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Optical Fiber inertial focusing based micro Flowcytometer
KTH, Skolan för teknikvetenskap (SCI), Tillämpad fysik.
KTH. mafaridi@kth.se. (Clinical Microfluidics)ORCID-id: 0000-0003-1176-0905
KTH, Skolan för bioteknologi (BIO), Proteomik och nanobioteknologi. (Clinical Microfluidics)ORCID-id: 0000-0001-5199-0663
Vise andre og tillknytning
(engelsk)Inngår i: Nature Communications, ISSN 2041-1723, E-ISSN 2041-1723Artikkel i tidsskrift (Fagfellevurdert) Submitted
Abstract [en]

Flow cytometry is a powerful method for analysis of cells and particles. Fueled by the need for point of care diagnostic applications, a significant effort has been made to miniaturize flow cytometry. However, despite recent advances, current microflow cytometers remain less versatile and much slower than their large-scale counterparts. Here, we present a portable all-silica optofluidic device that integrates particle focusing in flow through cylindrical silica capillaries and light delivery in optical fibers to simultaneously measure fluorescence and scattering from cells and particles at a rate of 2500 particles/s – a throughput comparable to conventional cytometers. Precise 3D cell focusing and ordering is accomplished using extended elasto-inertial focusing (EEF), a key enabler for eliminating the sheath fluid commonly employed in flow cytometry with maintained high throughput. We demonstrate simultaneously two-color fluorescence and scattering measurement of different sized particles and cells. This robust and low-cost optofluidic device, assembled without the need of clean-room facilities, is ideal suited for point of care applications.

HSV kategori
Identifikatorer
URN: urn:nbn:se:kth:diva-200303OAI: oai:DiVA.org:kth-200303DiVA, id: diva2:1068018
Forskningsfinansiär
Swedish Research CouncilSwedish Childhood Cancer Foundation
Merknad

QCR 20170124

Tilgjengelig fra: 2017-01-24 Laget: 2017-01-24 Sist oppdatert: 2017-11-29bibliografisk kontrollert
Inngår i avhandling
1. Bioparticle Manipulation using Acoustophoresis and Inertial Microfluidics
Åpne denne publikasjonen i ny fane eller vindu >>Bioparticle Manipulation using Acoustophoresis and Inertial Microfluidics
2017 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

Despite the many promising advances made in microfluidics, sample preparation remains the single largest challenge and bottleneck in the field of miniaturised diagnostics. This thesis is focused on the development of sample preparation methods using active and passive particle manipulation techniques for point of care diagnostic applications. The active technique is based on acoustophoresis (acoustic manipulation) while the passive method is based on inertial microfluidics (hydrodynamic manipulation). In paper I, acoustic capillary-based cavity resonator was used to study aggregation of silica and polystyrene particles. We found that silica particles show faster aggregation time (5.5 times) and larger average area of aggregates (3.4 times) in comparison to polystyrene particles under the same actuation procedure. The silica particles were then used for acoustic based bacteria up-concentration. In paper II, a microfluidic-based microbubbles activated acoustic cell sorting technique was developed for affinity based cell separation. As a proof of principle, separation of cancer cell line in a suspension with better than 75% efficiency is demonstrated. For the passive sample preparation, inertial and elasto-inertial microfluidic approach that uses geometry-induced hydrodynamic forces for continuous size-based sorting of particles in a flow-through fashion were studied and applied for blood processing (paper III-V). In paper III, a simple ushaped curved channel was used for inertial microfluidics based enrichment of white blood cells from diluted whole blood. A filtration efficiency of 78% was achieved at a flow rate of 2.2 ml/min. In paper IV, elasto-inertial microfluidics where viscoelastic flow enables size-based migration of cells into a non- Newtonian solution, was used to continuously separate bacteria from unprocessed whole blood for sepsis diagnostics. Bacteria were continuously separated at an efficiency of 76% from undiluted whole blood sample. Finally, in paper V, the inertial and elasto-inertial techniques were combined with a detection platform to demonstrate an integrated miniaturized flow cytometer. The all-optical-fiber technology based system allows for simultaneous measurements of fluorescent and scattering data at 2500 particles/s. The use of inertial and acoustic techniques for sample preparation and development of an integrated detection platform may allow for further development and realization of point of care testing (POCT) systems.

sted, utgiver, år, opplag, sider
Stockholm, Sweden: Kungliga Tekniska högskolan, 2017. s. 68
Serie
TRITA-BIO-Report, ISSN 1654-2312 ; 2017:4
HSV kategori
Forskningsprogram
Bioteknologi
Identifikatorer
urn:nbn:se:kth:diva-200304 (URN)978-91-7729-264-7 (ISBN)
Disputas
2017-02-16, Gard-Aulan, Nobels vägen 18, Solna, Stockholm, 10:00 (engelsk)
Opponent
Veileder
Merknad

QC 20170124

Tilgjengelig fra: 2017-01-24 Laget: 2017-01-24 Sist oppdatert: 2017-01-24bibliografisk kontrollert

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