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1.
SLAS Technol ; 23(1): 16-29, 2018 02.
Article in English | MEDLINE | ID: mdl-29355087

ABSTRACT

Tumor tissue biopsies are invasive, costly, and collect a limited cell population not completely reflective of patient cancer cell diversity. Circulating tumor cells (CTCs) can be isolated from a simple blood draw and may be representative of the diverse biology from multiple tumor sites. The VTX-1 Liquid Biopsy System was designed to automate the isolation of clinically relevant CTC populations, making the CTCs available for easy analysis. We present here the transition from a cutting-edge microfluidic innovation in the lab to a commercial, automated system for isolating CTCs directly from whole blood. As the technology evolved into a commercial system, flexible polydimethylsiloxane microfluidic chips were replaced by rigid poly(methyl methacrylate) chips for a 2.2-fold increase in cell recovery. Automating the fluidic processing with the VTX-1 further improved cancer cell recovery by nearly 1.4-fold, with a 2.8-fold decrease in contaminating white blood cells and overall improved reproducibility. Two isolation protocols were optimized that favor either the cancer cell recovery (up to 71.6% recovery) or sample purity (≤100 white blood cells/mL). The VTX-1's performance was further tested with three different spiked breast or lung cancer cell lines, with 69.0% to 79.5% cell recovery. Finally, several cancer research applications are presented using the commercial VTX-1 system.


Subject(s)
Automation, Laboratory/methods , Blood Cells , Cell Separation/methods , Liquid Biopsy/methods , Microfluidics/methods , Neoplastic Cells, Circulating , Automation, Laboratory/instrumentation , Cell Separation/instrumentation , Humans , Liquid Biopsy/instrumentation , Microfluidics/instrumentation , Reproducibility of Results
2.
Biotechniques ; Suppl: 70-2, 74, 76-7, 2002 Jun.
Article in English | MEDLINE | ID: mdl-12083401

ABSTRACT

Single nucleotide polymorphism (SNP) genotyping is playing an increasing role in genome mapping, pharmacogenetic studies, and drug discovery. To date, genome-wide scans and studies involving thousands of SNPs and samples have been hampered by the lack of a system that can perform genotyping with cost-effective throughput, accuracy, and reliability. To address this need, Orrhid has developed an automated, ultra-high throughput system, SNPstream UHT, which uses multiplexed PCR in conjunction with our next generation SNP-IT tag array single base extension genotyping technology The system employs oligonucleotide microarrays manufactured in a 384-well format on a novel glass-bottomed plate. Multiplexed PCR and genotyping are performed in homogeneous reactions, and assay results are read by direct two-color fluorescence on the SNPstream UHTArray Imager. The systems flexibility enables large projects involving thousands of SNPs and thousands of samples as well as small projects that have hundreds of SNPs and hundreds of samples to be done cost effectively. We have successfully demonstrated this system in greater than 1,000,000 genotyping assays with >96% of samples giving genotypes with >99% accuracy


Subject(s)
DNA Mutational Analysis/instrumentation , Drug Design , Gene Frequency , Genotype , Oligonucleotide Array Sequence Analysis/instrumentation , Pharmacogenetics/instrumentation , Polymorphism, Single Nucleotide , Alleles , DNA Primers , Equipment Design , Feasibility Studies , Humans , Oligonucleotide Array Sequence Analysis/methods , Pharmacogenetics/methods , Polymerase Chain Reaction , Quality Control , Reproducibility of Results , Sensitivity and Specificity , Sequence Analysis, DNA
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