Development of porous PLGA/PEI1.8k biodegradable microspheres for the delivery of mesenchymal stem cells (MSCs)

被引:41
作者
Lee, Young Sook [1 ]
Lim, Kwang Suk [1 ]
Oh, Jung-Eun [2 ]
Yoon, A-Rum [2 ]
Joo, Wan Seok [3 ]
Kim, Hyun Soo [3 ]
Yun, Chae-Ok [2 ]
Kim, SungWan [1 ,2 ]
机构
[1] Univ Utah, Ctr Controlled Chem Delivery, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT 84112 USA
[2] Hanyang Univ, Dept Bioengn, Seoul 133791, South Korea
[3] Pharmicell Co Ltd, Songnam, South Korea
关键词
PLGA; Porous microparticle; Mesenchymal stem cell; Human stem cell; Cell therapy; PEI1.8k; POTENTIAL APPLICATIONS; GENE DELIVERY; IN-VITRO; THERAPY; THERAPEUTICS; CARRIERS; BIOLOGY; REPAIR;
D O I
10.1016/j.jconrel.2015.01.004
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Multipotent 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.
引用
收藏
页码:128 / 133
页数:6
相关论文
共 27 条
[1]
Our Top 10 Developments in Stem Cell Biology over the Last 30 Years [J].
Armstrong, Lyle ;
Lako, Majlinda ;
Buckley, Noel ;
Lappin, Terry R. J. ;
Murphy, Martin J. ;
Nolta, Jan A. ;
Pittenger, Mark ;
Stojkovic, Miodrag .
STEM CELLS, 2012, 30 (01) :2-9
[2]
Stem Cells and Their Role in Renal Ischaemia Reperfusion Injury [J].
Bagul, Atul ;
Frost, Jodie H. ;
Drage, Martin .
AMERICAN JOURNAL OF NEPHROLOGY, 2013, 37 (01) :16-29
[3]
Bone marrow stromal stem cells: Nature, biology, and potential applications [J].
Bianco, P ;
Riminucci, M ;
Gronthos, S ;
Robey, PG .
STEM CELLS, 2001, 19 (03) :180-192
[4]
Biodegradable porous beads and their potential applications in regenerative medicine [J].
Choi, Sung-Wook ;
Zhang, Yu ;
Yeh, Yi-Chun ;
Wooten, A. Lake ;
Xia, Younan .
JOURNAL OF MATERIALS CHEMISTRY, 2012, 22 (23) :11442-11451
[5]
Hierarchical scaffold design for mesenchymal stem cell-based gene therapy of hemophilia B [J].
Coutu, Daniel L. ;
Cuerquis, Jessica ;
El Ayoubi, Rouwayda ;
Forner, Kathy-Ann ;
Roy, Ranjan ;
Francois, Moira ;
Griffith, May ;
Lillicrap, David ;
Yousefi, Azizeh-Mitra ;
Blostein, Mark D. ;
Galipeau, Jacques .
BIOMATERIALS, 2011, 32 (01) :295-305
[6]
Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement [J].
Dominici, M. ;
Le Blanc, K. ;
Mueller, I. ;
Slaper-Cortenbach, I. ;
Marini, F. C. ;
Krause, D. S. ;
Deans, R. J. ;
Keating, A. ;
Prockop, D. J. ;
Horwitz, E. M. .
CYTOTHERAPY, 2006, 8 (04) :315-317
[7]
PLGA/PEG-derivative polymeric matrix for drug delivery system applications:: Characterization and cell viability studies [J].
Fernandez-Carballido, A. ;
Pastoriza, P. ;
Barcia, E. ;
Montejo, C. ;
Negro, S. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2008, 352 (1-2) :50-57
[8]
From the laboratory bench to the patients bedside: An update on clinical trials with mesenchymal stem cells [J].
Giordano, Antonio ;
Galderisi, Umberto ;
Marino, Ignazio R. .
JOURNAL OF CELLULAR PHYSIOLOGY, 2007, 211 (01) :27-35
[9]
Influence of PEI as a core modifying agent on PLGA microspheres of PGE1, a pulmonary selective vasodilator [J].
Gupta, Vivek ;
Ahsan, Fakhrul .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2011, 413 (1-2) :51-62
[10]
Water-soluble lipopolymer for gene delivery [J].
Han, SO ;
Mahato, RI ;
Kim, SW .
BIOCONJUGATE CHEMISTRY, 2001, 12 (03) :337-345