ( |
DNA: Deoxyribonucleic acid
ELISA: Enzyme-linked immunosorbent assay
CFU: Colony forming unit
Detection methods for improved sensing capabilities in food samples
| Detection type | Type of LOC | Unique characteristics | Food sample | Conditions | Conclusions | References |
|---|---|---|---|---|---|---|
| Electrochemical detection | Impedance LOC | The cell membrane of the sample prevents the electric field lines from penetrating the cell. When a signal frequency is applied, the total impedance decreases due to short-circuiting. The properties of the sample can then be evaluated | Cow milk | Amplitude: 100 mV Frequency range: 100 Hz–1 MHz | Analysis of impedance and conventional measurements indicate that the former can be used to sense the presence of soap adulteration of 0.9% toxicity in milk | Brazey et al. ( |
| Carbon nanotube LOC | Such LOCs can be used to minimize the contact surface between microfluidic device channels giving higher precision during fluid control. The unique characteristic of this type of LOC is its electronic properties, higher sensitivities, and lower voltages | Vegetable extracts | Solution concentration: 4.75 × 10–5 mol/L Current: 4 A pH: 5 | Composite carbon paste (60:40 w/w) and paraffin binder gave the best results. The device proved effective in detecting pesticides, vitamins, and pro-vitamins thus showing high activity and catalytic properties | Oliveira et al. ( | |
| Optical detection | Lateral flow assay (or dipstick assay) | Simplest form of sensing technology. First applied during pregnancy tests. The user either applies the drop of sample onto the strip or dips the strip into the liquid sample. This causes a reaction between the strip and sample showing color changes, or line | Corn | Dissolving solution: tris-HCl (10 mL) pH: 8.5 Concentration of corn sample: 3,10, 30 ng/mL | Improvement in the recovery of mycotoxins in corn samples from 96.4 to 104.67% | Zhang et al. ( |
| Drinking water | Pesticide samples were diluted with 1 mg/mL acetonitrile, 5 mM phosphate buffer. pH: 7 Storage temperature: 4ºC | Lateral flow sensors showed the rate of inhibition reaction. Rate was determined by sensor output system. The calibration curve obtained for chlorpyrifos was 2–45 µg/L and for carbaryl, 0.24–2 µg/L. Reproducibility obtained was 4.2–5%. No specific sample preparation was required | Fernández-Ramos et al. ( | |||
| ELISA LOC | Generally performed on a microplate. The target solution continuously flows into the microchannel. This continuous flow makes the rinsing very effective and detects pathogens | Potato and corn chips | Amount of sample taken: 1 g Incubation temperature and time: 50 °C for 60 min | Analytical recovery for detection of acrylamide in potato and corn chips: 91.8% to 96%. Limit of detection: 5 ng/mL. High specificity with the technique having the potential for quick, simple, and reliable screening analysis | Franek et al. ( | |
| Gluten-free pieces of bread, sandwich spreads, and fried foods | Sample size: 0.25 g to 1 g | An evaluation of gluten cross-contact was done. 93.6% of results showed no significant cross contacts | Parsons et al. ( | |||
| Surface plasmon resonance LOC | Unique technology involving no labeling step with multiple rinsing as compared to lateral flow assay and ELISA. Surface plasmon resonance uses the total internal reflection principle causing variation in the refractive index of metal and liquid. The sample detection is done using concepts of polarization and oscillations | Milk | Limit of detection: 0.164 µg/mL | Antibody capturing using the sensor. This method proved better as compared to the ELISA-based technique for food allergen risk management in food manufacturing | Ashley et al. ( | |
| Peanut | Limit of detection: 5.54 ng/mL | Polyclonal antibodies enhanced the sensitivities using surface plasmon resonance and proved as a better method of detection as compared to ELISA | Wu et al. ( | |||
| PCR detection | Stationary chamber PCR | The technology uses heat transfer principles. The sample is heated at different temperatures to achieve thermocycling. The volume taken is the least (in microliters) thus yielding a faster heat transfer. Generally used for detecting pathogens or adulterants in foods | Meat mixtures | Initial activation: 95 °C for 5 min Denaturation: 95 °C for 15 s Annealing: 60 °C at 15 s Extension: 72 °C for 10 s | Pork DNA detection in binary meat mixtures was conducted using conventional and real-time PCR. Real-time PCR detected pork DNA at 0.0001 ng/µL or less. Detection limits of pork DNA in meat mixtures were 0.22, 0.047, 0.048, 0.015 ng/µL | Al-Kahtani et al. ( |
| Cashew | Limit of detection: 10 ppm Initial boiling: 121 °C for 15 min and 135 °C for 30 min | Real-time PCR detection proved better as compared to ELISA. Boiling did not affect cashew detectability | Sanchiz et al. ( | |||
| Isothermal PCR LOCs | The principle of isothermal PCR is based on the amplification of a target sample under a specific temperature. The technique is fast, ultrasensitive, and takes place within a single step. Monitoring is then generally done using a fluorescent reader. Much easier to fabricate and operate as compared to real-time PCR | Sample usage: 1 mL Time: 5 h Temperature for enrichment: 42 °C | Isothermal PCR required less expertise, was economical and reliable. It proved a rapid testing tool for interpretation. Detection time was obtained in less than 8 h including enrichment and DNA extraction steps | Tsen et al. ( | ||
| Colorimetric detection | Tree-shaped self-calibrating device | Widely applied for the analysis of proteins, chemicals, and metals. This tree-shaped device integrates self-calibration on the test strip due to which effects of environmental conditions can be minimized | Proteins | Bovine serum assay usage: 0–5 mg/mL | The device showed its potential to be coupled with digital transmission of images for remote sensing systems in food control and environmental analysis | Wang et al. ( |
| Chemiluminescence | Lab-on-paper device | Type of detection requiring less instrumentation and providing high sensitivity. Paper was chosen as a fabricating material considering cost efficiency for sample analysis | Cabbage leaves and tomato skin | Skins and leaves were washed using 20 mL distilled water for 40 s and then filtered before adding into analytical devices | Limit of detection of dichlorvos in the vegetables 0.8 ng/mL Sensitivity determination of dichlorvos in vegetables ranged between 3 ng/mL and 1 µg/mL making the technology a promising approach for environmental monitoring and food analysis | Liu et al. ( |
LOC: Lab-on-a-chip
ELISA: Enzyme-linked immunosorbent assay
PCR: Polymerase chain reaction
DNA: Deoxyribonucleic acid
Target groups for food safety applications
| Category | Target group | Technique used | Food sample | Limit of detection | Reference |
|---|---|---|---|---|---|
| Pathogen | Loop-mediated isothermal amplification | Tomato | 5 × 10–3 ng/µL | Sayad et al. ( | |
| Photolithography | Chicken | 103 CFU/mL | Kim et al. ( | ||
| Nanofiber light sensor | Orange juice | 102 CFU/mL | Shaibani et al. ( | ||
| Surface plasmon resonance | Cheese | 103–105 CFU/mL | Bouguelia et al. ( | ||
| Polymerase chain reaction detection | Meat products | 102 CFU/ 40 mL | Poltronieri et al. ( | ||
| Biotoxins | Aflatoxins | Platinum nanoparticle-based microfluidic chip | Beer | 0.55 ppb | Ma et al. ( |
| Aflatoxins | Enzyme-linked immunosorbent assay | Wheat | 0.33–0.4 ppb | Uludag et al. ( | |
| Aflatoxin M1 | Colorimetric detection | Milk | 3 pM to 10 pM | Kasoju et al. ( | |
| Ricin | Edge embossing (cell-free protein synthesis) | Orange juice, diet soda | Orange juice: 2 pM Diet soda: 170 pM | Khnouf et al. ( | |
| Heavy metal | Copper ions | Colorimetric detection | Tomato, rice, water | 1 ng/mL | Chaiyo et al. ( |
| Pesticides and other compounds | Carbaryl paraoxon parathion, malathion, diazinon, chlorpyrifos (Pesticides) | Ink-based printing | Tap water, apple juice, rice | Carbaryl 29 ng/mL Paraoxon: 22 ng/mL Parathion: 32 ng/mL Malathion: 17 ng/mL Diazinon: 45 ng/mL Chlorpyrifos: 36 ng/mL | Bordbar et al. ( |
| Chlorpyrifos | Screen printing | Tomato juice | 3 ng/L | Nagabooshanam et al. ( |
CFU: Colony forming unit
Fig. 5Mechanism of conventional emulsion process and lab-on-a-chip-based approach. Droplet size, droplet size distribution, and composition of the phases are critical factors that affect the stability of emulsions
Fig. 6Comparison of the human nose with an electronic nose based on mimicking human olfaction. The e-nose devices are powerful analytical instruments for evaluating the quality and freshness of drinks, foods, volatile compounds, aromatic oils at a shorter time with precise results
Fig. 7Vortex fluid device (VFD) with two sample inlets and one sample outlet. The device is a simple, low-cost platform that operates based on the principles of different shear regimes and organic reactions resulting in the formation of a suitable emulsion
Fig. 8Application of radio frequency identification (RFID) technology for product identification. These tags are attached to almost all food products to aid in reducing shoplifting and counterfeiting in addition to improvements in the supply chain
Characteristics of indicators used in the food industry
| Indicator name | Characteristics | Target to be detected | Application in foods | References |
|---|---|---|---|---|
| Gas indicators | To determine the scavenging activities in the food commodity. They offer an alternative approach for identifying any leakages or sealing issues in the pack. The chip detects the leak and converts the signals into visual colorimetric change | Gases like CO2, O2 | Oxygen inhibitor films using an alginate polymer coating | Vu and Won ( |
| Freshness indicators | Provide immediate product quality data regarding microbial growth or any chemical changes or modifications in the packaged food. Generally used for maintaining shelf life | Monitoring of nitrogen, amines, ammonia, CO2 pH sensing in food packages | Meat and fish | Kuswandi ( |
| Time–temperature indicators | Used for measuring food deterioration. Lab-on-a-chip device provides visual information concerning food quality, distribution, spoilage issues, and storage | Bacterial adulteration | Milk and other perishable foods | Zhang et al. ( |