Automating Cell Biology Annual general meeting, September 7, 2015. Phase Holographic Imaging www.phiab.se



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Transcription:

Automating Cell Biology Annual general meeting, September 7, 2015 www.phiab.se 1

PHASE HOLOGRAPHIC IMAGING (PHI) Began as a research project at Lund University, Sweden, in 2000 Founded in 2004 Sales in 2014/15: 2.7 (1.4) MSEK Over 40 units in operation at customers and key opinion leaders 12 granted patents Number of employees: 11 Publically traded since 2014 Website: www.phiab.se PHI leads the ground-breaking development of time-lapse cytometry instrumentation and software. With the first instrument introduced in 2011, the company today offers a range of products for longterm quantitative analysis of living cell dynamics that circumvent the drawbacks of traditional methods requiring toxic stains. Headquartered in Lund, Sweden, PHI trades through a network of international distributors. Committed to promoting the science and practice of time-lapse cytometry, PHI is actively expanding its customer base and scientific collaborations in cancer research, inflammatory and autoimmune diseases, stem cell biology, gene therapy, regenerative medicine and toxicological studies. 2

WHAT IS CELL CULTURE? Experiments using cultured cells is the cornerstone of drug development and preclinical research Such experiments are the only opportunity to work on human cells before clinical trials In specialized cell laboratories, cells are artificially cultured in plastic containers inside a cell incubator Cell culturing in a cell incubator Cell culture preparation 3

CELL ANALYSIS To understand biological processes scientist study cultured cells using cell analysis, often after treating the cells with a drug Technical limitations of the past has led to that scientists predominantly observe cells when fixed and dead fixed cell analysis Live cell analysis allows investigation of dynamic processes of living cells instead of only providing a snapshot of a cell s current state To characterize cellular behavior, cells are commonly labeled with chemicals or genetic modifications which emit light However, these labels are toxic and alter the natural behavior of cells Scientists therefore increasingly move to live cell analysis without using toxic labels, enabling repeated observations of the same cells over time label-free live cell analysis Intoxicated humans do not display their natural behavior. The same applies to their building blocks cells 4

MARKET SIZE Cell Analysis Flourishes Scientifically, Prospers Commercially Genetic Engineering and Biotechnology news, 2015 The global market is estimated to be valued at $8.7 billion USD in 2013 and will grow at a CAGR of 11.1% from 2013 to 2018 Cell-based Assays Market by Product, Application, End-user, Markets & Markets, 2014 Estimated number of labs performing cell analysis worldwide = 126 804 The Market for Cell-based Assays, Bioinformatics, gene2drug.com, 2015 Asia 19% Europe 26% RoW 5% North America 50% Other 2% Contract Research 16% Academia 33% Pharma Biotech 48% Government initiatives and publicprivate partnerships along with drying drug pipeline in pharma industry have led to increase in drug discovery activities; which is stimulating the market growth. Presently, the market is all set to witness trends such as labelfree detection, drug discovery outsourcing, 3D culture and stem cells Cell-based Assays Market by Product, Application, End-user, Markets & Markets, 2014 5

KEY MARKET TRENDS Rising incidence of cancer and neurodegenerative diseases propel the cell analysis market Advancements in biotechnology, optics, electronics and image analysis continue to create market opportunities Need for standardization and maintaining cell viability/optimal environment drive automation of cell culture systems Integration of microfluidics and nanobiotechnology with microscopy imaging platforms enables scientists to conduct more biologically relevant investigations, unattainable with conventional techniques Increased use of 3D cell culture methods drives the need for new analytical imaging technologies Present and future cell culturing. Labon-a-chip technology allows cells to be cultured in a micro-environment. 6

TARGET CUSTOMERS Academic Research Every academic lab involved in cell based preclinical research Pharmaceutical Mechanism of action studies Secondary screening Toxicology Bio-production HoloMonitor gives a totally new dimension to our work Prof. Stina Oredsson, Lund University Biotechnology Every company attempting to automate cell culturing process Every company performing cell-culture experiments (including household, cosmetics, tobacco, etc.) 7

END-POINT VS. TIME-LAPSE CELL ANALYSIS Fixed cell analysis and the limitations of labeled live cell analysis has led to that most cell culture based experiments are only analyzed at the end of the experiment end-point cell analysis Label-free live cell analysis allows cell culture based experiments to be continuously monitored and analyzed through out the experiment time-lapse cell analysis Time-lapse analysis End-point analysis Time Time 8

MARKET OPPORTUNITY Transition from end-point to time-lapse cell analysis Time-lapse microscopy allows cell based preclinical research to transition from end-point to time-lapse cell analysis End-point cell analysis Single observation at the end of the experiment One cell culture one data point Analysis of dead cells Time-lapse cell analysis Multiple observations during the experiment One cell culture multiple data points Analysis of living cells Time-lapse of a dividing cell Quantifying over time is crucial for a full understanding of cell systems. I am convinced that time-lapse microscopy will enable the next level of insight Prof. Timm Schroeder, ETH Zurich 9

TIME-LAPSE MICROSCOPY Modern computer technology makes it in principle very easy to record time-lapse microscopy movies of living cells However, the nature of cells and limitations of conventional microscopes make time-lapse recording and analysis challenging in practice 1. Cultured cells quickly die outside an incubator environment 2. To keep the cells in focus some type of autofocus is needed 3. Toxic stains are needed to automatically track cells 4. Cytometric software is needed to process the huge amount of data in time-lapse movies 5. Toxic stains are needed to quantitatively observe molecular specificity Addressed issues Microscope type Cost (K USD) 1 2 3 4 5 Conventional +10 Low-end time-lapse ~10 High-end time-lapse +100 20-10

HOLOMONITOR M4 Label-free live cell analysis Addresses issues 1-4 Over 40 units in operation with customers and key opinion leaders Harvard and Northeastern University, Boston University of California, San Francisco Israel Institute for Biological Research For additional users see www.phiab.se/publications/users After customer feedback several pilot builds have been manufactured Production will move into series production in Q3 2015 For additional product information see www.phiab.se/products/products The HoloMonitor platform offers unique 4-dimensional imaging capabilities that greatly enhance our understanding of both functions, which was previously unachievable by other technologies Ed Luther, Northeastern University, Boston 11

HOLOMONITOR M5 Minimally invasive live cell analysis Addresses issues 1-5 Cell biologists use fluorescent labels to identify biochemical compounds Fluorescent labels are activated by light of a specific wavelength. These labels are toxic, especially when activated By combining HoloMonitor technology with fluorescence detection capabilities, the activation of fluorescent labels can be dramatically reduced to minimize the toxic effect on cell behavior HoloMonitor M5 is being developed in collaboration with Lund University. Funding is provided by the Swedish Research Council (Vetenskapsrådet) HoloMonitor M4 + fluorescent capability = HoloMonitor M5 Fluorescent labelled cells 12

COMPETITION Microscope type Cost (K USD) Conventional +10 1: Incubator environment Low-end time-lapse ~10 High-end time-lapse +100 Addressed issues 2: Autofocus 3: No toxic stains needed to track cells Competing holographic ~50-100 4: Cytometric software HoloMonitor M4 20-35 5: No toxic stains needed to observe molecular specificity HoloMonitor M5 Microscope type Conventional Low-end time-lapse High-end time-lapse Competing holographic Suppliers Nikon, Olympus, Zeiss Small technology companies (NanoEntek, Etaluma, CytoMate) Nikon, Olympus, Zeiss, Thermo Fisher, GE Healthcare Small technology companies (Ovizio, Lynceé Tec, NanoLive) 13

HSTUDIO Proprietary cell analysis software Dedicated cell analysis software is a key competitive advantage Current version is stable and very appreciated by customers. Few issues have been reported by customers Development focus on facilitating distributed data analysis to provide additional revenue source Multiple Hstudio licenses for distributed data analysis Single Hstudio license for data collecting Cell incubator with multiple HoloMonitor Database server 14

CONSUMABLES PIPELINE To take full advantage of time-lapse cell analysis a new generation of cell culture vessels is needed Conventional cell culture vessels are designed for end-point cell analysis PHI is currently developing a new generation of cell culture vessels and other consumables Key to the long term profitability Makes HoloMonitor technology more convenient to use The PHI petri dish lid eliminates disturbances from condensation droplets and surface vibrations 15

INTELLECTUAL PROPERTY 2 registered trademarks, HoloMonitor and HoloMetrics 6 patent families 12 granted patents METHOD AND APPARATUS FOR HOLOGRAPHIC REFRACTOMETRY Patent Country Expiry date 4 739 214 Japan 2024-Oct-07 1 676 121 Denmark 2024-Oct-07 1 676 121 France 2024-Oct-07 60 2004 030 928.1 Germany 2024-Oct-07 1 676 121 The Netherlands 2024-Oct-07 1 676 121 Sweden 2024-Oct-07 1 676 121 Switzerland- Liechtenstein 2024-Oct-07 1 676 121 UK 2024-Oct-07 METHOD AND APPARATUS FOR ANALYSIS OF A SAMPLE OF CELLS Patent Country Expiry date ZL200680048900.7 China 2026-Dec-22 5 182 945 Japan 2026-Dec-22 7 948 632 USA 2027-Sep-30 METHOD FOR AND USE OF DIGITAL HOLOGRAPHIC MICROSCOPY AND IMAGING ON LABELLED CELL SAMPLES Patent Country Expiry date 8 937 756 USA 2030-Feb-09 16

EXIT STRATEGY Establish HoloMonitor technology through initial sales in key markets: US, Germany, Switzerland, UK, Japan and China collaborations with key opinion leaders Expand use of technology through Centers of Excellence in life science hotspots Boston, San Diego, San Francisco London, Basel, Heidelberg Tokyo To create visibility in the US, establish direct PHI presence in the Boston area Complete development of HoloMonitor M5 and consumables pipeline Seek global distribution through major life science tools companies Divest business when substantial market traction has been achieved 17

SUMMARY PHI s technology allows cell based preclinical research to transition from end-point to time-lapse cell analysis The global market is estimated to be valued at $8.7 billion USD Company sales in 2014/15: 2.7 (1.4) MSEK Over 40 units in operation at customers and key opinion leaders Production moves into series production in Q3 2015 Exit strategy increase sales, expand strategic marketing and divest the business 18

Time-lapse cytometry for biologists, by biologists Thank You www.phiab.se 19