575 0

Full metadata record

DC FieldValueLanguage
dc.contributor.author윤채옥-
dc.date.accessioned2016-12-08T02:02:51Z-
dc.date.available2016-12-08T02:02:51Z-
dc.date.issued2015-05-
dc.identifier.citationJOURNAL OF CONTROLLED RELEASE, v. 205, Page. 128-133en_US
dc.identifier.issn0168-3659-
dc.identifier.issn1873-4995-
dc.identifier.urihttp://www.sciencedirect.com/science/article/pii/S016836591500005X-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/24745-
dc.description.abstractMultipotent mesenchymal stem cells (MSCs) promise a therapeutic alternative for many debilitating and incurable diseases. However, one of the major limitations for the therapeutic application of human MSC (hMSC) is the lengthy ex vivo expansion time for preparing a sufficient amount of cells due to the low engraftment rate after transplantation. To solve this conundrum, a porous biodegradable polymeric microsphere was investigated as a potential scaffold for the delivery of MSCs. The modified water/oil/water (W-1/O/W-2) double emulsion solvent evaporation method was used for the construction of porous microspheres. PEI1.8k was blended with poly(lactic-co-glycolic acid) (PLGA) to enhance electrostatic cellular attachment to the microspheres. The porous PLGA/PEI1.8k (PPP) particles demonstrated an average particle size of 290 mu m and an average pore size of 14.3 mu m, providing a micro-carrier for the MSC delivery. PPP particles allowed for better attachment of rMSCs than non-porous PLGA/PEI1.8k (NPP) particles and non-porous (NP) and porous PLGA (PP) microspheres. rMSC successfully grew on the PPP particles for 2 weeks in vitro. Next, PPP particles loaded with 3 different amounts of hMSC showed increased in vivo engraftment rates and maintained the stemness characteristics of hMSC compared with hMSCs-alone group in rats 2 weeks after intramyocardial administration. These customized PPP particles for MSC delivery are a biodegradable and injectable scaffold that can be used for clinical applications. (C) 2015 Elsevier B.V. All rights reserved.en_US
dc.description.sponsorshipThis work was financially supported by a grant HL065477 from the National Institute of Health. We would like to thank Sheryl R. Tripp and Blake K. Anderson (ARUP Institute for Clinical & Experimental Pathology, Salt Lake City, UT) for the IHC staining (CD44, CD34).en_US
dc.language.isoenen_US
dc.publisherELSEVIER SCIENCE BVen_US
dc.subjectPLGAen_US
dc.subjectPorous microparticleen_US
dc.subjectMesenchymal stem cellen_US
dc.subjectHuman stem cellen_US
dc.subjectCell therapyen_US
dc.subjectPEI1.8ken_US
dc.titleDevelopment of porous PLGA/PEI1.8k biodegradable microspheres for the delivery of mesenchymal stem cells (MSCs)en_US
dc.typeArticleen_US
dc.relation.volume205-
dc.identifier.doi10.1016/j.jconrel.2015.01.004-
dc.relation.page128-133-
dc.relation.journalJOURNAL OF CONTROLLED RELEASE-
dc.contributor.googleauthorLee, Young Sook-
dc.contributor.googleauthorLim, Kwang Suk-
dc.contributor.googleauthorOh, Jung-Eun-
dc.contributor.googleauthorYoon, A-Rum-
dc.contributor.googleauthorJoo, Wan Seok-
dc.contributor.googleauthorKim, Hyun Soo-
dc.contributor.googleauthorYun, Chae-Ok-
dc.contributor.googleauthorKim, SungWan-
dc.relation.code2015002880-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF ENGINEERING[S]-
dc.sector.departmentDEPARTMENT OF BIOENGINEERING-
dc.identifier.pidchaeok-
dc.identifier.researcherIDP-3698-2015-
dc.identifier.orcidhttp://orcid.org/0000-0002-9466-4531-
Appears in Collections:
COLLEGE OF ENGINEERING[S](공과대학) > BIOENGINEERING(생명공학과) > Articles
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML


qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE