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Multidimensional Ultrasonic Standing Wave Manipulation in Microfluidic Chips
KTH, Skolan för teknikvetenskap (SCI), Tillämpad fysik, Biomedicinsk fysik och röntgenfysik. (Biomedical & X-Ray Physics)ORCID-id: 0000-0002-4720-2756
2009 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

The use of ultrasonic standing waves for contactless manipulation of microparticles in microfluidic systems is a field with potential to become a new standard tool in lab-on-chip systems. Compared to other contactless manipulation methods ultrasonic standing wave manipulation shows promises of gentle cell handling, low cost, and precise temperature control. The technology can be used both for batch handling, such as sorting and aggregation, and handling of single particles.

This doctoral Thesis presents multi-dimensional ultrasonic manipulation, i.e., manipulation in both two and three spatial dimensions as well as time-dependent manipulation of living cells and microbeads in microfluidic systems. The lab-on-chip structures used allow for high-quality optical microscopy, which is central to many bio-applications. It is demonstrated how the ultrasonic force fields can be spatially confined to predefined regions in the system, enabling sequential manipulation functions. Furthermore, it is shown how frequency-modulated signals can be used both for spatial stabilization of the force fields as well as for flow-free transport of particles in a microchannel. Design parameters of the chip-transducer systems employed are investigated experimentally as well as by numerical simulations. It is shown that three-dimensional resonances in the solid structure of the chip strongly influences the resonance shaping in the channel.

sted, utgiver, år, opplag, sider
Stockholm: KTH , 2009. , s. ix, 83
Serie
Trita-FYS, ISSN 0280-316X ; 2009:44
HSV kategori
Identifikatorer
URN: urn:nbn:se:kth:diva-10919ISBN: 978-91-7415-398-9 (tryckt)OAI: oai:DiVA.org:kth-10919DiVA, id: diva2:231815
Disputas
2009-09-11, FD5, Roslagstullsbacken 21, Stockholm, 14:00 (engelsk)
Opponent
Veileder
Merknad
QC 20100730Tilgjengelig fra: 2009-09-01 Laget: 2009-08-18 Sist oppdatert: 2010-07-30bibliografisk kontrollert
Delarbeid
1. Proliferation and viability of adherent cells manipulated by standing-wave ultrasound in a microfluidic chip
Åpne denne publikasjonen i ny fane eller vindu >>Proliferation and viability of adherent cells manipulated by standing-wave ultrasound in a microfluidic chip
Vise andre…
2007 (engelsk)Inngår i: Ultrasound in Medicine and Biology, ISSN 0301-5629, E-ISSN 1879-291X, Vol. 33, s. 145-151Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Ultrasonic-standing-wave (USW) technology has potential to become a standard method for gentle and contactless cell handling in microfluidic chips. We investigate the viability of adherent cells exposed to USWs by studying the proliferation rate of recultured cells following ultrasonic trapping and aggregation of low cell numbers in a microfluidic chip. The cells form 2-D aggregates inside the chip and the aggregates are held against a continuous flow of cell culture medium perpendicular to the propagation direction of the standing wave. No deviations in the doubling time from expected values (24 to 48 h) were observed for COS-7 cells held in the trap at acoustic pressure amplitudes up to 0.85 MPa and for times ranging between 30 and 75 min. Thus, the results demonstrate the potential of ultrasonic standing waves as a tool for gentle manipulation of low cell numbers in microfluidic systems.

Emneord
mammalian-cells; retention; sedimentation; aggregation; perfusion; channels; driven; matrix; filter; trap
HSV kategori
Identifikatorer
urn:nbn:se:kth:diva-10913 (URN)10.1016/j.ultrasmedbio.2006.07.024 (DOI)000243243700017 ()2-s2.0-33845626925 (Scopus ID)
Merknad
QC 20100730Tilgjengelig fra: 2009-08-18 Laget: 2009-08-18 Sist oppdatert: 2017-12-13bibliografisk kontrollert
2. Temperature regulation during ultrasonic manipulation for long-term cell handling in a microfluidic chip
Åpne denne publikasjonen i ny fane eller vindu >>Temperature regulation during ultrasonic manipulation for long-term cell handling in a microfluidic chip
2007 (engelsk)Inngår i: Journal of Micromechanics and Microengineering, ISSN 0960-1317, E-ISSN 1361-6439, Vol. 17, s. 2469-2474Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Regulation by the use of ultrasonic standing wave technology in a microfluidic chip. The system is based on a microfabricated silicon structure sandwiched between two glass layers, and an external ultrasonic transducer using a refractive wedge placed on top of the chip for efficient coupling of ultrasound into the microchannel. The chip is fully transparent and compatible with any kind of high-resolution optical microscopy. The temperature regulation method uses calibration data of the temperature increase due to the ultrasonic actuation for determining the temperature of the surrounding air and microscope table, controlled by a warm-air heating unit and a heatable mounting frame. The heating methods are independent of each other, resulting in a flexible choice of ultrasonic actuation voltage and flow rate for different cell and particle manipulation purposes. Our results indicate that it is possible to perform stable temperature regulation with an accuracy of the order of +/- 0.1 degrees C around any physiologically relevant temperature (e.g., 37 degrees C) with high temporal stability and repeatability. The purpose is to use ultrasound for long-term cell and/or particle handling in a microfluidic chip while controlling and maintaining the biocompatibility of the system.

Emneord
technology; retention
HSV kategori
Identifikatorer
urn:nbn:se:kth:diva-10914 (URN)10.1088/0960-1317/17/12/012 (DOI)000251767100012 ()2-s2.0-36949032927 (Scopus ID)
Merknad
QC 20100730Tilgjengelig fra: 2009-08-18 Laget: 2009-08-18 Sist oppdatert: 2017-12-13bibliografisk kontrollert
3. Spatial confinement of ultrasonic force fields in microfluidic chips
Åpne denne publikasjonen i ny fane eller vindu >>Spatial confinement of ultrasonic force fields in microfluidic chips
Vise andre…
2009 (engelsk)Inngår i: Ultrasonics, ISSN 0041-624X, E-ISSN 1874-9968, Vol. 49, s. 112-119Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

We demonstrate and investigate multiple localized ultrasonic manipulation functions in series in microfluidic chips. The manipulation functions are based on spatially separated and confined ultrasonic primary radiation force fields, obtained by local matching of the resonance condition of the microfluidic channel. The channel segments are remotely actuated by the use of frequency-specific external transducers with refracting wedges placed on top of the chips. The force field in each channel segment is characterized by the use of micrometer-resolution particle image velocimetry ( micro-PIV). The confinement of the ultrasonic fields during single-or dual-segment actuation, as well as the cross-talk between two adjacent. fields, is characterized and quantified. Our results show that the field confinement typically scales with the acoustic wavelength, and that the cross-talk is insignificant between adjacent. fields. The goal is to define design strategies for implementing several spatially separated ultrasonic manipulation functions in series for use in advanced particle or cell handling and processing applications. One such proof-of-concept application is demonstrated, where. flow-through-mode operation of a chip with. flow splitting elements is used for two-dimensional pre-alignment and addressable merging of particle tracks.

Emneord
Ultrasonic manipulation; Acoustic radiation force; Microfluidic chip; Particle image velocimetry; Spatial confinement; Cell handling
HSV kategori
Identifikatorer
urn:nbn:se:kth:diva-10912 (URN)10.1016/j.ultras.2008.06.012 (DOI)000261834200017 ()2-s2.0-56949083339 (Scopus ID)
Merknad
QC 20100730Tilgjengelig fra: 2009-08-18 Laget: 2009-08-18 Sist oppdatert: 2017-12-13bibliografisk kontrollert
4. Wedge transducer design for two-dimensional ultrasonic manipulation in a microfluidic chip
Åpne denne publikasjonen i ny fane eller vindu >>Wedge transducer design for two-dimensional ultrasonic manipulation in a microfluidic chip
2008 (engelsk)Inngår i: Journal of Micromechanics and Microengineering, ISSN 0960-1317, E-ISSN 1361-6439, Vol. 18, s. 095025-Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

We analyze and optimize the design of wedge transducers used for the excitation of resonances in the channel of a microfluidic chip in order to efficiently manipulate particles or cells in more than one dimension. The design procedure is based on (1) theoretical modeling of acoustic resonances in the transducer-chip system and calculation of the force fields in the fluid channel, (2) full-system resonance characterization by impedance spectroscopy and (3) image analysis of the particle distribution after ultrasonic manipulation. We optimize the transducer design in terms of actuation frequency, wedge angle and placement on top of the chip, and we characterize and compare the coupling effects in orthogonal directions between single- and dual-frequency ultrasonic actuation. The design results are verified by demonstrating arraying and alignment of particles in two dimensions. Since the device is compatible with high-resolution optical microscopy, the target application is dynamic cell characterization combined with improved microfluidic sample transport.

Emneord
standing-wave; separation; particles; channels; bioassays; cells
HSV kategori
Identifikatorer
urn:nbn:se:kth:diva-10915 (URN)10.1088/0960-1317/18/9/095025 (DOI)000259590700025 ()2-s2.0-54749116541 (Scopus ID)
Merknad
QC 20100730Tilgjengelig fra: 2009-08-18 Laget: 2009-08-18 Sist oppdatert: 2017-12-13bibliografisk kontrollert
5. A three-dimensional ultrasonic cage for characterization of individual cells
Åpne denne publikasjonen i ny fane eller vindu >>A three-dimensional ultrasonic cage for characterization of individual cells
Vise andre…
2008 (engelsk)Inngår i: Applied Physics Letters, ISSN 0003-6951, E-ISSN 1077-3118, Vol. 93, s. 063901-Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

We demonstrate enrichment, controlled aggregation, and manipulation of microparticles and cells by an ultrasonic cage integrated in a microfluidic chip compatible with high-resolution optical microscopy. The cage is designed as a dual-frequency resonant filleted square box integrated in the fluid channel. Individual particles may be trapped three dimensionally, and the dimensionality of one-dimensional to three-dimensional aggregates can be controlled. We investigate the dependence of the shape and position of a microparticle aggregate on the actuation voltages and aggregate size, and demonstrate optical monitoring of individually trapped live cells with submicrometer resolution.

Emneord
optical manipulation; microfluidic chip; particles; traps
HSV kategori
Identifikatorer
urn:nbn:se:kth:diva-10916 (URN)10.1063/1.2971030 (DOI)000258491000076 ()2-s2.0-49749149572 (Scopus ID)
Merknad
QC 20100730Tilgjengelig fra: 2009-08-18 Laget: 2009-08-18 Sist oppdatert: 2017-12-13bibliografisk kontrollert
6. Selective bioparticle retention and characterization in a chip-integrated confocal ultrasonic cavity
Åpne denne publikasjonen i ny fane eller vindu >>Selective bioparticle retention and characterization in a chip-integrated confocal ultrasonic cavity
Vise andre…
2009 (engelsk)Inngår i: Biotechnology and Bioengineering, ISSN 0006-3592, E-ISSN 1097-0290, Vol. 103, s. 323-328Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

We demonstrate selective retention and positioning of cells or other bioparticles by ultrasonic manipulation in a microfluidic expansion chamber during microfluidic perfusion. The chamber is designed as a confocal ultrasonic resonator for maximum confinement of the ultrasonic force field at the chamber center, where the cells are trapped. We investigate the resonant modes in the expansion chamber and its connecting inlet channel by theoretical modeling and experimental verification during no-flow conditions. Furthermore, by triple-frequency ultrasonic actuation during continuous microfluidic sample feeding, a set of several manipulation functions performed in series is demonstrated: sample bypass-injection-aggregation and retention-positioning. Finally, we demonstrate transillumination microscopy imaging Of Ultrasonically trapped COS-7 cell aggregates.

Emneord
ultrasonic manipulation; cell characterization; microfluidic chip
HSV kategori
Identifikatorer
urn:nbn:se:kth:diva-10917 (URN)10.1002/bit.22255 (DOI)000266078200009 ()19170245 (PubMedID)2-s2.0-65549156499 (Scopus ID)
Merknad
QC 20100730Tilgjengelig fra: 2009-08-18 Laget: 2009-08-18 Sist oppdatert: 2017-12-13bibliografisk kontrollert
7. Flow-free transport of cells in microchannels by frequency-modulated ultrasound
Åpne denne publikasjonen i ny fane eller vindu >>Flow-free transport of cells in microchannels by frequency-modulated ultrasound
2009 (engelsk)Inngår i: Lab on a Chip, ISSN 1473-0197, E-ISSN 1473-0189, Vol. 9, s. 833-837Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

We demonstrate flow-free transport of cells and particles by the use of frequency-modulated ultrasonic actuation of a microfluidic chip. Two different modulation schemes are combined: A rapid (1 kHz) linear frequency sweep around similar to 6.9 MHz is used for two-dimensional spatial stabilization of the force field over a 5 mm long inlet channel of constant cross section, and a slow (0.2-0.7 Hz) linear frequency sweep around similar to 2.6 MHz is used for flow-free ultrasonic transport and positioning of cells or particles. The method is used for controlling the motion and position of cells monitored with high-resolution optical microscopy, but can also be used more generally for improving the robustness and performance of ultrasonic manipulation micro-devices.

Emneord
manipulation; particles; chip; separation; channels
HSV kategori
Identifikatorer
urn:nbn:se:kth:diva-10918 (URN)10.1039/B816675G (DOI)000263847000012 ()2-s2.0-61849133822 (Scopus ID)
Merknad
QC 20100730Tilgjengelig fra: 2009-08-18 Laget: 2009-08-18 Sist oppdatert: 2017-12-13bibliografisk kontrollert

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