← Common Core coursesBMS 114 · General Microbiology I
BMS 114 · Common Core (Tronc commun)Section 8.1 · Controlling microbial growth
Section 31 of 33

Sterilisation, disinfection and asepsis

Choose the right word — sterilisation, disinfection, antisepsis, sanitisation or degerming — for a real nursing situation, and justify it from what must be destroyed and what is being treated.

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  1. Learn gives you one short idea at a time. Each idea starts with a single sentence, then explains it, gives an example, and asks you a small question you can answer straight away.
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Why this matters

The words on this page decide what you do with your hands. If you call a wipe-down “sterilisation”, you may put a contaminated instrument into a wound; if you treat an antiseptic as just a disinfectant, you may use a floor cleaner on a patient’s skin. The ladder in this section — sterilisation, disinfection, antisepsis, sanitisation, degerming — is a ladder of claims, and every rung tells you what must be destroyed, what may survive and what the object will touch next. Choosing the right word is choosing the safe action.

What you need to know first

You need only the idea that some microbes are harder to kill than others. The key words are defined as we go and collected in the recap: sterilisation, disinfection, antisepsis, sanitisation and degerming, together with asepsis, bactericidal and bacteriostatic. Nothing else is assumed; the physical methods named here are expanded in section 8.2, while the chemical vocabulary — disinfectants and antiseptics — is treated in this section itself.

Words to know (8)
Sterilisation
The process that destroys all forms of microbial life on an object or in a material, including bacterial endospores. An autoclave cycle at 121 °C for 15 minutes at 15 psi sterilises a surgical instrument.
Disinfectant
A chemical applied to an object or a material that tends to reduce or inhibit microbial growth and usually does not sterilise. A chlorine-releasing solution used on a commode is a disinfectant.
Antiseptic
A chemical agent applied to living tissue to kill microbes, and which must not be so harsh that it damages that tissue. Chlorhexidine or povidone-iodine used on skin before an injection is an antiseptic.
Sanitisation
The process of reducing microbial contamination to an accepted safe level, which cleans an object without necessarily sterilising it. Washing a ward floor with detergent and drying it sanitises the floor.
Degerming
The removal of microbes from a limited area, such as the skin around an injection site, mainly by mechanical action. An alcohol-soaked swab of the skin before an injection degerms that small area.
Asepsis
The absence of pathogens from an object or an area; an aseptic technique is designed to prevent pathogens from entering the body. Setting up a sterile field for a dressing is aseptic technique.
Bactericidal
Describing an agent that kills bacteria, as opposed to one that only stops them growing. A bactericidal agent leaves fewer living cells behind, so the count falls after it is used.
Bacteriostatic
Describing an agent that inhibits the growth of microorganisms without killing them, so growth can resume when it is removed. A bacteriostatic drug holds an infection in check while the immune system clears the bacteria.
One idea at a timeIdea 1 / 6

In one sentence Sterilisation is the destruction of all forms of microbial life on an object or in a material, including the endospores that resist almost everything else.

Sterilisation destroys all microbial life, endospores included

Sterilisation is the strongest claim on the ladder: it means that no living microorganism remains, and it is the only rung that includes bacterial endospores. An endospore is a dormant, dehydrated form that a few bacteria build when conditions turn hostile; it survives boiling, drying, many chemicals and radiation, which is why it is called the most resistant form of microbial life. A method that kills only growing cells therefore leaves endospores alive: it can disinfect, but it cannot sterilise. The reference conditions are moist heat at 121 °C for 15 minutes at 15 psi in an autoclave, and dry heat in a hot-air oven. The supplied notes give dry heat as 170 °C for 120 minutes, which is not the standard figure; the reference pair is 160 °C for 2 hours, or 170 °C for 1 hour.

For example

A pair of surgical scissors that will cut tissue must come out of an autoclave cycle; wiping it with a chemical and drying it is disinfection, and a boiled instrument is only disinfected, because endospores can survive boiling.

Pause and check yourself

Why is boiling an instrument in water at 100 °C not enough to call it sterile?

Show the answer

Boiling kills most growing bacteria and many viruses, but bacterial endospores survive it. Sterility means the destruction of all microbial life, so a method that leaves endospores alive can only disinfect.

Read detailed explanations
Kill kinetics: why sterility is a probability, not a moment

Two objects can leave the same machine carrying very different numbers of survivors, which is why sterilisation is taught as a probability rather than a moment. When a population is exposed to a lethal agent, killing follows first-order kinetics: in each unit of time the same fraction of the surviving cells dies, not the same number. That is why microbiologists count in powers of ten. A one-log reduction destroys 90 % of the population, a two-log reduction 99 %, and a six-log reduction leaves one survivor in a million. The decimal reduction time, or D-value, is the time needed at a given temperature to reduce the population by one power of ten; for a heat-resistant endospore former such as Geobacillus stearothermophilus, D at 121 °C may be one to two minutes, whereas a fragile vegetative cell may have a D of a few seconds. A sterilisation cycle is then designed from two numbers: the bioburden, meaning how many organisms are present before treatment, and the required sterility assurance level, conventionally a probability of no more than one surviving organism in a million units. If the bioburden is one million spores, a six-log reduction leaves about one; if cleaning first cuts the load to one hundred, the same six-log kill leaves one in ten thousand. This explains a rule that surprises beginners: instruments must be cleaned before they are sterilised, because blood, pus and dried organic matter shield organisms and raise the effective bioburden. It also explains why a six-log reduction is not the same as sterility. Six logs is a numerical target for a defined starting load, while sterility is an absolute statement about the object in front of you; moreover, the survivor curve is extrapolated from a sample, so the residual risk is a probability, never a direct count. For the same reason, true sterilisation requires a sporicidal process, because endospores have the highest D-values and are the last cells to die; a chemical that reliably kills vegetative bacteria but not spores can disinfect, yet it cannot be called a sterilant.

What is being treated decides the word: matrix, tissue and toxicity

Whether a method counts as sterilisation, disinfection or antisepsis depends less on the chemical than on the surface it touches and on what is allowed to survive. Sterilisation is asked of inanimate objects that will enter sterile tissue or the bloodstream: surgical instruments, implants, infusion fluids. Disinfection is asked of inanimate surfaces and equipment that touch intact skin or mucous membranes: a commode, a stethoscope, a blood-pressure cuff. Antisepsis is asked of living tissue, and there the requirement changes direction, because the agent must kill microbes without destroying the cells it is meant to protect. This is why the same molecule can appear under two labels. Chlorhexidine and povidone-iodine are antiseptics at skin concentrations and disinfectants at higher concentrations on a floor; sodium hypochlorite is an excellent disinfectant and a tissue irritant, so it is never left on a wound. Efficacy is never a property of the agent alone. It depends on concentration, contact time, temperature, pH and, above all, on the organic load: blood, serum and pus inactivate chlorine, oxidise peroxides and physically shield organisms inside clots. It also depends on whether the organisms form a biofilm, the slimy community that adheres to catheters, drains and water pipes and can be hundreds of times more tolerant than the same species growing freely. Some agents, called high-level disinfectants, kill all vegetative bacteria plus mycobacteria and most viruses but not large numbers of spores; glutaraldehyde, ortho-phthalaldehyde and peracetic acid belong here, and they are used for heat-sensitive endoscopes. Prions, the misfolded proteins that cause Creutzfeldt–Jakob disease, are not living and are not killed by ordinary cycles at all; instruments contaminated with them need specific, much harsher protocols. Nursing follows directly from this: an endoscope and a scalpel are handled by two different departments, skin preparation is timed to dry before the needle is inserted, and soaking time is read from a clock rather than guessed, because a shorter contact time silently converts a disinfection step into a decorative one.

Antibiotics are drugs, not disinfectants: selective toxicity and the wrong drug

An antibiotic is a drug that must travel through a patient to reach an infection, and that journey is what separates it from a disinfectant. The founding idea is selective toxicity: the agent must damage a structure or a pathway that the microbe has and the human cell does not. Penicillins and cephalosporins attack the peptidoglycan wall, which human cells never build; aminoglycosides and macrolides bind the 70S bacterial ribosome, which differs from our 80S ribosome; quinolones disable DNA gyrase; sulphonamides block a folate pathway the bacterium cannot borrow. Because these targets are bacterial, an antibiotic has no target at all in a virus. A virus is not a cell: it is a genome inside a protein coat that hijacks the host’s own machinery, so a drug that blocks bacterial walls or bacterial ribosomes has nothing to grip. This is why giving amoxicillin for a cold, a sore throat caused by rhinovirus or influenza is not a mild mistake but a complete category error: the drug cannot shorten the illness, cannot prevent pneumonia, and cannot protect contacts. It does real harm. Every course of antibiotics selects resistant survivors and damages the patient’s own microbiota; broad-spectrum agents are worst, because they clear the colon’s protective flora and leave the field open to Clostridioides difficile, the cause of antibiotic-associated colitis. Antiviral drugs work on the opposite principle: they target viral enzymes, such as the neuraminidase of influenza or the polymerase of hepatitis B, and they are useful only when they match the virus and are started early. The nursing consequences are specific. Take a specimen before the first dose, so that the laboratory can still grow the organism. Ask whether the illness is likely bacterial or viral, and do not press for a drug when the prescriber has correctly withheld one. Teach the patient to finish the prescribed course and to expect that some antibiotics lower the effectiveness of oral contraceptives or interact with warfarin. None of that makes an antibiotic a surface cleaner; a disinfectant acts outside the body, at a concentration far too toxic to swallow, while an antibiotic acts inside it, at a concentration the body can tolerate.

Explore the diagram

Look at the whole drawing first. Then select one numbered part and connect it to the idea you just read.

The ladder of microbial control: from an absolute claim to a clean surface

Read the ladder downwards. Each rung is a weaker promise than the one above it: sterilisation allows nothing living to remain, disinfection destroys growing pathogens, antisepsis acts on living tissue, sanitisation reaches an accepted safe level, and degerming simply removes organisms from a small area. The question to ask is always what the object will touch next.

New to diagrams? Read this first
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  2. Press Play, or use the arrows, to move through the numbered parts in order. The drawing stays still; only the highlight moves.
  3. Click a number, or its name in the list below, to read what that part is and why it matters. Use “Hide labels” when you want to test your memory.
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01 / 5Sterilisation: the absolute rung

The ladder of microbial control: from an absolute claim to a clean surfaceRead the ladder downwards. Each rung is a weaker promise than the one above it: sterilisation allows nothing living to remain, disinfection destroys growing pathogens, antisepsis acts on living tissue, sanitisation reaches an accepted safe level, and degerming simply removes organisms from a small area. The question to ask is always what the object will touch next.The ladder of microbial controlFrom the strongest claim to a clean surface1 · Sterilisation — the absolute claimDestroys all life, endospores includedMoist heat 121 °C · 15 min · 15 psiDry heat 160 °C · 2 h or 170 °C · 1 h2 · Disinfection — growing pathogensEndospores and some viruses may surviveChemical on objects; rarely sterilises3 · Antisepsis — living tissueMust not damage skin or mucosaLess toxic than a surface disinfectant4 · Sanitisation — an accepted levelReduces contamination to a safe levelA standard defines the safe level5 · Degerming — a limited areaMostly mechanical: swab or handwashRemoves microbes; does not kill allAlongside the ladder: decontaminationTreats an object or surface to be safeRanks the claim, not chemical strengthSterile has no degrees · clean by norm

If the drawing is wider than this panel, scroll it sideways. Labels stay readable; the numbered explanations below show the same ideas.

Sterilisation: the absolute rung

Sterilisation is the top rung because it is the only claim that includes endospores. Moist heat at 121 °C for 15 minutes at 15 psi, or dry heat at 160 °C for 2 hours or 170 °C for 1 hour, destroys all microbial life; anything less is disinfection. Boiling at 100 °C leaves spores alive, so a boiled instrument is never sterile.

A ranking of claims, not a scale of chemical strength or a list of methods: section 8.2 describes the physical techniques, the chemical vocabulary of disinfectants and antiseptics is defined in section 8.1 itself, and the times and concentrations shown here are reference values for the named processes, not the only valid cycles. A boiled instrument is disinfected, never sterile.

Key points to remember

  • Sterilisation destroys all microbial life, including endospores: moist heat at 121 °C for 15 minutes at 15 psi, or dry heat at 160 °C for 2 hours or 170 °C for 1 hour.
  • Disinfection destroys vegetative pathogens but not necessarily endospores or all viruses; a disinfectant acts on objects and usually does not sterilise.
  • Asepsis is the absence of pathogens and a way of working; antisepsis is chemical disinfection of living tissue, with an agent mild enough not to damage it.
  • Biocide, germicide, sporicide, bactericide, fungicide, virucide and amoebicide name what is killed; bactericidal kills while bacteriostatic only inhibits growth.
  • Degerming removes microbes from a limited area, decontamination makes an object safe to handle, and sanitisation reduces contamination to an accepted safe level without sterilising.
Go deeper

Worked example

Four decisions on one ward round. You are the nurse in charge of a treatment room. In the next ten minutes you must prepare for a deep intramuscular injection, receive a laryngoscope blade used on a patient with a difficult airway, deal with a blood spill on the floor, and decide how to clean the patient’s bedside table. For each one, say which word on the ladder applies and what must happen to the instrument or surface.

  1. Identify what will touch what. The injection needle breaks the skin and enters muscle, so it must be sterile and single-use. The laryngoscope blade touches mucous membrane and must be sterilised before reuse. The floor is touched only by shoes and cleaning equipment, so disinfection and decontamination are enough. The bedside table is touched by intact skin and by objects, so disinfection and sanitisation apply.
  2. Skin preparation is antisepsis, not sterilisation. Clean the injection site with an antiseptic and let it dry for the time the product requires. The skin cannot be sterilised, and a shortened drying time reduces the killing effect, because the agent needs contact time to act.
  3. The blade is cleaned first, then sterilised. Visible organic matter must be removed before sterilisation, because blood and tissue protect organisms and consume the sterilising agent. If the blade is heat-sensitive, use a validated low-temperature sterilisation process; a chemical wipe is disinfection only.
  4. The blood spill is decontaminated and disinfected. Put on gloves and an apron, remove the bulk with absorbent material, clean the area with detergent, then apply a disinfectant at the correct concentration and contact time. This makes the surface safe to handle; it does not sterilise the floor.
  5. Handwashing and the bedside table close the loop. Hand hygiene before and after each action is degerming, and the table is cleaned to an accepted safe level, which is sanitisation. Record what was used and how long it was left in contact, because the written record is part of the claim.

The ladder is not a ranking of effort but a ranking of claims. Say “sterile” only when nothing living remains, “disinfected” when vegetative pathogens have been destroyed, “antisepsis” when the surface is living tissue, and “sanitised” or “degermed” when you have made something safe rather than sterile. The word you choose is the promise you are making about the object in your hand.

Common misconception

The commonest beginner error is to treat disinfectants and antiseptics as the same thing, or to assume that a stronger chemical is always the safer choice. A disinfectant may be far too harsh for skin, and using it on tissue can damage the very barrier that keeps infection out. A second error is to believe that boiling, alcohol wipes or sunlight achieve sterilisation, when all three leave endospores alive. A third is to think that an antibiotic sterilises the body: it acts at a specific target, at a tolerable dose, and the patient’s own defences and normal microbiota are part of the outcome.

Check your reasoning

Think of a task you have performed or watched: cleaning a wound, preparing an injection, washing a bedpan, wiping a mattress. Which word on the ladder did that task really achieve, and what would have to change for the claim to move one rung higher?

Reveal an answer

Take washing a bedpan under running water with detergent. That is decontamination plus sanitisation: the object is made safe to handle and the microbial load is reduced to an accepted level, but endospores and some viruses may remain. To move one rung higher, the bedpan would have to be treated with a disinfectant at the correct concentration and contact time, which destroys vegetative pathogens. To reach the top rung it would have to be sterilised by a validated process such as an autoclave or a chemical sterilant, because only then are endospores destroyed as well.

Where this comes from

  • BMS 114 General Microbiology I lecture notes (supplied) · Lecture notes thirteen, “Terminologies relating to control of microbial growth”, lines 1730–1769
  • Correction to the supplied notes — dry-heat sterilisation values · Correction to the supplied notes: lines 1736–1737 give dry heat as 170 °C for 120 minutes. The standard reference pair is 160 °C for 2 hours, or 170 °C for 1 hour, and the section teaches that pair instead.
  • Correction to the supplied notes — spelling of bactericidal · Correction to the supplied notes: line 1759 writes “bacteriocidal”. The correct English term is bactericidal; the notes’ description of bacteriostatic agents at line 1760 is retained.
  • Beyond the supplied notes — kill kinetics, absolute sterility and agent selection · the log-kill concept, the D-value and the sterility assurance level, the argument that “sterile” is absolute, the resistance of non-enveloped viruses and mycobacteria to alcohol, the action of named antiseptics and high-level disinfectants, the role of organic load and biofilm, and the selective toxicity of antibiotics are standard microbiology and infection-control knowledge; the notes cover the vocabulary at lines 1730–1769 but not these mechanisms.

Lesson progress is saved on this device for the current learner. Practice answers stay separate and are not stored.

About this course and its sources

Bilingual lessons organised from the supplied BMS 114 General Microbiology I lecture notes (Mr Ngotelo F. Ambene, Mr Lyonga B. Lyonga & Mr Fumbui Louis Ngong). Diagrams are original educational schematics; sections that correct the notes or go beyond them say so in their sources. Nursing and French-language review are pending.