Light Seminars
February 20, 2013
L4H Seminar ANDREU LLOBERA 'Photonic Lab on a Chip: Mergence of Photonics and Microfluidics for Real Time Cell Screening'
L4H Seminar ANDREU LLOBERA 'Photonic Lab on a Chip: Mergence of Photonics and Microfluidics for Real Time Cell Screening'
ANDREU LLOBERA
Wednesday, February 20, 2013, 10:30. Seminar Room
ANDREU LLOBERA
Institut de Microelectrònica de Barcelona, SPAIN
ANDREU LLOBERA
Institut de Microelectrònica de Barcelona, SPAIN
One of the premises of the so called lab-on-a-chip paradigm is the integration of as many as possible processing stages of a chemical or biochemical analytical procedure together with microfluidics and detection methods. This latter aspect entails reliability, sensitivity and specificity of the analytical systems. Although electrochemical and mechanical approaches are common, optical detection remains predominant, mainly because its non-invasiveness, its high sensitivity and its small footprint. In this respect, many research groups – including our own – have concentrated their efforts in developing photonic lab-on-a-chip (PhLoC), where many different microoptical and photonic elements are monolithically integrated together with microfluidic devices.
Amongst the many applications to which these systems have been dedicated, cell culture has been identified as having great potential for improving throughput and reliability though miniaturization. In this seminar we will firstly, introduce the microoptical elements required to define PhLoC. Then, as a main example of such systems, it will be introduced the multiple internal reflection (MIR) systems, where simultaneous scattering and absorbance measurements can be performed. Key aspects in both PhLoC such as multiparametrical analysis, sensitivity, limit of detection, and growth rate will also be discussed. In the second part of this seminar, we will start discussing more advanced configurations such as the Dual Lab on a Chip (DLOC) that enables simultaneous optical and electrochemical detection working in continuous flow regime. Both detection modes are integrated for the first time into a single detection volume and operate simultaneously with no evidence of cross-talk. Such system was applied to the analysis of L-lactate via a bi-enzymatic reaction involving lactate oxidase (LOX) and horseradish peroxidase (HRP). Here, the consumption of the reagent of the reaction (ferrocyanide) was continuously monitored by amperometry whereas the product of the reaction (ferricyanide) was recorded by absorbance. Finally, some insights regarding the twin biophotonic lab on a chip with integrated size-exclusion microfilters for simultaneous monitoring of cell retention, proliferation and metabolism will also be given.
Wednesday, February 20, 2013, 10:30. Seminar Room
Hosted by Dr. Susana Santos
Amongst the many applications to which these systems have been dedicated, cell culture has been identified as having great potential for improving throughput and reliability though miniaturization. In this seminar we will firstly, introduce the microoptical elements required to define PhLoC. Then, as a main example of such systems, it will be introduced the multiple internal reflection (MIR) systems, where simultaneous scattering and absorbance measurements can be performed. Key aspects in both PhLoC such as multiparametrical analysis, sensitivity, limit of detection, and growth rate will also be discussed. In the second part of this seminar, we will start discussing more advanced configurations such as the Dual Lab on a Chip (DLOC) that enables simultaneous optical and electrochemical detection working in continuous flow regime. Both detection modes are integrated for the first time into a single detection volume and operate simultaneously with no evidence of cross-talk. Such system was applied to the analysis of L-lactate via a bi-enzymatic reaction involving lactate oxidase (LOX) and horseradish peroxidase (HRP). Here, the consumption of the reagent of the reaction (ferrocyanide) was continuously monitored by amperometry whereas the product of the reaction (ferricyanide) was recorded by absorbance. Finally, some insights regarding the twin biophotonic lab on a chip with integrated size-exclusion microfilters for simultaneous monitoring of cell retention, proliferation and metabolism will also be given.
Wednesday, February 20, 2013, 10:30. Seminar Room
Hosted by Dr. Susana Santos
Light Seminars
February 20, 2013
L4H Seminar ANDREU LLOBERA 'Photonic Lab on a Chip: Mergence of Photonics and Microfluidics for Real Time Cell Screening'
L4H Seminar ANDREU LLOBERA 'Photonic Lab on a Chip: Mergence of Photonics and Microfluidics for Real Time Cell Screening'
ANDREU LLOBERA
Wednesday, February 20, 2013, 10:30. Seminar Room
ANDREU LLOBERA
Institut de Microelectrònica de Barcelona, SPAIN
ANDREU LLOBERA
Institut de Microelectrònica de Barcelona, SPAIN
One of the premises of the so called lab-on-a-chip paradigm is the integration of as many as possible processing stages of a chemical or biochemical analytical procedure together with microfluidics and detection methods. This latter aspect entails reliability, sensitivity and specificity of the analytical systems. Although electrochemical and mechanical approaches are common, optical detection remains predominant, mainly because its non-invasiveness, its high sensitivity and its small footprint. In this respect, many research groups – including our own – have concentrated their efforts in developing photonic lab-on-a-chip (PhLoC), where many different microoptical and photonic elements are monolithically integrated together with microfluidic devices.
Amongst the many applications to which these systems have been dedicated, cell culture has been identified as having great potential for improving throughput and reliability though miniaturization. In this seminar we will firstly, introduce the microoptical elements required to define PhLoC. Then, as a main example of such systems, it will be introduced the multiple internal reflection (MIR) systems, where simultaneous scattering and absorbance measurements can be performed. Key aspects in both PhLoC such as multiparametrical analysis, sensitivity, limit of detection, and growth rate will also be discussed. In the second part of this seminar, we will start discussing more advanced configurations such as the Dual Lab on a Chip (DLOC) that enables simultaneous optical and electrochemical detection working in continuous flow regime. Both detection modes are integrated for the first time into a single detection volume and operate simultaneously with no evidence of cross-talk. Such system was applied to the analysis of L-lactate via a bi-enzymatic reaction involving lactate oxidase (LOX) and horseradish peroxidase (HRP). Here, the consumption of the reagent of the reaction (ferrocyanide) was continuously monitored by amperometry whereas the product of the reaction (ferricyanide) was recorded by absorbance. Finally, some insights regarding the twin biophotonic lab on a chip with integrated size-exclusion microfilters for simultaneous monitoring of cell retention, proliferation and metabolism will also be given.
Wednesday, February 20, 2013, 10:30. Seminar Room
Hosted by Dr. Susana Santos
Amongst the many applications to which these systems have been dedicated, cell culture has been identified as having great potential for improving throughput and reliability though miniaturization. In this seminar we will firstly, introduce the microoptical elements required to define PhLoC. Then, as a main example of such systems, it will be introduced the multiple internal reflection (MIR) systems, where simultaneous scattering and absorbance measurements can be performed. Key aspects in both PhLoC such as multiparametrical analysis, sensitivity, limit of detection, and growth rate will also be discussed. In the second part of this seminar, we will start discussing more advanced configurations such as the Dual Lab on a Chip (DLOC) that enables simultaneous optical and electrochemical detection working in continuous flow regime. Both detection modes are integrated for the first time into a single detection volume and operate simultaneously with no evidence of cross-talk. Such system was applied to the analysis of L-lactate via a bi-enzymatic reaction involving lactate oxidase (LOX) and horseradish peroxidase (HRP). Here, the consumption of the reagent of the reaction (ferrocyanide) was continuously monitored by amperometry whereas the product of the reaction (ferricyanide) was recorded by absorbance. Finally, some insights regarding the twin biophotonic lab on a chip with integrated size-exclusion microfilters for simultaneous monitoring of cell retention, proliferation and metabolism will also be given.
Wednesday, February 20, 2013, 10:30. Seminar Room
Hosted by Dr. Susana Santos
All Insight Seminars
Light Seminars
December 11, 2013
L4H SEMINAR JEAN FRANCOIS LEGER 'Exploring the Functions of the Brain in Vivo with Two-Photon Microscopy: the Case of the Tactile Cortex of Rat'
Light Seminars
November 26, 2013
L4H SEMINAR KHALID SALAITA 'Using Light to Visualize Molecular Forces in Cells'
Light Seminars
November 14, 2013
L4H SEMINAR HATICE ALTUG 'Integrated Nanoplasmonic Systems for Ultrasensitive Spectroscopy and High-Throughput Bio-Detection'
Light Seminars
November 6, 2013
L4H Seminar MARIE-CLAIRE SCHANNE-KLEIN'In Situ Visulalization of Collagen Architecture in Biological Tissues Using Polarization-Resolved SHG Microscopy'
Light Seminars
October 30, 2013
L4H Seminar ALFRED J. MEIXNER 'Tip-Enhanced Nanometer Scale Optical Imaging And Spectroscopy'
Light Seminars
October 18, 2013
L4H SEMINAR DAVID RUEDA 'Watching AID/APOBEC3G Scanning Single Stranded and Transcribed DNA with Single Molecule Resolution'
Light Seminars
September 27, 2013
L4H SEMINAR SEBASTIAN DEINDL 'A novel nucleosome remodeling mechanism revealed by single-molecule fluorescence microscopy'
Light Seminars
September 23, 2013
L4H SEMINAR VALENTINA EMILIANI 'Two-photon optogenetics by wave front shaping of ultrafast pulses'
Light Seminars
September 18, 2013
L4H SEMINAR TERESA NEVES PETERSEN 'Photonic cancer therapy: modulating cellular metabolism with light'
Light Seminars
September 4, 2013
L4H SEMINAR MIKE HEILEMANN 'Quantitative single-molecule super-resolution microscopy of cellular structures'
Light Seminars
July 3, 2013
L4H SEMINAR PAUL W. WISEMAN 'Mapping Adhesion, Cytoskeletal and Signaling Protein Transport and Interactions in Living Cells by Image Correlation Methods'
Light Seminars
June 12, 2013
L4H Seminar JONAS RIES 'Novel Labeling Schemes for Single-Molecule Localization Microscopy'
Light Seminars
May 29, 2013
Light Seminars
May 21, 2013
L4H Seminar XAVIER INTES 'Towards Whole-Body Foster Resonance Energy Transfer Pre-Clinical Imaging'
Light Seminars
April 22, 2013
L4H SEMINAR CORINNE LORENZO 'Development of 3D Imaging of Large Spheroid Tumor Models Using Light Sheet Microscopy'
Light Seminars
March 13, 2013
L4H Seminar JORGE RIPOLL 'From ballistic to diffusive regimes: Light Propagation Models and Applications for In-vivo Optical Tomography'