STREM-1 based sepsis detection with centrifugal microfluidics incorporating active valves and image analysis

dc.contributor.advisorMartinez Chapa, Sergio Omaren_US
dc.contributor.advisorMehdi Aeinehvand, Mohammaden_US
dc.contributor.authorMedrano Danés, Jonathanen_US
dc.contributor.committeememberDieck Assad, Gracianoen_US
dc.contributor.committeememberMartins Fernandes, Rute Fabianaen_US
dc.date.accessioned2018-05-22T20:13:30Z
dc.date.available2018-05-22T20:13:30Z
dc.date.issued2017-11-17
dc.description.abstractSepsis is the main cause of neonate death in hospitals. According to WHO, around one million neonatal deaths are caused each year because of sepsis. Rapid and early sepsis detection, are necessary for effective treatment of the patients to reduce the mortality rate, however this is still a big challenge, especially in low income countries with a poor healthcare system. Recently, soluble triggering receptor expressed on myeloid cells-1 (sTREM-1) biomarker has showed to be an accurate indicator for sepsis detection in neonates. When compared to conventional tests that take several days up to a week, sTREM-1 immunoassay is a faster approach for sepsis detection as it can be performed in five hours. However, the sTREM-1 immunoassay must be performed in a clinic laboratory by specialized staff and require several expensive and bulky equipment. One way to enable the sTREM-1 immunoassay outside specialized labs or at point-of-care (POC) is the integration of the complex assay into a centrifugal microfluidic platform. The disc-shaped microfluidic platform also known as lab-on-disc (LoD), employs centrifugal force from spinning of the disc to manipulate samples and reagents. The centrifugal force that exist everywhere on the disc prevents the need for several expensive syringe pumps. However, it makes simultaneous control over the retention and flow of several reagents/samples on a LoD challenging. To overcome this problem and automate sTREM-1 immunoassay for POC settings, this document presents the development of a new sacrificial polyethylene and a novel reversible valving mechanism on LoD. Based on the two valving mechanisms, a sTREM-1 immunoassay LoD is developed for sepsis detection. Integrating a series of sacrificial valves in the disc allowed for storage of reagents in the disc and their controlled release to a reaction chamber. The reversible valve, was used for the retention of each reagent in the detection chamber during incubation periods, and then transferring it to a waste chamber. A portable spinning system was developed to run the assay by microfluidic disc at POC. The successful automation of sTREM1 immunoassay on the microfluidic disc can provide a significant contribution in the reduction of complexity of the resources needed for sepsis detection at POC settings, particularly in remote areas.
dc.identifier.urihttp://hdl.handle.net/11285/629755
dc.language.isoengen_US
dc.rightsOpen Accessen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.disciplineCiencias / Sciencesen_US
dc.subject.keywordCentrifugal Microfluidicsen_US
dc.subject.keywordLab on a CDen_US
dc.subject.keywordLoDen_US
dc.subject.keywordSepsisen_US
dc.subject.keywordsTREM-1en_US
dc.subject.keywordELISAen_US
dc.subject.keywordelectronic systemsen_US
dc.subject.keywordengineeringen_US
dc.titleSTREM-1 based sepsis detection with centrifugal microfluidics incorporating active valves and image analysisen_US
dc.typeTesis de maestría
html.description.abstract<html> <head> <title></title> </head> <body> <p>Sepsis is the main cause of neonate death in hospitals. According to WHO, around one million neonatal deaths are caused each year because of sepsis. Rapid and early sepsis detection, are necessary for effective treatment of the patients to reduce the mortality rate, however this is still a big challenge, especially in low income countries with a poor healthcare system. Recently, soluble triggering receptor expressed on myeloid cells-1 (sTREM-1) biomarker has showed to be an accurate indicator for sepsis detection in neonates. When compared to conventional tests that take several days up to a week, sTREM-1 immunoassay is a faster approach for sepsis detection as it can be performed in five hours. However, the sTREM-1 immunoassay must be performed in a clinic laboratory by specialized staff and require several expensive and bulky equipment. One way to enable the sTREM-1 immunoassay outside specialized labs or at point-of-care (POC) is the integration of the complex assay into a centrifugal microfluidic platform. The disc-shaped microfluidic platform also known as lab-on-disc (LoD), employs centrifugal force from spinning of the disc to manipulate samples and reagents. The centrifugal force that exist everywhere on the disc prevents the need for several expensive syringe pumps. However, it makes simultaneous control over the retention and flow of several reagents/samples on a LoD challenging. To overcome this problem and automate sTREM-1 immunoassay for POC settings, this document presents the development of a new sacrificial polyethylene and a novel reversible valving mechanism on LoD. Based on the two valving mechanisms, a sTREM-1 immunoassay LoD is developed for sepsis detection. Integrating a series of sacrificial valves in the disc allowed for storage of reagents in the disc and their controlled release to a reaction chamber. The reversible valve, was used for the retention of each reagent in the detection chamber during incubation periods, and then transferring it to a waste chamber. A portable spinning system was developed to run the assay by microfluidic disc at POC. The successful automation of sTREM1 immunoassay on the microfluidic disc can provide a significant contribution in the reduction of complexity of the resources needed for sepsis detection at POC settings, particularly in remote areas.</p> </body> </html>en_US
refterms.dateFOA2018-05-22T20:13:31Z
thesis.degree.disciplineSchool of Engineering and Sciencesen_US
thesis.degree.grantorInstituto Tecnológico y de Estudios Superiores de Monterreyes
thesis.degree.levelMaster of Science in Electronic Systemsen_US
thesis.degree.nameMaestría en Ciencias con Especialidad en Ingeniería Electrónicaen_US
thesis.degree.programCampus Monterreyen_US

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