Pharmacokinetics

Pharmacokinetics describes how the body affects a specific xenobiotic/chemical after administration through the mechanisms of absorption and distribution, as well as the metabolic changes of the substance in the body (e.g. by metabolic enzymes such as cytochrome P450 or glucuronosyltransferase enzymes), and the effects and routes of excretion of the metabolites of the drug.[2] Pharmacokinetic properties of chemicals are affected by the route of administration and the dose of administered drug. These may affect the absorption rate.[3]

Models have been developed to simplify conceptualization of the many processes that take place in the interaction between an organism and a chemical substance. One of these, the multi-compartmental model, is the most commonly used approximations to reality; however, the complexity involved in adding parameters with that modelling approach means that monocompartmental models and above all two compartmental models are the most-frequently used. The various compartments that the model is divided into are commonly referred to as the ADME scheme (also referred to as LADME if liberation is included as a separate step from absorption):

• Liberation – the process of release of a drug from the pharmaceutical formulation.[4][5] See also IVIVC.
• Absorption – the process of a substance entering the blood circulation.
• Distribution – the dispersion or dissemination of substances throughout the fluids and tissues of the body.
• Metabolism (or biotransformation, or inactivation) – the recognition by the organism that a foreign substance is present and the irreversible transformation of parent compounds into daughter metabolites.
• Excretion – the removal of the substances from the body. In rare cases, some drugs irreversibly accumulate in body tissue.

The two phases of metabolism and excretion can also be grouped together under the title elimination. The study of these distinct phases involves the use and manipulation of basic concepts in order to understand the process dynamics. For this reason in order to fully comprehend the kinetics of a drug it is necessary to have detailed knowledge of a number of factors such as: the properties of the substances that act as excipients, the characteristics of the appropriate biological membranes and the way that substances can cross them, or the characteristics of the enzyme reactions that inactivate the drug.

All these concepts can be represented through mathematical formulas that have a corresponding graphical representation. The use of these models allows an understanding of the characteristics of a molecule, as well as how a particular drug will behave given information regarding some of its basic characteristics such as its acid dissociation constant (pKa), bioavailability and solubility, absorption capacity and distribution in the organism.

The model outputs for a drug can be used in industry (for example, in calculating bioequivalence when designing generic drugs) or in the clinical application of pharmacokinetic concepts. Clinical pharmacokinetics provides many performance guidelines for effective and efficient use of drugs for human-health professionals and in veterinary medicine.

The following are the most commonly measured pharmacokinetic metrics:[6] The units of the dose in the table are expressed in moles (mol) and molar (M). To express the metrics of the table in units of mass, instead of Amount of substance, simply replace 'mol' with 'g' and 'M' with 'g/dm3'. Similarly, other units in the table may be expressed in units of an equivalent dimension by scaling.

Characteristic	Description	Symbol	Unit	Formula	Worked example value
Dose	Amount of drug administered.	${\displaystyle D}$	${\displaystyle \mathrm {mol} }$	Design parameter	500 mmol
Dosing interval	Time between drug dose administrations.	${\displaystyle \tau }$	${\displaystyle \mathrm {s} }$	Design parameter	24 h
Cmax	The peak plasma concentration of a drug after administration.	${\displaystyle C_{\text{max}}}$	${\displaystyle \mathrm {M} }$	Direct measurement	60.9 mmol/L
tmax	Time to reach Cmax.	${\displaystyle t_{\text{max}}}$	${\displaystyle \mathrm {s} }$	Direct measurement	3.9 h
Cmin	The lowest (trough) concentration that a drug reaches before the next dose is administered.	${\displaystyle C_{{\text{min}},{\text{ss}}}}$	${\displaystyle \mathrm {M} }$	Direct measurement	27.7 mmol/L
Volume of distribution	The apparent volume in which a drug is distributed (i.e., the parameter relating drug concentration in plasma to drug amount in the body).	${\displaystyle V_{\text{d}}}$	${\displaystyle \mathrm {m} ^{3}}$	${\displaystyle {\frac {D}{C_{0}}}}$	6.0 L
Concentration	Amount of drug in a given volume of plasma.	${\displaystyle C_{0},C_{\text{ss}}}$	${\displaystyle \mathrm {M} }$	${\displaystyle {\frac {D}{V_{\text{d}}}}}$	83.3 mmol/L
Elimination half-‍life	The time required for the concentration of the drug to reach half of its original value.	${\displaystyle t_{\frac {1}{2}}}$	${\displaystyle \mathrm {s} }$	${\displaystyle {\frac {\ln(2)}{k_{\text{e}}}}}$	12 h
Elimination rate constant	The rate at which a drug is removed from the body.	${\displaystyle k_{\text{e}}}$	${\displaystyle \mathrm {s} ^{-1}}$	${\displaystyle {\frac {\ln(2)}{t_{\frac {1}{2}}}}={\frac {CL}{V_{\text{d}}}}}$	0.0578 h−1
Infusion rate	Rate of infusion required to balance elimination.	${\displaystyle k_{\text{in}}}$	${\displaystyle \mathrm {mol/s} }$	${\displaystyle C_{\text{ss}}\cdot CL}$	50 mmol/h
Area under the curve	The integral of the concentration-time curve (after a single dose or in steady state).	${\displaystyle AUC_{0-\infty }}$	${\displaystyle \mathrm {M} \cdot \mathrm {s} }$	${\displaystyle \int _{0}^{\infty }C\,\operatorname {d} t}$	1,320 mmol/L·h
		${\displaystyle AUC_{\tau ,{\text{ss}}}}$	${\displaystyle \mathrm {M} \cdot \mathrm {s} }$	${\displaystyle \int _{t}^{t+\tau }C\,\operatorname {d} t}$
Clearance	The volume of plasma cleared of the drug per unit time.	${\displaystyle CL}$	${\displaystyle \mathrm {m} ^{3}/\mathrm {s} }$	${\displaystyle V_{\text{d}}\cdot k_{\text{e}}={\frac {D}{AUC}}}$	0.38 L/h
Bioavailability	The systemically available fraction of a drug.	${\displaystyle f}$	Unitless	${\displaystyle {\frac {AUC_{\text{po}}\cdot D_{\text{iv}}}{AUC_{\text{iv}}\cdot D_{\text{po}}}}}$	0.8
Fluctuation	Peak trough fluctuation within one dosing interval at steady state.	${\displaystyle \%PTF}$	${\displaystyle \%}$	${\displaystyle {\frac {C_{{\text{max}},{\text{ss}}}-C_{{\text{min}},{\text{ss}}}}{C_{{\text{av}},{\text{ss}}}}}\cdot 100\%}$ where ${\displaystyle C_{{\text{av}},{\text{ss}}}={\frac {1}{\tau }}AUC_{\tau ,{\text{ss}}}}$	41.8%

In pharmacokinetics, steady state refers to the situation where the overall intake of a drug is fairly in dynamic equilibrium with its elimination. In practice, it is generally considered that steady state is reached when a time of 4 to 5 times the half-life for a drug after regular dosing is started.

The time course of drug plasma concentrations over 96 hours following oral administrations every 24 hours. Note that in steady state and in linear pharmacokinetics AUCτ=AUC∞.[7] Steady state is reached after about 5 × 12 = 60 hours. The graph depicts a typical time course of drug plasma concentration and illustrates main pharmacokinetic metrics

Pharmacokinetic modelling is performed by noncompartmental or compartmental methods. Noncompartmental methods estimate the exposure to a drug by estimating the area under the curve of a concentration-time graph. Compartmental methods estimate the concentration-time graph using kinetic models. Noncompartmental methods are often more versatile in that they do not assume any specific compartmental model and produce accurate results also acceptable for bioequivalence studies. The final outcome of the transformations that a drug undergoes in an organism and the rules that determine this fate depend on a number of interrelated factors. A number of functional models have been developed in order to simplify the study of pharmacokinetics. These models are based on a consideration of an organism as a number of related compartments. The simplest idea is to think of an organism as only one homogenous compartment. This monocompartmental model presupposes that blood plasma concentrations of the drug are a true reflection of the drug's concentration in other fluids or tissues and that the elimination of the drug is directly proportional to the drug's concentration in the organism (first order kinetics).

However, these models do not always truly reflect the real situation within an organism. For example, not all body tissues have the same blood supply, so the distribution of the drug will be slower in these tissues than in others with a better blood supply. In addition, there are some tissues (such as the brain tissue) that present a real barrier to the distribution of drugs, that can be breached with greater or lesser ease depending on the drug's characteristics. If these relative conditions for the different tissue types are considered along with the rate of elimination, the organism can be considered to be acting like two compartments: one that we can call the central compartment that has a more rapid distribution, comprising organs and systems with a well-developed blood supply; and a peripheral compartment made up of organs with a lower blood flow. Other tissues, such as the brain, can occupy a variable position depending on a drug's ability to cross the barrier that separates the organ from the blood supply.

This two compartment model will vary depending on which compartment elimination occurs in. The most common situation is that elimination occurs in the central compartment as the liver and kidneys are organs with a good blood supply. However, in some situations it may be that elimination occurs in the peripheral compartment or even in both. This can mean that there are three possible variations in the two compartment model, which still do not cover all possibilities.[8]

This model may not be applicable in situations where some of the enzymes responsible for metabolizing the drug become saturated, or where an active elimination mechanism is present that is independent of the drug's plasma concentration. In the real world each tissue will have its own distribution characteristics and none of them will be strictly linear. If we label the drug's volume of distribution within the organism Vd_F and its volume of distribution in a tissue Vd_T the former will be described by an equation that takes into account all the tissues that act in different ways, that is:

${\displaystyle Vd_{F}=Vd_{T1}+Vd_{T2}+Vd_{T3}+\cdots +Vd_{Tn}\,}$

This represents the multi-compartment model with a number of curves that express complicated equations in order to obtain an overall curve. A number of computer programs have been developed to plot these equations.[8] However complicated and precise this model may be, it still does not truly represent reality despite the effort involved in obtaining various distribution values for a drug. This is because the concept of distribution volume is a relative concept that is not a true reflection of reality. The choice of model therefore comes down to deciding which one offers the lowest margin of error for the drug involved.

Graph representing the monocompartmental action model.

Multi-compartmental models

Graphs for absorption and elimination for a non-linear pharmacokinetic model.

The graph for the non-linear relationship between the various factors is represented by a curve; the relationships between the factors can then be found by calculating the dimensions of different areas under the curve. The models used in non-linear pharmacokinetics are largely based on Michaelis–Menten kinetics. A reaction's factors of non-linearity include the following:

• Multiphasic absorption: Drugs injected intravenously are removed from the plasma through two primary mechanisms: (1) Distribution to body tissues and (2) metabolism + excretion of the drugs. The resulting decrease of the drug's plasma concentration follows a biphasic pattern (see figure).
  

  Plasma drug concentration vs time after an IV dose
  • Alpha phase: An initial phase of rapid decrease in plasma concentration. The decrease is primarily attributed to drug distribution from the central compartment (circulation) into the peripheral compartments (body tissues). This phase ends when a pseudo-equilibrium of drug concentration is established between the central and peripheral compartments.
  • Beta phase: A phase of gradual decrease in plasma concentration after the alpha phase. The decrease is primarily attributed to drug elimination, that is, metabolism and excretion.[9]
  • Additional phases (gamma, delta, etc.) are sometimes seen.[10]
• A drug's characteristics make a clear distinction between tissues with high and low blood flow.
• Enzymatic saturation: When the dose of a drug whose elimination depends on biotransformation is increased above a certain threshold the enzymes responsible for its metabolism become saturated. The drug's plasma concentration will then increase disproportionately and its elimination will no longer be constant.
• Induction or enzymatic inhibition: Some drugs have the capacity to inhibit or stimulate their own metabolism, in negative or positive feedback reactions. As occurs with fluvoxamine, fluoxetine and phenytoin. As larger doses of these pharmaceuticals are administered the plasma concentrations of the unmetabolized drug increases and the elimination half-life increases. It is therefore necessary to adjust the dose or other treatment parameters when a high dosage is required.
• The kidneys can also establish active elimination mechanisms for some drugs, independent of plasma concentrations.

It can therefore be seen that non-linearity can occur because of reasons that affect the entire pharmacokinetic sequence: absorption, distribution, metabolism and elimination.

Different forms of tablets, which will have different pharmacokinetic behaviours after their administration.

At a practical level, a drug's bioavailability can be defined as the proportion of the drug that reaches its site of action. From this perspective the intravenous administration of a drug provides the greatest possible bioavailability, and this method is considered to yield a bioavailability of 1 (or 100%). Bioavailability of other delivery methods is compared with that of intravenous injection (absolute bioavailability) or to a standard value related to other delivery methods in a particular study (relative bioavailability).

${\displaystyle B_{A}={\frac {[ABC]_{P}\cdot D_{IV}}{[ABC]_{IV}\cdot D_{P}}}}$

${\displaystyle {\mathit {B}}_{R}={\frac {[ABC]_{A}\cdot {\text{dose}}_{B}}{[ABC]_{B}\cdot {\text{dose}}_{A}}}}$

Once a drug's bioavailability has been established it is possible to calculate the changes that need to be made to its dosage in order to reach the required blood plasma levels. Bioavailability is therefore a mathematical factor for each individual drug that influences the administered dose. It is possible to calculate the amount of a drug in the blood plasma that has a real potential to bring about its effect using the formula:

${\displaystyle De=B\cdot Da\,}$

where De is the effective dose, B bioavailability and Da the administered dose.

Therefore, if a drug has a bioavailability of 0.8 (or 80%) and it is administered in a dose of 100 mg, the equation will demonstrate the following:

De = 0.8 × 100 mg = 80 mg

That is the 100 mg administered represents a blood plasma concentration of 80 mg that has the capacity to have a pharmaceutical effect.

This concept depends on a series of factors inherent to each drug, such as:[14]

• Pharmaceutical form
• Chemical form
• Route of administration
• Stability
• Metabolism

These concepts, which are discussed in detail in their respective titled articles, can be mathematically quantified and integrated to obtain an overall mathematical equation:

${\displaystyle De=Q\cdot Da\cdot B\,}$

where Q is the drug's purity.[14]

${\displaystyle Va={\frac {Da\cdot B\cdot Q}{\tau }}}$

where ${\displaystyle Va}$ is the drug's rate of administration and ${\displaystyle \tau }$ is the rate at which the absorbed drug reaches the circulatory system.

Finally, using the Henderson-Hasselbalch equation, and knowing the drug's ${\displaystyle pKa\,}$ (pH at which there is an equilibrium between its ionized and non ionized molecules), it is possible to calculate the non ionized concentration of the drug and therefore the concentration that will be subject to absorption:

${\displaystyle \mathrm {pH} =\mathrm {pKa} +\log {\frac {B}{A}}}$

When two drugs have the same bioavailability, they are said to be biological equivalents or bioequivalents. This concept of bioequivalence is important because it is currently used as a yardstick in the authorization of generic drugs in many countries.

A number of phases occur once the drug enters into contact with the organism, these are described using the acronym LADME:

• Liberation of the active substance from the delivery system,
• Absorption of the active substance by the organism,
• Distribution through the blood plasma and different body tissues,
• Metabolism that is inactivation of the xenobiotic substance, and finally
• Excretion or elimination of the substance or the products of its metabolism.

Some textbooks combine the first two phases as the drug is often administered in an active form, which means that there is no liberation phase. Others include a phase that combines distribution, metabolism and excretion into a disposition phase. Other authors include the drug's toxicological aspect in what is known as ADME-Tox or ADMET.

Each of the phases is subject to physico-chemical interactions between a drug and an organism, which can be expressed mathematically. Pharmacokinetics is therefore based on mathematical equations that allow the prediction of a drug's behavior and which place great emphasis on the relationships between drug plasma concentrations and the time elapsed since the drug's administration.

Population pharmacokinetics is the study of the sources and correlates of variability in drug concentrations among individuals who are the target patient population receiving clinically relevant doses of a drug of interest.[21][22][23] Certain patient demographic, pathophysiological, and therapeutical features, such as body weight, excretory and metabolic functions, and the presence of other therapies, can regularly alter dose-concentration relationships and can explain variability in exposures. For example, steady-state concentrations of drugs eliminated mostly by the kidney are usually greater in patients suffering from renal failure than they are in patients with normal renal function receiving the same drug dosage. Population pharmacokinetics seeks to identify the measurable pathophysiologic factors and explain sources of variability that cause changes in the dose-concentration relationship and the extent of these changes so that, if such changes are associated with clinically relevant and significant shifts in exposures that impact the therapeutic index, dosage can be appropriately modified. An advantage of population pharmacokinetic modelling is its ability to analyse sparse data sets (sometimes only one concentration measurement per patient is available).

Clinical pharmacokinetics (arising from the clinical use of population pharmacokinetics) is the direct application to a therapeutic situation of knowledge regarding a drug's pharmacokinetics and the characteristics of a population that a patient belongs to (or can be ascribed to).

An example is the relaunch of the use of ciclosporin as an immunosuppressor to facilitate organ transplant. The drug's therapeutic properties were initially demonstrated, but it was almost never used after it was found to cause nephrotoxicity in a number of patients.[24] However, it was then realized that it was possible to individualize a patient's dose of ciclosporin by analysing the patients plasmatic concentrations (pharmacokinetic monitoring). This practice has allowed this drug to be used again and has facilitated a great number of organ transplants.

Clinical monitoring is usually carried out by determination of plasma concentrations as this data is usually the easiest to obtain and the most reliable. The main reasons for determining a drug's plasma concentration include:[25]

• Narrow therapeutic range (difference between toxic and therapeutic concentrations)
• High toxicity
• High risk to life.

Ecotoxicology is the branch of science that deals with the nature, effects, and interactions of substances that are harmful to the environment.[26][27]