Superporous agarose scaffolds for encapsulation of adult human islets and human stem-cell-derived β cells for intravascular bioartificial pancreas applications.
Superporous agarose scaffolds for encapsulation of adult human islets and human stem-cell-derived β cells for intravascular bioartificial pancreas applications.
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用于封装成人胰岛和人类干细胞衍生的 β 细胞的超孔琼脂糖支架,用于血管内生物人工胰腺应用。
DOI:
10.1002/jbm.a.37236
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发表时间:
2021
期刊:
影响因子:
--
通讯作者:
Roy,Shuvo
中科院分区:
文献类型:
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作者:
Shaheen,Rebecca;Gurlin,RachelE;Gologorsky,Rebecca;Blaha,Charles;Munnangi,Pujita;Santandreu,Ana;Torres,Alonso;Carnese,Phichitpol;Nair,GopikaG;Szot,Gregory;Fissell,WilliamH;Hebrok,Matthias;Roy,Shuvo
Type 1 diabetic patients with severe hypoglycemia unawareness have benefitted from cellular therapies, such as pancreas or islet transplantation; however, donor shortage and the need for immunosuppression limits widespread clinical application. We previously developed an intravascular bioartificial pancreas (iBAP) using silicon nanopore membranes (SNM) for immunoprotection. To ensure ample nutrient delivery, the iBAP will need a cell scaffold with high hydraulic permeability to provide mechanical support and maintain islet viability and function. Here, we examine the feasibility of superporous agarose (SPA) as a potential cell scaffold in the iBAP. SPA exhibits 66‐fold greater hydraulic permeability than the SNM along with a short (<10 μm) diffusion distance to the nearest islet. SPA also supports short‐term functionality of both encapsulated human islets and stem‐cell‐derived enriched β‐clusters in a convection‐based system, demonstrated by high viability (>95%) and biphasic insulin responses to dynamic glucose stimulus. These findings suggest that the SPA scaffold will not limit nutrient delivery in a convection‐based bioartificial pancreas and merits continued investigation.
DOI:
--
发表时间:
2003
期刊:
影响因子:
--
作者:
P. Gustavsson;P. Larsson
通讯作者:
P. Larsson
DOI:
--
发表时间:
2009
期刊:
影响因子:
--
作者:
P. Gustavsson;Peter Tiainen;P. Larsson
通讯作者:
P. Larsson