Intraperitoneal Insulin Delivery: Evidence of a Physiological Route for Artificial Pancreas From Compartmental Modeling
Creators
- 1. Department of Woman's and Child's Health, University of Padova, Padova, Italy
- 2. Department of Woman's and Child's Health, University of Padova, Padova, Italy and Hôpital Necker-Enfants Malades, Paris, France
- 3. Harvard John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA
- 4. Department of Chemical Engineering, University of California, Santa Barbara, Santa Barbara, CA, USA
- 5. Department of Endocrinology, Diabetes, Nutrition and INSERM Clinical Investigation Center 1411, University Hospital of Montpellier, Montpellier, France Institute of Functional Genomics, CNRS, INSERM, University of Montpellier, Montpellier, France
- 6. Department of Electrical, Computer and Biomedical Engineering, University of Pavia, Pavia, Italy
Description
Background: Intraperitoneal insulin delivery has proven to safely overcome a major limit of subcutaneous delivery—meal announcement—and has been able to optimize glycemic control in adults under controlled experimental conditions. In addition, intraperitoneal delivery avoids peripheral hyperinsulinemia resulting from the subcutaneous route and restores a physiological liver gradient.
Methods: Relying on a unique data set of intraperitoneal closed-loop insulin delivery obtained with a Model Predictive Controller (MPC), we develop a compartmental model of intraperitoneal insulin kinetics, which, once included in the UVa/Padova T1D simulator, will facilitate the investigation of various control strategies, for example, the simpler Proportional Integral Derivative controller versus MPC.
Results: Intraperitoneal insulin kinetics can be described with a 2-compartment model including liver and plasma.
Conclusion: Intraperitoneal insulin transit is fast enough to render irrelevant the addition of a peritoneal compartment, proving the peritoneum being a virtual—not actual—transit space for insulin delivery.
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