Please use this identifier to cite or link to this item: https://doi.org/10.1038/s41598-018-20516-9
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dc.titlePolymerization-Induced Phase Separation Formation of Structured Hydrogel Particles via Microfluidics for Scar Therapeutics
dc.contributor.authorGuo, S
dc.contributor.authorKang, G
dc.contributor.authorPhan, D.T
dc.contributor.authorHsu, M.N
dc.contributor.authorPor, Y.C
dc.contributor.authorChen, C.H
dc.date.accessioned2020-09-09T03:04:54Z
dc.date.available2020-09-09T03:04:54Z
dc.date.issued2018
dc.identifier.citationGuo, S, Kang, G, Phan, D.T, Hsu, M.N, Por, Y.C, Chen, C.H (2018). Polymerization-Induced Phase Separation Formation of Structured Hydrogel Particles via Microfluidics for Scar Therapeutics. Scientific Reports 8 (1) : 2245. ScholarBank@NUS Repository. https://doi.org/10.1038/s41598-018-20516-9
dc.identifier.issn20452322
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/175030
dc.description.abstractExcessive scar formation can form disabling contractures that result in a debilitating psychological outcome. Sustainable hydrophobic corticosteroid release in vivo is essential to regulate the wound healing process. Functional hydrogel particles are widely applied for sustainable release. However, due to the limited aqueous solubility of hydrophobic compounds, most of the corticosteroid is released from the hydrogels within seconds, causing undesirable scar formation and recurrence. In this study, a novel polymerization-induced phase separation is investigated to form well-defined polyethylene glycol diacrylate (PEGDA) core/alginate shell structured hydrogel particles using microfluidics without toxic organic solvents. Based on their wettability preference, hydrophobic corticosteroid-loaded poly(lactic-co-glycolic acid) (PLGA) nanoparticles are compartmentalized in the PEGDA core during polymerization to control the corticosteroid release. The distribution of the PLGA nanoparticles is precisely regulated by the phase separation boundary and characterized using a fluorescent dye. The thickness of the shell and partition coefficients are determined using the UV intensity and irradiation period. Upon encapsulation of the PLGA nanoparticles within the poly(PEGDA) core, a long-term corticosteroid treatment is developed and effective scar therapeutic outcomes are evaluated using both in vitro and in vivo models. © 2018 The Author(s).
dc.sourceUnpaywall 20200831
dc.subjectcorticosteroid
dc.subjectdrug carrier
dc.subjectnanoparticle
dc.subjectpolyethylene glycol dimethacrylate hydrogel
dc.subjectanimal
dc.subjectchemical phenomena
dc.subjectchemistry
dc.subjectdrug therapy
dc.subjectfemale
dc.subjecthydrogel
dc.subjectLeporidae
dc.subjectmicrofluidics
dc.subjectphysiology
dc.subjectprocedures
dc.subjectscar
dc.subjectwound healing
dc.subjectAdrenal Cortex Hormones
dc.subjectAnimals
dc.subjectCicatrix
dc.subjectDrug Carriers
dc.subjectFemale
dc.subjectHydrogel, Polyethylene Glycol Dimethacrylate
dc.subjectHydrogels
dc.subjectHydrophobic and Hydrophilic Interactions
dc.subjectMicrofluidics
dc.subjectNanoparticles
dc.subjectPolylactic Acid-Polyglycolic Acid Copolymer
dc.subjectRabbits
dc.subjectWound Healing
dc.typeArticle
dc.contributor.departmentBIOMEDICAL ENGINEERING
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.1038/s41598-018-20516-9
dc.description.sourcetitleScientific Reports
dc.description.volume8
dc.description.issue1
dc.description.page2245
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