Drug absorption/elimination formulas

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In summary, the conversation discusses the amount of a drug present over time and the basic assumption that the rate of change of the amount is determined by the difference between the rate of absorption and the rate of elimination. The solution to this is a function with parameters related to the rate of absorption and elimination, and it has a peak value and half-life. The conversation also mentions the possibility of constructing a sum to study the long term behavior of the drug, but acknowledges that the properties and interactions of drugs with our metabolism vary and there is already a lot of available information on individual drugs.
  • #1
phoenixthoth
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let [tex]A[/tex] be the amount of a drug present [tex]t[/tex] units of time after its administration. this amount could be in terms of drug concentration.

the basic assumption i made was that the rate of change of [tex]A[/tex] is the difference between the rate of absorption and the rate of elimination where the rate of absorption is constant until the initial amount administered is gone and the rate of elimination is proportional to the amount present:

[tex]\frac{dA}{dt}=k_{1}u\left( k_{2}-t\right) -k_{3}A\left( t\right) [/tex].

here, [tex]u[/tex] is the unit step function defined so that [tex]u\left( t\right) =1[/tex] if [tex]t\geq 0[/tex] and is 0 otherwise. [tex]k_{1}[/tex] is related to the rate of absorption and [tex]k_{3}[/tex] is related to the rate of elimination. the absorption aspect
remains activated until [tex]t=k_{2}[/tex] which corresponds to when the intitial amount administered runs out.

the solution to this with [tex]A\left( 0\right) =0[/tex] is [tex]A\left( t\right) =\frac{e^{-k_{3}t}k_{1}}{k_{3}}\left( -1+e^{k_{3}t}+\left( e^{k_{2}k_{3}}-e^{k_{3}t}\right) u\left( t-k_{2}\right) \right) [/tex].

it became clear that [tex]A[/tex] must achieve a maximum value when [tex]t=k_{2};[/tex] here, [tex]A^{\prime }[/tex] is undefined whereas otherwise it is nonzero. let [tex]t_{peak}=k_{2}[/tex]. [tex]\ A\left( t_{peak}\right) =\frac{k_{1}}{k_{3}}\left(
1-e^{-t_{peak}k_{3}}\right) [/tex]; this is the peak amount present. let [tex]A_{peak}=A\left( t_{peak}\right) [/tex].

if we let [tex]t_{half}[/tex] be the element in the set [tex]\left\{ t>t_{peak}:A\left( t\right) =\frac{1}{2}A\left( t_{peak}\right) \right\} [/tex] and solve, we obtain that [tex]t_{half}=\frac{\log 2+t_{half}k_{3}}{k_{3}}[/tex], where the log is the natural log.

now that we know [tex]t_{peak}[/tex], [tex]A_{peak}[/tex], and [tex]t_{half}[/tex] in terms of [tex]k_{1}[/tex], [tex]k_{2}[/tex], and [tex]k_{3}[/tex], we can solve for [tex]k_{1}[/tex], [tex]k_{2}[/tex], and [tex]k_{3}[/tex] to get
[tex]k_{1}=\frac{A_{peak}\log 2}{\left( 2^{\frac{t_{peak}}{t_{peak}-t_{half}}}-1\right) \left( t_{peak}-t_{half}\right) }[/tex]

[tex]k_{2}=t_{peak}[/tex]

[tex]k_{3}=\frac{\log 2}{t_{half}-t_{peak}}[/tex].

putting these together, we get [tex]A\left( t\right) =\frac{A_{peak}\left( 1-2^{\frac{t}{t_{peak}-t_{half}}}+\left( 2^{\frac{t-t_{peak}}{t_{peak}-t_{half}}}-1\right) u\left( t-t_{peak}\right) \right) }{1-2^{\frac{t_{peak}}{t_{peak}-t_{half}}}}[/tex]. the graph of this looks like something of the form [tex]ate^{bt}[/tex] though that formula doesn't allow one to control the time to reach peak absorption, the peak amount, and the half-life which makes sense because it only has two parameters while the defining differential equation for the other formula has three parameters.

one can now construct a sum where the terms added are of the form [tex]A\left(t-kt_{int}\right) u\left( t-kt_{int}\right) [/tex] where [tex]k[/tex] are natural numbers and [tex]t_{int}[/tex] is the fixed time interval in between administrations of the drug though one could, of couse, add things of the form [tex]A\left(t-t_{k}\right) u\left( t-t_{k}\right) [/tex] where [tex]\left[ t_{k},t_{k+1}\right] [/tex] are not intervals of constant length. if the intervals are fixed, one can study the long term behavior of the drug.
 
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  • #2
Sadly the rate of absorption is not constant nor is the elimination dependent on the amount present. Every drug has a range of properties and interacts with our metabolism differently. There is already a lot of information available about individual drugs.
 

1. What is drug absorption?

Drug absorption refers to the process by which a drug enters the body and is transported to its site of action. This typically occurs through the gastrointestinal tract, but can also occur through other routes such as inhalation or injection.

2. How is drug absorption measured?

Drug absorption can be measured using various techniques such as blood sampling, urine analysis, and imaging techniques. These methods can help determine the amount of a drug that reaches the systemic circulation and the rate at which it is absorbed.

3. What factors affect drug absorption?

The rate and extent of drug absorption can be influenced by several factors, including the physicochemical properties of the drug, the route of administration, the health and age of the patient, and the presence of other drugs or food in the gastrointestinal tract.

4. What is drug elimination?

Drug elimination refers to the process by which a drug is removed from the body. This can occur through various routes, such as metabolism by the liver, excretion through the kidneys, or exhalation through the lungs.

5. How are drug elimination formulas used in pharmacokinetics?

Drug elimination formulas are used in pharmacokinetics to calculate the rate at which a drug is eliminated from the body, as well as to estimate the time it takes for the drug to be eliminated. This information is important in determining the appropriate dosage and dosing frequency of a drug to achieve the desired therapeutic effect.

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