Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/158602
Full metadata record
DC FieldValueLanguage
dc.contributor.authorLim, Jia Jiaen_US
dc.date.accessioned2022-06-04T11:26:00Z-
dc.date.available2022-06-04T11:26:00Z-
dc.date.issued2022-
dc.identifier.citationLim, J. J. (2022). Microfluidic isolation of extracellular vesicles using a short arcuated channel. Final Year Project (FYP), Nanyang Technological University, Singapore. https://hdl.handle.net/10356/158602en_US
dc.identifier.urihttps://hdl.handle.net/10356/158602-
dc.description.abstractExtracellular vesicles (EVs) are cell-derived nanoscale (~ 50 to 200 nm) membrane-bound particles which are important for cell-to-cell communication and are implicated in various diseases. While EVs present great potential as future disease biomarkers or drug delivery agents, it remains technically challenging to isolate EVs from complex biofluids like whole blood. Conventional EV isolation methods, such as ultracentrifugation (UC) and size exclusion chromatography (SEC) require manual centrifugation to remove cells and debris, which is labour intensive and time consuming. Therefore, there is an unmet need to develop a more robust, user-friendly and convenient EVs isolation method. In this paper, we report the development of a short arcuated microfluidic platform, ExoArc, to directly isolate EVs from whole blood in a label-free manner without manual centrifugation. Fluorescent imaging showed that 50 nm and 500 nm beads (representative of EV size range) could be efficiently separated from 1 μm beads at high flow rate (0.2 mL/min of whole blood), thus indicating minimal contamination of platelets and apoptotic bodies (~ 1 to 3 μm) in the isolated EVs. Nanoparticle tracking analysis (NTA) revealed that ExoArc had 2x and 500x higher particle yield than SEC and UC respectively. Protein level of ExoArc-eluted EVs was ~ 10 mg/mL which is 10x lower than plasma samples. To further reduce protein contamination, a 2-step EV isolation process (ExoArc + SEC) was proposed in which we demonstrated comparable EV yield of CD9+ as commercial SEC (using plasma), and 10 times higher yield than UC. Overall, ExoArc provides an easy-to-use, compact, and efficient method to isolate EVs, which can be readily automated for point-of-care application such as clinical diagnostics or process control of EVs manufacturing.en_US
dc.language.isoenen_US
dc.publisherNanyang Technological Universityen_US
dc.relationB080en_US
dc.subjectEngineering::Mechanical engineering::Fluid mechanicsen_US
dc.titleMicrofluidic isolation of extracellular vesicles using a short arcuated channelen_US
dc.typeFinal Year Project (FYP)en_US
dc.contributor.supervisorHou Han Weien_US
dc.contributor.schoolSchool of Mechanical and Aerospace Engineeringen_US
dc.description.degreeBachelor of Engineering (Mechanical Engineering)en_US
dc.contributor.supervisoremailhwhou@ntu.edu.sgen_US
item.grantfulltextembargo_restricted_20240519-
item.fulltextWith Fulltext-
Appears in Collections:MAE Student Reports (FYP/IA/PA/PI)
Files in This Item:
File Description SizeFormat 
Lim Jia Jia_U1821505G_FYP_Project_B080_Final_Report.pdf
  Until 2024-05-19
2.17 MBAdobe PDFUnder embargo until May 19, 2024

Page view(s)

24
Updated on Aug 15, 2022

Google ScholarTM

Check

Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.