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Microfluidic Brain-on-a-Chip: testbed for stroke damage, therapies

Microfluidic Brain-on-a-Chip: testbed for stroke damage, therapies
Figure 1: Schematic of brain tissue damaged from a stroke (Image © 2023 The Royal Society of Chemistry)

New research published in Lab on a Chip (September 21st) by researchers from the Ayuso lab (University of Wisconsin) and the Euan MacDonald Centre (University of Edinburgh) is an elegant example of a microfluidic organ-on-a-chip device. In this case, the organ is the brain, and the target disease is stroke. Stroke, or “brain attack”, is the brain equivalent of a heart attack. The majority of strokes are ischemic, typically caused by blood vessel blockage that leads to cell death in the brain tissue area served by that vessel.

The two research groups showed impressive results using rat astrocyte brain cells (which are a kind of “glia” — cells that support the brain’s neurons) to model the damage resulting from ischemic strokes, the response to reperfusion of nutrients to the deprived cells, and the viability of tissue grafting in an area damaged by stroke.

Figure 2: Cross-section of microfluidic device. (Image © 2023 The Royal Society of Chemistry)

Their microfluidic brain-on-a-chip device was made from a 384-well microtiter plate with various bottom chamber configurations machined out via CNC milling, and sealed with a polystyrene laminate using double-sided tape or solvent-assisted bonding. The chambers were filled with a collagen gel/astrocyte suspension (a proxy to mimic brain tissue) through the upper well openings, and then covered by filling the wells with either a nourishing medium, to simulate normal conditions, or a simple phosphate/borate pH buffer solution (PBS) lacking nutrients, to simulate deprivation during a stroke; see Figure 2 above.

Experiments were performed to show that their simulated normal and stroke conditions over different periods of time were reflected in terms of cell viability. In addition, the extent to which cells deprived of nutrients and oxygen during a simulated stroke were able to recover when replenished with nourishing medium was explored. The schematic shown below at left in Figure 3 illustrates a simple stroke simulation experiment (E), while the microscope image at right (F) and below (G) show the resultant effects on the astrocyte cells. Live cells are stained with with a green fluorescent dye (Cell Tracker Green), and dead cells with a red dye (propidium iodide). Magnified views of the cells directly beneath, nearby, or far from the nourishing medium are also shown (G); the further from the medium, the higher the proportion of dead cells.

Figure 3: Stroke simulation. Nutrient gradient created with medium and pH buffer (E); resulting zones of live and dead astrocyte cells (green and red, resp.), roughly correlating to their proximity to the nourishing medium (F & close-ups in G). (Image © 2023 The Royal Society of Chemistry)

Adding different labelling and assaying approaches to the microscopy techniques above, they were able to model several other key stroke features. They demonstrated that reperfusion of the damaged pseudo-tissue area with nutrients from the medium after the simulated stroke did not reverse the damage done, replicating what has been observed clinically. Stroke damage was also evident in the deprived and reperfused cells vs. healthy cells by the dysregulation of certain genes critical to governing glucose metabolism; these experiments were performed by quantifying up- and down-regulation of genes using RT-qPCR on RNA obtained by bead extraction from the astrocyte-gel matrix at different stages of the experiment.

Lastly, and perhaps most excitingly, the researchers were able to show the brain-on-a-chip’s ability to potentially evaluate therapeutic treatment candidates. They punched a hole in the astrocyte gel matrix, added a suspension of macrophages (aka white blood cells; they are said to be “key players in the inflammatory response that follows stroke damage”) to the space, and imaged their movement over time with fluorescence and confocal microcroscopy. A schematic of the experiment is shown in Figure 4 below. Significant penetration into the surrounding pseudo-tissue was seen at 24h vs. 30 min.

Figure 4: Biopsy and cell grafting experiment. (Image © 2023 The Royal Society of Chemistry)

The importance of these results is significant. The research team has shown that it can monitor the health and location of astrocyte cells with a number of analytical techniques including live- and dead-cell fluorescent tagging, and monitoring of gene regulation. It has also demonstrated that their attempt at tissue grafting showed successful cell penetration. This at least means that their brain-on-a-chip device should be tested more rigorously to explore its capabilities on several fronts — for example, monitoring movement and viability of different cells within a variety of tissues/proxies, evaluating the effectiveness of emerging, unproven stroke therapeutic treatments, etc. Furthering this research could provide invaluable insight into stroke tissue damage and regeneration techniques. Also, there is no reason to think that a similar approach could not be taken with other tissue models to characterise diseases and conditions, and evaluate therapies.

Survey: metrology in microfluidics

Survey: metrology in microfluidics

The Microfluidics Association is participating in a workshop on November 13th-14th, 2023 focussed on on metrology in microfluidics, and hosted by the metrology wing of the French Cetiat institution. In preparation, we at the Microfluidics Association (I’m on the Board) want to brush up on what the microfluidics community wants and needs as regards metrology. Here’s a letter from Henne van Heeren, fellow board member.


“For our work in developing standards and metrology protocols it is crucial that we know what the community needs. Therefor you you are invited to participate in our survey concerning prioritizing metrology and standardization work for the coming years.
Your participation in this study is completely voluntary, so if you feel uncomfortable answering any questions, you can skip questions or withdraw from the survey at any point.
The information you will supply will be coded and will remain strictly confidential.

Thank you very much for your time and support. Please start with the survey now by clicking on https://www.surveymonkey.com/r/D6RF9JM

This survey is held in preparation for the November workshop “on the road to standardization in microfluidics and organ-on-chip”. For more information on this workshop, please click here.

Best regards on behalf of the Microfluidics Association

Henne van Heeren
henne@enablingMNT.com
0031 78 6300748

Download our published whitepapers: https://microfluidics-association.org

We acknowledge the support of the MFMET project, https://mfmet.eu/ and the European Metrology Programme for Innovation and Research: EMPIR.”


On behalf of the Microfluidics Association, I would like to encourage any and all working in microfluidics to provide your input about metrology via our survey. I gave my 2¢ this morning! 🙂

Sensitive microfluidic detection of dopamine

Sensitive microfluidic detection of dopamine

Impressive detection of very low concentrations of the neurotransmitter dopamine have just been demonstrated in research coming from the Wang and Tu research groups at the Department of Bioscience and Biotechnology at the National Taiwan Ocean University and the Institute of Chemistry at the Academia Sinica, respectively, in Taiwan. The work was recently published as an on-line article in ACS Sensors.

Figure 1: chemical structure of 3,4-dihydroxyphenethylamine, or dopamine (Source: Wikipedia)

Dopamine, shown at right for like-minded chemistry nerds, is a small molecule that acts as a neurotransmitter in the brain and as a hormone with different functions elsewhere in the body including blood vessels, kidneys, the pancreas and the immune system. The ability to detect dopamine is of great interest, since abnormal dopamine levels are indicative of neurological conditions such as depression, schizophrenia, attention deficit hyperactivity disorder (ADHD) and Parkinson’s disease.

Figure 2: coating material, device structure and electropolymerisation of working electrode (Image © 2023 American Chemical Society)

The researchers created a microfluidic device to act as the dopamine biosensor. The glass base layer had an indium tin oxide (ITO) coating patterned with a CO2 laser to form the 3-electrodes used for electrochemical detection. The fluidic cover was made by soft lithography: cast moulding of PDMS over a photolithographically patterned SU-8 master. An additional novel coating was applied to the working electrode to afford the selective sensing of dopamine. The coating, “N7-P”, was electro-polymerised via cyclic voltammetry from a solution of an indium phosphate-organic linker hybrid and analine. The graphic at right from their paper shows a) the structure of the yellow/cyan InPO4/organic linker crystalline structure (left) with added green polyaniline (right), b) electrode base (grey) and fluidic cover (blue), together with N7-P coating materials input well (top) and neuroblastoma cell/dopamine input well (middle), c) photo of assembled chip, and d) microscope imagery of working electrode during coating process of the N7-P.

Performance demonstrated by the groups’ microfluidic dopamine sensors was impressive in terms of the low detection limits and dynamic ranges seen in static and flowing configurations. With no flow, the linear range was 1 pM to 10 nM, while under flow (optimised at 50 µL/h), the range was 1 aM to 100 fM, with an LoD of 0.183 aM. Unfortunately, the authors did not disclose the dimensions of the device’s fluidic channels and detection chamber, which become significant when low concentration levels approach the need for single molecule detection, as in this case.

Figure 3: selectivity for dopamine vs. other interfering neurotransmitters (Image © 2023 American Chemical Society)

Also important was the excellent selectivity shown by the devices for sensing dopamine in the presence of five other neurotransmitters with similar structures — acetylcholine, epinephrine, norepinephrine, gamma-aminotbutyric acid and serotonin. A plot showing the amperometric response of the sensor to dopamine (DA) versus these other five potential interferents at 10-fold concentrations (labelled Ace, EP, NEP, GABA and Ser, respectively) is shown at right.

In their experiments looking at biologically produced dopamine from rat cells (> 1000 cells/mL), the concentrations measured by the microfluidic biosensor tracked very closely with the results obtained using a commercial ELISA system when larger numbers of cells were used (> 1000 cells/mL); no comparison of results could be made for smaller numbers, as the commercial system failed to generate any signal. Signal from as few as 21 cells could be sensed at dopamine concentrations of ~15 aM.

If I’ve lost you with a bunch of chemistry concentrations jargon, please accept my apologies! The salient point is, the system has exquisite sensitivity, and that can be very useful in many situations where e.g. human biopsy or research cell samples are very small, and the impact of the cells’ environment or the effectiveness of a therapeutic drug for a neurological disorder is being evaluated. Having more sensitivity is like having more horsepower: it’s (almost) always a good thing!

Another important point is that the devices are manufacturable with what look to be fairly mainstream or easily implemented microfabrication methods. They mention that the closest rival electrode coating material to afford the selectivity for dopamine are “metal organic frameworks”, or MOFs. In a table they provide (Table S2 of their supplementary information), the current biosensor’s linear range is at least 8 orders of magnitude (i.e. 80 million times) more sensitive than that seen with MOF-based electrochemical detection. It’s not clear how ease-of-microfabrication compares between MOFs and the present coating technology.

Microfabrication of Zn-air microbatteries via 3-D printing

Microfabrication of Zn-air microbatteries via 3-D printing
Figure 1: 3-D printing of 2 interdigitated electrodes, silicone enclosure and gel electrolyte components of battery (Image © 2023 American Chemical Society)

Guoxian Li and Chuizhou Meng’s groups in Mechanical Engineering at the Hebei University of Technology recently published an interesting article pre-print from the American Chemical Society’s Applied Materials & Interfaces. Their research paper shows the simple microfabrication of rechargeable batteries in the form of 3-D printed interdigitated electrodes (IDEs) on a variety of substrates. The appearance and simplified fabrication process of the batteries are illustrated in Figure 1 above right.

The paper and supplementary information provide a fair amount of detail regarding the fabrication process used to make the electrodes. Four slurries were prepared for the air electrode, zinc electrode, interelectrode gel polymer electrolyte, and silicone rubber to close the cell. Figure 2 below left shows the printing process, chemical composition, sizes and examples of the IDE batteries. The air electrode incorporated tricobalt tetraoxide (Co3O4) to catalyse the oxygen reduction during discharge and oxidation (evolution) during charging.

Figure 2: Microfabrication via 3-D printing (a), electrode layout & composition (b-c) as well as photographs of IDE batteries of different sizes (d-h). (Image © 2023 American Chemical Society)

Different sizes (x, y) and thicknesses (z, depending on the number of layers deposited) of IDEs were prepared and characterised; electrode arrays were on the order of 1 cm x 1 cm, with thicknesses on the order of 1.5 mm. Arrangements with batteries in parallel (high current and power), in series (high voltage) or both were evaluated. Figure 3 below shows four batteries arranged in series (a), in parallel (c), and the polarisation & power curves for the single and 4-battery arrangements in each case for series and parallel circuits (b & d, respectively). Open circuit potential (i.e. voltage with no load) of the battery arrangements are also shown in (a) and (c). They claim high power density performance at 77.2 mW•h/cm². Lifetime of full power output varied approximately with the number of layers deposited.

Several examples of printing options and applications were also provided, demonstrating the use of the batteries in powering a fan motor (Figure 3, e-g), LEDs (h-i) and charging a cell phone (j). Interestingly, different Zn/air electrode alignments are possible, as in (h), as are different substrates. Normally, polyethylene terephthalate (PET, a common thermoplastic used for blowmoulding e.g. pop bottles, clamshell produce packages, etc.) in a flat sheet is used, but flexible wristbands (i) and cloth patches (j) were also demonstrated.

Figure 3: Serial and parallel battery circuits and performance (a to d), and application examples to power fans, LEDs and recharge cell phones (e-j). (Image © 2023 American Chemical Society)

This technology shows significant promise. The use of cobalt oxide as a catalyst and zinc as a metal are important advantages. Compared to the use of expensive noble metals like platinum and ruthenium, the use of Co3O4 as a catalyst is both more economical and environmentally sustainable. Likewise, the authors and others point out that zinc-air batteries have about five times the energy density of lithium-ion batteries, and are a potentially greener alternative. I was also struck by several potential benefits in the context of MEMS and microfluidic devices. The ability to integrate microfabricated batteries to power on-board components, without requiring an additional button cell, presents more opportunities. The battery size (capacity) can be tailored to device needs, reducing costs and waste impact for single-use scenarios. Also, the fact that these batteries are rechargeable opens the door to the development of multi-use or longer use MEMS and microfluidic devices, which can significantly decrease COGS and environmental footprint in an eventual product.

Reproducible pH control in microfluidic chambers for combinatorial chemistry

Reproducible pH control in microfluidic chambers for combinatorial chemistry

Researchers from César Pascual García’s group at the Luxembourg Institute of Science and Technology as well as Wouter Olthuis from the MESA+ Institute at the University of Twente in the Netherlands have designed, built and characterised a microfluidic device capable of controlling pH between acidic and neutral pH values. Their work was recently published on-line as an ACS Omega pre-print article.

Why does on-chip pH control matter? Control of acidity allows many molecular states and reactions to be regulated, e.g. for the synthesis of oligonucleotides (DNA), polypeptides (proteins), saccharides (carbohydrates), all of which are key in many areas of analytical, organic and pharmaceutical chemistry. One important area is combinatorial chemistry, which allows an array of related chemical compounds to be meticulously synthesised, and then evaluated against a target molecule for a given purpose, such as therapeutic effect of a drug, or receptor affinity as a bio marker of a disease or condition to be diagnosed. Regulating a large number of such reactions in a dense matrix array aboard a microfluidic chip means that many more reaction options can be screened simultaneously with very small amounts of reagents in an automated fashion, making for more effective drugs and diagnostics with lower development costs.

Their microfluidic devices have a Si/SiO2 base with Pt working, counter and reference electrodes, SU-8 patterned fluidic channels and removable glass lid. Ti/Au electrodes were lithographically patterned using lift-off, with subsequent electrochemical deposition of Pt and functionalisation with the electro-active species 4-aminothiophenol (4-ATP) thereafter. A photo of a 4-cell arrangement of their system, pH response and reversible reaction controlling the chamber pH are shown below.

Left: two of the four three-electrode cells used to adjust pH. Middle: trace depicting the alternating bias applied to the two cells, and resulting pH response. Right: electroactive species 4-ATP shown reacting reversibly between oxidised (purple) and reduced (red) configurations. (Image © American Chemical Society/Divya Balakrishnan et al.)

Fairly reproducible control of pH through 100+ cycles was achieved, with pH stability lasting through holding times of up to 10 minutes. pH can also be tailored to given values between pH = 3-7 ±0.4, based on the fluorescence intensity of the carboxy semi-napthorhodafluors dye used to validate performance.

The authors have taken previous work by others using photoactive compounds for pH regulation ahead a step, by removing the need for optical interrogation of the cell. This eliminates expensive optics instrumentation and alignment issues, replacing them with mass-manufacturable electrochemical control. While the current design is not configured for high density, the 2.5 nL reaction volumes are already quite small, and it is not hard to imagine a high density layout for manufacturing. Application of this technology to the development of therapeutic drug candidates, disease diagnostics and other areas seems promising.

Zeon acquires Edge Precision Manufacturing

Zeon acquires Edge Precision Manufacturing

According to recent LinkedIn posts and a press release, polymer manufacturing leader Zeon Specialty Materials Inc. (subsidiary of Zeon Corporation, Japan) recently acquired Edge Precision Manufacturing, a microfabrication manufacturing house based in the Boston, MA area. In the world of microfluidics, Zeon is a well known manufacturer of its cyclic olefin copolymers (COPs) Zeonor® and Zeonex®, widely used in the injection moulding of microfluidic products.

The manufacture of plastic microfluidic devices is most often performed with injection moulding, given its economic edge at high volumes, and less often with hot embossing, given its slower throughput, however hot embossing has the edge for devices with more demanding fine features and fidelity requirements. Edge Precision Manufacturing, formerly Edge Embossing, is able to combine the best of both worlds with a high volume, high precision hybrid approach, where hot embossing is used for the most demanding areas of a component, and injection moulding for the more routine feature sizes.

Zeon’s acquisition of Edge Precision Manufacturing is the latest in a series of microfluidics and MEMS fab house acquisitions that has seen Invenios acquired by Corning and thinXXS acquired by IDEX in 2017, miniFAB acquired by Schott and Micralyne acquired by Teledyne in 2019, and most recently microLIQUID acquired by TE Connectivity in 2021.

Skin-on-chip system for modelling herpes simplex virus (HSV) infection

Skin-on-chip system for modelling herpes simplex virus (HSV) infection
Structure of skin-on-chip microfluidic vascular network and epidermis. (Image © Nature Communications/Jia Zhu et al.)

Impressive work out of the Zhu lab at the University of Washington’s Department of Laboratory Medicine & Pathology and Institute for Stem Cell & Regenerative Medicine appears to effectively mimic human skin by combining a microfluidic “blood vessel-like” vascular network and a stratified epidermis structure. The research was published in September in Nature Communications, and profiled by the UW’s Fred Hutch Cancer Centre.

The skin-on-chip device was constructed in several steps. First, a microfluidic network with 100 µm-wide channels was patterned via soft lithography/injection moulding in a collagen matrix with dermal fibroblasts. The channels were perfused with vascular endothelial cells that lined the surface and formed a vascular network. Second, at the outer surface of the collagen chip, the epidermis was constructed: epidermal keratinocytes were seeded for 3 days, and later exposed to air to differentiate into a multilayered epidermis. The graphic above shows diagrams and a confocal micrograph that illustrate the skin-on-chip device.

The growth of the seeded keratinocytes into a fully stratified epidermis over ~2 weeks was characterised with cross-sectional images and a variety of fluorescent dyes to show the growth of the layers. Comparisons of different fluorescently stained keratinocyte markers (K14 & K10), basement membrane markers (Col IV) and vimentin in the skin-on-chip model and in native skin showed the model to accurately mimic the natural structures in native skin.

Many experiments were performed to illustrate the abilities of their platform; two are showcased here. In one experiment, the effectiveness of herpes simplex virus 1 and 2 (HSV-1 and -2) infection was tracked at various stages of dermal growth, pinpointing dramatic decreases in infection rate with completed layers of dermal growth as days progressed. After just 1 day of exposure to air and differentiation of the dermal layer, the number of infected cells dropped from 67 to 16% for HSV-1, and from 100 to 36% for HSV-2. It’s no surprise that, as skin forms or heals, its ability to prevent infection improves, but accurately determining at what time, stage of growth and to what extent this happens via a real model is powerful indeed.

White blood cell neutrophils (red) migrating up to HSV- infected skin (green) in an on-chip immune response. (Image © Nature Communications/Jia Zhu et al.)

In another experiment, the authors showed that neutrophils (the most abundant type of the white blood cells used in our body’s immune response) would adhere to the walls within minutes of perfusion through the microfluidic vascular network for a chip that was infected with HSV, vs. essentially no adhesion in a control chip. After hours, the neutrophils continued to accumulate, transmigrated through the endothelium and entered into the layered dermis on the chip surface. A confocal microscopy image, reproduced at right, shows the presence of red-stained neutrophils in the cross-shaped microfluidic vasculature below, and migrating upwards towards the HSV-infected skin layers above, stained green.

The effectiveness and utility of this skin-on-chip model system to monitor immune responses to disease is obvious. The authors discuss an array of investigations that can be undertaken to better understand the chemistry of immune responses. If we consider the 3-D spatial information content provided by confocal microscope imagery in the context of their stratified, vascular-epidermal microfluidic system, it seems like the sky is the limit for recreating immune and other skin-based biological/biochemical processes, and perhaps with other tissue types as well. There is a good reason this paper was accepted by Nature Communications. 🙂

Microfluidic fabrication of hydrogels that consume environmental pollutants

New work from Patrick Doyle’s group at MIT, just published in ACS’ Applied Polymer Materials and highlighted in MIT News, shows the simple microfluidic manufacture of hydrogel particles that can be used to remove hydrophobic (non-polar, water ‘fearing’) micropollutants from water. Their hydrogel ‘filtres’ show enhanced performance compared to activated carbon (AC); in addition, and critically, they can easily be regenerated.

Microfluidic synthesis of micelle-based hydrogel particles. (Image © American Chemical Society/Applied Polymer Materials)

The hydrogel particles are made from acrylate-based micelles that are covalently bound into a cross-linked acrylate gel. The diagram above from their paper illustrates the nature of the micelle monomers and cross-linkers (A); the polymerisation reaction (B – I’ll pretend I understand exactly what’s going on, there …;-); the solution (left) before polymerisation, with free micelles spontaneously formed, and (right) after (UV) polymerisation, with the micelles fixed in the gel polymer (C); the microfluidic cross used for droplet/particle formation (D); a micrograph of the 500 µm gel particles (E); and a diagram showing the formation of the droplets in the microfluidic reactor that polymerise under UV light to form the gel particles.

The microfluidic reactor in this case is simply made from off-the-shelf components: a microcross such as from Idex (150 µm through-hole) and 1/16″ OD tubing. For R&D, this is an ideal set-up: fairly cheap with parts delivered in days and set up in minutes. For manufacturing, it’s only a small leap to replicate this structure in polymer or glass and set multiple microfluidic synthesis networks up together in parallel to reduce the cost contribution of the microfluidic reactor.

Hydrogel column used to clean water. (Image © American Chemical Society/Applied Polymer Materials)

To remove the pollutants from a water sample, water is passed through a column filled with this hydrogel, and the hydrophobic pollutants partition into the hydrophobic micelle centres, analogous to reverse-phase chromatography, with the pollutants being highly retained in the stationary phase. Once the hydrogel is saturated with pollutants, it can be regenerated with an ethanol flush, purging the column of bound pollutants; the authors claim it will maintain performance over years of such regenerative cycles. Different micelle monomer hydrophobic tails can be used to optimise the affinity and partitioning coefficient for a variety of pollutant targets.

Uptake of 2-napthol by F127DA hydrogel at different concentrations, compared to activated carbon. (Image © American Chemical Society/Applied Polymer Materials)

The performance of the hydrogels stacks up very nicely against activated carbon filtres which are the current gold standard in many applications. Doyle’s group measured the performance of a variety of different micelle compounds in their hydrogels against each other and activated carbon for their micropollutant model compound, 2-napthol (used in the manufacture of dyes, fungicides, insecticides, pharmaceuticals and perfumes; carries the H400 classification of “very toxic to aquatic life”). The graph at right plots pollutant removal over time for a particular micelle formulation, F127DA. The ordinate is c/c(o), or the concentration of pollutant left in the test solution vs. initial concentration; the faster and greater this drops, the better the performance. The four different exponential decay curves (blue) correspond to different quantities of micelle surfactants bound in the hydrogel: 0 to 40% surfactant concentration in the gel; the grey curve is for Brita activated carbon. The plot shows that higher percent quantities of micelles bound in the hydrogel lead to pollutant removal in greater quantities and at faster rates. On time scales under 10 minutes, typical for water treatment contact times, both the 15 and 40% F127DA formulations handily outperform the activated carbon, although longer timescales favour the AC.

The authors highlight the fact that their hydrogels can be regenerated with ethanol, using between one thousandth to one billionth the volume of EtOH vs. water treated, and show good performance for cycles subsequent to regeneration. They also note the very energy-intensive process needed for regenerating AC filtres. While it seems they have effectively shown good performance from their hydrogels for both filtration and re-usability, what is missing in the comparison, in my view, is a clearer contrast of economic and environmental drivers. For example, potential costs/year for filtre replacement, ethanol/energy consumption, releases to the environment, etc. That is arguably the product developer’s job, and perhaps this paper’s performance will pique the interest of some entrepreneurs, hopefully with well-heeled partners.

Simplicity through capillarity: automatic microfluidic analyses

New research from David Juncker’s lab at McGill University’s Biomedical Engineering Department show’s impressive progress along the path to sophisticated diagnostics or analyses performed on low-cost microfluidic devices in resource-limited environments. Their work was just published last month in Nature and also profiled in an article in McGill’s Health e-News.

Juncker’s group excels at capillarity-driven microfluidic devices, and they wrote an excellent critical review paper in Lab on a Chip a few years ago on ‘capillaric circuits’. It provides a full description of the physical chemistry of Laplace pressure and surface chemistry that underpin the capillarity-driven microfluidic operations used in these devices. While the full depth of the chemistry and physics is beyond the scope of this blog article (and the author’s RAM capacity ;-), they may be explored separately in a future post. Suffice it to say that, while somewhat involved, the capillarity-based pumping, valving and timing technology is well understood and and fairly well developed by this group, amongst others.

‘Microfluidic Chain Reaction’ device for COVID-19 detection (image © McGill University Health e-News)

In this work, they are moving from the ‘mere’ sequential delivery of a few liquids at a channel intersection to fully configured, multi-step analyses using hundreds of sequential pre-programmed liquid manipulations. A first chip enables sequential delivery of 300 sample aliquots, while the second, shown above, performs the 8-step ELISA detection of COVID-19 antigen found in a patient’s saliva sample . Some impressive videos showing the performance of the 300 aliquot chip and the COVID-19 diagnostic chip can be found in the McGill article.

For someone like myself working in the field of microfluidics, perhaps the most thought-provoking aspect of this article is the potential for the technology to dramatically simplify the operation of fairly complex microfluidic devices. Being able to programme sequential volumetric flows with precise timing with a virtually unrestricted number of on-chip steps, all under autonomous operation, has far-reaching implications. It means that, after addition of sample(s), the device will simply start its protocol, with no interaction needed from an instrument or human operator. Using existing, fully developed on-board technologies such as lyophilised reagents and mixing procedures together with simple visible bands for detection such as with COVID-19 rapid tests, the door to many other more complex medical diagnostics, industrial or environmental assays is now open.

Development of products to meet these application needs will no doubt carry challenges, but at the end is a cheaply manufactured, complex device that can be used at the point of care or need; this represents a huge foundation on which to build any number of enabling, disruptive products.

Quantitative visual detection via microfluidic V-chip

Quantitative visual detection via microfluidic V-chip

Xiujun Li’s group at the University of Texas at El Paso recently published an article in Analytical Chemistry that builds on the “V-chip” concept from a 2012 Nature Communications publication by the Qin group. The chip uses the position of a visible liquid in a channel to allow the user to quantitatively determine the concentration of an analyte of interest by simple visual inspection – no detector needed!

Thermometer-like readout device from Li group at UTEP
(Copyright: American Chemical Society)

The chip (schematic at right) operates similarly to an alcohol or mercury thermometer in which the user reads the liquid meniscus level against a scale to determine the temperature. In the case of these microfluidic V-chip devices, the liquid level moves in response to the concentration of an analyte. In the seminal paper by Qin in 2012, the liquid plug was driven by gaseous products generated in a reaction with the analyte. A sandwich ELISA (enzyme-linked immunosorbent assay) reaction was used in which the unbound antibody was labelled with nanoparticles conjugated to a catalase enzyme. At the end of the ELISA reaction, the bound catalase labels reacted with preloaded hydrogen peroxide in the solution to produce oxygen gas in proportion to the amount of analyte initially present. The liquid ink was driven along connected ‘thermometer’ microfluidic channels and measured accordingly to determine the concentration of analyte. This volumetric relationship gives rise to the V in V-chip.

Result from a sample with 64 ng/mL PSA in phosphate buffered solution (PBS)
(Copyright: American Chemical Society)

In the work of Li’s group, a sandwich ELISA is also used, but the labelling and gas generation are different, and arguably improved. Instead of generating gas enzymatically with catalase, it is generated photothermally with a near infrared (NIR) laser. In their work, the analyte of interest is the prostate cancer biomarker PSA (prostate-specific antigen), and the unbound antibody is labelled with an Fe3O4 nanoparticle. The nanoparticle is chemically converted to a Prussian Blue (PB) nanoparticle which is a strong NIR-absorbing photothermal agent. At the end of the ELISA reaction, an NIR laser is shone onto the sample chamber and the incident radiation is converted by the PB nanoparticles to heat and generates vapour, causing liquid to be driven along the thin radiating ‘thermometer’ channels. The extent of displacement of the liquid again depends directly on the amount of PB nanoparticle-labelled antibodies present, which is a function of the concentration of PSA to which they bind. An example with blue dye showing the liquid after ELISA reaction and photothermal interrogation is shown above right.

The V-chips in both studies offer the huge benefit of not requiring any measuring instrumentation for detection; no optical or electrochemical detector, signal processing and display required. With a properly designed microfluidic chip and calibrated scale, the results of an ELISA-based cancer biomarker assay can be read directly from the chip like a thermometer. The dramatic reduction in complexity and cost can be a huge gain in a derived product concept. In addition, Li’s work uses a photothermal heating process in lieu of the second enzymatic reaction (catalase) in the analysis chain, which both simplifies the procedure, and is likely to make it more robust, since photothermal heating is more controllable and reproducible than an enzymatic reaction. The cost for this is an added on- or off-board NIR laser and lens, both of which can be mass-fabricated cheaply. This approach potentially improves analytical performance, which could in turn be an enabling piece of the technology foundation for a related product.

908 Devices: an investment opportunity?

908 Devices: an investment opportunity?

In a recent Forbes profile, author Peter Cohan suggests that 908 Devices, based in Boston, may be a good company to consider for investment. He notes that they are doing several things right that are keeping them nimble, including attracting top talent, empowering employees closest to clients, launching products quickly and fighting bureaucracy.

Zip Chip ESI microfluidic device.
Copyright: 908 Devices

The company uses microfluidic chips for electrophoresis-based sample preparation and electrospray ionisation (ESI) for sample introduction into their revolutionary desktop or hand-held, low power, high (atmospheric) pressure mass spectrometers (HPMS) that perform the sample analysis. In some cases the HPMS operates alone. More information is available on their website, including a listing of their suite of patents relating to both the microfluidic ESI and HPMS aspects of their core technology. Applications vary from cell biology analysis, detection of drugs (e.g. fentanyls, opioids and amphetamines), explosives and chemical warfare agents. Importantly, the chips are easy to use, and instrumentation is coupled to powerful electronics and software to automate all operations and analysis computations, and thus afford a simplified, practical interface suitable for a broad base of operators.

MX 908 system. Copyright: 908 Devices

The company was founded 9 years ago, and had its IPO in December, 2020. It’s stock has dipped slightly, but revenue grew by 50% last year to USD $26.9 M and is projected to grow another 45% in 2021. The company also just landed a USD $25M purchase contract from the US Army for 350 of its MX908® portable MS instruments for on-site explosive threat detection and evaluation applications.

Cohan notes that 908 Devices avoids agility potholes such as forcing valuable employees who intimately understand the technology, customers and competition to do “tooth-cleaning-like reviews” for C-suite executives. CEO Kevin Knopp noted in his interview with Cohan that they intentionally maintain a fairly flat organisational structure, hire high-calibre talent, and empower their employees to listen to customers and react accordingly.

Cohan summarises: “If 908 can figure out an easy button for sustaining 50% annual revenue growth, its stock is a buy.”

Ultra-sensitive fire accelerant detection by dogs

Ultra-sensitive fire accelerant detection by dogs
Our beloved dog Fezzik … equipped with standard superior olfactory prowess

As both a proud and loving owner of a loyal golden doodle (Fezzik) and an analytical chemist, I couldn’t resist this one! I also can’t resist posting a photo of our family’s lovable hot dog burglar, Fezzik. He’s in his winter attire in this photo from last Saturday morning’s breezy -34°C walk. He’s amazingly well adapted to the cold, with enough circulation to keep his exposed nose and thin ears nice and warm no matter what!

But I digress. Did you know that man’s best friend is an analytical chemistry superhero? Well, I guess we are all familiar with the notion that dogs have incredibly sensitive noses. We may have seen handlers harnessing their dog’s superpower for good, such as with drug sniffer dogs at airports and accelerant sniffer dogs at arson crime scene. A dog/hander team photo of German Sheppard Ezra and Jeff Lunder of CADA Fire Dogs from the Harynuk paper described below is shown below.

Ezra and handler Jeff Lunder at work in a forensic fire investigation. Picture from Forensic Chemistry article.

It should perhaps come as no surprise that there’s some really cool biology behind their abilities. Chemist and founder of Chemistry Matters Dr. Court Sandau recently posted a link on LinkedIn to an excerpt of a talk he gave describing the special design of canine olfactory systems – have a look. Dogs have 300 million sensing cells (~50x as many as humans), direct over 10% of their inhaled air over these sensors, and can expand the area at will to allow for expanded sensitivity … absolutely fascinating!

It may come as a surprise, however, to learn that their olfactory power is more sensitive than the best analytical chemistry methods and instrumentation, and that this actually causes us problems as they work their magic. The dilemma arises when a forensic lab cannot detect the presence of an accelerant that a dog very likely correctly identified, due to the lab’s inferior limit of detection (LoD, the lowest amount or concentration for which something can be detected by a dog, detector, etc.); such a situation can potentially render arson evidence inadmissible.

A paper published in Forensic Chemistry last year by Professor James Harynuk’s group at the University of Alberta tackled the first step in addressing the gap between canine and analytical instrumentation/methodology performance: determining the canine limit of detection for an accelerant. With an idea of dogs’ capabilities, analytical chemists would at least know the target they are trying to hit!

Sample being applied to tile, left, and after 10s to allow the dichloromethane solvent to evaporate, left. Picture from Forensic Chemistry article.

A great deal of effort was required by Harynuk’s group to conceive of and validate methods to clean and prepare slate tile substrates to receive accelerant samples; the extent of initial contaminants and cleaning effectiveness was demonstrated with solid phase microextraction followed by gas chromatographic – mass spectrometry headspace analysis. They also had to research and chose suitable solvents and stabilisers in which to prepare diluted accelerant solutions. Taking great care to eliminate any source of bias for the dog and handler during the identification trials, Harynuk’s team applied an increasingly diluted range of accelerants such as lighter fluid, regular gasoline and diesel gasoline, to slate tile substrates located amongst blank and control tile samples with other petroleum components typical of a scene. An example of a sample being applied to a tile substrate is shown at right. For the trials, two dog/handler teams were brought in to determine their ability to correctly identify the spiked tile from the group, and at increasingly weaker doses. Both dog/handler teams were able to correctly detect tiles spiked with as little as 5 pL of gasoline (1 pL is one billionth of 1 mL)!

And so now we know why it is that, when we quietly peel the film wrap off steaks to be prepared for the grill, our dog smells it from the other end of the house, two stories up, and comes running with eyes full of hope and obedience … before the first dash of steak spice has hit the meat!

Microfluidic droplet generation via on-chip microwave heating

Microfluidic droplet generation via on-chip microwave heating

A recent technical note in Analytical Chemistry from Professor Carolyn Ren’s lab at the University of Waterloo demonstrates an efficient and controlled approach for on-demand microfluidic droplet generation.  The technique is used in a variety of important bio-medical and industrial applications such as: single or multiple cell sorting, culturing and incubation; droplet-based PCR and DNA sequencing; and chemical synthesis including micro- and nanoparticle synthesis.

overal device2Microfluidic droplet generation at a tee intersection on a chip can be initiated or controlled by several approaches or factors such as balancing input pressures, channel intersection geometry, and surface tension at the interface.  The latter offers an opportunity for fine control: input pressures for immiscible carrier and droplet fluids are nearly matched, and alteration of the surface tension and thus Laplace pressure at the interface meniscus will lead to on-demand droplet generation.  Surface tension is a function of the chemical composition of the carrier and droplet fluids as well as temperature, so localised heating at the meniscus can enable fine control of droplet generation.  On-chip resistive thermal heating works well, but has a slow response; laser cavitation is much faster, but requires expensive, delicate optically aligned off-chip instrumentation.  The authors’ choice of on-chip microwave heating, shown at right above, has very rapid response times, is implemented with very simple (and cost-effective) microfabricated heating resonator electrodes, and affords precisely localised heating based on electrode design and chemically selective absorption of microwave energy by the aqueous droplet fluid (and not the carrier oil or PDMS device material).

droplet generationTime-lapsed photographs of droplet generation of water (vertical channel) in carrier oil (horizontal channel) using their system are shown at right below; the curved black line is the electrode under the vertical channel.  The research showed a relationship between applied microwave power and generation time, but with droplet sizes remaining at a constant ~1.8 nL in their 40 µm deep x 210 µm wide channels.

The advantage of repeatable, precisely controlled on-demand droplet generation for the many fields in which droplet-based microfluidics is used could be important.  The fact that it should be manufacturable from different microfluidic device materials without expensive instrumentation is a considerable advantage as well.  The localised nature of the heating could also be beneficial in thermally sensitive assays where excessive and/or prolonged heating is detrimental.

Ovarian cancer culturing and chemotherapy testing on microfluidic device

Ovarian cancer culturing and chemotherapy testing on microfluidic device

Impressive research coming out of the Revzin group at the Mayo Clinic’s Department of Physiology and Biomedical Engineering shows an improved approach to first culture and then evaluate cell responses to chemotherapy treatments using polydimethyl siloxane (PDMS) microfluidic devices cast from silicon masters.  The research was published in Microsystems & Nanoengineering in October (DOI: 10.1038/s41378-020-00201-6).

different approachesOvarian cancer often has a very poor prognosis when detected due in large part to the inaccessibility of the ovaries for many diagnostic methods, and the late-stage in which diagnoses are usually made.  As a result, there is a strong focus on improved therapeutic strategies to best use the brief window available for treatment of the advanced disease.  One such strategy is to use ‘patient-derived xenografts’ (PDXs) where tumour tissue cells are implanted in a mouse to allow the cancer to be monitored in parallel to that of the patient.  While valuable to determine the effectiveness of various chemotherapies, PDX requires research animals, experienced animal researchers, high costs and long timelines.  As a result, in vitro ‘organoid’ or ‘spheroid’ 3-D cancer cultures are being explored on 96-well microtiter plates, Matrigel plates and other array platforms to arrive at suitable replacement environments.  As comparison standards for their microfluidic design, the authors used Matrigel and microtiter plates approaches, with the latter having PDMS inserts with microwells identical in size to the microfluidic counterpart.  A graphic depicting the three approaches is shown above at right.

viability, spheroid growthA first advantage of their microfluidic platform is that it can easily make use of the miniscule amounts of cells afforded by a fine needle biopsy sample.  Secondly, the on-chip incubation environment appears to be superior to that of standard microtiter plates when using identical media and culturing methods.  After 14 days, 0n-chip viability was typically ~90% vs. ~60% & ~80% for standard microtiter and Matrigel plates, respectively; growth of the spheroid cluster of cancer cells was also significantly better using the chip platform. Figure at right shows micrographs of the spheroid cell clusters in the microfluidic wells (a), and a comparison of viability (b) and spheroid size growth multiple (c) over 2 weeks.  Lastly, a multiplexed design shown below multiplexed designat right was created to allow serial and parallel perfusion across eight chambers.  Chambers are filled serially from left as in (a), and in parallel via discrete inputs as in (b); fluidic control is achieved by opening and closing red valves surrounding each chamber.  This device was used to determine the chemotherapy agent doxorubicin’s IC50 (50% inhibitory concentration) for two types of cancer cells via viability curves drawn from parallel injections of agent concentrations ranging from 10 nM to 100 µM.  The injected amount for the multiplexed study was ~100,000 cells, stated as the minimum amount obtained from a fine needle aspirate (biopsy).

Application of this microfluidic analysis approach to very small masses of biopsy, or other, samples is compelling as demonstrated in the case of ovarian cancer.  It may be that many disease biopsies from other organs or perhaps forensic or other bio-samples could also benefit from the efficient approach.

On-demand microfluidic devices in Petri dish

On-demand microfluidic devices in Petri dish

principleNew research from Edmond Walsh’s group at the University of Oxford and Iota Sciences demonstrates rapid in situ device prototyping in a plastic Petri dish using robotic jet printing.  The work was published in Advanced Science 2 weeks ago.

Beginning with a Petri dish containing an aqueous cell medium, the procedure entails covering the medium with a second immiscible layer of FC40 fluorocarbon, and then jetting the fluorocarbon through the medium to make contact with and stick to the Petri dish via preferential wetting.  The moving jet nozzle can thus define channel & chamber walls bonded to the Petri dish surface and directly write a fluidic channel network according to a CAD layout input.  The jet stays in the fluorocarbon, making the fabrication contactless.  Writing time depends on the design complexity, but may be about five minutes.  A diagram of the fabrication procedure is shown at right above, and a fluidic maze structure created with this technique is show at right below.  First author Cristian Soitu’s Twitter feed (@CristianSoitu) has an impressive video showing the creation of some devices.

mazeThe authors have done a nice job of characterising the various parameters relevant to creating walls or features from the fluorocarbon, such as jet nozzle height, diameter, flow rate, lateral speed, wall thickness and channel widths.  The ability to pipet into enclosed chamber arrays was also explored in terms of volume ranges and resistance to cross-contamination.  Preliminary cloning studies with different cells suggested comparable cloning efficiency vs. normal Petri dishes without fluorocarbon structures.

The possibilities afforded by such a direct-write technique are compelling.  An ability to create custom microfluidic structures for a given pattern of cells or conceivably other analytes adsorbed on a solid substrate with secluded, sterile and controllable environments seems like a window into new analytical techniques enabled by powerful sampling and work-up strategies.  Iota Sciences appears to be moving the technology forward for cell cloning purposes.

Quantitation of dopamine from blood and CSF from mice with Parkinson’s via electrochemical sensor in microfluidic device

Quantitation of dopamine from blood and CSF from mice with Parkinson’s via electrochemical sensor in microfluidic device

overall schematic A very thorough characterisation paper was published a few weeks ago in Analytical Chemistry by researchers in Amal Alachkar’s group at UC Irvine, and Nicolas Voelcker‘s and Victor Cadarso‘s groups at Monash University.  The collaboration made a microfluidic dopamine sensor that detected dopamine in blood or cerebrospinal fluid (CSF) obtained from mice used to model Parkinson’s disease.  Dopamine is a small molecule that acts as a neurotransmitter in the brain and as a hormone with different functions elsewhere in the body including blood vessels, kidneys, the pancreas and the immune system.

device schematicThe microfluidic devices were fairly simple in structure, with a three-electrode configuration used for the amperometric detection patterned on the oxide layer of a silicon substrate, and a single channel/chamber fluidic structure fabricated in PDMS that was bonded to the silicon baseplate.

Characterisation tests showed robust performance.  Good repeatability was seen across ten replicate devices, linear ranges extended through 4 decades and included an LoD at 0.1 nM in both CSF and phosphate buffer.  The current plots showing the dynamic range appeared quite steady and smooth at 0.1 nM, and well apart from the baseline, so I wonder if a 3-standard deviation mark would lie well below 0.1 nM?  Regardless, this was adequate to easily sense the physiological levels of dopamine in the test mice CSF in the range of 0.1-1 nM.  It also showed good selectivity in the presence of interferents.  The good analytical performance is likely attributable to the small 2.4 µL chamber, relatively large electrode array (~1 mm²) and narrow (50 µm) separation between the electrodes.

The ability to detect dopamine is of great interest, since abnormal dopamine levels are indicative of neurological conditions such as depression, schizophrenia, attention deficit hyperactivity disorder (ADHD) and Parkinson’s disease.  In the case of Parkinson’s disease, an effective sensor can help both with diagnosis and with treatment, as patients are often treated with  L-DOPA, a chemical precursor to dopamine, to help reach optimal levels.

Microfluidic biopsy tissue sample analysis

Microfluidic biopsy tissue sample analysis

Tissue uF dvcInteresting research regarding a microfluidic chip that facilitates multiplex analysis on a single biopsy tissue sample was recently published in a Microsystems & Nanoengineering article from José Luis García-Cordero’s group at Unidad Monterrey.  The technique allows highly irregular surfaces to be simply examined without further modification.

The PDMS chip, shown in upper image (©Nature – Microsystems & Nanoengineering), uses a ~3 x 7 mm chamber for the biopsy tissue sample, allows media to perfuse around the sample (orange fluid).  Once the valve is pneumatically actuated (7-35 kPa), theTissue uF dvc - no X-talk tissue is pressed against the lid to seal the microfluidic channels and allow the simultaneous introduction of discrete drug or tissue culture solutions through each of the eight channels.  Characterisation studies shown in the lower image (©Nature – Microsystems & Nanoengineering) demonstrate good permanent sealing and no cross-talk between channels.  Also, the continuous periperfusion of media around the sample increased tissue cell viability over the first several hours in the microfluidic device vs. in a petri dish.

The authors discuss the possibility of using biopsy samples in devices to perform drug efficacy, safety and toxicology studies before clinical trials, as well as facilitating research in physiology, metabolism and tissue regeneration.

Controlled microfluidic reagent dissolution via capillarity

Controlled microfluidic reagent dissolution via capillarity

Fig 2 Onur Gökçe at University of Zurich/ETH and Yuksel Temiz and Emmanuel Delamarche at IBM in Zurich, Switzerland, together with Samuel Castonguay and Thomas Gervais at École Polytechnique in Montréal, Canada recently authored a clever article in Nature that shows beautiful control of dried reagent dissolution and diffusion into the liquid buffer flowing over-top of the reagents in a microfluidic channel.

The authors demonstrated that, by including a partial-height longitudinal wall to act as a “capillary pinning line”, liquid flows through an empty channel and back along the adjoining channel with spotted reagents to create zones of dissolved reagents – a process they term ‘self-coalescing flow’ or SCM.  This is in contrast with the frontal accumulation of  reagents spotted conventionally along a single channel.  Further, by adjusting channel dimension, the concentration profiles could easily be manipulated to produce short zones of high-concentration or longer zones of lower concentration, with fairly homogeneous concentration profiles in all cases.  Several additional examples showed the ability to either segregate or coalesce such zones for a given reagent, mix and react with downstream reagents, etc.

Fig 3From the perspective of microfluidic product development, this development is very interesting for several reasons.  First, it provides this control of reagents in solution with very simple channel structures that can be fabricated existing standard methods for any substrate material (plastic, glass, silicon).  Secondly, it may obviate the need for more complex channel networks and associated pumps and valves required to physically segregate parallel reactions of a single analyte with several target reagents for multiplexed analyses, common in many microfluidic products currently.  This could reduce the size, complexity and cost of the chip consumable, making the price and profitability of such products much more attractive.

Stabilisation of hydrogen peroxide on paper microfluidics with poly(vinyl alcohol)

Stabilisation of hydrogen peroxide on paper microfluidics with poly(vinyl alcohol)

printed spotsResearchers from Wanida Wonsawat‘s group at Suan Sunandha Rajabhat University (Bangkok) and Takashi Kaneta‘s group at Okayama University recently published an article in Nature Research showing a relatively simple but elegant procedure to greatly increase the stability of hydrogen peroxide reagent absorbed into the fibres of the patterned Whatman filtre paper used the paper microfluidic devices in the study.  Hydrogen peroxide is an oxidising agent that is often used in enzymatic assays that may create or remove a separate species that can be measured via indirect optical detection using colourimetry, fluorescence, chemiluminescence, etc.

The paper microfluidic devices (or paper-based analytical devices, PADs) were created by with a commercial wax printer, and the exposed paper areas were treated  with the colourimetric reagents.  For these trials, simple circular areas were patterned for the proof-of-principle studies undertaken, in lieu of channel networks.  The reagents used were 3, 3′, 5, 5′-tetramethylbenzidine (TMB, the substrate and also colourimetric reagent), bovine serum albumin (BSA), phosphate buffer and hydrogen peroxide, with or without the poly(vinyl alcohol) (PVA).  Horseradish peroxidase (HRP, the enzyme ) was contained in the sample solution.  TMB changes to blue in the presence of HRP and hydrogen peroxide.

The authors discovered that blue colour seen upon initial reaction faded after a day, and isolated the cause to decomposition of the hydrogen peroxide on the PAD during this time.  The figure above shows PADs with the enzymatic assay occurring in the patterned dots, where a) both hydrogen peroxide and TMB were added to the PAD, and the results are captured shortly after reaction; or the PAD with only b) hydrogen peroxide or c) TMB is prepared and stored at room temperature for one day, and then the other reagents are added and the results captured.  Degradation of the hydrogen peroxide causes the near total loss of signal in b).

extended refrigerated lifetimesTo stabilise the hydrogen peroxide, they added PVA to the hydrogen peroxide solutions prior to addition to the PAD, and found dramatic improvements in hydrogen peroxide stability.  The extent of the improvement varying with PVA concentration and chain length, as well as storage temperature.  2% solutions of PVA with a length of ~1650 monomers extended the life of the reaction at ~100 intensity to 10 days with storage at room temperature, while refrigeration at 4°C extended that to 30 days for PVA lengths of ~1650 or 2000 monomers.  The PVA is thought to protect the hydrogen peroxide by forming a liquid- and air-tight barrier, thus preventing attack by hydroxide anion that catalyses the degradation.

The importance of extending reagent lifetimes in microfluidic devices is a critical building block for the development of point-of-care/use devices.  In this case, isolation and stabilisation of the hydrogen peroxide reagent, in widespread use for enzymatic assays, is of obvious benefit.  30 days of refrigerated storage is much better than a few hours, but a long way from the requirements for a robust product with a minimum 6-month shelf-life.  However, one could imagine product development efforts with currently available packaging technology, e.g. desiccation followed by vacuum packaging or dry inert gas packaging, might easily eliminate the moisture-catalysed degradation, and thus extend product life significantly.  There are also other stabilising polymers to choose from that may be better optimised for other types of reagents requiring a liquid/gas barrier.

 

Wood microfluidics devices

Wood microfluidics devices

device-arrayI guess it’s not a big stretch to go from paper to wood for microfluidic substrates, but I’m impressed nonetheless!  Govind Rao‘s group in Chemical Engineering at the University Maryland recently published an ASAP article in Analytical Chemistry (alternatively use this DOI) about microfluidic devices made in plywood.

The Rao group machined channels and features in 35 chips laid out on 12″ x 12″ plywood sheets using a CO2 laser printer.  Devices were treated with a 0.1-1% PMMA or Teflon solution to seal up pores and inhibit capilarity which would otherwise promote seepage of sample and running buffers in the substrate.  Wooden channel layer substrate was bonded with cyanoacrylate glue to wooden cover plate with through-holes accommodating Luer lock fittings; PMMA covers were sometimes used for visualisation.  Channels were ~0.68 mm-deep X 1 mm-wide, and the system tolerated pressures of ~2 psi.  Different laser rastering speeds and line thicknesses were explored.  Identical devices were made out of PMMA for performance comparison purposes.

t-and-y-mixerRuns with blue and red food dye mixed at Y- and T-intersection mixers were performed and imaged to compare performance in a simple flow experiment.  The figure at right shows comparable performance (PMMA in left column, wood in right column), though for both geometries, the wood chips do not provide an even amount of the two dyes (less red dye), and the signal is noisier, as shown by the black standard deviation lines above and below the red average signal lines.  No discussion was found concerning these two discrepancies.

The authors discuss the biodegradable advantage that wooden devices have vs. their polymer or glass counterparts, and how this is becoming increasingly important with new legislation banning single-use plastics coming into force in many jurisdictions.