Synthetic material selection method, material manufacturing method, synthetic material selection data structure, and manufacturing method
US-2024420808-A1 · Dec 19, 2024 · US
US10169544B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10169544-B2 |
| Application number | US-201414902731-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 3, 2014 |
| Priority date | Jul 3, 2013 |
| Publication date | Jan 1, 2019 |
| Grant date | Jan 1, 2019 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
A simulator for in-silico testing of Type 1 diabetes patients uses a model that puts in relation plasma concentrations, i.e., glucose G and insulin /, with glucose fluxes, i.e. endogenous glucose production (EGP), glucose rate of appearance (Ra), glucose utilization by the tissues (U), renal extraction (E), and insulin fluxes, i.e., rate of insulin appearance from the subcutaneous tissues (SC) and insulin degradation (D). A module is also included to describe counter-regulation, i.e. glucagon kinetics, secretion and action. A glucagon subcutaneous absorption model enables simulation of dual hormone control.
Opening claim text (preview).
What is claimed is: 1. An electronic system that simulates a glucose-insulin metabolic system of a T1DM subject, comprising: an electronic subsystem configured to model dynamic glucose concentration in the T1DM subject, including an electronic module configured to model glucagon action on endogenous glucose production (EGP(t)), an electronic module configured to model meal glucose rate of appearance (Ra(t)), an electronic module configured to model insulin-dependent glucose utilization (U id (t)), according to following equation: U id ( t ) = [ V m 0 + V mx · X ( t ) · ( 1 + r 1 · risk ) ] · G t ( t ) K m 0 + G t ( t ) where G t (t) is an amount of glucose in tissue, X(t) is insulin action on glucose utilization and [V m0 , V mx , K m0 , p 2U ] are model parameters, where V m0 governs amplitude of insulin action on glucuose utilization at basal steady state, V mx governs amplitude of insulin action on glucuose utilization, K m0 governs glucose control on glucose utilization, p 2U accounts for delay between insulin signal and insulin action on glucose utilization, and risk = { 0 if G ≥ G b 10 · [ f ( G ) ] 2 if G th ≤ G < G b 10 · [ f ( G th ) ] 2 if G < G th with G being total glucose, G b being patient basal glucose, G th a hypoglycemic threshold, which is set at 60 mg/d1, and risk is a measure of risk of hypoglycemia, f ( G ) = log ( G G b
for simulation or modelling of medical disorders · CPC title
Analysis or design of chemical reactions, syntheses or processes · CPC title
Physics · mapped topic
Physics · mapped topic
Subject matter not provided for in other main groups of this subclass · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.