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• W2331769508 abstract "Problems associated with islet transplantation for Type 1 Diabetes (T1D) such as shortage of donor cells, use of immunosuppressive drugs remain as major challenges. Immune isolation using encapsulation may circumvent the use of immunosuppressants and prolong the longevity of transplanted islets. The encapsulating membrane must block the passage of host's immune components while providing sufficient exchange of glucose, insulin and other small molecules. We report the development and characterization of a new generation of semipermeable ultrafiltration membrane, the silicon nanopore membrane (SNM), designed with approximately 7 nm-wide slit-pores to provide middle molecule selectivity by limiting passage of pro-inflammatory cytokines. Moreover, the use of convective transport with a pressure differential across the SNM overcomes the mass transfer limitations associated with diffusion through nanometer-scale pores. The SNM exhibited a hydraulic permeability of 130 ml/hr/m(2)/mmHg, which is more than 3 fold greater than existing polymer membranes. Analysis of sieving coefficients revealed 80% reduction in cytokines passage through SNM under convective transport. SNM protected encapsulated islets from infiltrating cytokines and retained islet viability over 6 hours and remained responsive to changes in glucose levels unlike non-encapsulated controls. Together, these data demonstrate the novel membrane exhibiting unprecedented hydraulic permeability and immune-protection for islet transplantation therapy." @default.
• W2331769508 created "2016-06-24" @default.
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• W2331769508 date "2016-03-24" @default.
• W2331769508 modified "2023-10-16" @default.
• W2331769508 title "Silicon nanopore membrane (SNM) for islet encapsulation and immunoisolation under convective transport" @default.
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• W2331769508 doi "https://doi.org/10.1038/srep23679" @default.
• W2331769508 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4806308" @default.
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• W2331769508 hasPublicationYear "2016" @default.
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