Parallel microfluidic synthesis of size-tunable polymeric nanoparticles using 3D flow focusing towards in vivo study

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dc.contributor.authorLim, Jong-Minko
dc.contributor.authorBertrand, Nicolasko
dc.contributor.authorValencia, Pedro M.ko
dc.contributor.authorRhee, Minsoungko
dc.contributor.authorLanger, Rko
dc.contributor.authorJon, Sangyongko
dc.contributor.authorFarokhzad, Omid C.ko
dc.contributor.authorKarnik, Rohitko
dc.date.accessioned2014-09-01T08:35:02Z-
dc.date.available2014-09-01T08:35:02Z-
dc.date.created2014-03-12-
dc.date.created2014-03-12-
dc.date.issued2014-02-
dc.identifier.citationNANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, v.10, no.2, pp.401 - 409-
dc.identifier.issn1549-9634-
dc.identifier.urihttp://hdl.handle.net/10203/189580-
dc.description.abstractMicrofluidic synthesis of nanoparticles (NPs) can enhance the controllability and reproducibility in physicochemical properties of NPs compared to bulk synthesis methods. However, applications of microfluidic synthesis are typically limited to in vitro studies due to low production rates. Herein, we report the parallelization of NP synthesis by 3D hydrodynamic flow focusing (HFF) using a multilayer microfluidic system to enhance the production rate without losing the advantages of reproducibility, controllability, and robustness. Using parallel 3D HFF, polymeric poly(lactide-co-glycolide)-b-polyethyleneglycol (PLGA-PEG) NPs with sizes tunable in the range of 13-150 nm could be synthesized reproducibly with high production rate. As a proof of concept, we used this system to perform in vivo pharmacokinetic and biodistribution study of small (20 nm diameter) PLGA-PEG NPs that are otherwise difficult to synthesize. Microfluidic parallelization thus enables synthesis of NPs with tunable properties with production rates suitable for both in vitro and in vivo studies. (C) 2014 Elsevier Inc. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER SCIENCE BV-
dc.subjectMASS-PRODUCTION-
dc.subjectDRUG-DELIVERY-
dc.subjectTHROUGHPUT PRODUCTION-
dc.subjectCLINICAL TRANSLATION-
dc.subjectDESIGN-
dc.subjectBIODISTRIBUTION-
dc.subjectFORMULATION-
dc.subjectEMULSIONS-
dc.subjectDROPLETS-
dc.subjectPLATFORM-
dc.titleParallel microfluidic synthesis of size-tunable polymeric nanoparticles using 3D flow focusing towards in vivo study-
dc.typeArticle-
dc.identifier.wosid000330728400013-
dc.identifier.scopusid2-s2.0-84895071390-
dc.type.rimsART-
dc.citation.volume10-
dc.citation.issue2-
dc.citation.beginningpage401-
dc.citation.endingpage409-
dc.citation.publicationnameNANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE-
dc.identifier.doi10.1016/j.nano.2013.08.003-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorJon, Sangyong-
dc.contributor.nonIdAuthorLim, Jong-Min-
dc.contributor.nonIdAuthorBertrand, Nicolas-
dc.contributor.nonIdAuthorValencia, Pedro M.-
dc.contributor.nonIdAuthorRhee, Minsoung-
dc.contributor.nonIdAuthorLanger, R-
dc.contributor.nonIdAuthorFarokhzad, Omid C.-
dc.contributor.nonIdAuthorKarnik, Rohit-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorNanoparticles-
dc.subject.keywordAuthorNanoprecipitation-
dc.subject.keywordAuthor3D flow focusing-
dc.subject.keywordAuthorMicrofluidics-
dc.subject.keywordAuthorBlock copolymers-
dc.subject.keywordPlusMASS-PRODUCTION-
dc.subject.keywordPlusDRUG-DELIVERY-
dc.subject.keywordPlusTHROUGHPUT PRODUCTION-
dc.subject.keywordPlusCLINICAL TRANSLATION-
dc.subject.keywordPlusDESIGN-
dc.subject.keywordPlusBIODISTRIBUTION-
dc.subject.keywordPlusFORMULATION-
dc.subject.keywordPlusEMULSIONS-
dc.subject.keywordPlusDROPLETS-
dc.subject.keywordPlusPLATFORM-
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