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1661 ISS N 1757-6180 10.4155/BIO.10.145 © 2010 Future Science Ltd  Bioanalysis  (2010) 2 (10), 1661–1 662 During the past 15 years, one of the greatest research efforts in the eld of miniaturization has been in analytical science, with the main goal of this research being to develop miniatur- ized total analytical systems [1]. This interest in miniaturization has been due to the ever-increas- ing requirement for utilizing less material, for a variety of reasons. This, in turn, has prompted the design and development of novel miniatur- ized platforms, hence, the term ‘lab-on-a-chip’,  with corresponding high-throughput methods to accomplish the same tasks as found in larger and older benchtop instruments. For years, the literature has hig hlighted the ‘coming revolution’ in microuidic technology and applications. The term microuidics is generally used to describe any technology that moves microscopic and nanoscale volumes of uid through microsized channels on a microelectro mechanical system. Microuidics is the combination of a variety of disciplines including uid mechanics, surface science, chemistry, physics and biology (and in many cases optics, microscopy, electronics, con- trol systems and microfabrication). The term lab- on-a-chip is practically passé now for the numbe rs of papers, patents, inventions and researchers who seek to miniaturize everything larger than a n- ger. One must now wonder if there is a l imit as to  what should and can be miniatur ized. Microuidics has attracted much attention due to the many benets that miniaturi zed plat- forms offer researchers. Adva ntages include, but are not limited to, small sample volumes lead- ing to greater efciency of chemical reagents; low production costs per microuidic device (MD), thereby allowing for disposability; high- throughput synthesis and screening of biologi- cal species and drug targets; parallel processing of samples; fast sampling times; accurate and precise control of samples reagents reducing the need for pipetting; low power consumption; and versatile format for integration of various detec- tion schemes thereby leading to g reater sensitiv- ity. Fabri cation of MDs involves techniques that are well known in the semiconductor industry and manufacturing and have been used in the developmen t of complex dev ices.  A PubMed query indicates that the citation rate for the word ‘microuidics’ increased ve- fold between 2001 and 2004 and doubled to 500 between 2003 and 20 04. In 1998, the number of issued patents detailing the use of microuidic platforms in commercial applications was less than 25; by 2004 the number had risen to over 350. The microuidics market for life-science applications reached US$750 million in 2004 and was expected to reach US$2 billion by this year. In 2014, the market of MDs is expected to exceed over US$3 billion. Drug discovery remains the largest microuidics market and  will continue to grow signica ntly ov er the next decade. This is particularly true for the tech- nologies that enable multiplexing. However , the largest growth is expected in the eld of point of-care (POC) diag nostics and related technolo- gies. With this being said, there are a myriad of companies that offer MDs for a variety of mostly bioanalytical applications including  Ag ilent, Cel li x, Fluid igm, Nanostream and Rainda nce T echnologies. The past 20 years has seen a huge growth in the number of potential applications of micro- uidics focusing on biotechnology, pharma- ceuticals, life sciences, defense, public health and agriculture. In the bioanalytical area these applications have included single-cell ana lysis (cell sorting, cell-based assays and stem cell and neuroscience research) [2], nucleic acid analysis (microarrays and RNA ana lysis) [3], PCR ampli- cation [4], enzyme reactors and assays [5], gene Bioanalytical applications in microuidics ...applications for microuidic devices have proliferated at a speed reminiscent of the use of electronics shortly after the invention of the integrated circuit. Frank A Gomez Department of Chemistry & Biochemistry, California State University, Los Angeles, 51 51 State University Drive, LA, CA 90032-8202, USA Tel.: +1 323 343 2368 Fax: +1 323 343 6490 E-mail: [email protected] Special F ocuS: MicroFluidicS F oreword Keywords: bioanalysis n lab-on-a-chip n microelectromechanical system n microuidics n micro total analysis system

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1661ISSN 1757-618010.4155/BIO.10.145 © 2010 Future Science Ltd   Bioanalysis  (2010) 2 (10), 1661–1662

During the past 15 years, one of the greatestresearch efforts in the field of miniaturization

has been in analytical science, with the maingoal of this research being to develop miniatur-ized total analytical systems [1]. This interest inminiaturization has been due to the ever-increas-ing requirement for utilizing less material, for avariety of reasons. This, in turn, has promptedthe design and development of novel miniatur-ized platforms, hence, the term ‘lab-on-a-chip’, with corresponding high-throughput methodsto accomplish the same tasks as found in largerand older benchtop instruments. For years, theliterature has highlighted the ‘coming revolution’in microfluidic technology and applications. Theterm microfluidics is generally used to describeany technology that moves microscopic andnanoscale volumes of fluid through microsizedchannels on a microelectromechanical system.Microfluidics is the combination of a variety ofdisciplines including fluid mechanics, surfacescience, chemistry, physics and biology (and inmany cases optics, microscopy, electronics, con-trol systems and microfabrication). The term lab-on-a-chip is practically passé now for the numbersof papers, patents, inventions and researchers whoseek to miniaturize everything larger than a fin-

ger. One must now wonder if there is a limit as to what should and can be miniaturized.

Microfluidics has attracted much attentiondue to the many benefits that miniaturized plat-forms offer researchers. Advantages include, butare not limited to, small sample volumes lead-ing to greater efficiency of chemical reagents;low production costs per microfluidic device(MD), thereby allowing for disposability; high-throughput synthesis and screening of biologi-cal species and drug targets; parallel processingof samples; fast sampling times; accurate and

precise control of samples reagents reducing the

need for pipetting; low power consumption; andversatile format for integration of various detec-

tion schemes thereby leading to greater sensitiv-ity. Fabrication of MDs involves techniques thatare well known in the semiconductor industryand manufacturing and have been used in thedevelopment of complex devices.

 A PubMed query indicates that the citationrate for the word ‘microfluidics’ increased five-fold between 2001 and 2004 and doubled to 500between 2003 and 2004. In 1998, the number ofissued patents detailing the use of microfluidicplatforms in commercial applications was lessthan 25; by 2004 the number had risen to over350. The microfluidics market for life-scienceapplications reached US$750 million in 2004and was expected to reach US$2 billion by thisyear. In 2014, the market of MDs is expectedto exceed over US$3 billion. Drug discoveryremains the largest microfluidics market and will continue to grow significantly over the nextdecade. This is particularly true for the tech-nologies that enable multiplexing. However, thelargest growth is expected in the field of pointof-care (POC) diagnostics and related technolo-gies. With this being said, there are a myriadof companies that offer MDs for a variety of

mostly bioanalytical applications including Agilent, Cel lix, Fluidigm, Nanostream andRaindance Technologies.

The past 20 years has seen a huge growth inthe number of potential applications of micro-fluidics focusing on biotechnology, pharma-ceuticals, life sciences, defense, public healthand agriculture. In the bioanalytical area theseapplications have included single-cell analysis(cell sorting, cell-based assays and stem cell andneuroscience research) [2], nucleic acid analysis(microarrays and RNA analysis) [3], PCR ampli-

fication [4], enzyme reactors and assays [5], gene

Bioanalytical applications in microuidics

“...applications for microuidic devices have proliferated at a speed reminiscent of the use of electronics shortly

after the invention of the integrated circuit.”

Frank A Gomez

Department of Chemistry

& Biochemistry, California StateUniversity, Los Angeles,5151 State University Drive, LA,CA 90032-8202, USA

Tel.: +1 323 343 2368Fax: +1 323 343 6490E-mail: [email protected]

Special FocuS: MicroFluidicS

Foreword

Keywords: bioanalysis n lab-on-a-chip n microelectromechanical system n microuidics n micro totalanalysis system

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Foreword | Gomez

Bioanalysis  (2010) 2(10)1662 future science group

isolation and transformation [6], biochemicalmonitorization [7], in vitro  diagnostics (clini-cal and veterinary diagnostics) [8] and proteincrystallization [9]. In fact, applications for MDshave proliferated at a speed reminiscent of the

use of electronics shortly after the invention ofthe integrated circuit.

This special issue on bioanalytical applica-tions in microfluidics brings together the workof scientists and researchers from across severaldisciplines, to demonstrate the strong overlapbetween their efforts and how their work typi-fies the exciting potential of microfluidics in thebioanalytical realm. As can be seen, people withdiverse educational backgrounds and traininghave found microfluidics to be an interestingarea of study and it is my hope that this spe-

cial issue will inspire future scientists to con-sider studying microfluidics. Only by bringingtogether people of varied backgrounds can thisfield reach its full potential.

In this issue, Li et al. detail a study involvingtransfection of molecular beacons in microflu-idic channels. Ueda developed a microfluid-ics-based noncompetitive immunodetectionchip system using anti-T4 antibody frag-ments obtained from a phage display library. Amasia et al.  describe the development andvalidation of a large-volume centrifugal orCD-based device for blood plasma separation

that is capable of processing 2 ml of undilutedblood samples. Lahann highlights the use ofreactive coatings for surface modification appli-cations focusing on microfluidic systems. Wangprovides an overview of current MDs used in

islet studies and analyzes their strengths andexperimental suitability. Shadpour reviews the1D and 2D microchip profiling of proteins forPOC applications. Kim reviews the technicalaspects and application of image cytometers,recent progress in the field and available com-mercial devices. The Mora article is a productreview of the Gyrolab® microfluidics platformused in ligand binding assays. I hope that read-ers of this special issue will gain a balancedview of a few of the bioanalytical applicationsin microfluidics, and entertain the thought of

integrating them into their research program.

Financial & competing interests disclosure

The author gratefully acknowledges financial support for

this research by grants from the National Science

Foundation (CHE-0515363, DMR-0351848 and CBET-

0723271). The author has no other relevant affiliations or

 financial involvement with any organization or entity with

a financial interest in or financial conflict with the subject

matter or materials discussed in the manuscript apart from

those disclosed.

No writing assistance was utilized in the production of

this manuscript.

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