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1.
Opt Express ; 29(3): 3882-3890, 2021 Feb 01.
Article in English | MEDLINE | ID: mdl-33770978

ABSTRACT

We present an in-line metrology solution for dimensional characterization of roll-to-roll imprinted nanostructures. The solution is based on a scatterometric analysis of optical data from a hyperspectral camera deployed at a production facility, where nanostructures are produced at speeds of 10m/min. The system combines the ease of use of a real-space imaging system with the spectral information used in scatterometry. We present nanoscale dimensional measurements on one-dimensional line gratings with various periods and orientations. The depths of the produced structures are accurately characterized with uncertainties on the scale of a few nanometers. The hyperspectral imaging capabilities of the system can also be used to avoid vibrational effects.

2.
Proc Natl Acad Sci U S A ; 115(44): 11192-11197, 2018 10 30.
Article in English | MEDLINE | ID: mdl-30322920

ABSTRACT

To elucidate cellular diversity and clonal evolution in tissues and tumors, one must resolve genomic heterogeneity in single cells. To this end, we have developed low-cost, mass-producible micro-/nanofluidic chips for DNA extraction from individual cells. These chips have modules that collect genomic DNA for sequencing or map genomic structure directly, on-chip, with denaturation-renaturation (D-R) optical mapping [Marie R, et al. (2013) Proc Natl Acad Sci USA 110:4893-4898]. Processing of single cells from the LS174T colorectal cancer cell line showed that D-R mapping of single molecules can reveal structural variation (SV) in the genome of single cells. In one experiment, we processed 17 fragments covering 19.8 Mb of the cell's genome. One megabase-large fragment aligned well to chromosome 19 with half its length, while the other half showed variable alignment. Paired-end single-cell sequencing supported this finding, revealing a region of complexity and a 50-kb deletion. Sequencing struggled, however, to detect a 20-kb gap that D-R mapping showed clearly in a megabase fragment that otherwise mapped well to the reference at the pericentromeric region of chromosome 4. Pericentromeric regions are complex and show substantial sequence homology between different chromosomes, making mapping of sequence reads ambiguous. Thus, D-R mapping directly, from a single molecule, revealed characteristics of the single-cell genome that were challenging for short-read sequencing.


Subject(s)
Chromosome Mapping/methods , DNA/genetics , Genome/genetics , High-Throughput Nucleotide Sequencing/methods , Sequence Analysis, DNA/methods , Cell Line, Tumor , Chromosomes, Human, Pair 19/genetics , Chromosomes, Human, Pair 4/genetics , Clonal Evolution/genetics , Colorectal Neoplasms/genetics , Genomics/methods , Humans , Sequence Deletion/genetics
3.
Lab Chip ; 15(24): 4598-606, 2015 Dec 21.
Article in English | MEDLINE | ID: mdl-26510401

ABSTRACT

In this paper, the microfluidic size-separation technique pinched flow fractionation (PFF) is used to separate cancer cells from white blood cells (WBCs). The cells are separated at efficiencies above 90% for both cell types. Circulating tumor cells (CTCs) are found in the blood of cancer patients and can form new tumors. CTCs are rare cells in blood, but they are important for the understanding of metastasis. There is therefore a high interest in developing a method for the enrichment of CTCs from blood samples, which also enables further analysis of the separated cells. The separation is challenged by the size overlap between cancer cells and the 10(6) times more abundant WBCs. The size overlap prevents high efficiency separation, however we demonstrate that cell deformability can be exploited in PFF devices to gain higher efficiencies than expected from the size distribution of the cells.


Subject(s)
Cell Separation/instrumentation , Leukocytes/cytology , Microfluidic Analytical Techniques/instrumentation , Neoplastic Cells, Circulating/pathology , Biomechanical Phenomena , Cell Line, Tumor , Cell Size , Equipment Design , Humans
4.
Opt Express ; 23(9): 11586-99, 2015 May 04.
Article in English | MEDLINE | ID: mdl-25969252

ABSTRACT

We present a new technique for permanent metamaterial reconfiguration via optically induced mass transfer of gold. This mass transfer, which can be explained by field-emission induced electromigration, causes a geometric change in the metamaterial sample. Since a metamaterial's electromagnetic response is dictated by its geometry, this structural change massively alters the metamaterial's behavior. We show this by optically forming a conducting pathway between two closely spaced dipole antennas, thereby changing the resonance frequency by a factor of two. After discussing the physics of the process, we conclude by presenting an optical fuse that can be used as a sacrificial element to protect sensitive components, demonstrating the applicability of optically induced mass transfer for device design.

5.
Opt Express ; 20(20): 22770-82, 2012 Sep 24.
Article in English | MEDLINE | ID: mdl-23037428

ABSTRACT

In this article, we propose a simple scheme to make a metallic film on a semi-infinite substrate optically transparent, thus obtaining a completely transparent electrode in a desired frequency range. By placing a composite layer consisting of dielectric and metallic stripes on top of the metallic one, we found that the back-scattering from the metallic film can be almost perfectly canceled by the composite layer under certain conditions, leading to transparency of the whole structure. We performed proof-of-concept experiments in the terahertz domain to verify our theoretical predictions, using carefully designed metamaterials to mimic plasmonic metals in optical regime. Experiments are in excellent agreement with full-wave simulations.


Subject(s)
Electrodes , Models, Theoretical , Computer Simulation , Computer-Aided Design , Equipment Design , Equipment Failure Analysis , Light , Refractometry , Scattering, Radiation , Terahertz Radiation
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