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dc.contributor.authorKirtane, Ameya R.
dc.contributor.authorKaravasili, Christina
dc.contributor.authorWahane, Aniket
dc.contributor.authorFreitas, Dylan
dc.contributor.authorBooz, Katelyn
dc.contributor.authorLe, Dao Thi Hong
dc.contributor.authorHua, Tiffany
dc.contributor.authorScala, Stephen
dc.contributor.authorLopes, Aaron
dc.contributor.authorHess, Kaitlyn
dc.contributor.authorCollins, Joy
dc.contributor.authorTamang, Siddartha
dc.contributor.authorIshida, Keiko
dc.contributor.authorKuosmanen, Johannes L. P.
dc.contributor.authorRajesh, Netra Unni
dc.contributor.authorPhan, Nhi V.
dc.contributor.authorLi, Junwei
dc.contributor.authorKrogmann, Annlyse
dc.contributor.authorLennerz, Jochen K.
dc.contributor.authorHayward, Alison
dc.contributor.authorLanger, Robert
dc.contributor.authorTraverso, Giovanni
dc.date.accessioned2024-05-23T13:51:13Z
dc.date.available2024-05-23T13:51:13Z
dc.date.issued2022-05-27
dc.identifier.issn2375-2548
dc.identifier.urihttps://hdl.handle.net/1721.1/155044
dc.description.abstractAdministering medicines to 0- to 5-year-old children in a resource-limited environment requires dosage forms that circumvent swallowing solids, avoid on-field reconstitution, and are thermostable, cheap, versatile, and taste masking. We present a strategy that stands to solve this multifaceted problem. As many drugs lack adequate water solubility, our formulations used oils, whose textures could be modified with gelling agents to form “oleogels.” In a clinical study, we showed that the oleogels can be formulated to be as fluid as thickened beverages and as stiff as yogurt puddings. In swine, oleogels could deliver four drugs ranging three orders of magnitude in their water solubilities and two orders of magnitude in their partition coefficients. Oleogels could be stabilized at 40°C for prolonged durations and used without redispersion. Last, we developed a macrofluidic system enabling fixed and metered dosing. We anticipate that this platform could be adopted for pediatric dosing, palliative care, and gastrointestinal disease applications.en_US
dc.language.isoen
dc.publisherAmerican Association for the Advancement of Scienceen_US
dc.relation.isversionof10.1126/sciadv.abm8478en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceAmerican Association for the Advancement of Scienceen_US
dc.titleDevelopment of oil-based gels as versatile drug delivery systems for pediatric applicationsen_US
dc.typeArticleen_US
dc.identifier.citationAmeya R. Kirtane et al. ,Development of oil-based gels as versatile drug delivery systems for pediatric applications.Sci. Adv.8,eabm8478(2022).en_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MIT
dc.contributor.departmentMassachusetts Institute of Technology. Division of Comparative Medicine
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineering
dc.relation.journalScience Advancesen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2024-05-23T13:46:38Z
dspace.orderedauthorsKirtane, AR; Karavasili, C; Wahane, A; Freitas, D; Booz, K; Le, DTH; Hua, T; Scala, S; Lopes, A; Hess, K; Collins, J; Tamang, S; Ishida, K; Kuosmanen, JLP; Rajesh, NU; Phan, NV; Li, J; Krogmann, A; Lennerz, JK; Hayward, A; Langer, R; Traverso, Gen_US
dspace.date.submission2024-05-23T13:46:43Z
mit.journal.volume8en_US
mit.journal.issue21en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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