Title:
Formulation and clinical translation of microneedles for vaccination in developing countries

dc.contributor.advisor Prausnitz, Mark R.
dc.contributor.advisor Colton, Jonathan S.
dc.contributor.advisor Champion, Julie A.
dc.contributor.advisor Roy, Krishnendu
dc.contributor.advisor Weldon, William
dc.contributor.author Arya, Jaya
dc.contributor.department Chemical and Biomolecular Engineering
dc.date.accessioned 2017-08-17T18:56:31Z
dc.date.available 2017-08-17T18:56:31Z
dc.date.created 2016-08
dc.date.issued 2016-05-20
dc.date.submitted August 2016
dc.date.updated 2017-08-17T18:56:32Z
dc.description.abstract Most vaccines are currently administered by healthcare personnel using a needle and syringe, which poses significant hurdles especially in developing countries. We propose dissolving microneedle patches to be a suitable alternative to needle and syringe vaccination in developing countries. Dissolving microneedle patches contain micron-sized needles made out of water-soluble biodegradable polymers that dissolve in the skin to deliver the vaccine. They offer the simplicity of patch application and the possibility to mitigate the logistical and safety challenges associated with conventional hypodermic needles. The overall goal of this thesis was to develop dissolving microneedle patches to further clinical translation of this technology in the context of vaccinations in developing countries. We studied two specific scenarios, development of microneedle patches for rabies vaccination of dogs and assessment of dissolving microneedle patches in human subjects. The central hypothesis was that rabies vaccine can be stabilized in a dissolving microneedle patch and be at least as immunogenic as conventional needle and syringe while enabling simple administration and that dissolving microneedle patches could be easily administered without the need of an applicator, be well tolerated in the skin and preferred over needle and syringe administration. This was assessed by engineering patches for veterinary rabies vaccination and evaluating immune response in dogs and determining tolerability, usability and acceptability of placebo microneedle patches in human subjects. Altogether, the results from this thesis should further clinical translation of microneedles for vaccination in developing countries.
dc.description.degree Ph.D.
dc.format.mimetype application/pdf
dc.identifier.uri http://hdl.handle.net/1853/58577
dc.language.iso en_US
dc.publisher Georgia Institute of Technology
dc.subject Microneedle patch
dc.subject Transdermal drug delivery
dc.subject Intradermal skin vaccination
dc.subject Veterinary vaccination of dogs
dc.subject Human study
dc.title Formulation and clinical translation of microneedles for vaccination in developing countries
dc.type Text
dc.type.genre Dissertation
dspace.entity.type Publication
local.contributor.advisor Prausnitz, Mark R.
local.contributor.advisor Champion, Julie A.
local.contributor.advisor Colton, Jonathan S.
local.contributor.advisor Roy, Krishnendu
local.contributor.corporatename School of Chemical and Biomolecular Engineering
local.contributor.corporatename College of Engineering
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thesis.degree.level Doctoral
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