Lab On A Chip

We present a laterally emitting, coupled cavity micro fluidic dye ring laser, suitable for integration into lab-on-a-chip micro systems. The micro-fluidic laser has been successfully designed, fabricated, characterized and modelled. The resonator is formed by a micro-fluidic channel bounded by two isosceles triangle mirrors. The micro-fluidic laser structure is defined using photo lithography in 10 microns thick SU-8 polymer on a glass substrate. The micro fluidic channel is sealed by a glass lid, using PMMA adhesive bonding. The laser is characterized using the laser dye Rhodamine 6G dissolved in ethanol or ethylene glycol as the active gain medium, which is pumped through the micro-fluidic channel and laser resonator. The dye laser is optically pumped normal to the chip plane at 532 nm by a pulsed, frequency doubled Nd:YAG laser and lasing is observed with a threshold pump pulse energy flux of around 55 micro-Joule/square-milimeter. The lasing is multi-mode, and the laser has switchable output coupling into an integrated polymer planar waveguide. Tuning of the lasing wavelength is feasible by changing the dye/solvent properties.

A lab-on-a-disc is a unique microfluidic platform that utilizes centrifugal force to pump liquids. This offers many benefits for point-of-care devices because it eliminates the need for connections to multiple pumps and complex tubing connections. A wide range of applications including clinical chemistry, immunoassay, cell analysis, and nucleic acid tests could be demonstrated on a spinning disc. To enable the performance of assays in a fully integrated and automated manner, the robust actuation of integrated valves is a prerequisite. However, conventional passive-type valves incur a critical drawback in that their operation is dependent on the rotational frequency, which is easily influenced by the channel geometry and chemistry, in addition to the physical properties of the liquids to be transferred. Even though a few active-type valving techniques permit the individual actuation of valves, independent of the rotational frequency, complex procedures for the fabrication as well as ...

We have developed a super compact optical fluorescence spectrometer. Our innovative design combines advantages of guided wave planar optics and free-space microoptics. This innovation allows for miniaturization that is not achievable with pure planar or pure free-space optics. A prototype device has volume of its optical part below 1cm3. The spectrometer covers 450nm-650nm spectral range, and provides spectral resolution of

Lab on Chip technologies have enabled the possibility of novel μTAS devices (micro Total Analysis System) that could drastically improve health care services for billions of people around the world. However, serious drawbacks that reside in fluid handling technology currently available for these systems often restrict the commercialization of such devices. This work demonstrates a novel fluid handling method as a possible alternative to current micropumping techniques for disposable microfluidic chips. This technology is based on a single use, low cost, thermal micropumping system in which expandable microsphere mixtures are activated by commercial grade laser diodes to achieve flow rates as high as 2.2 μl/s and total volumes over 160 μl. With the addition of a volume dependent shut off valve, nanoliter repeatability is realized. Pressure and heat transfer related data are presented. Finally, the possible prospects and limitations of this technology as a core element in unified optofluidic systems are discussed.

3D printed biomaterials with spatial and temporal functionality could enable interfacial manipulation of fluid flows and motile cells. However, such dynamic biomaterials are challenging to implement since they must be responsive to multiple, biocompatible stimuli. Here, we show stereolithographic printing of hydrogels using noncovalent (ionic) crosslinking, which enables reversible patterning with controlled degradation. We demonstrate this approach using sodium alginate, photoacid generators and various combinations of divalent cation salts, which can be used to tune the hydrogel degradation kinetics, pattern fidelity, and mechanical properties. This approach is first utilized to template perfusable microfluidic channels within a second encapsulating hydrogel for T-junction and gradient devices. The presence and degradation of printed alginate microstructures were further verified to have minimal toxicity on epithelial cells. Degradable alginate barriers were used to direct collect...

An integrated lab-on-a-chip system has been developed and successfully utilized for real-time forensic short tandem repeat (STR) analysis. The microdevice comprises a 160-nL polymerase chain reaction reactor with an on-chip heater and a temperature sensor for thermal cycling, microvalves for fluidic manipulation, a co-injector for sizing standard injection, and a 7-cm-long separation channel for capillary electrophoretic analysis. A 9-plex autosomal STR typing system consisting of amelogenin and eight combined DNA index system (CODIS) core STR loci has been constructed and optimized for this real-time human identification study. Reproducible STR profiles of control DNA samples are obtained in 2h and 30min with <or=0.8bp allele typing accuracy. The minimal amount of DNA required for a complete DNA profile is 100 copies. To critically evaluate the capabilities of our portable microsystem as well as its compatibility with crime scene investigation processes, real-time STR analyses were carried out at a mock crime scene prepared by the Palm Beach County Sheriff's Office (PBSO). Blood stain sample collection, DNA extraction, and STR analyses on the portable microsystem were conducted in the field, and a successful "mock" CODIS hit was generated on the suspect's sample within 6h. This demonstration of on-site STR analysis establishes the feasibility of real-time DNA typing to identify the contributor of probative biological evidence at a crime scene and for real-time human identification.

Bacterial cells attachment onto solid surfaces and the following growth into mature microbial biofilms may result in highly antibiotic resistant biofilms. Such biofilms may be incidentally formed on tissues or implanted devices, or intentionally formed by directed deposition of microbial sensors on whole- cell bio-chip surface. A new method for electrical characterization of the later on-chip microbial biofilm buildup is presented in this paper. Measurement of impedance vs. frequency in the range of 100 mHz to 400 kHz of Escherichia coli cells attachment to indium-tin-oxide-coated electrodes was carried out while using optical microscopy estimating the electrode area coverage. We show that impedance spectroscopy measurements can be interpreted by a simple electrical equivalent model characterizing both attachment and growth of the biofilm. The correlation of extracted equivalent electrical lumped components with the visual biofilm parameters and their dependence on the attachment and growth phases is confirmed.

The open-source release of self-replicating rapid prototypers (RepRaps) has created a rich opportunity for low-cost distributed digital fabrication of complex 3-D objects such as scientific equipment. For example, 3-D printable reactionware devices offer the opportunity to combine open hardware microfluidic handling with lab-on-a-chip reactionware to radically reduce costs and increase the number and complexity of microfluidic applications. To further drive down the cost while improving the performance of lab-on-a-chip paper-based microfluidic prototyping, this study reports on the development of a RepRap upgrade capable of converting a Prusa Mendel RepRap into a wax 3-D printer for paper-based microfluidic applications. An open-source hardware approach is used to demonstrate a 3-D printable upgrade for the 3-D printer, which combines a heated syringe pump with the RepRap/Arduino 3-D control. The bill of materials, designs, basic assembly, and use instructions are provided, along with a completely free and open-source software tool chain. The open-source hardware device described here accelerates the potential of the nascent field of electrochemical detection combined with paper-based microfluidics by dropping the marginal cost of prototyping to nearly zero while accelerating the turnover between paper-based microfluidic designs.

The development of passively driven microfluidic labs on chips has been increasing over the years. In the
passive approach, the microfluids are usually driven and operated without any external actuators, fields,
or power sources. Passive microfluidic techniques adopt osmosis, capillary action, surface tension,
pressure, gravity-driven flow, hydrostatic flow, and vacuums to achieve fluid flow. There is a great need
to explore labs on chips that are rapid, compact, portable, and easy to use. The evolution of these
techniques is essential to meet current needs. Researchers have highlighted the vast potential in the field
that needs to be explored to develop rapid passive labs on chips to suit market/researcher demands. A
comprehensive review, along with patent analysis, is presented here, listing the latest advances in passive
microfluidic techniques, along with the related mechanisms and applications.