Fedegari: Highlights on “Equivalent Time” F0

| By | Fedegari
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This paper summarizes the concept of Fo and its related parameters (D, z). Essential notions on sterilization kinetics are explained. The idea of physical and biological “equivalent time” is presented and its application in moist-heat sterilization processes is discussed.

Essentials on Sterilization Kinetics

It has been experimentally shown that the reaction of thermal degradation of micro-organisms obeys the laws of a first order chemical reaction (i.e. like a chemical decomposition reaction) in which the reaction rate is proportional, in each moment, only to the amount of product still to be degraded (or decomposed).

If N0 is the initial microbial population, after an exposure time t to defined and steady conditions, the population N will be expressed by each one of the following formulas:

Log (N0/N) = t/D;
Log N0 – Log N = t/D;
N = N0*10 (-t / D)

Parameter D in these formulas is physically a time and is defined decimal (or decadal) decay (or reduction). This parameter expresses in a quantitative way the resistance of a microbial species to a sterilizing treatment; for this reason, the Parenteral Drug Association of USA (PDA) calls it resistance value. In a thermal sterilization process, D-value is the time required to reduce down to one tenth of the initial value the population of:

· a specified microbial species
· prepared in a defined way
· treated on a specific substrate
· under specified and ideally steady process conditions.

Resistance value D is:

· expressed in minutes and tenths of minutes
· referred always and explicitly to a temperature, that is usually indicated as foot index: DT, for example D121, D134
· independent of the residual amount of the microbial population.

If liquid H2O (superheated water or condensing steam) is steadily in contact with the microorganisms to inactivate, the process is called moist heat sterilization. As well as on all the above conditions, in this type of process the resistance value D depends very strongly on the temperature T. If there is no contact between microorganisms and liquid H2O, the process is called dry heat sterilization. In this type of process, D-values useful for industry can be obtained only at notably higher temperature than in the case of moist heat sterilization, and their dependency on temperature is less sensible.

For the moist heat sterilization of most microbial species, the reference temperature is 121°C (formerly 250°F, exactly 121.11°C). The following are experimental facts:

· provided that all the other conditions, including the steady contact between microorganisms and liquid H2O remain unchanged, the resistance value DT becomes smaller if the temperature increases;
· inversely, D-values grow bigger if the temperature decreases.

For each microorganism at a given temperature, the knowledge of its Resistance value DT derives from experimental evaluations of initial microbial population N0 and of the surviving population N after the exposure time tT at the ideally constant temperature T. The value of DT is calculated as:

DT = tT/Log N00 – Log N

The real difficulty when using this formula lies both in the reliable knowledge of N0 and N and in the correct evaluation of the dwelling time tT at the foreseen conditions of constant temperature T under steady contact with liquid H2O. Regardless to the mathematical calculation finally involved, D-values are intrinsically experimental data and can not be predicted on a theoretical basis.

The effect of temperature

A temperature coefficient and is the common way to express the dependence of D-value on temperature for a specified microorganism. Temperature coefficient is defined as the number z of degrees of temperature variation required to change ten times a D-value. As already said, the D-value increases if the temperature decreases and decreases if the temperature increases.

Parameter z is:
· expressed in temperature degrees
· relevant to a specified microbial species
· referred to a small temperature range.

The definition of z-coefficient involves that:

D(T-z) = DT*10

Thanks to the definition of Parameter z, D-value undergoes a ten-fold variation if the temperature varies by z°C. For 1°C, the variation of D is given by the formula:

DT/D(T-1) = z√10

For instance:
· if z = 10°C, the ratio of D-values at two temperatures which differs by 1°C is given by 10√10 = 1.2589, i.e. D changes by about 26 % every degree centigrade
· if z = 5°C, the ratio of D-values at two temperatures which differs by 1°C is given by 5√10 = 1.5849, i.e. D changes by more than 58 % every degree centigrade
· if z = 20°C, the ratio of D-values at two temperatures which differs by 1°C is given by 20√10 = 1.1220, i.e. D changes by about 12 % every degree centigrade

It may be easily verified that by iteration of these variations over all the temperature range equal to z-coefficient, the D-values change by ten times, according to the definition of z. z-coefficient for a specified microorganism within a given temperature range is calculated by the following formula from two experimentally known values D2 e D1 at two temperatures T2 e T1:

z = (T2 – T1)/(LogD1 – Log D2)

It is worthy to repeat that a value of z-coefficient is reliable only within the bounds of the temperature range to which are referred the experimentally known D-values used for the calculation of it. The use of a z-coefficient outside this temperature range is not sound (extrapolations are always very risky). Inside the meaningful range, z-coefficient provides the instrument to calculate D-values at intermediate temperatures as mathematical issues of the two experimental ones at the bounds of the temperature range.

The Equivalent time

The trend of Resistance value D vs Temperature T may thus be known by the calculation of z-coefficient from at least two experimental D-values. To provide this mathematical relationship with a biological meaning, a continuous presence of liquid H22O (superheated water or condensing steam) in contact with the microorganisms is necessary.

The following question may now be discussed:

how many minutes of sterilization at an ideally constant reference temperature (i.e. 121°C) are tantamount to t minutes of sterilization at a different and/or variable temperature?

To answer this question, one has to start from the different resistance of a reference microorganism to the moist heat at different temperatures; this fact is expressed through the parameter D by the above formula:

DT = D0*10 (T0 – T)/z

The equivalent time at the reference temperature will be the time that yields the same reduction of the microbial population as under the actual conditions. In finite terms, this time is given by the formula:

F(T0,z) = t*10 (T – T0)/z

where Δt is a constant and suitably short interval of time between next measurements of actual exposure temperature T. When using this finite formula, T is regarded as constant during a time interval Δt. This equivalent time F is also called by PDA Lethality (factor). Lethality is thus the integration over the exposure time to moist heat of the Lethal rates L expressed by the formula:

L(T0,z) = 10 (T – T0)/z

Lethal rates are dimensionless and thus have no unit of measurement. They are a function only of the difference between actual temperature and reference temperature and of the value of z-coefficient.

If the references temperature T0 is set equal to 121°C (formerly 250°F, i.e. 121.11°C) and z-coefficient is set equal to 10°C (formerly 18°F), the equivalent time is conventionally called F0. In finite terms, it is given by the formula:

F0 = Δt*Σ10 (T – 121[.11])/10

where Δt is the constant and suitably short interval of time between next measurements of actual exposure temperature T. When using this finite formula, T is regarded as constant during a time interval Δt.

If the actual temperature T is lower than the reference temperature, the equivalent time is always shorter than the actual one, as the exponent of 10 in the formula is negative and the resulting power of 10 is lower than 1. On the other side, if the actual temperature T is higher than the reference temperature, the equivalent time is always bigger than the actual one, as the exponent of 10 in the formula is in this case positive and the resulting power of 10 bigger is than 1. Exactly at the reference temperature, equivalent time and actual time are identical, and the formula confirms this obvious fact because the exponent of 10 is exactly nought and the power of 10 is exactly 1. In other words, these formulas are valid throughout the entire temperature range within which the z-coefficient is deemed to be constant.

“Physical” and “biological” equivalent time

The “physical” equivalent time, FPHY, is that one calculated from the actual data of time and temperature measured during a sterilization process. If an autoclave maintained exactly the reference temperature for a time t, the consequence would be FPHY = t, regardless to the value of z-coefficient. On the contrary, assuming for instance z = 10°C:

· while the temperature is 0.5°C lower than the reference one, the equivalent time is equal to t*10(-0.5/10) = 0.89 t
· while the temperature is 2.0°C higher than the reference one, the equivalent time is equal to t * 10(2/10) = 1.585 t.

As said above, the number that multiplies the actual time to produce equivalent time is called L, lethal rate.

The formulas to calculate the lethal rates and the equivalent time are obtained by comparing D-values at the bounds of a temperature range within which the D-values undergoes a ten-fold change. This means that the concept of L (and F) depends on the concept of D, but this origin does not entail that any D-value of microorganisms is to be used in the calculation of the lethal rates L and of the physical equivalent time FPHY produced by an autoclave. Lethal rates and physical equivalent time depend only on the actual temperature, on the reference temperature and on z-value, i.e. the temperature range within which the Resistance of a microorganism assumed as reference changes by ten times, regardless to the actual values that express it.

Independently of the above, the exposure time tT necessary to obtain the aimed reduction of a given microbial population at sterilization temperature T is often called “biological” equivalent time, FBIO. Thanks to the definition of DT, FBIO is given by the formula:

FBIO = tT = DT*(Log N0 – Log N)

FBIO may be regarded as the equivalent target time of a sterilization process. If:

FPHY ≥ FBIO

the sterilization process reduces the microbial species deemed to be initially present with a population N0 to a final population of N. Thanks to the formulas of FPHY and of FBIO, the condition may also be written as:

Δt*Σ10(T–T0)/z DT*(Log N0 – Log N)

Another parameter has been introduced to “rectify” the actual FPHY-value, in order to comply directly with the actual D-value of a reference microorganism: the ratio F0/D0. has been called FD. By dividing the above equations through D and using this parameter the above equations may also be written:

FD ≥ Log N0 – Log N

This simplified way of writing must not hide the essential requirement that the reference temperature has always to be the same for FPHY and D.

How to use equivalent time F0

To speak of equivalent sterilization time, it is always necessary that the essential conditions for the effectiveness of sterilization are complied with. In the case of moist heat sterilization, the exposure to temperature is effective as purported to be only as long as the microorganisms are in contact with liquid H2O (superheated water o condensing steam). If this condition is not complied with, equivalent time becomes only a mathematical formula without any biological meaning and to use it is a non-sense.

If water containing products are sterilized (including simple saline solutions and most of the food specialities in sealed containers), no doubt that liquid H2O (in this case superheated water) is present in contact with microorganisms, because it is already contained in the bulk of the items to be sterilized. This case is also called bulk sterilization and the calculation of equivalent time may usefully include heating and cooling phases, even if temperatures lower that 110°C supply no appreciable lethality to load. In this first case, the steam fed into the autoclave or the water circulated in it is not a sterilizing agent, but only the heating one.

On the contrary, the sterilization of so called porous/hard goods (P/HG) is a surface sterilization process and the effective contact of the microorganisms with liquid H2O (in this case almost always condensing steam) may be obtained only after a complete removal of the air initially surrounding the load and by the presence of saturated steam in contact with the external surfaces, and internal if any, of the load. In this second case, the steam fed into the autoclave or the water circulating is both the heating agent and the sterilizing one.

As the effectiveness of the sterilization of P/HG does not depend only on temperature, it makes no sense to start the calculation of the equivalent time for such goods before all the sterilization conditions are fully attained, i.e. in advance of the so called plateau period, when no residual air is supposed to be any longer present in the chamber and around the load. The equivalent time itself may be regarded in this case only as an additional instrument of control. If a programmable temperature threshold is provided to start the calculation of the equivalent sterilization time, this threshold has thus to be set equal or very close to the minimum sterilization temperature. This is very important not only before the exposure phase, but also after it, because both the drying vacuum and the cooling by air circulation immediately destroy the condition of contact of condensing steam with the load.

Also in the case of some special products, as dialysis filters or multibag systems for blood, the calculation of equivalent sterilization time is not useful and may be very misleading, regardless to the fact that a counterpressure autoclave is often used to sterilize them.

For these products, the effective sterilization conditions depend on equilibria of partial steam and air pressure inside the products and the validation exercise must include an accurate biological study. Due to the possible presence of residual air or other non-condensable gases inside these products, the sterilization effective temperature, i.e. the steam condensation temperature, is often different in a non predictable way from the measurable temperature inside. Therefore, for these products it makes no sense to speak of equivalent sterilization time on the basis of thermometric data: the calculation of the temperature-time function F would become meaningless and its results would be misleading.


By V. Mascherpa,
Senior consultant R&D

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