25,493 research outputs found
Lab-on-a-chip Raman sensors outperforming Raman microscopes
We demonstrate that the signal-to-noise ratio and signal collection efficiency in evanescent waveguide-based Raman spectroscopy exceeds that in Raman microscopes. We investigate the effect of silicon-nitride waveguide geometry to further improve the performance
Advances in Microfluidics and Lab-on-a-Chip Technologies
Advances in molecular biology are enabling rapid and efficient analyses for
effective intervention in domains such as biology research, infectious disease
management, food safety, and biodefense. The emergence of microfluidics and
nanotechnologies has enabled both new capabilities and instrument sizes
practical for point-of-care. It has also introduced new functionality, enhanced
sensitivity, and reduced the time and cost involved in conventional molecular
diagnostic techniques. This chapter reviews the application of microfluidics
for molecular diagnostics methods such as nucleic acid amplification,
next-generation sequencing, high resolution melting analysis, cytogenetics,
protein detection and analysis, and cell sorting. We also review microfluidic
sample preparation platforms applied to molecular diagnostics and targeted to
sample-in, answer-out capabilities
Recommended from our members
Simulation of droplet-based microfluidic lab-on-a-chip applications
This paper was presented at the 3rd Micro and Nano Flows Conference (MNF2011), which was held at the Makedonia Palace Hotel, Thessaloniki in Greece. The conference was organised by Brunel University and supported by the Italian Union of Thermofluiddynamics, Aristotle University of Thessaloniki, University of Thessaly, IPEM, the Process Intensification Network, the Institution of Mechanical Engineers, the Heat Transfer Society, HEXAG - the Heat Exchange Action Group, and the Energy Institute.Miniaturization of biological and chemical assays in lab-on-a-chip systems is a highly topical field of research. Droplet-based microfluidic chips are types of these miniaturized systems. They expand the capability of assays with special features that are unreached by traditional workflows. In particular, small sample volumes, independent separated reaction units, high throughput, automation and parallelization of assays are prominent features of droplet-based microfluidic devices. Full custom centric design of droplet-based microfluidic lab-on-a-chip technology implicates a high system integration level and design complexity. Therefore advanced development methodologies are needed, comparable with the methods in electronic design automation. Our design and simulation toolkit meets these requirements for an agile and low-risk development of custom lab-on-a-chip devices. The system simulation approach enables a fast and precise prediction of complex microfluidic networks. This fact is confirmed by reference and benchmark
experiments. The results show that the simulation correctly reproduces the experimental measurements.The German BMBF and the EU in the projects DiNaMiD, signature 0315591B and NoE Photonics4Life, Grant Agreement number: 224014
Themed issue: Optofluidics
The term optofluidics defines a growing
research area that integrates optics and
microfluidics in ways that enable unique
strengths and advantages for a broad range
of applications. The First International
Conference on Optofluidics (Optofluidics-
2011) organized by Xi’an Jiaotong
University and Lab on a Chip on 11–12
December 2011 featured work in this field,
with an exciting two-day program of presentations
and discussions. We are happy
that Lab on a Chip, a major publication
destination for optofluidic research, has
scheduled this themed issue on Optofluidics.
We are especially heartened that the optofluidics
community has responded enthusiastically
with a large number of excellent
manuscript submissions
Flat fiber: the flexible format for distributed lab-on-a-chip
Integrated optical devices offer dense, multifunctional capability in a single robust package but are rarely considered compatible with the fields of remote or distributed sensing or long-haul 'one-dimensional' fibers. Here we aim to change that by introducing a 'flat-fiber' process that combines the advantages of existing low-cost fiber drawing with the functionality of planar lightwave circuits in a novel hybrid format. By taking this approach, we hope to extend beyond the limitations of traditional planar and fiber substrates - allowing exotic material compositions, device layouts, and local sensing functions to be distributed over extended distances with no coupling or compatibility concerns in highly functional distributed lab-on-a-chip devices
Liquid-infiltrated photonic crystals - enhanced light-matter interactions for lab-on-a-chip applications
Optical techniques are finding widespread use in analytical chemistry for
chemical and bio-chemical analysis. During the past decade, there has been an
increasing emphasis on miniaturization of chemical analysis systems and
naturally this has stimulated a large effort in integrating microfluidics and
optics in lab-on-a-chip microsystems. This development is partly defining the
emerging field of optofluidics. Scaling analysis and experiments have
demonstrated the advantage of micro-scale devices over their macroscopic
counterparts for a number of chemical applications. However, from an optical
point of view, miniaturized devices suffer dramatically from the reduced
optical path compared to macroscale experiments, e.g. in a cuvette. Obviously,
the reduced optical path complicates the application of optical techniques in
lab-on-a-chip systems. In this paper we theoretically discuss how a strongly
dispersive photonic crystal environment may be used to enhance the light-matter
interactions, thus potentially compensating for the reduced optical path in
lab-on-a-chip systems. Combining electromagnetic perturbation theory with
full-wave electromagnetic simulations we address the prospects for achieving
slow-light enhancement of Beer-Lambert-Bouguer absorption, photonic band-gap
based refractometry, and high-Q cavity sensing.Comment: Invited paper accepted for the "Optofluidics" special issue to appear
in Microfluidics and Nanofluidics (ed. Prof. David Erickson). 11 pages
including 8 figure
SERS-Enabled Lab-on-a-Chip Systems
Surface-enhanced Raman spectroscopy (SERS) has been combined with microfluidic Lab-on-a-Chip (LoC) systems for sensitive optofluidic detection for more than a decade. However, most microfluidic SERS devices still suffer from analyte contamination and signal irreproducibility. In recent years, both the microfluidics and SERS communities have developed their own solutions that are complementary to each other; their combination even has potential for commercialization. In this review, the recent advances in both fields are summarized with regard to the development of reliable multifunctional SERS-enabled LoC systems and their broad applications. Starting from SERS fundamentals, reproducible SERS substrates and dynamic microfluidic trapping are discussed. Based on their combination, on-chip applications beyond SERS are presented, and insight can be gained into the commercialization of portable SERS chips.postprin
Selective low concentration ammonia sensing in a microfluidic lab-on-a-chip
In the medical community, there is a considerable interest in a diagnostic breath analyzer for ammonia that is selectively enough to measure in exhaled air and small enough for the small volumes available in such an application. An indirect measurement system for low gaseous ammonia concentrations has been miniaturized and integrated on a chip in order to reach this goal. The detection limit of the system was calculated to be 1.1 parts per billion (ppb). The response time was determined to be 1.6 min with a gas How of 50 ml/min. The required gas volume for one measurement is therefore sufficiently small, although sampling assistance is required for breath analysis. The selectivity of the system is sufficient to measure ammonia concentrations in the low-ppb range. The system is even sufficiently selective to be used in environments that contain elevated carbon dioxide levels, like exhaled air. The lower ammonia concentration expected in diagnostic breath analysis applications, 50 ppb, was demonstrated to be detectable
LTCC packaging for Lab-on-a-chip application
LTCC -pakkaus Lab-on-a-chip -sovellukseen. Tiivistelmä. Tässä työssä suunniteltiin, valmistettiin ja testattiin uusi pakkaustekniikka ”Lab-on-a-chip” (LOC) -sovellukseen. Pakkaus tehtiin pii-mikrosirulle, jolla voidaan mitata solujen kiinnittymistä sirun pintaan solujen elinkelpoisuuden indikaattorina. Luotettavuustestaukset tehtiin daisy-chain -resistanssimittauksilla solunkasvatusolosuhteissa. Lisäksi työssä selvitettiin LTCC- ja ”Lab-on-a-chip” -teknologioiden perusteet teoreettiselta pohjalta.
Mikrosirun pakkauksessa käytettiin joustavaa LTCC-teknologiaa. Sähköisiin kontakteihin ja niiden suojauksiin käytettiin sekä johtavia että eristäviä epoksi-liimoja.
LOC-sovelluksiin on tärkeää kehittää uusia pakkausmenetelmiä jotta näiden laitteiden kaikki ominaisuudet saadaan toimimaan luotettavasti. Pakkaus testattiin samoissa olosuhteissa missä sitä tullaan käyttämään ja pakkaus kesti kaikki nämä haasteet. Lisäksi esitetty valmistusprosessi on sellainen, että sitä voidaan käyttää myös muihin ”Lab-on-a-chip” -sovelluksiin.Abstract. This work presents design, manufacturing and testing of new packaging method for Lab-on-a-chip (LOC) application. Packaging was made for silicon microchip which can measure cell adhesion on chips surface as indication of cell viability. Reliability testing was done with daisy-chain resistance measurement in real conditions. Moreover basic theory of LTCC and Lab-on-a-chip technology is presented.
Resilient LTCC technology was used for packaging material and conductive/insulating epoxies were applied for electrical contacts and barriers against the environment.
It is fundamentally important to develop new packaging methods for LOC applications, so all the properties can be utilized reliably. Packaging was tested under the cell growth conditions and the package showed to withstand all these challenges. Moreover the presented packaging method is possible to use also in other Lab-on-a-chip applications
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