Emerging paper microfluidic devices

The Analyst ◽  
2019 ◽  
Vol 144 (22) ◽  
pp. 6497-6511 ◽  
Author(s):  
Bingbing Gao ◽  
Xin Li ◽  
Yaqiong Yang ◽  
Jianlin Chu ◽  
Bingfang He

Paper has unique advantages over other materials, including low cost, flexibility, porosity, and self-driven liquid pumping, thus making it widely used in various fields in biology, chemistry, physics and materials science.

2020 ◽  
Author(s):  
Dharitri Rath ◽  
Bhushan Toley

<p>Paper-based microfluidic devices are popular for their ability to automate multi-step assays for chemical or biological sensing at a low cost, but the design of paper microfluidic networks has largely relied on experimental trial and error. A few mathematical models of flow through paper microfluidic devices have been developed and have succeeded in explaining experimental flow behaviour. However, the reverse engineering problem of designing complex paper networks guided by appropriate mathematical models is largely unsolved. In this article, we demonstrate that a two-dimensional paper network (2DPN) designed to sequentially deliver three fluids to a test zone on the device can be computationally designed and experimentally implemented without trial and error. This was accomplished by three new developments in modelling flow through paper networks: i) coupling of the Richards equation of flow through porous media to the species transport equation, ii) modelling flow through assemblies of multiple paper materials (test membrane and wicking pad), and iii) incorporating limited-volume fluid sources. We demonstrate the application of this model in the optimal design of a paper-based signal-enhanced immunoassay for a malaria protein, P<i>f</i>HRP2. This work lays the foundation for the development of a computational design toolbox to aid in the design of paper microfluidic networks.</p>


Crystals ◽  
2018 ◽  
Vol 9 (1) ◽  
pp. 12 ◽  
Author(s):  
Mathieu Gonidec ◽  
Josep Puigmartí-Luis

Materials science is a fast-evolving area that aims to uncover functional materials with ever more sophisticated properties and functions. For this to happen, new methodologies for materials synthesis, optimization, and preparation are desired. In this context, microfluidic technologies have emerged as a key enabling tool for a low-cost and fast prototyping of materials. Their ability to screen multiple reaction conditions rapidly with a small amount of reagent, together with their unique physico-chemical characteristics, have made microfluidic devices a cornerstone technology in this research field. Among the different microfluidic approaches to materials synthesis, the main contenders can be classified in two categories: continuous-flow and segmented-flow microfluidic devices. These two families of devices present very distinct characteristics, but they are often pooled together in general discussions about the field with seemingly little awareness of the major divide between them. In this perspective, we outline the parallel evolution of those two sub-fields by highlighting the key differences between both approaches, via a discussion of their main achievements. We show how continuous-flow microfluidic approaches, mimicking nature, provide very finely-tuned chemical gradients that yield highly-controlled reaction–diffusion (RD) areas, while segmented-flow microfluidic systems provide, on the contrary, very fast homogenization methods, and therefore well-defined super-saturation regimes inside arrays of micro-droplets that can be manipulated and controlled at the milliseconds scale. Those two classes of microfluidic reactors thus provide unique and complementary advantages over classical batch synthesis, with a drive towards the rational synthesis of out-of-equilibrium states for the former, and the preparation of high-quality and complex nanoparticles with narrow size distributions for the latter.


2020 ◽  
Author(s):  
Dharitri Rath ◽  
Bhushan Toley

<p>Paper-based microfluidic devices are popular for their ability to automate multi-step assays for chemical or biological sensing at a low cost, but the design of paper microfluidic networks has largely relied on experimental trial and error. A few mathematical models of flow through paper microfluidic devices have been developed and have succeeded in explaining experimental flow behaviour. However, the reverse engineering problem of designing complex paper networks guided by appropriate mathematical models is largely unsolved. In this article, we demonstrate that a two-dimensional paper network (2DPN) designed to sequentially deliver three fluids to a test zone on the device can be computationally designed and experimentally implemented without trial and error. This was accomplished by three new developments in modelling flow through paper networks: i) coupling of the Richards equation of flow through porous media to the species transport equation, ii) modelling flow through assemblies of multiple paper materials (test membrane and wicking pad), and iii) incorporating limited-volume fluid sources. We demonstrate the application of this model in the optimal design of a paper-based signal-enhanced immunoassay for a malaria protein, P<i>f</i>HRP2. This work lays the foundation for the development of a computational design toolbox to aid in the design of paper microfluidic networks.</p>


2013 ◽  
Vol 562-565 ◽  
pp. 601-607
Author(s):  
Zong An Li ◽  
Li Ya Hou ◽  
Wei Yi Zhang ◽  
Li Zhu

Paper-based microfluidic devices have a significant potential for low-cost diagnostics in the developing world. This study reported a simple fabrication method based on the digitallization of microfluidic technology for paper based microfluidic devices. Melted wax was jetted steadily with PZT actuated microfluidic pulse inertia driving system and pulled-forged glass micronozzle in the form of droplets. The wax melted into filter paper to form hydrophobic wall and different patterns for paper microfluidic devices were made. The influence of system parameters such as driving force, frequency, the fabrication process and the tip diameter of glass micronozzle on the wax line width was experimentally studied. 75 μm500 μm wax lines were achieved with the wax printing system. The paper microfluidic devices fabricated could lead the capillary action of black ink and the color change reaction of NaOH and phenolphthalein solution. Result showed that the wax printing system is simple structured and this method suggests a novel path to develop simple, inexpensive, and portable diagnostic assays.


The Analyst ◽  
2019 ◽  
Vol 144 (4) ◽  
pp. 1178-1186 ◽  
Author(s):  
Hiroyuki Shibata ◽  
Yuki Hiruta ◽  
Daniel Citterio

Fully inkjet-printed and low-cost microfluidic paper-based analytical devices (μPADs) demonstrate the simple naked-eye colorimetric determination of calcium ions in drinking and tap water samples.


Polymers ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 607
Author(s):  
Lucero M. Hernandez-Cedillo ◽  
Francisco G. Vázquez-Cuevas ◽  
Rafael Quintero-Torres ◽  
Jose L. Aragón ◽  
Miguel Angel Ocampo Mortera ◽  
...  

In this article, we show an alternative low-cost fabrication method to obtain poly(dimethyl siloxane) (PDMS) microfluidic devices. The proposed method allows the inscription of micron resolution channels on polystyrene (PS) surfaces, used as a mold for the wanted microchip’s production, by applying a high absorption coating film on the PS surface to ablate it with a focused low-power visible laser. The method allows for obtaining micro-resolution channels at powers between 2 and 10 mW and can realize any two-dimensional polymeric devices. The effect of the main processing parameters on the channel’s geometry is presented.


1998 ◽  
Vol 70 (1-2) ◽  
pp. 153-158 ◽  
Author(s):  
W.K. Schomburg ◽  
R. Ahrens ◽  
W. Bacher ◽  
C. Goll ◽  
S. Meinzer ◽  
...  

2009 ◽  
Vol 20 (1) ◽  
pp. 015026 ◽  
Author(s):  
Mona Rahbar ◽  
Sumanpreet Chhina ◽  
Dan Sameoto ◽  
M Parameswaran

2021 ◽  
Author(s):  
Samantha Richardson ◽  
Samira Al Hinai ◽  
Jesse Gitaka ◽  
Will Mayes ◽  
Mark Lorch ◽  
...  

&lt;p&gt;Routine monitoring of available soil nutrients is required to better manage agricultural land&lt;sup&gt;1&lt;/sup&gt;, especially in many lower and middle income countries (LMICs). Analysis often still relies on laboratory-based equipment, meaning regular monitoring is challenging.&lt;sup&gt;2&lt;/sup&gt; The limited number of in situ sensors that exist are expensive or have complex workflows, thus are not suitable in LMICs, where the need is greatest.&lt;sup&gt;3&lt;/sup&gt; We aim to develop a simple-to-use, low-cost analysis system that enable farmers to directly monitor available nutrients and pH on-site, thus making informed decisions about when and where to apply fertilisers.&lt;/p&gt;&lt;p&gt;We combine nutrient extraction via a cafetiere-based filtration system with nutrient readout on a paper microfluidic analysis device (PAD) employing colour producing reactions that can be captured via a smartphone camera through an app. Image analysis of colour intensity permits quantitation of analytes. We initially focus on key nutrients (phosphate, nitrate) and pH analysis.&lt;/p&gt;&lt;p&gt;For extraction of phosphate, we mixed soil and water in the cafetiere and quantified the extracted phosphate via phosphomolybdenum blue chemistry. For example, for 5 g of soil, a water volume of about 160 mL led to optimum extraction. Active mixing, by pushing coffee filter plunger up and down, aided extraction. A mixing period of 3 min yielded maximum extraction; this time period was deemed suitable for an on-site workflow.&lt;/p&gt;&lt;p&gt;Following nutrient extraction, a simple-to-use readout system is required. For this, we developed colourimetric paper-based microfluidic devices; these are simply dipped into the decanted soil supernatant from the cafetiere and wick fluids based on capillary forces. Chemical reagents are pre-stored in reaction zones, created by patterning cellulose with wax barriers. Our devices contain multiple paper layers with different reagents; these are folded, laminated and holes cut for sample entry. Following the required incubation time, the developed colour is captured using a smartphone. This constitutes a portable detector, already available to envisaged end users, even in LMICs. We have previously developed an on-paper reaction for monitoring phosphates in fresh water in the mg L&lt;sup&gt;-1&lt;/sup&gt; working range, with readout after an incubation period of 3 min. This method was adapted here to enable storage at ambient temperatures up to 1 week by incorporating additional acidic reagents. Further pad devices were developed in our group for colour-based readout of nitrate, involving a two-step reaction chemistry. Within a relatively short incubation period (&amp;#8804;8 min) a pink coloured was formed following reduction of nitrate to nitrite with zinc and subsequent reaction to form an azo-dye. This system achieved detection in the low mg L&lt;sup&gt;-1&lt;/sup&gt; range. Moreover, a pad to monitor pH was developed, employing chlorophenol red indicator, with linear response achieved over the relevant pH 5-7 range. &amp;#160;&lt;/p&gt;&lt;p&gt;Our analysis workflow combines a simple-to-use cafetiere-based extraction method with paper microfluidic colour readout and smart-phone detector. This has the potential to enable farmers to monitor nutrients in soils on-site. Future work will aim at integrating multiple analytes into a single analysis card and to automate image analysis.&lt;/p&gt;&lt;p&gt;[1] &lt;em&gt;Europ. J. Agronomy&lt;/em&gt;, 55, 42&amp;#8211;52, &lt;strong&gt;2014.&lt;/strong&gt;&lt;/p&gt;&lt;p&gt;[2] &lt;em&gt;Nutr. Cycling Agroecosyst.,&lt;/em&gt; 109, 77-102, &lt;strong&gt;2017.&lt;/strong&gt;&lt;/p&gt;&lt;p&gt;[3] Sens Actuators B, 30, 126855, &lt;strong&gt;2019.&lt;/strong&gt;&lt;/p&gt;


Sign in / Sign up

Export Citation Format

Share Document