Team:UCL/Science/MicroF
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<ul class="tabs"><li><a href="#view1">Our Microfluidics Project</a></li><li><a href="#view2">Microfluidic Design</a></li><li><a href="#view3">Basic Principles</a></li></ul> | <ul class="tabs"><li><a href="#view1">Our Microfluidics Project</a></li><li><a href="#view2">Microfluidic Design</a></li><li><a href="#view3">Basic Principles</a></li></ul> | ||
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+ | <div class="textTitle"><h4>Application of microfluidic techniques to test performance of <a data-tip="true" class="top large" data-tip-content="Downstream processing units: each stage indicated in our downstream process flowsheet." href="javascript:void(0)"><b>DPUs</b></a> in scalable synbio azo-remediation technology</h4></div><br> | ||
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- | + | The Role of Microfluidic Analysis to Evaluate the Scalable Synbio Azo-Remediation Solution | |
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- | - | + | We have <a data-tip="true" class="top large" data-tip-content="Design of a complete industrial-scale process application, and testing of module units using customized microfluidic devices." href="javascript:void(0)"><b>designed and tested</b></a> a novel approach to azo-remediation, which allows sustainable and scalable bioprocessing. Our bioprocess integrates elements from <a data-tip="true" class="top large" data-tip-content="Investigation of bioreactor design and performance." href="javascript:void(0)"><b>upstream</b></a> and <a data-tip="true" class="top large" data-tip-content="Identification of downstream processing requirements, and design of a novel immobilisation module." href="javascript:void(0)"><b>downstream</b></a> processing. |
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- | + | In order to develop and improve the functionality of our bioprocess, key steps must be tested to quantify <a data-tip="true" class="top large" data-tip-content="Such as flow rates to determine residence time." href="javascript:void(0)"><b>process variables</b></a>, and allow for preliminary mass transfer calculations and detection of azo dye degradation rates. | |
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- | - | + | We have created microfluidic prototype devices to test the mixing in our reactors, and to test the performance of our novel immobilisation module, allowing for process optimisation and testing, without the <a data-tip="true" class="top large" data-tip-content="Microfluidic testing maintains low fabrication costs and reagent consumption, ideal for our testing stages." href="javascript:void(0)"><b>burdens</b></a> of expensive pilot scale testing. |
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- | + | The process testing timeline demonstrates that effective microfluidic testing can be used in replacement to conventional small-scale testing approaches. This is ideal for our project, especially when optimising whole unit operations. | |
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+ | <iframe width="600" height="380" style="padding:2.5%; border:0.5% #000" src="//www.youtube.com/embed/sRc_-zurwUE" frameborder="0" allowfullscreen align="right"></iframe> | ||
+ | Since our project involves designing a novel <a data-tip="true" class="top large" data-tip-content="Microfluidics allows us to test downstream processing units without the need to construct expensive small scale reactors." href="https://2014.igem.org/Team:UCL/Science/Bioprocessing"><b>bioprocess</b></a> using whole-cell biocatalysts, we constructed a <a><b>microfluidic scale immobilisation module</b></a> to investigate and evaluate our industrial scale module, the <a><b>video is shown on the right</b></a>. | ||
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+ | Investigation into reactor design and reaction constraints can be performed with ease and with low reagent cost, as all variables are scaled down to a micro-level. | ||
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+ | Most importantly, the scale-down can be carried out <a><b>without losing any of the accuracy or quantification of data output</a></b>; this is due the number of sensors and control mechanisms which can be integrated into the microfluidic system. | ||
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+ | For our <a><b>microfluidic bioreactor</b></a>, we will be using a <a><b>magnetic free floating bar</b></a> as our mixing system. This is an effective method of mixing at a microfluidic scale, as demonstrated in the video on the right. <a><b>The video on the left is of a microfluidic chemostat bioreactor</b></a> designed by Davies et al. 2014 UCL, using a free-floating bar to mix two dyes.</p></div> | ||
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+ | Construction of Microfluidic Mixing Device to Analyse Optimal Mixing Methods & Conditions | ||
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+ | On the left, is an image of a microfluidic device constructed and designed by Lewis Brayshaw; which was then tested using facilities in the UCL Microfluidics and Anatomy Labs.</p> | ||
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- | <div class=" | + | <a data-tip="true" class="top large" data-tip-content="This is Lewis' microfluidic device being tested to examine mixing conditions." href="javascript:void(0)" style="width: 32%;float: left;margin-left:0%"><img src="https://static.igem.org/mediawiki/2014/6/69/UCLMF123.jpg" style="max-width: 100%;"></a> |
- | + | <a data-tip="true" class="top large" data-tip-content="This is the overall schematic of the microfluidic device designed by Lewis Brayshaw." href="javascript:void(0)" style="width: 32%;float: left;margin-left:2%;margin-right:2%"><img src="https://static.igem.org/mediawiki/2014/3/36/Lewis_igem_device_exploded-1.png.jpg" style="max-width: 100%;"></a> | |
- | + | <a data-tip="true" class="top large" data-tip-content="The annotated view allows us to comprehend the simplicity and size of the microfluidic device." href="javascript:void(0)" style="width: 32%;float: left;margin-right:0%"><img src="https://static.igem.org/mediawiki/2014/5/5b/Lewis_igem_device_overall_drawing-1.png.jpg" style="max-width: 100%;"></a> | |
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- | + | The images above demonstrate the microfluidic device constructed by Lewis Brayshaw. The device was designed initially using computer-aided design, then constructed using rapid polymer prototyping techniques.</p></div> | |
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<div class="textTitle"><h4>Design & construct of a microfluidic device</h4></div> | <div class="textTitle"><h4>Design & construct of a microfluidic device</h4></div> | ||
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<p>We will use rapid polymer prototyping techniques to generate microfluidic chips that will allow us to test our reaction and aid in the construction of a realistic bioprocess, which can be successfully scaled-up for industrial use. <br><br>As we optimise and change our bioprocess, we can also quickly design new microfluidic chips that can mimic its development on a micro-scale. For example, it is our goal to integrate multiple downstream steps, such as chromatography, in order to isolate potential useful products. Demonstrating this in a microfluidic system is less time-consuming and far more cost effective than doing so at a larger scale.</p><br> | <p>We will use rapid polymer prototyping techniques to generate microfluidic chips that will allow us to test our reaction and aid in the construction of a realistic bioprocess, which can be successfully scaled-up for industrial use. <br><br>As we optimise and change our bioprocess, we can also quickly design new microfluidic chips that can mimic its development on a micro-scale. For example, it is our goal to integrate multiple downstream steps, such as chromatography, in order to isolate potential useful products. Demonstrating this in a microfluidic system is less time-consuming and far more cost effective than doing so at a larger scale.</p><br> | ||
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<a data-tip="true" class="top large" data-tip-content="AutoCAD allowed us to quickly generate multiple device designs, and accurately develop 3D views of both simple and complex designs." href="javascript:void(0)" style="width: 32%;float: left;margin-left:0%"><img src="https://static.igem.org/mediawiki/2014/thumb/b/b8/AutoCAD_Device.png/800px-AutoCAD_Device.png" style="max-width: 100%;"></a> | <a data-tip="true" class="top large" data-tip-content="AutoCAD allowed us to quickly generate multiple device designs, and accurately develop 3D views of both simple and complex designs." href="javascript:void(0)" style="width: 32%;float: left;margin-left:0%"><img src="https://static.igem.org/mediawiki/2014/thumb/b/b8/AutoCAD_Device.png/800px-AutoCAD_Device.png" style="max-width: 100%;"></a> | ||
<a data-tip="true" class="top large" data-tip-content="Our custom made devices have all sorts of unique designs which we wanted to test out. Each device can range from the size of your phone to the width of a 2 pound coin!" href="javascript:void(0)" style="width: 32%;float: left;margin-left:2%;margin-right:2%"><img src="https://static.igem.org/mediawiki/2014/thumb/7/71/MicrofluidicsDevice.jpg/800px-MicrofluidicsDevice.jpg" style="max-width: 100%;"></a> | <a data-tip="true" class="top large" data-tip-content="Our custom made devices have all sorts of unique designs which we wanted to test out. Each device can range from the size of your phone to the width of a 2 pound coin!" href="javascript:void(0)" style="width: 32%;float: left;margin-left:2%;margin-right:2%"><img src="https://static.igem.org/mediawiki/2014/thumb/7/71/MicrofluidicsDevice.jpg/800px-MicrofluidicsDevice.jpg" style="max-width: 100%;"></a> | ||
<a data-tip="true" class="top large" data-tip-content="Once designed and constructed, it's time to hook it up and run some tests!" href="javascript:void(0)" style="width: 32%;float: left;margin-right:0%"><img src="https://static.igem.org/mediawiki/2014/1/1e/Fluidics_Chip.JPG" style="max-width: 100%;"></a> | <a data-tip="true" class="top large" data-tip-content="Once designed and constructed, it's time to hook it up and run some tests!" href="javascript:void(0)" style="width: 32%;float: left;margin-right:0%"><img src="https://static.igem.org/mediawiki/2014/1/1e/Fluidics_Chip.JPG" style="max-width: 100%;"></a> | ||
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Above are some examples of the microfluidics devices developed by our team for use in the lab at the UCL ACBE. The devices are initially designed using AutoCAD (2D and 3D computer-aided design software), once the designs are finalised they can be 3D-printed using the facilities provided by the UCL Institute of Making and UCL ACBE; allowing our bioprocess and laboratory team to experiment and improve designs.</p></div><br> | Above are some examples of the microfluidics devices developed by our team for use in the lab at the UCL ACBE. The devices are initially designed using AutoCAD (2D and 3D computer-aided design software), once the designs are finalised they can be 3D-printed using the facilities provided by the UCL Institute of Making and UCL ACBE; allowing our bioprocess and laboratory team to experiment and improve designs.</p></div><br> | ||
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<p>One of the major hurdles in microfluidics is the fact that fluids are very difficult to mix at small volumes as a result of low <a data-tip="true" class="top large" data-tip-content="To learn more about Reynolds number, click here!" href="http://en.wikipedia.org/wiki/Reynolds_number"><b>Reynolds numbers</b></a>. Reynolds number describes flow patterns in various flow situations; a low Reynolds number indicates laminar flow, whereas a large Reynolds number indicates turbulent flow. Turbulent flow allows highly effective mixing in comparison to laminar flow. However, in microfluidics several device designs are available, which (to a greater or lesser degree) allow sufficient mixing. The flip side of this is that diffusion is often the only method of mixing. This in itself can be very useful, particularly when investigating enzyme kinetics. </p><br> | <p>One of the major hurdles in microfluidics is the fact that fluids are very difficult to mix at small volumes as a result of low <a data-tip="true" class="top large" data-tip-content="To learn more about Reynolds number, click here!" href="http://en.wikipedia.org/wiki/Reynolds_number"><b>Reynolds numbers</b></a>. Reynolds number describes flow patterns in various flow situations; a low Reynolds number indicates laminar flow, whereas a large Reynolds number indicates turbulent flow. Turbulent flow allows highly effective mixing in comparison to laminar flow. However, in microfluidics several device designs are available, which (to a greater or lesser degree) allow sufficient mixing. The flip side of this is that diffusion is often the only method of mixing. This in itself can be very useful, particularly when investigating enzyme kinetics. </p><br> | ||
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+ | <a data-tip="true" class="top large" data-tip-content="This device and equipment is provided for by the UCL microfluidics lab." href="javascript:void(0)" style="width: 35%;float: right;margin-left:2%"><img src="https://static.igem.org/mediawiki/2014/4/49/Microfluidic_set-up_iGEM.JPG" style="max-width: 100%;"></a> | ||
+ | The videos above were recorded in the UCL ACBE Microfluidics labs by members of our team. The video on the left is a demonstration of laminar flow across a T-junction microfluidic device. The video on the right demonstrates one of the methods of mixing made possible by microfluidics (herring bone channels etched into the chip). | ||
+ | <br><br>The image on the right displays the microfluidics set-up used by our iGEM team.</p></div> | ||
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<p><a data-tip="true" class="top large" data-tip-content="Here's a picture of Dave Jackson 'working hard' in the microfluidics lab." href="javascript:void(0)" style="width: 20%;float: right;margin-left:2%"><img src="https://static.igem.org/mediawiki/2014/2/22/UCLDAVEJACKSONMF.jpg" style="max-width: 100%;"></a> | <p><a data-tip="true" class="top large" data-tip-content="Here's a picture of Dave Jackson 'working hard' in the microfluidics lab." href="javascript:void(0)" style="width: 20%;float: right;margin-left:2%"><img src="https://static.igem.org/mediawiki/2014/2/22/UCLDAVEJACKSONMF.jpg" style="max-width: 100%;"></a> | ||
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Latest revision as of 19:24, 17 October 2014
Application of microfluidic techniques to test performance of DPUs in scalable synbio azo-remediation technology
In order to develop and improve the functionality of our bioprocess, key steps must be tested to quantify process variables, and allow for preliminary mass transfer calculations and detection of azo dye degradation rates.
We have created microfluidic prototype devices to test the mixing in our reactors, and to test the performance of our novel immobilisation module, allowing for process optimisation and testing, without the burdens of expensive pilot scale testing.
The process testing timeline demonstrates that effective microfluidic testing can be used in replacement to conventional small-scale testing approaches. This is ideal for our project, especially when optimising whole unit operations.
Since our project involves designing a novel bioprocess using whole-cell biocatalysts, we constructed a microfluidic scale immobilisation module to investigate and evaluate our industrial scale module, the video is shown on the right.
Investigation into reactor design and reaction constraints can be performed with ease and with low reagent cost, as all variables are scaled down to a micro-level.
Most importantly, the scale-down can be carried out without losing any of the accuracy or quantification of data output; this is due the number of sensors and control mechanisms which can be integrated into the microfluidic system.
For our microfluidic bioreactor, we will be using a magnetic free floating bar as our mixing system. This is an effective method of mixing at a microfluidic scale, as demonstrated in the video on the right. The video on the left is of a microfluidic chemostat bioreactor designed by Davies et al. 2014 UCL, using a free-floating bar to mix two dyes.
Design & construct of a microfluidic device
We will use rapid polymer prototyping techniques to generate microfluidic chips that will allow us to test our reaction and aid in the construction of a realistic bioprocess, which can be successfully scaled-up for industrial use.
As we optimise and change our bioprocess, we can also quickly design new microfluidic chips that can mimic its development on a micro-scale. For example, it is our goal to integrate multiple downstream steps, such as chromatography, in order to isolate potential useful products. Demonstrating this in a microfluidic system is less time-consuming and far more cost effective than doing so at a larger scale.
Above are some examples of the microfluidics devices developed by our team for use in the lab at the UCL ACBE. The devices are initially designed using AutoCAD (2D and 3D computer-aided design software), once the designs are finalised they can be 3D-printed using the facilities provided by the UCL Institute of Making and UCL ACBE; allowing our bioprocess and laboratory team to experiment and improve designs.
An example of one of our microfluidic devices designed on AutoCAD can be downloaded here. This device utilises the basic concept of mixing the cells and dyes, producing a single output stream; much alike to the bioprocessing concept. During the course of designing the microfluidic device, several key considerations must be taken into account: ability to withstand high pressure without leakage; materials of construction to be inert and transparent; size constraints of inlet and outlet piping; ability to accurately 3D-print the device.
Basic principles of microfluidic technology
Microfluidics is the study, design, and fabrication of devices that can handle and process fluids on the microlitre scale. Over the past few decades, this field has been responsible for many commonly used, and sometimes life-dependant, tools that people rely on. For example, glucose sensors for diabetics, is one of the plethora of handheld devices made available through microfluidics. The tiny volumes involved allow niche environments to be studied (e.g. in understanding stem cells), as well as permitting the development of high throughput screening devices (e.g. in drug discovery and development).
One of the major hurdles in microfluidics is the fact that fluids are very difficult to mix at small volumes as a result of low Reynolds numbers. Reynolds number describes flow patterns in various flow situations; a low Reynolds number indicates laminar flow, whereas a large Reynolds number indicates turbulent flow. Turbulent flow allows highly effective mixing in comparison to laminar flow. However, in microfluidics several device designs are available, which (to a greater or lesser degree) allow sufficient mixing. The flip side of this is that diffusion is often the only method of mixing. This in itself can be very useful, particularly when investigating enzyme kinetics.
The videos above were recorded in the UCL ACBE Microfluidics labs by members of our team. The video on the left is a demonstration of laminar flow across a T-junction microfluidic device. The video on the right demonstrates one of the methods of mixing made possible by microfluidics (herring bone channels etched into the chip).
The image on the right displays the microfluidics set-up used by our iGEM team.
The scope and applications of microfluidics is truly immense and as time goes on, ever increasing amounts of investment is made. With more start-up companies and takeover bids in play, it is clear microfluidics is an exciting and emerging scientific field.
As a powerful biological research tool, microfluidics allows the adaptation of various molecular biology techniques - ranging from on-chip gene synthesis (protein expression from coding DNA) to the screening of protein interactions.