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|a dc
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|a Evron, Yoav
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|a Massachusetts Institute of Technology. Department of Chemical Engineering
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|a Colton, Clark K
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|a DiIenno, Amanda Rose
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|a Colton, Clark K.
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|a Ludwig, Barbara
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|a Weir, Gordon C.
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|a Zimermann, Baruch
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|a Maimon, Shiri
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|a Neufeld, Tova
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|a Shalev, Nurit
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|a Goldman, Tali
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|a Leon, Assaf
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|a Yavriyants, Karina
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|a Shabtay, Noa
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|a Rozenshtein, Tania
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|a Azarov, Dimitri
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|a DiIenno, Amanda R.
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|a Steffen, Anja
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|a de Vos, Paul
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|a Bornstein, Stefan R.
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|a Barkai, Uriel
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|a Rotem, Avi
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|a Colton, Clark K
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|a DiIenno, Amanda Rose
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|a Long-term viability and function of transplanted islets macroencapsulated at high density are achieved by enhanced oxygen supply
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|b Springer Nature,
|c 2018-10-22T18:49:14Z.
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|z Get fulltext
|u http://hdl.handle.net/1721.1/118745
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|a Transplantation of encapsulated islets can cure diabetes without immunosuppression, but oxygen supply limitations can cause failure. We investigated a retrievable macroencapsulation device wherein islets are encapsulated in a planar alginate slab and supplied with exogenous oxygen from a replenishable gas chamber. Translation to clinically-useful devices entails reduction of device size by increasing islet surface density, which requires increased gas chamber pO[subscript 2]. Here we show that islet surface density can be substantially increased safely by increasing gas chamber pO[subscript 2] to a supraphysiological level that maintains all islets viable and functional. These levels were determined from measurements of pO[subscript 2] profiles in islet-alginate slabs. Encapsulated islets implanted with surface density as high as 4,800 islet equivalents/cm[superscrip 3] in diabetic rats maintained normoglycemia for more than 7 months and provided near-normal intravenous glucose tolerance tests. Nearly 90% of the original viable tissue was recovered after device explantation. Damaged islets failed after progressively shorter times. The required values of gas chamber p[subscript O] were predictable from a mathematical model of oxygen consumption and diffusion in the device. These results demonstrate feasibility of developing retrievable macroencapsulated devices small enough for clinical use and provide a firm basis for design of devices for testing in large animals and humans.
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|a Israel. Ministry of Science
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|a Article
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|t Scientific Reports
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