Autoclave: Introduction, Fundamental structures, Principle, Types, Sterilization Control, Working Mechanisms, Uses, and Precautions
Table of Contents
An autoclave is the most common method of sterilization in the laboratory working on moist heat. Sterilization is the process of removing or destroying all microorganisms including viruses, bacteria, and their spores from the article or surface without destroying its quality and quantity. It is a physical method of sterilization due to moist heat. Factors influencing sterilization by heat are the nature of heat i.e dry or moist, temperature and time, number of microorganisms, nature of microorganisms, type of microorganism, and presence of organic material.
Mode of action, moist heat kills microorganisms by coagulating and denaturing their enzymes and their structural proteins. Heating in presence of water is preferred over dry heat because of its rapid killing and is effective even at a lower temperature than dry heat due to its latent heat. Temperature is above 100°C and sterilization by dry saturated steam under pressure. The most efficient method of sterilization is commonly called autoclaving and the instrument used is an autoclave.
Essentially a modified pressure cooker may be horizontal or vertical. It contains a double-walled or Jacketed chamber made of stainless steel or gunmetal with a supporting frame. In the modern type of autoclave, steam circulates within the jacket and is supplied under high pressure to the closed inner chamber where goods are kept for sterilization. One-fifth part of the cylinder is filled with water and the materials to be sterilized are placed inside. The lid is closed securely with a discharge tap on it open. A safety valve is present to permit the escape of steam from the chamber. It works on the principle of steam under pressure. It was invented by Charles Chamberland in 1879.
It utilizes the thermodynamics principle of water. Water boils when its vapor pressure equals that of the surrounding atmosphere. When the pressure inside the closed vessel increases, the temperature at which water boils also increases. Dry saturated steam at high pressure when strikes the cooler surfaces of the articles in the autoclave, condenses into water, and efficiently destroys all microorganisms along with thermal-resistant bacterial spores.
According to structure
According to the structures, autoclaves are of the following types and they are-
Simple non-jacketed autoclave, steam jacketed autoclave with automatic air and condensate discharge, and high pre-vacuum sterilizers.
According to function
According to function, autoclaves are of the following types and they are-Simple laboratory autoclaves, transportable benchtop autoclaves, large simple autoclaves, downward displacement laboratory autoclaves, media preparatory autoclaves, and multi-purpose laboratory autoclave
Sterilization cycle
The sterilization cycle includes warming of the chamber, vacuum extraction, pre-steam penetration time, steam penetration time, holding time, and cooling time.
Dynamics of sterilization
Thermal death time (TDT): It is the time in minutes required to kill all cells in a suspension at a given temperature. It is highly dependent on the inoculum size. Thermal death point(TDP): It is the temperature needed to kill all cells in suspension after a fixed exposure time. D Value(decimal reduction time, DRT): It is the time in minutes needed at a particular temperature to reduce the viable organisms by 90% i.e. to 10% or by 1 log 10. The d value is independent of inoculum size and is inversely related to temperature.
Sterilization time is inversely proportional to the temperature at constant pressure. For example 115°C, 10 lb/in 2 for 45 minutes; 121°C, 15 lb/in 2 for 15-20 minutes; 126°C, 20 lb/in 2 for 10 minutes and 134°C, 30 lb/in 2 for 3 minutes.
Common sterilization condition is at 121°C for 15-20 minutes at 15 lb/sq inch but it may vary as 10 lbs pressure for 10 minutes is for culture media. 15 lbs pressure is for 20 minutes for infected material. 20 lbs,30 minutes is for dressing and towels whereas 5 lbs-30 minutes is for gloves.
Automatic Process Control: It carries through the sterilization cycle according to a pre-selected scheme for the duration, temperature, and pressure of each stage. Recording Thermometer: Graphic record of temperature changes in the chamber discharge channel avoiding errors in timing the holding period. Thermocouple: It is when kept inside the test article and attached to a potentiometer, it indicates the temperature inside the test article during autoclaving. Chemical Indicators: Browne’s Sterilizer has a red solution that turns green when heated at 115°C for 25 minutes (type 1), or 15 minutes (type 2). Store it at 20°C to avoid pre-mature color change. Adhesive Tapes: Bowie-Dick autoclave tape test for steam penetration.
Biological indicators–Organism: Bacillus stearothermophilus (NCTC 10003 ATCC 7953), a thermophile that requires to be cultivated at 55-60°C. Its spores are killed at 121°C in 12 minutes. Preparation: culture grown aerobically on nutrient agar for 5 days is suspended in sterile water to a concentration of one million spores per milliliter. Small strips of filter paper soaked in the suspension are dried at room temp and packed in envelopes.
Initially check the water level. Place the articles to be sterilized in the center of the largest or most densely packed items and some in the coolest part. Now switch on the autoclave. Check the pressure and wait for the proper time (If there is an automated system, no need for these steps). After autoclaving, the envelope is cut with sterile scissors and the strip is transferred to a recovery medium, e.g. thioglycolate broth with strict precautions against contamination. Incubate the tube for 7 days at 55°C and examined for growth. An unautoclaved spore strip is used as the positive control and an uninoculated tube of the medium as a negative control. Use results in terms of the degree of heat resistance of preparation.
It is widely used for the following purposes -sterilization of culture media, aqueous solutions, empty bottles, impervious containers, surgical instruments, wrapped dry goods and dressings, gowns and dressings, rubber goods, syringes, etc.
Advantages: It is a very effective way of sterilization, quicker than a hot air oven.
Disadvantage: Articles may trapped air, and take a long time to cool.
Air must be completely removed until saturated steam is filled. Contents should be arranged loosely to ensure the free circulation of steam. It shouldn’t allow forming of supersaturated steam. The lid should be opened only after pressure gets down to normal. Follow manufacturers’ guidelines. Avoid standing directly in front of the autoclave door when opening it. Cool to below 80°C before opening.
There is no clear and proven concept but several theories are as follows-Spores have low water content and therefore essential factor in resistance.
-According to Warth (1985), the stability of protein could be intrinsic, or due to the presence of a substance ( might be Calcium-diplocolinate) that helps to stabilize or due to the removal of water. Several properties of spore i.e. thermotolerance, mineralization, and thermal adaptation might help in resistance. Small acid-soluble spore proteins(SASPs) may also play some role.
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