Document information
- University
- Politecnico di Milano
- Degree programme
- Biomedical Engineering
- Subject
- Bioengineering of Physiological Control Systems
- Classification
- Notes · By topic
- Original format
- Text
- Searchable text
Topic-based study materials for Bioengineering of Physiological Control Systems in the Biomedical Engineering degree programme at Politecnico di Milano. The document covers: ● ● Glucose-Insuline Regulation There is a physiological control system in charge of the regulation of glucose concentration in the plasmatic compartment, to keep glicemia levels within the normal range and avoid ipoglicemia or iperglicemia. The amount of glucose in inside the
Topic-based study materials for Bioengineering of Physiological Control Systems in the Biomedical Engineering degree programme at Politecnico di Milano. The document covers: ● ● Glucose-Insuline Regulation There is a physiological control system in charge of the regulation of glucose concentration in the plasmatic compartment, to keep glicemia levels within the normal range and avoid ipoglicemia or iperglicemia. The amount of glucose in inside the
Import quality: text was extracted directly from the original document.
Representative passages recognised in different parts of the material. The full extracted text remains available to search, while this compact preview makes the page easier to read.
● ● Glucose-Insuline Regulation There is a physiological control system in charge of the regulation of glucose concentration in the plasmatic compartment, to keep glicemia levels within the normal range and avoid ipoglicemia or iperglicemia. The amount of glucose in inside the body ( x ) is regulated by 3 main mechanisms: the RENAL LOSS, which is active only when the glucose level is above a certain value (theta) the TISSUE UTILIZATION, which is divided in two rates one insulin ( y ) dependent (depending also on the cell’s response to insulin, v) ● and one independent from it On the other hand, the insuline production depends on the glucose concentration and it is produced at a certain rate, but in the meantime is also destructed proportionally to its amount (alpha), furthermore it is active only when glucose exceeds a certain threshold: GLUCOSE- INSULINEDYNAMICMODEL ⊥= plasmaticoglncosecapacitance Cadj= Ut)- ti- vxy ✗<e CI= plasmaticiinsulinacapacitava{Ult)- Ix- vxy- µ(x-0)×>0 ✗= plasmatiglncoseconcentrazioni Y= plasmatiinsulinaconcentratori ✗<0Gdi= { - ✗y dt _ ay+plx- ¢)×>0 thatMealsthatthelevelofglncose 1. EQUILIBRIUM@Constant/NpviUlt)= Q, → {×")>× isalonetheminimumthresholdforinsulina✗(t)-Y Production,soit isenouglehighto produceinsulina,butnottotheextent 0= Ql- Xx- VXY ✗to thattheRENALlossisactivated ]soif ✗€(¢;f)0= Qe- ax- vxy- µ(x-0) ×>e 0= - xy ✗E { Q= IX+VXY (o. . ,.gg, ×,, y, qq.gg a. LINEARIZATIONAROUNDtheWORKINGPOINT(X,Y) assuming✗c-(0,0) Ult)= Q,+SUA) }ma Cadè= Qi- XIX+Sx)- v(✗+Sx)(Y+Sy)+SUA) { ✗A)= ✗+Sx Ylt)= Y+Sy CIOÈ= - ✗(Ytdy)+p(✗+Sx-0) 1 a.E:/= - a-VI E-'È!;" ⊥Silt)= asxlt)+Bsylt)+Csult) (☒it) {G.Sjlt)= Dsyit)+Esxct) ←È!- "☒ F-- ¥-1, +p [= 1 p3.TRANSFERFUNCTIONS@WP (g.s. SXCS)= - (✗+VY)SXCS)- VX (gg, +a)S✗(s)+SUIS) )⊥" °" """= ' ""+"")""' "×" """+&""…
First page of the document.