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Subsections


Introduction to convergence of sequences and series

Introduction

This lab introduces you to the concept of convergence of sequences and series with an application of geometric series involving a model for a drug being given to a patient at regular intervals. As the drug is broken down by the body, its concentration in the bloodstream decreases. However, it doesn't disappear completely before the next dose is given. This means that there is a tendency for the average drug concentration to increase over time. It turns out that a geometric series is the key to understanding how high the concentration can go.

Getting Started

To assist you, there is a worksheet associated with this lab that contains examples and even solutions to some of the exercises. You can copy that worksheet to your home directory by going to your computer's Start menu and choose run. In the run field type:

\\storage\academics\math\calclab

when you hit enter, you can then choose MA1023 and then choose the worksheet

Seq_series_drug_start_B14.mw

Remember to immediately save it in your own home directory. Once you've copied and saved the worksheet, read through the background on the internet and the background of the worksheet before starting the exercises.

Background

Sequences and Series

An infinite sequence is a list of numbers defined by the formula $a_n$ where $n$ is the set of positive integers ${1,2,3,...}$. A sequence is said to converge if the numbers in the in the list approach a single value as $n$ approaches $\infty$. If the numbers in the list increase or decrease without bound as $n$ gets larger, then we say that the sequence diverges.

An infinite series is the sum of an infinite sequence. More precisely, the sum of an infinite series is defined as the limit of the sequence of the partial sums of the terms of the series, provided this limit exists. If no finite limit exists, then we say that the series is divergent.

The sum of an infinite series is defined as $\displaystyle \lim_{n \rightarrow \infty} S_n$, where $S_n$ is the partial sum of the first n terms of the series. However, because of the algebraic difficulty of expressing $S_n$ as a function of n, it is not always possible to find sums by directly using the definition.

Exponential decay and effective medicine dosage

In this section, we describe an exponential decay model for the concentration of a drug in a patient's bloodstream. We assume that the drug is administered intravenously, so that the concentration of the drug in the bloodstream jumps almost immediately to its highest level. The concentration of the drug then decays exponentially. If we use $C(t)$ to represent the concentration at time t, and $C_0$ to represent the concentration just after the first dose is administered then our exponential decay model would be given by

\begin{displaymath}C(t) = C_0 e^{-kt} \end{displaymath}

where $k$ is the decay constant, and is a property of the particular drug being used. It is usually obtained experimentally. The Getting Started worksheet has examples of how to compute $k$ from experimental data.

Now suppose that an additional dose of the drug is given to the patient. Since we are assuming that when the drug is administered it is diffused so rapidly throughout the bloodstream that, for all practical purposes, it reaches its highest concentration instantaneously, we would see a jump in the concentration of the drug when the new dose is given, as shown in the graph below.

\includegraphics[height=4.0in]{drugfig1.ps}

After the additional dose is given, the concentration again decays over time.

A problem facing physicians is the fact that for most drugs, there is a concentration, $m$, below which the drug is ineffective and a concentration, $M$, above which the drug is dangerous. Thus the physician would like the have the concentration $C(t)$ satisfy

\begin{displaymath}m \leq C(t) \leq M \end{displaymath}

This requirement helps determine the initial dose of a drug and when the next dose should be administered. For example, the first dose should never raise the concentration above $M$. That is, we must have $C_0 \leq M$. To get a handle on the time between doses, we can calculate the maximum possible time between doses. That is, suppose an initial dose is given such that the concentration immediately after the dose is $M$, the maximum safe dose. If we calculate the time at which the concentration has decayed to $m$, then this gives the maximum time interval between doses. This gives us an upper bound on the time between doses. The worksheet contains examples of this kind of calculation. Note that many factors could be important in determining the time between doses that is actually used, including practical considerations like hospital schedules and shift changes.

Equal, regularly-spaced doses

We next consider what happens if equal doses of the drug are given at regular time intervals. Recall that a drug has a maximum safe concentration, $M$, and a minimum effective concentration, $m$. We say that a treatment program of equal, regularly-spaced doses is safe and effective if the concentration $C(t)$ of the drug satisfies

\begin{displaymath}m \leq C(t) \leq M \end{displaymath}

during the treatment.

In the first part of this lab, we presented the expression

\begin{displaymath}C(t) = C_0 e^{-kt} \end{displaymath}

for the concentration of the drug after the first dose. This expression is valid as long as only a single dose is given. However, suppose that at $t=L$ a second dose is given and that the amount of the drug administered is the same as the first dose. According to our model, the concentration will jump immediately by an amount equal to $C_0$ when the second dose is given. However, when the second dose is given, there is still some of the drug in the bloodstream remaining from the first dose. This means that to compute the concentration just after the second dose, we have to add the value $C_0$ to the concentration remaining from the first dose. During the time between the second and third doses, the concentration decays exponentially from this value. To find the concentration after the third dose, we would have to repeat this process, but now we have contributions from the first and second doses to include.

We can calculate the concentration just before the second dose is administered by setting $t=L$ in our equation

\begin{displaymath}C(t) = C_0 e^{-kt} \end{displaymath}

to get

\begin{displaymath}C(L^-) = C_0 e^{-kL} \end{displaymath}

where by $C(L^-)$ we mean the

\begin{displaymath}\lim_{t \rightarrow L^-} C(t) \end{displaymath}

Now, when the second dose is administered the concentration jumps by an increment $C_0$ so that the concentration just after the second dose is given is

\begin{displaymath}C_0 + C(L^-) = C_0+ C_0 e^{-kL} = C_0 (1 + e^{-kL}) \end{displaymath}

The concentration then decays from this value according to our exponential decay rule, but with a slight twist. The twist is that the ``initial'' concentration is at $t=L$, instead of the more familiar case of $t=0$. One way to handle this is to write the exponential term as

\begin{displaymath}e^{-k(t-L)} \end{displaymath}

so that at $t=L$, the exponent is $0$. If we do this, then we can write the concentration as a function of time as

\begin{displaymath}C(t) = C_0 (1 + e^{-kL}) e^{-k(t-L)} \end{displaymath}

This function is only valid after the second dose is administered and before the third dose is given. That is, for $L \leq t < 2L$.

Now, suppose that a third dose of the drug is given at $t=2L$. The concentration just before the third dose is given is $C(2L^-)$, which is

\begin{displaymath}C(2L^-) = C_0 (1 + e^{-kL}) e^{-kL} \end{displaymath}

which we can also write as

\begin{displaymath}C(2L^-) = C_0 (e^{-kL}+ e^{-2kL}) \end{displaymath}

When the third dose is given, the concentration would jump again by $C_0$ and the concentration just after the third dose would be

\begin{displaymath}C(2L) = C_0 (1 +e^{-kL}+ e^{-2kL}) \end{displaymath}

This process can be continued and leads to the following two formulas. The first is the concentration just before the $N\mathrm{th}$ dose of the drug. This is

\begin{displaymath}C((N-1)L^-) =C_0 \sum_{i=1}^{N-1} e^{-ikL} \end{displaymath}

The second result we need is the concentration just after the $N\mathrm{th}$ dose, which is

\begin{displaymath}C((N-1)L) =C_0 \sum_{i=0}^{N-1} e^{-ikL} \end{displaymath}

Geometric series

At this point, you are probably wondering how geometric series fit into this lab. The answer should be a lot clearer if we define a parameter $r$ by

\begin{displaymath}r = e^{-kL}\end{displaymath}

Note that $0 < r < 1$, since $k$ and $L$ are both positive constants. The properties of the exponential function can be used to show that

\begin{displaymath}r^i = e^{-ikL} \end{displaymath}

where $i$ is a non-negative integer. We can write our two fromulas for the concentration just before and after the $N\mathrm{th}$ dose in terms of $r$ as

\begin{displaymath}C((N-1)L^-) =C_0 \sum_{i=1}^{N-1} r^i = C_0 \frac{r-r^N}{1-r} \end{displaymath}

and

\begin{displaymath}C((N-1)L) =C_0 \sum_{i=0}^{N-1} r^i = C_0 \frac{1-r^N}{1-r}\end{displaymath}

where the formula for the partial sum of a geometric series has been used to obtain the last equality in each of the equations above.

Now, suppose a treatment program is to be continued indefinitely. The formulas above show that $ C((N-1)L^-)$ and $C((N-1)L)$ both increase with $N$. This means that the minimum concentration is the concentration just before the second dose or

\begin{displaymath}C_{\mathrm{min}} = C_0 r \end{displaymath}

and that the maximum concentration occurs just after the last dose. Thus we have that

\begin{displaymath}C_{\mathrm{max}} \leq \lim_{N \rightarrow \infty} C_0
\frac{1-r^N}{1-r} = \frac{C_0}{1-r} \end{displaymath}

Exercises

    1. Write the sequence $\displaystyle \frac{9n^2-4}{5n^2+6}$ as a function. List the first fifteen terms.
    2. Plot the first fifteen terms. Does it appear to converge or diverge? If it seems to converge, to what does it converge?
    3. Calculate the limit of the sequence as $n$ approaches $\infty$. Is your answer close to your approximation above?
    4. Write a function for the sum of the sequence. List the first ten terms of the sequence of partial sums.
    5. Plot the at least the first ten terms of the sequence of partial sums (You may want to restrict the $y$ range to $ 0 \leq y \leq 10$). Does it appear that the series converges or diverges? If it seems to converge, to what does it converge?
    6. Calculate the limit of the series as $n$ approaches $\infty$.
    1. Suppose that for a certain drug, which we'll refer to as drug A, the following results were obtained. Immediately after the drug was administered, the concentration was 3.3 mg/ml. Six hours later, the concentration had dropped to 1.55 mg/ml. Determine the value of $k$ for this drug.

    2. Consider drug A, assuming that doses are given every six hours, or $L=6$. Compute the minimum initial dose $C_0$ that will keep the concentration above the minimum effective level for the first six hours, i.e before the second dose is given.

    3. Consider drug A again, with doses to be given every six hours. Can you find a dose $C_0$ such that the concentration stays below $M=8$ and above $m=1.8$ for at least 72 hours?

    4. Trials of another drug, call it drug B, produced the following data. The concentration just after the drug was administered was 6 mg/ml and 5 hours later the concentration was 1.2 mg/ml. If the maximum safe concentration is 10 mg/ml and the minimum effective concentration is 2 mg/ml, find one set of values of $C_0$ and $L$ that provide a safe and effective treatment program. (Hint: Copy commands from part 1, 2, and 3 of this exercise and make the appropriate changes. You should also change the variable name for the constant $k$ from $k1$ to $k2$.)

    5. Suppose that new research with drug A shows that the maximum safe level is $M=7$ and the minimum effective dose is $m=2.5$ Can you find values of $C_0$ and $L$ that produce a safe and effective treatment program? Try at least two sets of values of $C_0$ and $L$.


next up previous
Next: About this document ... Up: lab_template Previous: lab_template
Dina J. Solitro-Rassias
2014-11-13