Abstract
dc:description.abstractIso-dielectrophoresis (IDS) can be used to characterize and separate cells by their electrical characteristics. An IDS system usually consist of a RF frequency voltage source up to 24 V, syringe pumps, microscope, and computer. Much of this equipment is difficult to transport, making off-site sample collection of time-sensitive samples, such as blood, difficult. The miniaturization of the IDS system would allow measurements to take place at the time of sample collection, improving the confidence in the measurement. This thesis details an attempt to miniaturize each system. The Raspberry Pi microcomputer was used to control and process signals from the hardware. A portable, affordable system for the electrical and optical equipment systems are described. A custom PCB was designed to provide voltage signals up to 3 MHz and 12 Vpp. A microscope using a Raspberry Pi camera and reversed webcam lens achieved 240x magnification with 13 [mu]m resolution. Alternatives to the syringe pump, including air pressure regulated pumps and peristaltic pumps, were considered for the fluidic component.
Degree
thesis:*- Department dc:contributor.department
- Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science.
- Grantor dc:publisher
- Massachusetts Institute of Technology
- Year dc:date.issued
- 2016
Author and committee
dc:creator, dc:contributor.*- Author dc:creator
-
- Liu, Lisa, M. Eng. Massachusetts Institute of Technology
- Advisor dc:contributor.advisor
-
- Joel Voldman.
Subjects
dc:subject × 1Rights
dc:rights- Statement dc:rights
-
- M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.
- Licence dc:rights.uri
- Language dc:language.iso
- eng
Identifiers
dc:identifier.*- Handle dc:identifier.uri
- http://hdl.handle.net/1721.1/105981
- OAI identifier oai:identifier
- oai:dspace.mit.edu:1721.1/105981