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SELECTBIO Conferences Lab-on-a-Chip & Microfluidics, Point-of-Care Diagnostics & Global Health Asia 2017

Lab-on-a-Chip & Microfluidics, Point-of-Care Diagnostics & Global Health Asia 2017 Agenda



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Lab-on-a-Chip & Microfluidics, Point-of-Care Diagnostics & Global Health Asia 2017 | 

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Thursday, 30 November 2017

08:00

Conference Registration, Materials Pick-Up, Morning Coffee and Breakfast Pastries


Session Title: Conference Opening Session -- Emerging Themes in the Microfluidics and Lab-on-a-Chip Fields

09:00

Chwee Teck LimKeynote Presentation

Microfluidic Technologies for Liquid Biopsy & Precision Medicine
Chwee Teck Lim, Provost's Chair Professor, Principal Investigator, Mechanobiology Institute, National University of Singapore, Singapore

Capturing of circulating Tumor Cells (CTCs) from the peripheral blood of patients (a.k.a. liquid biopsy) can potentially lead to applications in cancer diagnosis and personalized medicine.   Using a label-free approach via our developed microfluidic biochips, we not only show successful detection and retrieval of CTCs, but also how selective capturing of each single CTCs can lead to downstream single cell analysis and enable personalized treatment through the detection of specific actionable or druggable mutation.

09:45

Accelerating the Detection Speed of Circulating DNA/RNA by Electrokinetic Concentration in a Microfluidic Chip
Yong-Ak (Rafael) Song, Assistant Professor of Mechanical and Biomedical Engineering, New York University Abu Dhabi, United Arab Emirates

The cell-free DNA (cfDNA), which consists of fragments of DNA from dying cancer cells, and exosomes released during fusion of the multivesicular endosomes have demonstrated great promise as an alternative biomarker for cancer detection and assessment of treatment. To enhance the detection sensitivity and speed of “Liquid Biopsy” tools for cfDNA and exosomal RNA, we have developed a microfluidic concentrator chip based on ion concentration polarization (ICP) that can preconcentrate target nucleic acids electrokinetically from a ~µL fluidic sample into a ~pL plug in the vicinity of the molecular capture probes. ICP preconcentration not only reduces the analyte diffusion length but also increases the binding reaction rate, and as a result, ICP-enhanced biosensors allow much faster hybridization than standard diffusion-limited biosensors such as microarrays. Utilizing an ion-selective conductive polymer membrane, poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS), in a microfluidic channel, we could achieve a concentration increase of DNA by 6 orders of magnitude from an initial concentration of 100 fM at 50V within 10 min. As for the detection via surface hybridization on morpholino (MO) probes, a class of uncharged DNA mimics, DNA target concentration as low as 10 pM was detected within 15 min. In the case of an exosomal RNA, miR21, we could accelerate its surface hybridization on MO probes by 7-fold using the electrokinetic concentrator. It even allowed an increase of the concentration of exosomes (from human breast cancer cell lines, ~105/mL) locally for a sensitive fluorescence detection. These results demonstrate a potential application of the microfluidic electrokinetic concentrator for a rapid detection of cfDNA and exosomal RNA molecules down to few pico- and femtomolar regimes.

10:15

Microfluidic Processes For Advanced Pharmaceutical Manufacturing - From Drug Molecules to Novel Drug Products
Saif Khan, Associate Professor, Chemical and Biomolecular Engineering, National University of Singapore, Singapore

This presentation will focus on the development of advanced manufacturing processes based on microfluidic technology, which bridge both primary and secondary pharmaceutical manufacturing, while also enabling novel ways to envision the final drug product. In particular, recent research at the National University of Singapore on the development of microfluidics-based crystallization and formulation processes, which allows the manufacture of spherical microparticles with remarkably precise control over the solid form of the drug substance, will be discussed. Application of the developed processes to both model and commercial API molecules, and their combinations with several excipients, will be highlighted. The presentation will conclude with an outline of the challenges and opportunities.

10:45

Coffee and Tea Break and Networking in the Exhibit Hall

11:15

Microfluidic Platform For Personalized Medicine and Healthcare
Nien-Tsu Huang, Assistant Professor, Department of Electrical Engineering, National Taiwan University, Taiwan

A discussion regarding how to develop a fully integrated microfluidic platform enabling on-chip sample preparation and in-situ biomarkers detection. The platform can potentially be applied for personalized healthcare.

11:45

Victor UgazKeynote Presentation

Lab-on-a-Drone: Portable Robust Platforms for Mobile Point-of-Care Bioanalysis
Victor Ugaz, Professor & Holder of the Charles D. Holland ’53 Professorship, Artie McFerrin Department of Chemical Engineering, Texas A&M University, United States of America

We describe recent innovations aimed at overcoming many of the roadblocks that have traditionally hindered deployment of advanced biochemical diagnostic technologies in field/resource-limited settings. Nucleic acid-based approaches like the polymerase chain reaction (PCR) are generally considered to be diagnostic gold standards in terms of both sensitivity and specificity. But PCR is largely ruled out as a viable candidate for portable deployment, particularly in resource-limited settings, due to an unfavorable combination of excessive electrical power requirements associated with repeated heating and cooling of reagents during thermocycling, and complexities related to inexpensively implementing fluorescence-based detection of the reaction products. We show how a unique convergence of scientific and technological breakthroughs from multiple disciplines have now made it possible to overcome these limitations, laying the foundation for a new generation of simple ruggedized POC diagnostic platforms.

12:30

Networking Lunch in the Exhibit Hall -- Meet the Exhibitors and View Posters


Session Title: Point-of-Care Diagnostics Utilizing Microfluidics and LOAC-based Approaches

13:30

Hyun-Duck KimKeynote Presentation

Point-of–Care Diagnostics Using Saliva
Hyun-Duck Kim, Professor, Seoul National University, Korea South

Oral and systemic chronic diseases, which are prevalent, have common risk factors; while they have not early diagnostic tool. Rapid test kits using salivary POC could be useful for early screening of both diseases at home and its application could be useful for early diagnosis at clinics.

14:15

Liquid Crystals in Microfluidic Devices for Biosensing Applications
Kun-Lin Yang, Associate Professor, Department of Chemical and Biomolecular Engineering, National University of Singapore, Singapore

Microfluidic sensors possess several advantages such as smaller sample volume, shorter assay time and lower cost compared to conventional assays performed in 96-well plates. However, because of its miniaturized format, microfluidic sensors also faced serious challenges in signal detection because of inherent short light path length, small sample volume, and short residence time. To overcome these limitations in microfluidic sensors, ultrasensitive signal detection and amplification mechanism are required. In this presentation, integration of liquid crystal (LC) materials with microfluidic devices for various chemical and biological sensing applications will be discussed. Because molecules form a LC phase have polar functional groups which have long-range interactions, they respond collectively to surface molecular binding events and change their orientations accordingly. This working principle has been exploited to develop highly sensitive biosensors in microfluidic devices. Using LC for signal transduction and amplification is advantageous because it is highly sensitive, fast and simple. More importantly, optical outputs of LC can be observed with the naked eye directly without using any complex instrumentation. Interference colors of LC also offer a simple way for qualitative and spatial analysis of protein concentration in microfluidic devices. Using LC-based microfluidic sensors, different biomolecules such as antibodies and enzymes can be detected in microfluidic devices.

14:45

Miniaturized Devices for Point-of-Care Diagnostic Applications
Chien-Fu Chen, Assistant professor, Institute of Applied Mechanics, National Taiwan University, Taiwan

A discussion regarding the miniaturized systems utilizing micro/nanomaterials for biomedical point-of-care sensing applications.

15:15

Rapid Detection of Pathogenic Bacteria on a Microfluidic Disc
Izumi Kubo, Professor, Soka University, Japan

We have developed an originally designed microfluidic disc-like device with microchannels and microchambers for single cell isolation. For the detection of genes in isolated cells on the device, hot cell-direct polymerase chain reaction (PCR) method was invented. In this study, food pathogenic bacteria such as Salmonella enterica was isolated on the disc and determined by the amplification of its specific gene based on hot cell-direct PCR using fluorescent probe. Relative fluorescence of each microchamber after/before PCR was determined to detect the bacteria. By the method, rapid and simple detection of bacterial cells was performed.

15:45

Afternoon Coffee and Tea Break and Networking in the Exhibit Hall

16:15

Ultra Low-Cost Smartphone Optosensors for Mobile Point-of-Care Diagnostics
Lei Li, Assistant professor, School of Mechanical and Materials Engineering, Washington State University, United States of America

We have developed a series of opto-sensing platforms that cover a wide range of applications. Especially, we have developed an ultra low-cost miniaturized multichannel smartphone opto-sensing platform with high accuracy and sensitivity. Our unique opto-mechanical system design and manufacturing process made our platforms appropriate for low-cost in-field applications.

16:45

PeptaSensors Open up New Avenues For POC Diagnostics
Manish Biyani, Associate Professor, Japan Advanced Institute of Science and Technology, Japan

This talk will introduce peptide aptamer-based biosensor, so-called peptasensor, for making undetectable sensing possible for routine and fast-tracking molecular diagnostics. Small peptide chains, which can arrange themselves into tridimensional functional structures, exhibit a smaller binding footprint allowing for a more thorough and precise interrogation of the target molecule. We engineered these peptide chains by an iterative process of in vitro selection procedure and applied to recognize certain biomarkers with high affinity and specificity. The applicability of these peptide aptamer to fabricate the new age of integrated electronic biosensors to detect unreachable target molecules will be addressed in this presentation.

17:15

An-Bang WangKeynote Presentation

Promoting Microfluidics From the Lab to Real Biomedical Applications
An-Bang Wang, Professor, Institute of Applied Mechanics, National Taiwan University, Taiwan

Microfluidics could bring significant advantages in the applications of chemical reaction, process control and biomedical detection. In the past fifteen years, the research topics have been shifted from different microfluidic components in our lab, including micropump, microvalve, and micromixer etc., to various integration systems, e.g., micro-multiphase flow/multiemulsion generators, microreactor, high-throughput fluid/flow properties detection, and the maskless pattern coating technology by two-phase microfluidic method, etc. Recently, special efforts were made for the extension of microfluidic applications in the life science studies and clinical diagnoses with advantages of easy use, compact size and excellent cost performance, e.g., a lab-on-a-chip with sequential control for biomedical point-of-care testing and a new extremely material- and time-saving Western blotting method that is widely used in analytical chemistry.

18:00

Networking Cocktail Reception with Beer, Wine and Appetizers in the Exhibit Hall. Engage with Colleagues and Visit the Exhibitors

19:00

Close of Day 1 of the Conference

Friday, 1 December 2017

08:00

Morning Coffee, Tea and Networking


Session Title: Microfluidics in Organs-on-Chips, Single Cell and Single Molecule Analysis

08:30

Man Bock GuKeynote Presentation

Screening a Pair of Aptamers using GO-SELEX for Nanobiosensors and Lateral Flow Assays
Man Bock Gu, Professor & Chair, Department of Biotechnology, Korea University; Director, BK21 PLUS for Biotechnology, Korea South

Aptamers are single-stranded nucleic acids having molecular recognition properties similar to antibodies, and isolated by in vitro selection and amplification process, SELEX. This talk will start with how the aptamers are innovatively screened, for the first time in the world, by using a new nano-material, graphene, without the immobilization of targets and how a few aptamer duos, inevitable for being applied in a sandwich-type platform, a reliable platform for commercialization eventually, were successfully develpoed for different pandemic influenza viruses, from graphene oxide-based immobilization-free screening (GO-SELEX).  In addition, some examples obtained from the interactions among aptamers, nanoparticles, and targets will be shown for a single or flexible aptamers with their successful implementation to the aptasensors. In addition, the benefits of using nano-sized materials for biosensing applications including lateral flow and SPR assays will be presented with scientifically proven clear examples of different organic-inorganic hybrid forms of nanomaterials and aptamers.

09:15

Roger KammKeynote Presentation

Providing Vascular Perfusion to Organ-on-Chip Disease Models
Roger Kamm, Cecil and Ida Green Distinguished Professor of Biological and Mechanical Engineering, Massachusetts Institute of Technology (MIT), United States of America

10:00

Keisuke GodaKeynote Presentation

Extreme Imaging For Large-Scale Single Cell Analysis
Keisuke Goda, Professor of Physical Chemistry, University of Tokyo, Japan

Cellular heterogeneity is a central challenge of biology and medicine in which there are cell-to-cell differences even within the same species. Population-averaged measurements of cellular behaviors do not represent the behaviors of any individual cell. A few notable examples of cellular heterogeneity are the resistance of cancer cells to anticancer drugs and the metabolic heterogeneity of microorganisms. In this talk, I present extremely fast molecular imaging technology combined with artificial intelligence on a microfluidic platform for large-scale single-cell analysis. The technology enables the acquisition of information-rich molecular images of numerous single cells in a short period of time to address and exploit cellular heterogeneity for precision medicine and green energy.

10:45

Morning Coffee, Tea and Networking in the Exhibit Hall

11:30

Induction of Stem Cell Self-Assembly by Adhesion Restriction
Kennedy Okeyo, Senior Lecturer, Institute for Frontier Life and Medical Sciences, Kyoto University, Japan

We have recently developed a novel culture technique, namely, the shoji technique, which involves the use of micro-structured large porous meshes as substrates for cell culture and growth in a suspension under restricted adhesion condition. This talk will highlight our on-going work on stem cell culture by the shoji technique, specifically, how this results in induction of self-assembly organization and, ultimately, differentiation. We show that the latter occurs mechanically and results in dynamic morphogenetic transformations that yields unique 3D cysts from originally 2D stem cell sheets. Overall, we show that the shoji technique presents a novel approach to modulate the cell culture microenvironment, resulting in mechanical induction of directed stem cell differentiation.

12:00

PERSONAL PHOTOMETER “PHOTOPETTE” WITH “LAB-IN-A-TIP” TECHNOLOGY FOR LIFE-SCIENCE APPLICATIONS
Dieter Trau, Associate Professor, University of Singapore, Singapore

Here, we introduce two novel concepts, a personal photometer “PHOTOPETTE” combined with “Lab-in-a-Tip” technology. The “Lab-in-a-Tip” is based on colorimetric reactions of an analyte with a reagent incorporated into a disposable polymer tip. The “PHOTOPETTE” is used for optical read out. Less sample volume required and on-spot detection are the advantages of this technology. We demonstrated pH and protein measurements in our “Lab-in-a-Tip design”. The work was conducted in collaboration with Tip Biosystems Pte Ltd. (This work is supported by National Research Foundation Singapore, NRF2014NRF-POC002-045).

12:30

Flexible Microfluidic Control for Highly Functionalized LOAC Platform
Masahiro Motosuke, Associate Professor, Department of Mechanical Engineering, Tokyo University of Science, Japan

In this talk, I would like to introduce some our recent work in the development of sophisticated microfluidic control by using external-field for on-demand functionality in LOAC platform.

13:00

Networking Lunch in the Exhibit Hall -- Meet the Exhibitors and View Posters


Session Title: Biosensors

13:45

Jong-In HongKeynote Presentation

Electrochemiluminescent Sensors for Selective Detection of Biologically Important Analytes
Jong-In Hong, Professor, Department of Chemistry, Seoul National University, Korea South

A discussion regarding chemo-dosimetric and supramolecular approaches to selective detection of biologically important analytes for point-of-care (POC) detection.

14:30

Microfluidic Cell Culture Devices to Control Gaseous Microenvironments in vitro
Yi Chung Tung, Associate Research Fellow,Research Center for Applied Sciences, Academia Sinica, Taiwan

Introduction of microfluidic devices capable of controlling various gaseous concentrations and gradients for in vitro cell culture developed in my laboratory.

15:00

Binding Kinetic Constants Measurement by Using Fiber Optic Particle Plasmon Resonance Biosensor
Shau-Chun Wang, Professor and Director, Department of Chemistry and Biochemistry and the Center for Nano BioDetection, National Chung Cheng University, Taiwan

Biosensing methods have been a popular means to measure the binding affinity and rate constants of immuno-logical reactions. In particular, the quantitative investigation of binding kinetics provides important information regarding the interactions between the docking target molecule and the counterpart probe molecule. Fiber optic particle plasmon resonance (FOPPR) biosensor, one simple and label-free sensing platform, has been successfully used to determine binding kinetic constants. The FOPPR biosensor is based on an optical fiber modified on gold nanoparticles, where the surface of gold nanoparticles has been conjugated by a mixed self-assembled monolayer (SAM) and a molecular probe reporter to dock with the corresponding analyte species. The binding process is recorded in static mode when analyte solution is loaded in one static sensing cell. The ability to analyse biomolecules without flow may be especially useful when an experiment only has a small amount of analyte available to characterize a biomolecular interaction. We compare FOPPR biosensor with commercialized Biacore 3000 SPR biosensor to determine the binding kinetic constants, which is limited by analyte injection flow rate and the probe concentration on the chip in Biacore 3000 SPR biosensor whereas FOPPR is not affected by these two effects. In addition, we established the general mathematical model to estimate the binding kinetic rate constants based on the pseudo-first-order model. We will discuss the agreement of obtained association rate constants (ka) and dissociation rate constants (kd) of anti-ovalbumin with ovalbumin and IgG binding with anti-IgG, between the computational results using our mathematical model, and the measured values.

15:30

Direct Observation of Folding Stability of Individual Chromosomes Isolated From Single Mammalian Cells in a Microfluidic Channel
Hidehiro Oana, Associate Professor, The University of Tokyo, Japan

Chromosomes were isolated from single mammalian cells in a microfluidic channel. Then, the isolated chromosomes were tethered at microstructures and exposed to high-salt solution in the channel. As a result, the chromosomes were unfolded non-uniformly, which can provide insights into epigenetic mechanisms.

16:00

Highly-Sensitive Label-Free Optical Biosensors and Multiplex Immuno-Magnetic Platform for Point-of-Care Diagnostics
Petr Nikitin, Professor and Head of Laboratory, Prokhorov General Physics Institute, Russian Academy of Sciences, Russian Federation

Several types of original biosensors will be presented. Intelligent biosensing systems are developed based on nanoparticles that can employ molecular interactions to perform any Boolean logic function. These systems are efficiently used for logic-gated biosensing with lateral flow test-strips and 3D filters. Besides, multichannel label-free biosensors are designed based on the spectral correlation interferometry (SCI) for detection of various analytes by measuring changes in thickness of a biolayer on functionalized glass slips used as affordable single-use sensor chips. The SCI method is not sensitive to bulk refractive index of a solution under test and provides signals in metrological units (pm or nm). Using real-time monitoring of bioreactions by the SCI, a new multiplex dry-reagent immunomagnetic (DRIM) biosensing platform is developed for rapid high-precision quantitative analyses of complex mediums. It is based on the highly sensitive magnetic particle quantification (MPQ) method that provides detection limit of 60 zeptomoles or 0.4 ng of magnetic nanolabels and extremely wide linear dynamic range of 7 orders. The DRIM platform has permitted the detection in human serum of as low as 25 pg/ml total prostate specific antigen during 30-min assay. The featured 3-fold signal increase per every order of concentration within 3.5 orders of magnitude allows precise analysis of antigen concentrations in a wide range. In addition, based on the MPQ technique, a new cytometry method has been developed and successfully tested for rapid assessment of cancer HER2/neu status of cells, for estimation of expression level of various antigens on cell surfaces and cancer diagnostics.

16:30

Discrimination of Alzheimer’s Disease Patient From Normal Control with Amyloid Beta Concentration in Neuronal Exosomes From Blood
Ji Yoon Kang, Professor, Department of Biomedical Engineering, Korea Institute of Science and Technology, Korea South

We propose a novel method for electrical discrimination of Alzheimer’s disease (AD) patient with blood sample using a bead-based electrochemical impedance spectrometry (BEIS) sensor. The blood-based diagnosis of AD has been tackled by many research groups for more than 10 years, but just few groups have succeeded in identifying AD patients due to difficulties in measuring oligomer amyloid beta (Aß) in blood. Since the signal magnitude of a BEIS sensor is proportional to the size and total charges of the biomolecules, the sensor characteristics were utilized to detect the ratio of oligomer amyloid beta (Aß) to monomer Aß for accurate discrimination of AD patients with human blood. Our study found that the change in output responses of a BEIS increased as the Aß is aggregated. This implies that impedance changes are increased more rapidly in AD samples than in NC samples, according to the dilution ratio. Based on this assumption, the slope extracted from impedance changes is used as a diagnosis factor to differentiate the AD. The results with the neuronal exosomes of AD and NC samples showed clear difference, suggesting possible use as a diagnostic tool with a sensitivity and specificity of more than 90 % in both measurements. Especially, the results of the measurement of the slope can provide dramatically enhanced the sensitivity and specificity in the diagnosis of ADs from neuronal exosome samples.

17:00

Saving Lives With Brownian Motion
Han-Sheng Oswald Chuang, Associate Professor, Department of Biomedical Engineering, National Cheng Kung University, Taiwan

Sepsis is a fatal infectious disease claiming thousands of lives every year. Antimicrobial susceptibility testing (AST) plays a pivotal role in the success of treatments. However, the turnaround time for the outcome of conventional AST usually requires over 24 hours, resulting in high patient mortality. Moreover, antibiotics abuse can also incubate the booming of superbugs. A reliable and efficient drug screen becomes increasingly important to date to save lives in a timely fashion. To this end, a technique combining optical diffusometry and bead-based immunoassays is developed herein to achieve a rapid quantification of target microorganisms. The limit of detection of the method could achieve 100 CFU/mL. This study provides valuable information to timely treatments against poly-microbial diseases in the near future.

17:30

Single Cell Clinical Enzyme Analysis for Precision Medicine by Using Continuous Flow Microfluidics
Chia Hung Chen, Assistant Professor, National University of Singapore, Singapore

Precision medicine refers to giving the right therapeutics, to the right patient, at the right time. In the context of cancer, successful implementation of precision medicine, requires treatment individualization not only taking into account patient and tumor factors, but also tumor heterogeneity and tumor evolution over time. In this study, a continuous flow microfluidic device was developed as a functional flow cytometer (Droplet FACS) to detect secreted multiplexed protease activities at single cell resolution. The individual cells from patient samples are encapsulated within water-in-oil droplets for single cell multiplexed protease assay. We modified FRET (fluorescence resonance energy transfer)-based substrates to accommodate different fluorescent pairs with distinct excitation and emission wavelengths to obtain multiple signals from droplets containing single cells. Four substrate-protease reactions in a droplet were simultaneously monitored at three distinct pairs of fluorescent excitation (UV: 400nm, B: 470nm, G: 546nm, R: 635nm) and emission (B: 520nm, G: 580nm, R: 670nm) wavelengths. To infer a quantitative profile of multiple proteolytic activities from single cells, we applied the computational method Proteolytic Activity Matrix Analysis (PrAMA). The capability to determine multiple protease activities at single cell resolution has the potential to characterize tumor progress of individual patients.

18:00

Close of Day 2 of the Conference


Add to Calendar ▼2017-11-30 00:00:002017-12-01 00:00:00Europe/LondonLab-on-a-Chip and Microfluidics, Point-of-Care Diagnostics and Global Health Asia 2017Lab-on-a-Chip and Microfluidics, Point-of-Care Diagnostics and Global Health Asia 2017 in Taipei, TaiwanTaipei, TaiwanSELECTBIOenquiries@selectbiosciences.com