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Biological Waste Disposal

Biological agents are assessed before being placed in the appropriate waste stream.

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> Types of biological wasteÌý
> Deactivation and disposal of biological waste
>ÌýDisinfectionÌý
> Disinfectant effectiveness
> Autoclaves
> Incineration
>ÌýUltraviolet light

Departmental responsibilitiesÌý


The Ïã¸ÛÁùºÏ²Ê waste streams are managed by Estates who have produced the Ïã¸ÛÁùºÏ²Ê Clinical Waste Procedures.

All departments must have a hazardousÌýwaste plan which ensures waste produced by the department is identified and managed before entered into the waste stream.

Types of biological waste


Biological Waste can include the following:

  • Infectious waste - wild type microorganisms or materials containing pathogens
  • Genetically Modified Organism waste - the class of the GMO will determine the waste route
  • Offensive waste - not infectious and does not contain any pharmaceutical or chemical substances. Examples are sterilised masks, gowns and other PPE or hygiene waste such as nappies
  • Plasters and similar waste-dressing from non-infectious wounds (dentistry and fracture clinics)Ìýhave their own waste stream
  • Waste medicines -Ìýthis depends on the risk posed by the medicine – cytotoxic and cytostatic medicines are separated from other medicines
  • Sharp and related waste -ÌýdependingÌýon the type of contaminationÌý
  • Anatomical waste -Ìýdepends on whether the agent isÌýinfectious and if it has been chemically preserved

For more information refer to Laboratory wasteÌýweb page.Ìý

Deactivation and Disposal of WasteÌý


There are a range of options available for the inactivation and disposal of biological waste. The main methods used are through chemical disinfection, heat treatment through autoclave and incineration or UV.

Before disposing of biological agents, the following factors need to be considered and assessed:

  • The amount of agent
  • The medium that the agent is in
  • The infectious nature of the agent
  • The treatment of the agent before entry into the waste stream
  • Any other hazards e.g. toxic chemicals or radiation

    Disinfection


    Disinfection is not the same as sterilisation and is subject to many variables that may cause failure to adequately decontaminate material. It is best used to reduce the infectious hazard associated with small quantities of liquid or solid waste accumulated during laboratory activities and for the decontamination of surfaces and equipment.

    Chemical disinfectants should be selected with regards to the situation in which they will be used, and biological agents may be present. Do not assume all disinfectants will deactivate all microorganisms.

    Disinfection procedures should detail suitable concentrations, contact times and applications. For hazard group 3 and Class 3 GMOs disinfectants must be validated for the infectious agent being handled. Where practicable the number of different disinfectants should be restricted to a minimum to avoid mistakes in application.

    Disinfection is reliant on the following factors:

    • The disinfectant must be able to deactivate the biological agent that needs to be deactivated
    • The right concentration needs to be made for disinfectants that have to be made fresh
    • Disinfectants need time to be effective always adhere to the disinfection times

    Factors that can have a negative effect on the effectiveness of disinfectants:

    • Concentration of contaminant
    • Concentration of disinfectant
    • TypeÌýof disinfectant
    • Heat
    • pH
    • humidity
    • time

    Disinfectants and effectiveness


    This section provides information on the effectiveness of various types of disinfectant and provides information on their hazards, limitations and use.

    Hypochlorites e.g. Presept

    The tableÌýbelow shows the effectiveness of the hypochloriteÌýbased disinfectants at deactivating microorganisms.

    MicroorganismEffectivenessÌý
    FungiRecommended
    Vegetive bacteriaÌýRecommended
    MycobacteriaVariableÌý
    SporesÌýVariableÌý
    Lipid VirusesÌýRecommended
    Non lipid virusesRecommended
    TSEsRecommended

    Limitations:
    Inactivated by organic matter, corrosive to some metals, may cause damage to rubber, not compatible with cationic detergents. Working solutions need to be changedÌýdaily andÌýdo not autoclave.ÌýÌý

    Hazards:
    Corrosive in concentrated forms. Irritant in dilute. Releases chlorine gas on contact with acids, releases bis chloromethyl 3 ether, a carcinogen, on contact with formalin or formaldehyde.

    Typical Uses:
    1000ppm for general surface disinfection of benches and equipment.

    Peroxygen compounds e.g. Virkon

    The tableÌýbelow shows the effectiveness of the peroxygen compound based disinfectants at deactivating microorganisms.

    MicroorganismEffectivenessÌý
    FungiRecommended
    Vegetive bacteriaÌýRecommended
    MycobacteriaNot SuitableÌý
    SporesÌýVariableÌý
    Lipid VirusesÌýRecommended
    Non lipid virusesRecommended
    TSEsNot SuitableÌý

    Limitations:
    Corrosive to some metals, (releases hypochlorous acid), but less than hypochlorite. Can be inactivated by organic matter.Ìý

    Hazards:
    Powder form is an irritant when making up solutions. Harmful if inhaled swallowed or absorbed through the skin or eyes and skin.ÌýÌý

    Typical Uses:
    Due to its wide spectrum of activity, Virkon is suitable for a wide range of applications in routine bacteriology, virology and cell culture laboratories. The powder can be used to treat spills.Ìý

    Accellerated Hydrogen Peroxide (AHP) e.g. Oxivir TB

    The tableÌýbelow shows the effectiveness of the peroxygen compound based disinfectants at deactivating microorganisms.

    MicroorganismEffectivenessÌý
    FungiRecommendedÌý
    Vegetive bacteriaÌýRecommendedÌý
    MycobacteriaRecommendedÌý
    SporesÌýVariableÌý
    Lipid VirusesÌýRecommendedÌý
    Non lipid virusesRecommendedÌý
    TSEsNot SuitableÌý

    Limitations:
    Incompatible with rubber, some plastics, aluminium, copper, zinc, brass. Check product label for incompatibilities.Ìý

    Hazards:
    Do not mix with concentrated bleach products.ÌýÌý

    Typical Uses:
    Due to wide spectrum of activity,ÌýAHP is suitable for a wide range of applications in routine bacteriology, virology and cell culture laboratories. Contact time is typically 1 min, but could be more or less depending on the pathogen, thus check product label. Most products use 0.5% hydrogen peroxide which will break down to water and oxygen. High concentrations are typically needed to be effective against sporesÌýÌý

    Alcohol e.g. 70% Ethanol

    The tableÌýbelow shows the effectiveness of the alcohol basedÌýdisinfectants at deactivating microorganisms:

    MicroorganismsEffectiveness
    FungiVariableÌý
    Vegetive bacteriaÌýRecommended
    MycobacteriaVariableÌý
    SporesÌýNot suitableÌý
    Lipid VirusesÌýRecommended
    Non lipid virusesNot suitableÌý
    TSEsNot suitableÌý

    Limitations:
    Poor penetration of organic matter and should only be used on physically clean surfaces.Ìý

    Hazards:
    Flammable, irritant to eyes nose and throat at high airborne concentrations may cause drowsiness or dizziness.Ìý

    Typical Uses:
    Surface disinfection of clean surface, electrical equipment should be disconnected from the mains before treating.Ìý

    Quaternary Amine Compounds e.g. Chemegene HLD4

    The tableÌýbelow shows the effectiveness of the Quaternary Amine Compound basedÌýÌýdisinfectants at deactivating microorganisms:

    MicroorganismsEffectiveness
    FungiVariableÌý
    Vegetive bacteriaÌýRecommended
    MycobacteriaNot suitableÌý
    SporesÌýNot suitableÌý
    Lipid VirusesÌýRecommended
    Non lipid virusesVariableÌý
    TSEsNot suitableÌý

    Limitations:
    Inactivated by protein and some plastics, not compatible with anionic detergents. Inactivated by soaps and organic matter.Ìý

    Hazards:
    Non-toxic, however many are classified as skin, eye, respiratory and GI irritants may degrease skin on prolonged contact. Incompatible with Phenols.

    Typical Uses:
    General surface disinfectant, spillages and discard jars. Follow manufactures in instructions for appropriate dilutions.

    Chlorine dioxideÌý e.g Tristel Jet

    The tableÌýbelow shows the effectiveness of the chlorine dioxiceÌýbasedÌýdisinfectants at deactivating microorganisms:

    MicroorganismsEffectiveness
    FungiRecommended
    Vegetive bacteriaÌýRecommended
    MycobacteriaRecommended
    SporesÌýRecommended
    Lipid VirusesÌýRecommended
    Non lipid virusesRecommendedÌý
    TSEsNot suitableÌý

    Limitations:
    Trisel is an aqueous solution of chlorine dioxide and requires activation before useÌýÌý

    Hazards:
    NotÌý skin or respiratory sensitiser or irritant. Hazards may vary depending on composition, check SDSÌý

    Typical Uses:
    Surface disinfection, spills and discard jars where spores or resistant bacteria -e.g. mycobacteria may be presentÌý

    Autoclaves


    Autoclaves are used to treat waste to render it non-infectious before transporting to a licenced incinerator. This ensures that infectious waste is safe to transport on the public highway.

    Autoclaves work by generating steam at high temperatures such as 121oC under pressure. The steam penetrates the waste to kill any viable pathogens. There can be many different cycles for different agents and for liquid waste as well as solid waste. This is determined by risk assessment. Information should be available on what cycle to run and why, including information on how to load the autoclave to ensure the materials are efficiently autoclaved. People generating waste that needs autoclaving should ensure that steam can penetrate the waste by not sealing autoclave bags and bottles. If the steamÌýcannot penetrate the load, it can not be assured that the waste has been deactivated.

    The location of an autoclave will be determined by risk assessment and the level of hazard of the biological agent used. Where higher hazard material is handled the autoclave may be in the laboratory or suite (e.g. in CL3 areas), For lower hazard material the autoclave will be in the building for biological agents in hazard group 2 and Class 2 materials.

    Autoclaves are pressure systems and come under the Pressure Safety Systems Regulations (PSSR) which meansÌýthey are subject to statutory testing. All autoclaves need to be asset registered to ensure they under --autoclaves should undergo a through inspection for insurance as well as validation and calibrationÌýby a competent person to ensure autoclaves are safe and effective in theirÌýoperation. There should be an appointed person for pressure systems who is the first point of contact for new and existing pressure systems, such as autoclaves to ensure they are included in annual statutory testing and have maintenance plans in place.Ìý

    Validation of an autoclave can be through a 12 point thermocouple test to ensure the autoclave reaches and maintains the temperature of the cycle being validated. Other methods include Bowie Dick and Helix testsÌýprovide an indication of steam penetration but doesn't confirm a successfull cycle. However if these tests fail the autoclave should not be used until a competent person has confirmed the autoclave is operational.

    Insurance and through inspections information can be found in Crimson, whilst maintainance information can be found in Planet.

    Be aware that some material may not be suitable for autoclaving e.g. radioactive material or toxic chemicals

    Incineration


    Incinerators are facilities with a constant flame that burns waste and high temperatures to destroy the waste. This waste disposal route is used for low hazard biological waste and is also used to dispose of carcasses. For guidance on the packing of waste forÌýincineration can be found on the Laboratory waste page. Different bags are required for transporting different types of waste off campus.Ìý

    IncineratorsÌýdo not need to present in the building, and risk assessments should cover how waste will be packed toÌýtravel to the incinerator or what other disposal arrangements are in place. Some licensed incinerators convert waste to power. Ìý

    Ultraviolet light


    Ultraviolet light is a form of non-ionisingÌýradiation. Based on wavelength the UV spectrum can be split into 3 different bands UV-A, UV-B and UV-C.
    UV-C can be used for germicidal purposes to kill or inactivate microorganisms.

    There are a number of factors that influence the effectiveness of UV-C sterilisation.

    • Exposure: microorganisms need direct contact with UV-C for kill or inactivation of a microorganism. Dust and dirt can shield microorganisms which means that inactivation is not achieved.
    • Temperature: the optimum temperature output of UV-C is 25oC-27oC outside this range the effectiveness is reduced
    • Humidity: adversely affects UV. A relative humidity above 70% reduces the germicidal properties of UV.
    • Cleanliness of UV light: dust and dirt can block the UV. UV lights should be cleaned weekly
    • Age of UV lights: with increasing age the germicidal properties of UV will reduce over time. Periodic monitoring of the UV output will ensure efficiency.

    UV light also has health implications. Over-exposure can lead to erythema, photokeratitis and or conjunctivitis. UV exposure is known to increase the risk of developing skin cancer.

    Last updated: Tuesday, January 17, 2023