Clearance (pharmacology)
In pharmacology, clearance is a pharmacokinetic measurement of the volume of plasma from which a substance is completely removed per unit time. Usually, clearance is measured in L/h or mL/min.^{[1]} The quantity reflects the rate of drug elimination divided by plasma concentration. Excretion, on the other hand, is a measurement of the amount of a substance removed from the body per unit time (e.g., mg/min, μg/min, etc.). While clearance and excretion of a substance are related, they are not the same thing. The concept of clearance was described by Thomas Addis, a graduate of the University of Edinburgh Medical School.
Substances in the body can be cleared by various organs, including the kidneys, liver, lungs, etc. Thus, total body clearance is equal to the sum clearance of the substance by each organ (e.g., renal clearance + hepatic clearance + lung clearance = total body clearance). For many drugs, however, clearance is solely a function of renal excretion. In these cases, clearance is almost synonymous with renal clearance or renal plasma clearance. Each substance has a specific clearance that depends on how the substance is handled by the nephron. Clearance is a function of 1) glomerular filtration, 2) secretion from the peritubular capillaries to the nephron, and 3) reabsorption from the nephron back to the peritubular capillaries. Clearance is variable in zeroorder kinetics because a constant amount of the drug is eliminated per unit time, but it is constant in firstorder kinetics, because the amount of drug eliminated per unit time changes with the concentration of drug in the blood.^{[2]}^{[3]}
Clearance can refer to the volume of plasma from which the substance is removed (i.e., cleared) per unit time or, in some cases, intercompartmental clearances can be discussed when referring to redistribution between body compartments such as plasma, muscle, and fat.^{[1]}
Definition
When referring to the function of the kidney, clearance is considered to be the amount of liquid filtered out of the blood that gets processed by the kidneys or the amount of blood cleaned per time because it has the units of a volumetric flow rate [ volume per unit time ]. However, it does not refer to a real value; "the kidney does not completely remove a substance from the total renal plasma flow."^{[4]} From a mass transfer perspective^{[5]} and physiologically, volumetric blood flow (to the dialysis machine and/or kidney) is only one of several factors that determine blood concentration and removal of a substance from the body. Other factors include the mass transfer coefficient, dialysate flow and dialysate recirculation flow for hemodialysis, and the glomerular filtration rate and the tubular reabsorption rate, for the kidney. A physiologic interpretation of clearance (at steadystate) is that clearance is a ratio of the mass generation and blood (or plasma) concentration.
Its definition follows from the differential equation that describes exponential decay and is used to model kidney function and hemodialysis machine function:

(1)
Where:
 is the mass generation rate of the substance  assumed to be a constant, i.e. not a function of time (equal to zero for foreign substances/drugs) [mmol/min] or [mol/s]
 t is dialysis time or time since injection of the substance/drug [min] or [s]
 V is the volume of distribution or total body water [L] or [m^{3}]
 K is the clearance [mL/min] or [m^{3}/s]
 C is the concentration [mmol/L] or [mol/m^{3}] (in the United States often [mg/mL])
From the above definitions it follows that is the first derivative of concentration with respect to time, i.e. the change in concentration with time.
It is derived from a mass balance.
Clearance of a substance is sometimes expressed as the inverse of the time constant that describes its removal rate from the body divided by its volume of distribution (or total body water).
In steadystate, it is defined as the mass generation rate of a substance (which equals the mass removal rate) divided by its concentration in the blood.
Clearance, halflife and distribution volume
There is an important relationship between clearance, elimination halflife and distribution volume. The elimination rate constant of a drug Κel is equivalent to total clearance divided by the distribution volume (Κel=Cltot/Vd)(note the usage of Cl and not Κ, not to confuse with Κel). But Κel is also equivalent to ln2 divided by elimination rate halflife t1/2 (Κel=ln2t1/2). Thus, Cltot = ln2 Vd/t1/2. This means, for example, that an increase in total clearance results in a decrease in elimination rate halflife, provided distribution volume is constant. Derivation of these equations can be found in e.g. Rang and Dale's Pharmacology ^{[6]}
Effect of plasma protein binding
For substances that exhibit substantial plasma protein binding, clearance is generally dependent on the total concentration (free + proteinbound) and not the free concentration.^{[7]}
Most plasma substances have primarily their free concentrations regulated, which thus remains the same, so extensive protein binding increases total plasma concentration (free + proteinbound). This decreases clearance compared to what would have been the case if the substance did not bind to protein.^{[7]} However, the mass removal rate is the same,^{[7]} because it depends only on concentration of free substance, and is independent on plasma protein binding, even with the fact that plasma proteins increase in concentration in the distal renal glomerulus as plasma is filtered into Bowman's capsule, because the relative increases in concentrations of substanceprotein and nonoccupied protein are equal and therefore give no net binding or dissociation of substances from plasma proteins, thus giving a constant plasma concentration of free substance throughout the glomerulus, which also would have been the case without any plasma protein binding.
In other sites than the kidneys, however, where clearance is made by membrane transport proteins rather than filtration, extensive plasma protein binding may increase clearance by keeping concentration of free substance fairly constant throughout the capillary bed, inhibiting a decrease in clearance caused by decreased concentration of free substance through the capillary.
Derivation of equation
Equation 1 is derived from a mass balance:

(2)
where:
 is a period of time
 the change in mass of the toxin in the body during
 is the toxin intake rate
 is the toxin removal rate
 is the toxin generation rate
In words, the above equation states:
 The change in the mass of a toxin within the body () during some time is equal to the toxin intake plus the toxin generation minus the toxin removal.
Since

(3)
and

(4)
Equation A1 can be rewritten as:

(5)
If one lumps the in and gen. terms together, i.e. and divides by the result is a difference equation:

(6)
If one applies the limit one obtains a differential equation:

(7)
Using the Product Rule this can be rewritten as:

(8)
If one assumes that the volume change is not significant, i.e. , the result is Equation 1:
Solution to the differential equation
The general solution of the above differential equation (1) is:^{[8]}^{[9]}

(9)
Where:
 C_{o} is the concentration at the beginning of dialysis or the initial concentration of the substance/drug (after it has distributed) [mmol/L] or [mol/m^{3}]
 e is the base of the natural logarithm
Steadystate solution
The solution to the above differential equation (9) at time infinity (steady state) is:

(10a)
The above equation (10a) can be rewritten as:

(10b)
The above equation (10b) makes clear the relationship between mass removal and clearance. It states that (with a constant mass generation) the concentration and clearance vary inversely with one another. If applied to creatinine (i.e. creatinine clearance), it follows from the equation that if the serum creatinine doubles the clearance halves and that if the serum creatinine quadruples the clearance is quartered.
Measurement of renal clearance
Renal clearance can be measured with a timed collection of urine and an analysis of its composition with the aid of the following equation (which follows directly from the derivation of (10b)):

(11)
Where:
 K is the clearance [mL/min]
 C_{U} is the urine concentration [mmol/L] (in the USA often [mg/mL])
 Q is the urine flow (volume/time) [mL/min] (often [mL/24 h])
 C_{B} is the plasma concentration [mmol/L] (in the USA often [mg/mL])
When the substance "C" is creatinine, an endogenous chemical that is excreted only by filtration, the clearance is an approximation of the glomerular filtration rate. Inulin clearance is less commonly used to precisely determine glomerular filtration rate.
Note  the above equation (11) is valid only for the steadystate condition. If the substance being cleared is not at a constant plasma concentration (i.e. not at steadystate) K must be obtained from the (full) solution of the differential equation (9).
See also
References
 ^ ^{a} ^{b} Rowland M, Tozer TM (2011). Clinical Pharmacokinetics and Pharmacodynamics, Concepts and Applications (4th ed.). Baltimore MD: Lippincott Williams & Wilkins.
 ^ "Pharmacokinetics objectives". Pharmacology2000.com. 20061227. Retrieved 20130506.
 ^ Kaplan Step1 Pharmacology 2010, page 14
 ^ Seldin DW (2004). "The development of the clearance concept". Journal of Nephrology. 17 (1): 166–71. PMID 15151274.
 ^ Babb AL, Popovich RP, Christopher TG, Scribner BH (1971). "The genesis of the square meterhour hypothesis". Transactions of the American Society for Artificial Internal Organs. 17: 81–91. PMID 5158139.
 ^ Ritter J, Flower R, Henderson G, Rang H. Rang & Dale's Pharmacology. 8th ed. London. Churchill Livingstone; 2015
 ^ ^{a} ^{b} ^{c} Winter ME (2003). "Plasma protein binding". Basic clinical pharmacokinetics (4th ed.). Lippincott Williams & Wilkins. p. 32. ISBN 9780781741477.
 ^ Gotch FA (1998). "The current place of urea kinetic modelling with respect to different dialysis modalities". Nephrology, Dialysis, Transplantation. 13 (Suppl 6): 10–4. doi:10.1093/ndt/13.suppl_6.10. PMID 9719197. Full Text
 ^ Gotch FA, Sargent JA, Keen ML (August 2000). "Whither goest Kt/V?". Kidney International. 76 (Suppl 76): S318. doi:10.1046/j.15231755.2000.07602.x. PMID 10936795.
Further reading
 Sharifi M, Ghafourian T (January 2014). "Estimation of biliary excretion of foreign compounds using properties of molecular structure". The AAPS Journal. 16 (1): 65–78. doi:10.1208/s122480139541z. PMC 3889537. PMID 24202722.