Bioactive Materials for Use in Stem Cell Therapies for the Treatment of Type 1 Diabetes
Pluripotent Stem Cell Therapy for Diabetes, First Edition, Page: 221-250
2024
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
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Book Chapter Description
Diabetes is a major challenge to healthcare providers globally, with significant human and financial costs. Type 1 diabetes is expected to effect more than a million people concurrently, with over 130,000 newly identified cases every year (Standl et al., Eur J Prev Cardiol 26(2_suppl): 7-14, 2019; International Diabetes Federation. IDF Diabetes Atlas, 2017). Whilst treatments involving insulin injections have proven to be more successful than transplantations, the rising cost of insulin and donor shortages have prompted researchers to look for more permanent insulin replacement therapy (IRT) options. One of these proposed options has been the immune-isolation and implantation of healthy islets, which can maintain normoglycaemia whilst remaining “invisible” to the endogenous immune system (Correia, Adv Funct Mater 30(26): 1908061, 2020). This chapter will describe the bioactive materials used for Immunoisolative Insulin Replacement Therapy (IRT) and will evaluate the successes and failures of IRT devices, both in the laboratory and in the clinic. We will also discuss the proposed optimizations to the IRT device design for the development of a semi-artificial pancreas, to improve insulin release and islet viability, whilst reducing fibrotic overgrowth and immune response.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85204842386&origin=inward; http://dx.doi.org/10.1007/978-3-031-41943-0_11; https://link.springer.com/10.1007/978-3-031-41943-0_11; https://dx.doi.org/10.1007/978-3-031-41943-0_11; https://link.springer.com/chapter/10.1007/978-3-031-41943-0_11
Springer Science and Business Media LLC
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