Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/102614
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dc.contributor.advisorBi, Jingxiu-
dc.contributor.advisorZhang, Hu-
dc.contributor.advisorBiggs, Mark James-
dc.contributor.authorZhang, Mengjue-
dc.date.issued2016-
dc.identifier.urihttp://hdl.handle.net/2440/102614-
dc.description.abstractDevelopment and application of a microfluidic system for generating drug delivery carriers are investigated in this research. Various types of microfluidic devices are designed and fabricated for peptide nanotubes, liposome vesicles and double emulsions formation. The microfluidic system offers a better control over the formation process of all three drug delivery carriers. Comparing to traditional methods such as bulk mixing, the process efficiency, size and size distribution of the final products are significantly improved. The results generated show that tuning the flow rate ratios between different reagents from the inlet streams successfully controls the sizes and size distributions of liposomes vesicles. The relationship between the flow rate ratio and the size of the resulting vesicles is established. Macrocycle (AP-169) that was found to self-assemble into an anti-parallel ╬▓-sheet nanotube with a triggering agent is successfully synthesized and purified for peptide nanotube self-assembling process. A microfluidic device is designed and fabricated to control the interaction between AP-169 and its self-assembling triggering agent, dimethyl sulfoxide. Double emulsions with different radii are produced with the microfluidic system by adjusting the flow rate ratio between each phase of the solution, and changing the wetting properties of the microchannels. The stability of double emulsions is enhanced by introducing various surfactants. The sizes and size distributions of liposomes and double emulsions have been successfully controlled and optimized for drug delivery. In conclusion, various drug delivery carriers have been successfully generated and optimized with a designed and modified microfluidic system. These products can be further applied in drug encapsulation, biomolecular screening and in vitro compartmentalization in the future.en
dc.subjectmicrofluidicen
dc.subjectliposomesen
dc.subjectdouble emulsionsen
dc.titleMicrofluidic system development for drug deliveryen
dc.typeThesesen
dc.contributor.schoolSchool of Chemical Engineeringen
dc.provenanceThis electronic version is made publicly available by the University of Adelaide in accordance with its open access policy for student theses. Copyright in this thesis remains with the author. This thesis may incorporate third party material which has been used by the author pursuant to Fair Dealing exceptions. If you are the owner of any included third party copyright material you wish to be removed from this electronic version, please complete the take down form located at: http://www.adelaide.edu.au/legalsen
dc.description.dissertationThesis (M.Eng.Sc.) -- University of Adelaide, School of Chemical Engineering, 2016.en
dc.identifier.doi10.4225/55/582e673a0d955-
Appears in Collections:Research Theses

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