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dc.contributor.authorLangholz, Jana
dc.contributor.authorDavari Benam, Karim
dc.contributor.authorSharan, Bindu
dc.contributor.authorGros, Sebastien Nicolas
dc.contributor.authorFougner, Anders Lyngvi
dc.date.accessioned2023-08-15T10:51:25Z
dc.date.available2023-08-15T10:51:25Z
dc.date.created2023-06-16T12:04:51Z
dc.date.issued2023
dc.identifier.isbn978-3-907144-09-1
dc.identifier.urihttps://hdl.handle.net/11250/3084121
dc.description.abstractTreatment of type 1 diabetes mellitus is significantly improved by using commercially available hybrid closed-loop systems to deliver insulin. These systems, also called artificial pancreas (AP), use the subcutaneous (SC) route to deliver insulin. However, meal announcements are necessary due to the slow insulin absorption from the SC tissue. Thus due to the need for human intervention, it is called “hybrid closed loop” AP. In this work, a bi-hormonal AP with intraperitoneal (IP) infusion is designed to increase the time within the range of 3.9–10.0 mmol/l and alleviate the burden of meal announcements. A two-layer controller is designed to provide safe and effective insulin and glucagon delivery. The primary layer is based on classical PID controllers for insulin and glucagon, and the supervisory layer includes four parts: (A) Zone-based control settings, (B) Extrapolation of sensor data to compensate for sensor delay in SC tissue, (C) Auto-tuning of the PID parameters in the primary layer through simulation in an animal model, and (D) Safety barriers. The controller is designed to prevent hypoglycemia after meals and during physical activity, as well as prevent postprandial hyperglycemia. The designed AP achieved 92.5% of the time within the range of 3.9–10.0 mmol/l on a simulator trained on data from animal experiments. The results indicate that this two-layer control structure with IP infusions makes it feasible to achieve a fully automated artificial pancreas without the need for meal announcements, i.e. without human intervention.en_US
dc.language.isoengen_US
dc.publisherInstitute of Electrical and Electronics Engineers (IEEE)en_US
dc.relation.ispartofProceedings of the 2023 European Control Conference (ECC)
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectType 1 diabetesen_US
dc.subjectType 1 diabetesen_US
dc.subjectAutomatisk glukosereguleringen_US
dc.subjectClosed loop glucose controlen_US
dc.subjectIntraperitoneal insulininfusjonen_US
dc.subjectIntraperitoneal insulin infusionen_US
dc.subjectKunstig bukspyttkjertelen_US
dc.subjectArtificial Pancreasen_US
dc.titleFully Automated Bi-Hormonal Intraperitoneal Artificial Pancreas Using a Two-Layer PID Control Schemeen_US
dc.title.alternativeFully Automated Bi-Hormonal Intraperitoneal Artificial Pancreas Using a Two-Layer PID Control Schemeen_US
dc.typeChapteren_US
dc.description.versionacceptedVersionen_US
dc.subject.nsiVDP::Medisinsk teknologi: 620en_US
dc.subject.nsiVDP::Medical technology: 620en_US
dc.source.pagenumber186-193en_US
dc.identifier.doi10.23919/ECC57647.2023.10178295
dc.identifier.cristin2155243
dc.relation.projectNorges forskningsråd: 248872en_US
cristin.ispublishedtrue
cristin.fulltextpostprint


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Navngivelse 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Navngivelse 4.0 Internasjonal