Vascularization and cellular isolation potential of a novel electrospun cell delivery vehicle.
Vascularization and cellular isolation potential of a novel electrospun cell delivery vehicle.
复制标题
新型电纺细胞输送载体的血管化和细胞分离潜力。
DOI:
10.1002/jbm.a.34900
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发表时间:
2014
期刊:
影响因子:
--
通讯作者:
Williams,StuartK
中科院分区:
文献类型:
--
作者:
Krishnan,Laxminarayanan;Touroo,Jeremy;Reed,Robert;Boland,Eugene;Hoying,JamesB;Williams,StuartK
A clinical need exists for a cell delivery device that supports long‐term cell viability, cell retention within the device and retrieval of delivered cells if necessary. Previously, cell isolation devices have been based on hollow fiber membranes, porous polymer scaffolds, alginate systems, or micro‐machined membranes. We present the development and characterization of a novel dual porosity electrospun membrane based device, which supports cellular infiltration and vascularization of its outer porous layer and maintains cellular isolation within a lumen bounded by an inner low porosity layer. Electrospinning conditions were initially established to support electrospun fiber deposition onto nonconductive silicone surfaces. With these parameters established, devices forin vivoevaluations were produced using nylon as a nonconductive scaffold for deposition of dual porosity electrospun fibers. The outer porous layer supported the development of a penetrating microcirculation and the membrane supported the transfer of insulin from encapsulated sustained release pellets for 4 weeks. Viable cells implanted within the device could be identified after 2 weeks of implantation. Through the successful demonstration of survival and cellular isolation of human epithelial cells within the implanted devices and the ability to use the device to deliver insulin, we have established the utility of this device toward localized cell transplantation. The cell delivery device establishes a platform to test the feasibility of approaches to cell dose control and cell localization at the site of implantation in the clinical use of modified autologous or allogeneic cells. © 2013 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 102A: 2208–2219, 2014.
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DOI:
10.1016/s1054-8807(97)00061-6
发表时间:
1998
期刊:
Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology
影响因子:
--
作者:
K. Dědič;Tomas Klima;D. A. Cooley;O. Frazier;K. Kadipasaoglu;Hasan B. Cihan
通讯作者:
Hasan B. Cihan
DOI:
10.1557/proc-530-7
发表时间:
1998
期刊:
MRS Proceedings
影响因子:
--
作者:
T. Desai;D. Hansford;W. Chu;T. Huen;M. Ferrari
通讯作者:
M. Ferrari
影响因子:
0.9
作者:
J. Brauker;L. Martinson;R. Hill;S. Young;V. Carr;R. C. Johnson
通讯作者:
R. C. Johnson
影响因子:
2.8
作者:
Desai, Tejal A.;Chu, Wen Hwa;Ferrari, Mauro
通讯作者:
Ferrari, Mauro
影响因子:
--
作者:
Griffith, CK;Miller, C;George, SC
通讯作者:
George, SC