Preclinical Development of the Islet Sheet
: The Islet Sheet is a thin planar bioartificial endocrine pancreas fabricated by gelling highly purified alginate and islets of Langerhans. Acellular alginate layers form a uniform immunoprotective barrier to host rejection of the encapsulated cells, with the tissue nourished by passive diffusion f...
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Veröffentlicht in: | Annals of the New York Academy of Sciences 2001-11, Vol.944 (1), p.252-266 |
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creator | STORRS, RICHARD DORIAN, RANDY KING, SCOTT R. LAKEY, JONATHAN RILO, HORACIO |
description | : The Islet Sheet is a thin planar bioartificial endocrine pancreas fabricated by gelling highly purified alginate and islets of Langerhans. Acellular alginate layers form a uniform immunoprotective barrier to host rejection of the encapsulated cells, with the tissue nourished by passive diffusion from adjacent host tissue. The overall thickness of the Islet Sheet, 250 μm, is chosen to maximize nutrient diffusion. In this paper we describe the early development of the Islet Sheet, including purification and fractionation of the alginates used, difficulties in maintaining sheet planarity, and preliminary metabolic studies in pancreatectomized dogs. In a key experiment, approximately 75,000 allogeneic islet equivalents in six Islet Sheets were sutured to the omentum of a 7‐kg female beagle dog at the time of pancreatectomy. Fasting euglycemia was maintained for 84 days. Fed blood sugars were usually below 150 mg/dL. A single injection of 2 U insulin was administered on day 9, and antibiotics were administered for two weeks. No other drugs were used. IVGTT post implant was not normal, but seemed to improve between 30 and 60 days. Upon omentectomy and sheet removal the metabolic parameters deteriorated to a frankly diabetic state within seven days. The sheets did not remain flat, but fragments were recovered within hard, mostly acellular capsules. Dithizone staining showed islets within alginate sheets recovered from the interior of these capsules, suggesting that allogeneic islet tissue survived 84 days and was responsible for maintaining fasting euglycemia. |
doi_str_mv | 10.1111/j.1749-6632.2001.tb03837.x |
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Acellular alginate layers form a uniform immunoprotective barrier to host rejection of the encapsulated cells, with the tissue nourished by passive diffusion from adjacent host tissue. The overall thickness of the Islet Sheet, 250 μm, is chosen to maximize nutrient diffusion. In this paper we describe the early development of the Islet Sheet, including purification and fractionation of the alginates used, difficulties in maintaining sheet planarity, and preliminary metabolic studies in pancreatectomized dogs. In a key experiment, approximately 75,000 allogeneic islet equivalents in six Islet Sheets were sutured to the omentum of a 7‐kg female beagle dog at the time of pancreatectomy. Fasting euglycemia was maintained for 84 days. Fed blood sugars were usually below 150 mg/dL. A single injection of 2 U insulin was administered on day 9, and antibiotics were administered for two weeks. No other drugs were used. IVGTT post implant was not normal, but seemed to improve between 30 and 60 days. Upon omentectomy and sheet removal the metabolic parameters deteriorated to a frankly diabetic state within seven days. The sheets did not remain flat, but fragments were recovered within hard, mostly acellular capsules. Dithizone staining showed islets within alginate sheets recovered from the interior of these capsules, suggesting that allogeneic islet tissue survived 84 days and was responsible for maintaining fasting euglycemia.</description><identifier>ISSN: 0077-8923</identifier><identifier>EISSN: 1749-6632</identifier><identifier>DOI: 10.1111/j.1749-6632.2001.tb03837.x</identifier><identifier>PMID: 11797674</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>alginate ; Animals ; Anti-Bacterial Agents - administration & dosage ; Bioartificial Organs ; bioartificial pancreas ; Blood Glucose - analysis ; diabetes ; Dogs ; Female ; Glucose Tolerance Test ; Insulin - administration & dosage ; islet transplantation ; Islets of Langerhans ; Membranes, Artificial ; microencapsulation ; Microscopy, Electron, Scanning ; Pancreas, Artificial</subject><ispartof>Annals of the New York Academy of Sciences, 2001-11, Vol.944 (1), p.252-266</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4092-f7a9b4754c20303a92d0343c9e0ab135328ea643f5acd327c5b9d32949d88de23</citedby><cites>FETCH-LOGICAL-c4092-f7a9b4754c20303a92d0343c9e0ab135328ea643f5acd327c5b9d32949d88de23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1749-6632.2001.tb03837.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1749-6632.2001.tb03837.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11797674$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>STORRS, RICHARD</creatorcontrib><creatorcontrib>DORIAN, RANDY</creatorcontrib><creatorcontrib>KING, SCOTT R.</creatorcontrib><creatorcontrib>LAKEY, JONATHAN</creatorcontrib><creatorcontrib>RILO, HORACIO</creatorcontrib><title>Preclinical Development of the Islet Sheet</title><title>Annals of the New York Academy of Sciences</title><addtitle>Ann N Y Acad Sci</addtitle><description>: The Islet Sheet is a thin planar bioartificial endocrine pancreas fabricated by gelling highly purified alginate and islets of Langerhans. Acellular alginate layers form a uniform immunoprotective barrier to host rejection of the encapsulated cells, with the tissue nourished by passive diffusion from adjacent host tissue. The overall thickness of the Islet Sheet, 250 μm, is chosen to maximize nutrient diffusion. In this paper we describe the early development of the Islet Sheet, including purification and fractionation of the alginates used, difficulties in maintaining sheet planarity, and preliminary metabolic studies in pancreatectomized dogs. In a key experiment, approximately 75,000 allogeneic islet equivalents in six Islet Sheets were sutured to the omentum of a 7‐kg female beagle dog at the time of pancreatectomy. Fasting euglycemia was maintained for 84 days. Fed blood sugars were usually below 150 mg/dL. A single injection of 2 U insulin was administered on day 9, and antibiotics were administered for two weeks. No other drugs were used. IVGTT post implant was not normal, but seemed to improve between 30 and 60 days. Upon omentectomy and sheet removal the metabolic parameters deteriorated to a frankly diabetic state within seven days. The sheets did not remain flat, but fragments were recovered within hard, mostly acellular capsules. Dithizone staining showed islets within alginate sheets recovered from the interior of these capsules, suggesting that allogeneic islet tissue survived 84 days and was responsible for maintaining fasting euglycemia.</description><subject>alginate</subject><subject>Animals</subject><subject>Anti-Bacterial Agents - administration & dosage</subject><subject>Bioartificial Organs</subject><subject>bioartificial pancreas</subject><subject>Blood Glucose - analysis</subject><subject>diabetes</subject><subject>Dogs</subject><subject>Female</subject><subject>Glucose Tolerance Test</subject><subject>Insulin - administration & dosage</subject><subject>islet transplantation</subject><subject>Islets of Langerhans</subject><subject>Membranes, Artificial</subject><subject>microencapsulation</subject><subject>Microscopy, Electron, Scanning</subject><subject>Pancreas, Artificial</subject><issn>0077-8923</issn><issn>1749-6632</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkE1PwkAQhjdGI4j-BdN48GDSul_tdr0YggokBDVgjKfNdjsNxUKxWxT-vW3a4Nm5zGGeeSfzIHRFsEequl16RHDpBgGjHsWYeGWEWciEtztC3cPoGHUxFsINJWUddGbtskJpyMUp6hAipAgE76KblwJMlq5TozPnAb4hyzcrWJdOnjjlApyxzaB0ZguA8hydJDqzcNH2Hnp7epwPRu7keTge9Ceu4VhSNxFaRlz43FDMMNOSxphxZiRgHRHmMxqCDjhLfG1iRoXxI1l1yWUchjFQ1kPXTe6myL-2YEu1Sq2BLNNryLdWCcqxYJxU4F0DmiK3toBEbYp0pYu9IljVptRS1TpUrUPVplRrSu2q5cv2yjZaQfy32qqpgPsG-Ekz2P8jWk0_-jPq14-4TUJqS9gdEnTxqQLBhK_ep0M1mrzOqZhTNWO_hIiGOw</recordid><startdate>200111</startdate><enddate>200111</enddate><creator>STORRS, RICHARD</creator><creator>DORIAN, RANDY</creator><creator>KING, SCOTT R.</creator><creator>LAKEY, JONATHAN</creator><creator>RILO, HORACIO</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200111</creationdate><title>Preclinical Development of the Islet Sheet</title><author>STORRS, RICHARD ; DORIAN, RANDY ; KING, SCOTT R. ; LAKEY, JONATHAN ; RILO, HORACIO</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4092-f7a9b4754c20303a92d0343c9e0ab135328ea643f5acd327c5b9d32949d88de23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>alginate</topic><topic>Animals</topic><topic>Anti-Bacterial Agents - administration & dosage</topic><topic>Bioartificial Organs</topic><topic>bioartificial pancreas</topic><topic>Blood Glucose - analysis</topic><topic>diabetes</topic><topic>Dogs</topic><topic>Female</topic><topic>Glucose Tolerance Test</topic><topic>Insulin - administration & dosage</topic><topic>islet transplantation</topic><topic>Islets of Langerhans</topic><topic>Membranes, Artificial</topic><topic>microencapsulation</topic><topic>Microscopy, Electron, Scanning</topic><topic>Pancreas, Artificial</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>STORRS, RICHARD</creatorcontrib><creatorcontrib>DORIAN, RANDY</creatorcontrib><creatorcontrib>KING, SCOTT R.</creatorcontrib><creatorcontrib>LAKEY, JONATHAN</creatorcontrib><creatorcontrib>RILO, HORACIO</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Annals of the New York Academy of Sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>STORRS, RICHARD</au><au>DORIAN, RANDY</au><au>KING, SCOTT R.</au><au>LAKEY, JONATHAN</au><au>RILO, HORACIO</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preclinical Development of the Islet Sheet</atitle><jtitle>Annals of the New York Academy of Sciences</jtitle><addtitle>Ann N Y Acad Sci</addtitle><date>2001-11</date><risdate>2001</risdate><volume>944</volume><issue>1</issue><spage>252</spage><epage>266</epage><pages>252-266</pages><issn>0077-8923</issn><eissn>1749-6632</eissn><abstract>: The Islet Sheet is a thin planar bioartificial endocrine pancreas fabricated by gelling highly purified alginate and islets of Langerhans. Acellular alginate layers form a uniform immunoprotective barrier to host rejection of the encapsulated cells, with the tissue nourished by passive diffusion from adjacent host tissue. The overall thickness of the Islet Sheet, 250 μm, is chosen to maximize nutrient diffusion. In this paper we describe the early development of the Islet Sheet, including purification and fractionation of the alginates used, difficulties in maintaining sheet planarity, and preliminary metabolic studies in pancreatectomized dogs. In a key experiment, approximately 75,000 allogeneic islet equivalents in six Islet Sheets were sutured to the omentum of a 7‐kg female beagle dog at the time of pancreatectomy. Fasting euglycemia was maintained for 84 days. Fed blood sugars were usually below 150 mg/dL. A single injection of 2 U insulin was administered on day 9, and antibiotics were administered for two weeks. No other drugs were used. IVGTT post implant was not normal, but seemed to improve between 30 and 60 days. Upon omentectomy and sheet removal the metabolic parameters deteriorated to a frankly diabetic state within seven days. The sheets did not remain flat, but fragments were recovered within hard, mostly acellular capsules. Dithizone staining showed islets within alginate sheets recovered from the interior of these capsules, suggesting that allogeneic islet tissue survived 84 days and was responsible for maintaining fasting euglycemia.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>11797674</pmid><doi>10.1111/j.1749-6632.2001.tb03837.x</doi><tpages>15</tpages></addata></record> |
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subjects | alginate Animals Anti-Bacterial Agents - administration & dosage Bioartificial Organs bioartificial pancreas Blood Glucose - analysis diabetes Dogs Female Glucose Tolerance Test Insulin - administration & dosage islet transplantation Islets of Langerhans Membranes, Artificial microencapsulation Microscopy, Electron, Scanning Pancreas, Artificial |
title | Preclinical Development of the Islet Sheet |
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