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Related Concept Videos

Insulin Formulations: Types and Delivery01:27

Insulin Formulations: Types and Delivery

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Insulin preparations are categorized by their duration of action into short-acting and long-acting types. Two strategies are used to modify insulin's absorption and pharmacokinetic profile: slowing the absorption post-subcutaneous injection, or altering human insulin's amino acid sequence or protein structure. These changes retain the insulin's ability to bind to the insulin receptor, but alter its behavior in solution or after injection.
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Insulin: Biosynthesis, Chemistry, and Preparation01:25

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The endoplasmic reticulum (ER) of pancreatic β-cells synthesizes preproinsulin, which consists of a signal peptide, A and B chains, and a C-peptide. Preproinsulin is then cleaved and folded into proinsulin, which translocates to the Golgi apparatus for sorting and packaging into secretory granules. In these granules, enzymatic clipping generates insulin and C-peptide.
Damage or functional impairment of β-cells inhibits insulin production, leading to diabetes. Diabetes treatment...
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Insulin: Dosing Regimen and Adverse Effects01:16

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Insulin-replacement therapy usually includes both long-acting insulin (basal) and short-acting insulin (to cater to postprandial needs). In a diverse group of type 1 diabetes patients, the average daily insulin dose is typically 0.5-0.7 units/kg body weight. However, obese patients and pubertal adolescents may need more due to insulin resistance.
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Repaglinide (Prandin) and Nateglinide (Starlix), known as glinides, are oral insulin secretagogues that stimulate insulin release from pancreatic β cells by closing the ATP-sensitive potassium channels (KATP channel). Repaglinide controls insulin release from pancreatic β cells by managing potassium efflux. It shares two binding sites with sulfonylureas and also has a unique site, indicating overlapping mechanisms of action. With a rapid onset and a 4-7 hour duration, it effectively...
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Insulin secretory vesicles release insulin to stimulate blood glucose uptake and regulate carbohydrate metabolism. When the blood glucose levels increase, glucose enters the pancreatic β-islet cells through glucose transporters. Once inside, glucose is metabolized through glycolysis, the citric acid cycle, and the electron transport chain, producing ATP. This increase in ATP concentration closes ATP-sensitive potassium channels, leading to depolarization of the membrane and the opening of...
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Refining Insulin on Board with netIOB for Automated Insulin Delivery.

Michael C Riddell1, Dana M Lewis2, Lauren V Turner1

  • 1School of Kinesiology & Health Science, Muscle Health Research Centre, York University, Toronto, ON, Canada.

Journal of Diabetes Science and Technology
|August 15, 2024
PubMed
Summary

Automated insulin delivery (AID) systems improve glucose control, but the "insulin on board" (IOB) metric can be misleading. Current IOB displays don't accurately reflect real-time insulin action or dynamic adjustments in AID systems.

Keywords:
automated insulin deliverybasal insulinbolus insulincontinuous glucose monitoringcontinuous subcutaneous insulin infusioninsulin on boardmultiple daily injectionsopen-loop controltype 1 diabetes

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Area of Science:

  • Endocrinology
  • Biomedical Engineering
  • Diabetes Technology

Background:

  • Automated insulin delivery (AID) systems significantly improve glycemic control in diabetes management.
  • A common feature in AID systems is the display of "insulin on board" (IOB) to prevent insulin stacking and inform dosing decisions.
  • Current IOB metrics aim to help users understand insulin action and predict hypoglycemia risk.

Purpose of the Study:

  • To examine the evolution of the "insulin on board" (IOB) metric in automated insulin delivery (AID) systems.
  • To highlight the limitations of current IOB presentations in accurately reflecting real-time insulin action and dynamic adjustments.
  • To discuss the implications of misleading IOB data for users of AID systems.

Main Methods:

  • This is a commentary, not an experimental study.
  • Analysis of the historical development and current implementation of IOB in AID systems.
  • Discussion of the physiological and technological factors influencing insulin action.

Main Results:

  • The presentation of IOB in current AID systems can be misleading.
  • Existing IOB metrics do not fully capture the dynamic and automatic insulin adjustments made by AID systems.
  • IOB does not accurately reflect true insulin action across varying physiological states.

Conclusions:

  • The current "insulin on board" metric in AID systems has significant limitations.
  • There is a need for improved IOB representations that better reflect real-time insulin dynamics and AID system adjustments.
  • More accurate IOB metrics are crucial for safe and effective use of AID systems and preventing glucose management errors.