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OCTOBER 2010 issue n°100<br />

THE DISRUPTIVE SEMICONDUCTOR TECHNOLOGIES MAGAZINE<br />

MICROFLUIDICS<br />

New microfluidic device helps identify and capture breast cancer cells<br />

Researchers have developed a new disposable device that could help identify patients with advanced breast cancer<br />

awaiting drug <strong>the</strong>rapy with trastuzumab, and capture cancer cells that have an abnormal amount of <strong>the</strong> protein HER2.<br />

Benjamin Thierry, of <strong>the</strong> Ian Wark Research<br />

Institute at <strong>the</strong> University of South Australia,<br />

along with his colleagues, has created an<br />

elastic, disposable microfluidic device that can<br />

efficiently catch <strong>the</strong> protein HER2 – which is <strong>the</strong><br />

tyrosine kinase human epidermal growth factor<br />

receptor 2 – found in "aggressive breast cancers with<br />

poor prognosis."<br />

The only way to find out HER2 status in breast cancer<br />

patients now is through fluorescence in situ<br />

hybridization (FISH) or immunohistochemistry, both<br />

of which require biopsies. The problem with biopsybased<br />

testing is that it could lead to treatment that is<br />

ineffective, because <strong>the</strong> HER2 status of <strong>the</strong> primary<br />

tumor in 20 percent of breast cancers differs from <strong>the</strong><br />

HER2 status in that of a metastatic tumor. This<br />

information has led to <strong>the</strong> idea of isolating circulating<br />

tumor cells (CTCs), but this is difficult because<br />

circulating tumor cells exist at very low ratios of 1 to<br />

10 per billion blood cells.<br />

Establishing HER2 status is very critical because<br />

HER2 positive breast cancer patients have benefitted<br />

from drug <strong>the</strong>rapy with trastuzumab (Herceptin), which<br />

are humanized monoclonal antibodies against HER2.<br />

It also decreases recurrence risk by half. Also, <strong>the</strong> side<br />

effects and cost makes it a priority to identify patients<br />

who are HER2 positive. Now, Thierry and his colleagues'<br />

device has <strong>the</strong> ability to detect <strong>the</strong> status of HER2 and<br />

help capture circulating tumor cells. The device is made<br />

of organic silicon found in most contact lenses, and<br />

polydimethylsiloxane (PDMS), which are shampoos<br />

that are transparent, permeable to gasses, and<br />

compatible with soft molding techniques. The device<br />

also contains a polymeric layer on its surface, which has<br />

a large number of reactive molecules in it. Through <strong>the</strong><br />

use of a plasma-based polymerization process, this<br />

layer can attach to proteins that are able to catch cancer<br />

cells while leaving normal blood cells alone.<br />

Thierry's device showed an 80 percent immunocapture<br />

efficacy of HER2 positive cells, and is also<br />

cheaper and easier to make than previous<br />

microfabricated devices, which were developed to<br />

bind to cells of epi<strong>the</strong>lial tissues where <strong>the</strong> cancer<br />

originated, ultimately isolating CTCs.<br />

www.unisa.edu.au<br />

Lockheed Martin and ZyGEM accelerate DNA identification for law enforcement,<br />

homeland security and defense communities<br />

New, fast sample-to-answer DNA analysis platform previewed at 2010 Biometric Consortium conference.<br />

Lockheed Martin and ZyGEM Corp. Ltd. are<br />

unveiling a new DNA analysis system that has<br />

potential to transform how law enforcement,<br />

homeland security and defense communities use<br />

DNA-based identification in support of <strong>the</strong>ir missions.<br />

The prototype, called RapI.D., will be previewed at<br />

a 2010 Biometric Consortium Conference special<br />

session on Rapid DNA.<br />

Developed in collaboration with ZyGEM as a Lockheed<br />

Martin Technology Innovation Initiative, RapI.D.<br />

leverages <strong>the</strong> latest in microfluidic research and<br />

development to accelerate <strong>the</strong> DNA identification<br />

process – essentially building a laboratory on a small,<br />

single chip that reduces <strong>the</strong> processing steps and time<br />

needed for analysis. The RapI.D. platform is<br />

currently in prototype at ZyGEM's Charlottesville, Va.,<br />

MicroLab laboratories, with a Beta version expected<br />

to be released for testing in select laboratories early<br />

next year. The cost and complexity of current forensic<br />

DNA analysis methods has contributed to significant<br />

processing backlogs throughout <strong>the</strong> criminal justice<br />

system. Data from <strong>the</strong> Justice Department's FY 2009<br />

Forensic DNA Backlog Reduction Program suggest<br />

that <strong>the</strong> backlog has increased in recent years,<br />

indicating that <strong>the</strong> 2008 backlogged cases reported<br />

by state and local government applicants for funding<br />

under <strong>the</strong> program had nearly tripled compared to<br />

comparable data from 2005.<br />

www.lockheedmartin.com<br />

www.zygem.com<br />

Pacific Biosciences to raise up to $230 M in IPO<br />

Pacific Biosciences of California Inc said it<br />

expects to raise up to $230 million in an initial<br />

public offering of its common stock. The Menlo<br />

Park, California-based company expects to offer<br />

12.5 million shares at $15-$17 each, with an overallotment<br />

option of 1.9 million shares, it said in an<br />

amended filing.<br />

The life sciences company, which designs machines<br />

to speed up DNA sequencing in labs, sees net proceeds<br />

of $182.5 million, assuming <strong>the</strong> offering priced at $16<br />

per share, <strong>the</strong> mid-point of <strong>the</strong> range. The company<br />

plans to invest about $60-$70 million of <strong>the</strong> proceeds<br />

in its technology platform called single molecule, realtime,<br />

or SMRT technology. Pacific Biosciences initially<br />

filed for an IPO in August. The amended filing detailed<br />

<strong>the</strong> expected pricing of <strong>the</strong> common stock sale.<br />

JP Morgan, Morgan Stanley, Deutsche Bank and Piper<br />

Jaffray are underwriting <strong>the</strong> IPO, <strong>the</strong> company said.<br />

Pacific Biosciences plans to list its shares under <strong>the</strong><br />

ticker symbol "PACB" on Nasdaq.<br />

www.pacificbiosciences.com<br />

FluimediX closes financing round<br />

Funding Supports continued development of <strong>the</strong> NanoCycler platform to include a Warfarin Diagnostic Test.<br />

FluimediX announced that it has received<br />

funding for <strong>the</strong> continued development of <strong>the</strong><br />

NanoCycler, a diagnostic platform for <strong>the</strong><br />

measurement of relevant genetic mutations in<br />

patients. The proceeds of this financing round will be<br />

dedicated to developing a diagnostic test for Warfarin<br />

metabolism. The investment round was led by SEED<br />

Capital Denmark, a leading early stage investor<br />

managing more than € 200 million in total assets.<br />

Existing shareholders also participated in <strong>the</strong><br />

financing. The size of <strong>the</strong> round was not disclosed.<br />

Tomas Ussing, CEO and founder of FluimediX,<br />

commented: “Firstly, it is comprised of low cost, wellestablished<br />

components. Secondly, <strong>the</strong> use of<br />

plastic disposables enables extremely competitive<br />

molecular diagnostic testing, and will thus bring this<br />

type of testing closer to <strong>the</strong> patient. Thirdly, <strong>the</strong> built-in<br />

broad versatility of <strong>the</strong> NanoCycler device will allow<br />

o<strong>the</strong>r tests to be transferred to or developed for <strong>the</strong><br />

NanoCycler platform in <strong>the</strong> future.”<br />

The use of a diagnostic test for Warfarin metabolism<br />

would deliver important clinical benefits and cost<br />

savings to <strong>the</strong> healthcare system. Approximately two<br />

million people start taking Warfarin each year in <strong>the</strong><br />

U.S. Unfortunately, <strong>the</strong> optimal dose differs significantly<br />

due to patient-to-patient genetic variation in how<br />

quickly Warfarin is metabolized, and <strong>the</strong> medical<br />

consequences of under- or over-dosing <strong>the</strong> drug<br />

can be severe. Roughly one-third of <strong>the</strong> population<br />

carries a genetic mutation that results in slow<br />

metabolism of <strong>the</strong> drug, so <strong>the</strong> identification of those<br />

patients who have this mutation could help avoid <strong>the</strong><br />

consequences of under- or over-dosing.<br />

FX device lunch-box<br />

www.fluimedix.com<br />

FX chip<br />

Copyrights © Yole Développement SA. All rights reserved - Recycled paper<br />

11

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