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omation mbers - Society for Laboratory Automation and Screening

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TP023<br />

Katherine Dains<br />

Adeline Scientific<br />

Research<br />

1534 Plaza Lane, Suite 119<br />

Burlingame, Cali<strong>for</strong>nia 94010<br />

kdains@earthlink.net<br />

157<br />

Co-Author(s)<br />

Wensheng Chen<br />

In<strong>for</strong>mation <strong>and</strong> Data Management Software <strong>for</strong> Tracking Patient, Research, <strong>and</strong> Analysis<br />

Data in Small to Medium Clinical <strong>and</strong> Research Labs<br />

We have developed software <strong>for</strong> in<strong>for</strong>mation <strong>and</strong> data management <strong>for</strong> use in the small- to medium-sized life<br />

science research labs. The system is user configurable, uncomplicated, <strong>and</strong> af<strong>for</strong>dable. Most commercial data<br />

management software products available require sophisticated IT setup, in-house personnel or outside contractors<br />

to control <strong>and</strong> maintain the system. Our system will appeal to many laboratories that require flexibility <strong>and</strong><br />

specificity to their laboratory needs without the complexity <strong>and</strong> cost of a large <strong>and</strong> expensive product. At the<br />

center of the system is a configuration tool that can be set up to h<strong>and</strong>le various laboratory data management<br />

workflows such as recruitment <strong>and</strong> tracking of research study c<strong>and</strong>idates <strong>and</strong> related genetic studies. This<br />

intelligence tool is made possible through a proprietary data model cartridge technology. After completing the<br />

configuration process, the user can choose to deploy the data system or to merge data with existing systems. The<br />

system is designed with three-tier architecture in the <strong>for</strong>m of web applications thus allowing <strong>for</strong> easy upgrades <strong>and</strong><br />

remote access. Along with the simple web-based architecture, user-configurable data loading tools are provided<br />

that will adapt to most data importing tasks. In<strong>for</strong>mation can be entered <strong>and</strong> tracked over long periods of time,<br />

as well as easily retrieved through the web-based reporting structure. The system is built to support all major<br />

database products. We will present details on the architecture, detailed design specifications, <strong>and</strong> test results from<br />

collaborating research labs.<br />

TP024<br />

Juan Jose Diaz-Mochon<br />

University of Southampton<br />

Chemistry<br />

Highfield Campus<br />

Southampton SO17 1BJ United Kingdom<br />

jjd29@soton.ac.uk<br />

Novel PNA-Peptoid Conjugates as Antisense Drugs<br />

Co-Author(s)<br />

Laurent Bialy, Boon-ek Yingyongnarongkul,<br />

Adam Belson, Mark Bradley<br />

Peptide Nucleic Acid (PNA) has been developed in the last decade as a new DNA mimic which hybridises<br />

complementary DNA or RNA sequences with higher affinity than its counterparts. PNA presents a 2aminoethylglycine<br />

backbone instead of the DNA sugar-phosphonate moiety. This uncharged backbone allows<br />

PNA to display a stronger hybridisation with DNA or RNA <strong>and</strong> to be easily synthesised. These features prompted<br />

investigators to develop PNA analogues as promising c<strong>and</strong>idates <strong>for</strong> the antisense therapy strategies. Antisense<br />

drugs target genes that are active or over expressed in certain pathological processes thus disrupting the synthesis<br />

of disease-responsible proteins. However, the main drawback has been their lack of cellular permeability that<br />

has avoided their further development as efficient antisense drugs. A few promising PNA-conjugates have been<br />

reported but new models are necessary to improve cellular permeability <strong>and</strong> overall drug-like features. Herein a<br />

new type of PNA-conjugates with higher cellular permeability is introduced. These novel PNA oligomers are bound<br />

to peptoids that have been reported as successful transfection agents. A library of PNA analogues has been<br />

synthesised on solid phase using a novel deprotection strategy, <strong>and</strong> it has been tested on GFP-transfected cell<br />

cultures. Furthermore, this library will also be tested using a cell-based microchip assay.<br />

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