Separation of blood components is of high importance in healthcare and often require fractionation of blood in its subcomponents by centrifugation. There are several scenarios that calls for improved resolution:
1. When blood is...
ver más
¿Tienes un proyecto y buscas un partner? Gracias a nuestro motor inteligente podemos recomendarte los mejores socios y ponerte en contacto con ellos. Te lo explicamos en este video
Proyectos interesantes
pureCTC
A LAB ON A CHIP DEVICE FOR PURE CIRCULATING TUMOR CELL ISOLA...
173K€
Cerrado
FVDI13-4E-2653
Citómetro de Flujo Analizador BD FACSCalibur para el Centro...
39K€
Cerrado
EQC2018-004349-P
Adquisición de infraestructura científica para el Servicio d...
396K€
Cerrado
PTA2020-019342-I
Citometría de Flujo Analítica y Preparativa (Cell Sorting)
42K€
Cerrado
CSIC08-1E-033
Adquisición de un citómetro de flujo y separador celular
471K€
Cerrado
Información proyecto TAPAS
Duración del proyecto: 25 meses
Fecha Inicio: 2022-09-26
Fecha Fin: 2024-10-31
Líder del proyecto
LUNDS UNIVERSITET
No se ha especificado una descripción o un objeto social para esta compañía.
TRL
4-5
Presupuesto del proyecto
150K€
Fecha límite de participación
Sin fecha límite de participación.
Descripción del proyecto
Separation of blood components is of high importance in healthcare and often require fractionation of blood in its subcomponents by centrifugation. There are several scenarios that calls for improved resolution:
1. When blood is drawn from a donor and a specific cell type is extracted while returning remaining blood components.
2. In cancer immunotherapy where T-cells are isolated from the blood and then genetically reprogrammed to be re-infused in the patient where they seek up and destroy cancer cells.
3. Circulating tumor cells, which are involved in the process of formation of metastases in cancer patients, can be detected and monitored by extracting cancer cells in large volumes of blood.
4. Improving the quality and reducing the number of manual procedures in diagnostic instrumentation that analyzes blood.
Centrifugation has the fundamental drawback of having rotating parts, and thereby taking up space and being difficult to implement for flow-through processing which is desirable both for integration in analytical equipment and for processing blood for continuous re-infusion into a person.
We will investigate an alternative to centrifugation wherein blood components are separated by a sound field. Cells will be separated based on differences in density and size while flowing through an acoustic separator module. Recent ERC-funded research indicates that this approach is feasible, but three scientific questions has been identified with fundamental impact on the commercial potential of this technology:
1. How selectively can sub-groups of blood cells be separated by acoustic separation?
2. Can acoustic separation be scaled for high throughput applications?
3. Can acoustic separation affect blood cells?
To address this, my team will design and build two prototype systems for whole blood processing and evaluate the quality and throughput of the separation with the ultimate goal of bringing this technology to the market for the benefit of society.