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Extraction ratio

From Wikipedia, the free encyclopedia

Parameter Value
renal blood flow RBF = 1000 mL/min
hematocrit HCT = 40%
glomerular filtration rate GFR = 120 mL/min
renal plasma flow RPF = 600 mL/min
filtration fraction FF = 20%
urine flow rate V = 1 mL/min
Sodium Inulin Creatinine PAH
SNa = 150 mEq/L SIn = 1 mg/mL SCr = 0.01 mg/mL SPAH =
UNa = 710 mEq/L UIn = 150 mg/mL UCr = 1.25 mg/mL UPAH =
CNa = 5 mL/min CIn = 150 mL/min CCr = 125 mL/min CPAH = 420 mL/min
ER = 90%
ERPF = 540 mL/min

Extraction ratio is a measure in renal physiology, primarily used to calculate renal plasma flow in order to evaluate renal function. It measures the percentage of the compound entering the kidney that was excreted into the final urine.[1]

Measured in concentration in blood plasma, it may thus be expressed as:

, where Pa is the concentration in renal artery, and Pv is the concentration in the renal vein.

For instance, para aminohippuric acid (PAH) is almost completely excreted in the final urine, and thus almost none is found in the venous return (Pv ~0). Therefore, the extraction ratio of PAH ~1. This is why PAH is used in PAH clearance to estimate renal plasma flow.

YouTube Encyclopedic

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  • Clearance and Rate of Elimination - Pharmacokinetics - Pharmacology Lect 12
  • Renal Excretion of Drugs | Pharmacokinetics Lect 13
  • Plasma Protein Binding Drugs

Transcription

So now we finally get to talk about drug clearance. Let's start off with the definition. What is it? Clearance is the volume of plasma that is cleared of drug per unit time. It is a volume per unit time. So, let's discuss the 3 most important points to remember and front load this lecture and then develop each one of those points. So, the first point is the definition. What is the definition of clearance? Well we just said it's a volume per unit time and I want you to remember just that. The units of clearance. It is a volume. It is milliliters per minute. Note, that this says nothing about the amount of drug. Clearance does not tell us how much drug, it is telling us the volume of plasma that is cleared of drug per unit time. If I wanted to figure out the amount of drug that is being cleared, then I'm talking about the rate of drug elimination. So, clearance is used to determine the rate of drug elimination and the way that it does so is that clearance is the proportionality factor that is used to determine the rate of elimination. This is the definition used in many textbooks. So, what do I mean? Well, if I wanted to figure out the rate of elimination, what I need to do is take that clearance and multiply it by the plasma drug concentration. Let's talk about this for 1 moment. So, the rate of elimination of a drug. What the units are here or what I'm referring to is the amount of drug being eliminated per unit time. So, the amount of drug we can think of as the mass of the drug, the amount of milligrams of drug being eliminated per unit time and that's going to equal the clearance which we said is a volume per unit time multiplied by a concentration. So what are the units of concentration? You should be screaming at me concentration is equal to mass over volume. And so, notice volume cancels out and we get the units for the rate of elimination and that is mass over time or the amount of drug being eliminated over time. That is how clearance is used. It is a proportionality factor. The third point I want you to remember is how do we clear drugs. Well any organ that has access to the outside world. Our kidneys can excrete drugs into the urine, our liver can excrete drugs into our bile, our lungs can excrete drugs into the air. Those are all organs in which clearance occurs and to figure out the total clearance, I have to add up the clearance at each one of those individual organs. Now the most important one is the renal clearance. And so, if we think about what's going on at the kidney, we have our glomerulus which is filtering our blood of drug and we excrete it. So that is how we estimate clearance clinically. We use the glomerular filtration rate. The GFR, and the GFR is used to make clinical decisions regarding drug dosages and drug choice and this is a good thing because we can easily estimate the GFR and if we have less renal clearance, we might want to give less drug to avoid the build up of metabolites or we might want to give a drug that might be cleared via the liver. So, important points to remember. Let's discuss the first point, the definition. So clearance is a volume per unit time and what I've done here is I've created a little video to represent what's going on at the kidney. So, this is the filtering apparatus of the kidney. I just made a little filter. And this is the collection system of the kidney. We can think of this as the functional unit of the kidney or the nephron. So, the rate at which this picture is being filled up of fluid. Let's say this is a 1 liter pitcher and it fills up in a minute, that would tell me my clearance. So, the clearance is the rate at which we are clearing the blood or the plasma of drug. Now, it's important to remember that in order to figure out how much drug I am clearing, I would need to multiply this rate of clearance by the concentration in here and that would tell me the mass over time. Now, to point 2. Clearance is the proportionality factor used to determine the rate of elimination. So, here I have this equation that the rate of elimination is equal to the clearance times the concentration. And so, the way the constraints under which I can use this equation is when I'm dealing with first order kinetics. And this is something that we describe in the past and I'll briefly touch on it now. But if you're confused, refer to the prior video on that topic. So, on this graph, I have the rate of elimination on the Y axis and the plasma drug concentration on the X axis. And as we discussed in the past, as the plasma drug concentration increases, the rate of drug elimination goes up and when this happens, we call this first order kinetics or first order elimination. And so, notice that there is a proportional relationship here on this part of the graph and if I wanted to figure out that proportional relationship, I need the proportionality factor or the clearance but after I've saturated all of my enzymes, I reach a certain point where as I increase the plasma drug concentration, the rate of elimination does not go up anymore. That is zero order kinetics. and the way that I remember that is the slope of the graph here is approximately equal to zero. So, clearance really is a constant and it is a constant under the constraint of first order kinetics. First order kinetics. And what I mean here is when I have not saturated all of my enzymes. So, this is for most drugs at most dosages. Clearance is not constant when you hit this zero order kinetics. Just a little tidbit that you should know. Another point I want to make here is this is 1 equation you should know for clearance. There's also another equation and that equation is that the clearance is equal to the volume of distribution multiplied by something called the first order elimination rate constant. Now, we have a video on each one of these terms and I'd suggest that you go back and look at them if you are confused but this equation isn't too bad because if we look at the units for each one of these, the units for volume of distribution is just volume and the units for first order elimination rate constant is inverse time. So that's one over time. And if we multiply these two by each other, we get the units of volume over time which would be clearance. Now, I want to be clear here. No pun intended that we don't really use this equation to solve for clearance. This equation is really used for us to get a sense of that first order elimination constant which is equal to the clearance divided by the volume of distribution. This here makes sense to us because as our clearance is increasing more volume per unit time, the rate of elimination will also go up. Also, as the volume of distribution decreases and that means that you know if the drug is staying in the plasma, that drug now has a better chanceof being filtered by the kidney. So, lower volume of distribution also increases that first order elimination rate constant. These two terms here are constants for a given drug, so this is not something we really calculate using this equation but it gives us a sense of the first order elimination rate constant. Now, let's move on to our third point that the total clearance is the sum of clearance at each organ. And I mentioned to you that really organs that have access to the outside world are organs in which clearance occurs. So, in terms of the kidney, the renal clearance - this is excreting drugs into the urine. This is occurring for most drugs. At the liver, we are excreting drugs into the bile which then goes into the feces and we defecate that out and at the level of the lungs, we have our pulmonary clearance and the pulmonary clearance is important for really for inhaled anesthetics. These are drugs. These are volatile substances that we breathe in, they get access to our brain and then once we remove the you know gas, we can breathe out the drugs. And so, what's nice here is that the total clearance is the sum of each one of these. So, if a patient has a decrease in their renal clearance, let's say they have chronic kidney disease or they just get older, we can do a couple of things. We can choose a drug that might be hepatically cleared or we can decrease the dosage or increase the spacing between dosages so that we don't have a build up of drug from a lack of elimination or excretion. And like I was saying, clinically speaking, this is the most important term. and the way that we estimate our renal clearance is by looking at our glumerulofiltration rate. So, we use the GFR to estimate changes in the renal clearance of drugs and the way that we determine the GFR is by looking at something called the plasma creatinine concentration and so, what we're going to do in the next video is talk about these two terms in a little bit more detail. Subtitles by the Amara.org community

Hepatic extraction ratio

The "Hepatic Extraction Ratio" is a similar measurement for clearance of a substance (usually a pharmacological drug) by the liver. It is defined as the fraction of drug removed from blood by the liver, and depends on 3 factors— the hepatic blood flow, the uptake into the hepatocytes, and the enzyme metabolic capacity. Examples of drugs with a high hepatic extraction ratio include propranolol, opiates, and lignocaine.

References

  1. ^ Renal Mathematics Texas Tech University Health Sciences Center
This page was last edited on 4 May 2021, at 15:02
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