Alternatives to animal testing

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Alternatives to animal testing are the development and implementation of test methods that avoid the use of live animals.

Contents

There is widespread agreement that a reduction in the number of animals used and the refinement of testing to reduce suffering should be important goals for the industries involved. [1] Two major alternatives to in vivo animal testing are in vitro cell culture techniques and in silico computer simulation. However, some claim they are not true alternatives because simulations use data from prior animal experiments and cell cultures often require animal derived products, such as serum or cells. Others say that they cannot replace animals completely as they are unlikely to ever provide enough information about the complex interactions of living systems. [2] Other alternatives include the use of humans for skin irritancy tests and donated human blood for pyrogenicity studies. Another alternative is so-called microdosing, in which the basic behaviour of drugs is assessed using human volunteers receiving doses well below those expected to produce whole-body effects. [3] While microdosing produces important information about pharmacokinetics and pharmacodynamics it does not reveal information about toxicity or toxicology. [4] Furthermore, it was noted by the Fund for the Replacement of Animals in Medical Experiments that despite the use of microdosing, "animal studies will still be required". [5]

Guiding principles for more ethical use of animals in testing are the Three Rs (3Rs) first described by Russell and Burch in 1959. [6] These principles are now followed in many testing establishments worldwide.

  1. Replacement refers to the preferred use of non-animal methods over animal methods whenever it is possible to achieve the same scientific aim.
  2. Reduction refers to methods that enable researchers to obtain comparable levels of information from fewer animals, or to obtain more information from the same number of animals.
  3. Refinement refers to methods that alleviate or minimize potential pain, suffering, or distress, and enhance animal welfare for the animals used.

Cell culture and tissue engineering

Cell culture in a special tissue culture dish Cell Culture in a tiny Petri dish.jpg
Cell culture in a special tissue culture dish

Cell culture can be an alternative to animal use in some cases. For example, cultured cells have been developed to create monoclonal antibodies; prior to this, production required animals to undergo a procedure likely to cause pain and distress. [7] However, even though cell or tissue culture methods may reduce the number of experiments performed on intact animals, the maintenance of cells in culture normally requires the use of animal-derived serum. Although exact figures are difficult to obtain, some have estimated that one million foetal cows are sacrificed each year to obtain the world's supply of foetal bovine serum, used to grow cultured cells. [8] The testing of cosmetic products directly onto an animal can be minimized or eliminated by the use of in vitro cell growth and development. This can be generalized as the growth of cells outside of the body and tested on without causing harm or pain on the test subject. Much of the time this method of cosmetic testing is less time-consuming and less expensive than alternative choices. [9]

Skin corrosion and skin irritation

Skin irritation and skin corrosion refer to localized toxic effects resulting from a topical exposure of the skin to a substance. Human skin equivalent tests can be used to replace animal-based corrosive and irritative studies. EpiDerm from Mattek [10] and EpiSkin [11] and SkinEthic RHE model [12] are derived from human skin cells which have been cultured to produce a model of human skin. These methods are currently accepted replacements in Canada and the European Union (EU). [13] In August 2010, the Organisation for Economic Co-operation and Development (OECD) published the Test Guideline 439 which describes the new procedure for in vitro hazard identification of irritant chemicals. [14]

Another synthetic replacement uses a protein membrane to simulate a skin barrier and is approved as a partial replacement by the US Department of Transportation and European Union. [15]

Skin absorption

Several tissue culture methods that measure the rate of chemical absorption by the skin have been approved by the OECD. [16]

Phototoxicity

Phototoxicity is a rash, swelling, or inflammation, like a severe sunburn, caused by exposure to light following exposure to a chemical. The 3T3 Neutral Red Uptake (NRU) Phototoxicity Test, approved by the OECD, detects the viability of 3T3 cells after exposure to a chemical in the presence or absence of light. [17] The 3T3 cell line was developed in 1962 and is derived from mouse embryonic fibroblast cells. [18]

Fungal model for mammalian drug metabolism

Fungi like Cunninghamella elegans can be used as a microbial model of mammalian drug metabolism [19] [20] [21] [22] thereby reducing the need for laboratory animals. [23]

Prokaryotes are often used as an alternative to animal testing. Prokaryotes include bacteria such as Escherichia coli (E. coli) or Bacillus subtilis . These bacteria are the ideal model for genetic and molecular studies. Fungi is also used as an alternative for animal testing. Certain fungi can be used for genetic studies or circadian rhythms studies. This may include Neurospora crassa , otherwise known as a type of red mould. Invertebrates are another ideal candidate for testing. One of the most common invertebrates tested on include Drosophila melanogaster , the fruit fly. Fruit flies are used to find human diseases.

Organoids (3D cell cultures)

Russell and Burch writing six decades ago could not have anticipated some of the technologies that have emerged today. One of these technologies, 3D cell cultures, also known as organoids or mini-organs, have replaced animal models for some types of research. In recent years, scientists have produced organoids that can be used to model disease and test new drugs. Organoids grow in vitro on scaffolds (biological or synthetic hydrogels such as Matrigel) or in a culture medium. Organoids are derived from three kinds of human or animal stem cells—embryonic pluripotent stem cells (ESCs), adult somatic stem cells (ASCs), and induced pluripotent stem cells (iPSCs). These organoids are grown in vitro and mimic the structure and function of different organs such as the brain, liver, lung, kidney, and intestine. Organoids have been developed to study infectious disease. Scientists at Johns Hopkins University have developed mini-brain organoids to model how COVID-19 can affect the brain. [24] Researchers have used brain organoids to model how the Zika virus disrupts foetal brain development. Tumoroids—3D cell cultures derived from cells biopsied from human patients—can be used in studying the genomics and drug resistance of tumours in different organs. Organoids are also used in modelling genetic diseases such as cystic fibrosis, neurodegenerative diseases such as Alzheimer's and Parkinson's, infectious diseases such as MERS-CoV and norovirus, and parasitic infections such as Toxoplasma gondii . Human- and animal-cell-derived organoids are also used extensively in pharmacological and toxicological research.

Human-based

Skin irritation

A skinpatch test has been designed and is used in Canada to measure development of rashes, inflammation, swelling or abnormal tissue growth on human volunteers. [25] Unlike corrosives, substances defined as irritants cause only reversible skin damage.

Another approach has been the development of test methods that use cultured human cells. Human epidermal keratinocytes have been cultured to mimic the human epidermis, and are used to measure skin irritation and dermal corrosion. This method has been accepted by the EU and is intended to replace the Draize rabbit skin irritation test. [26]

Pyrogenicity

Pyrogens are most often pharmaceutical products or intravenous drugs that may cause inflammation or fever when they interact with immune system cells. This interaction can be quickly and accurately tested in vitro.

Modular immune in vitro construct

The modular immune in vitro construct (MIMIC) uses human cells to create a model of the human immune system on which the efficacy of new vaccines and other compounds may be tested, replacing some steps of the vaccine development process that would otherwise be performed on animals. This process is faster and more flexible than previous methods but critics worry that it may be too simple to be useful on a large scale. [27]

Medical imaging

Medical imaging is able to demonstrate to researchers both how drugs are metabolised by use of microdosing, and the detailed condition of organ tissue. [28]

Computer simulation

Crash test dummies have been used to replace live animals in impact testing. IIHS crash test dummy in Hyundai Tucson.jpg
Crash test dummies have been used to replace live animals in impact testing.

Examples of computer simulations available include models of asthma, [29] though potential new medicines identified using these techniques are currently still required to be verified in animal and human tests before licensing.

Computer operated mannequins, also known as crash test dummies, complete with internal sensors and video, have replaced live animal trauma testing for automobile crash testing. The first of these was "Sierra Sam" built in 1949 by Alderson Research Labs (ARL) Sierra Engineering. These dummies continue to be refined. [30] Prior to this, live pigs were used as test subjects for crash testing. [31]

Computer models have been constructed to model human metabolism, to study plaque build-up and cardiovascular risk, and to evaluate toxicity of drugs, tasks for which animals are also used. [32] In 2007, US researchers using the world's fastest computer at the time, BlueGene L, modelled half a mouse brain for just 10 seconds. However, due to limitations in computing power, the simulation could only be run at one-tenth the speed of an actual mouse brain. [33] Although this was an advance in science, its representative power as a model was limited and the researchers were quoted as saying that "although the simulation shared some similarities with a mouse's mental make-up in terms of nerves and connections it lacked the structures seen in real mice brains." [33]

In pharmacology and toxicology, physiologically based pharmacokinetic models can be used for in vitro to in vivo extrapolation and to predict the time-dependent distribution of chemicals in the organism, while quantitative structure-activity relationship (QSAR) models can be used to predict the physicochemical and hazard properties of chemicals.

Microfluidic chips

Microfluidic chips, which are just 2 cm (0.79 in) wide, can be engraved into a series of small chambers, each containing a sample of tissue from a different part of the body. A substitute of blood flows through micro-channels where the compartments of chips linked. When injected, the test drug circulates around the device, mimicking what goes in the body on a micro scale. Sensors in the chip transfer information for computer analysis. [34]

Another name for this chip is the microfluidic chip is cell-bio chips. With the capacity to "perform perfusion culture" and reproduce "physiological conditions such three-dimensional architectures, circulatory flowrate and zonation and multi cellular co-cultures", the biochips have set themselves apart from basic cell cultures analysed in a Petri dish. [35] The effectiveness of these systems is constantly being increased with various new materials that can be used to make it. An ideal material would be gas permeable but still be able to absorb molecules that would be expected to be found in various drugs [35]

The choice of the material for chips is still challenging. One of the major materials that can be possibly used in chips is known as polydimethylsiloxane (PDMS). However, due to lack of facilities for mass production and drug clearance issue, the use of PDMS is still being speculated, even though it has great properties as microfluidic chip. Also, the biological process involved in proliferation and metabolism might be modified when compared to larger scales, because the materials have micro-structured scales comparable in size to cells. [36]

Future alternatives

Organs on a chip

The Wyss Institute for Biologically Inspired Engineering (US) intends to develop in-vitro organs for drug screening and thereby eliminate the use of animals for this type of testing. One model is the "lung-on-a-chip". [37] This combines microfabrication techniques with modern tissue engineering and mimics the complicated mechanical and biochemical behaviours of a human lung.

Human toxome

Toxicity testing typically involves studying adverse health outcomes in animals subjected to high doses of toxicants with subsequent extrapolation to expected human responses at lower doses. The system relies on the use of a 40+year-old patchwork of animal tests that are expensive (costing more than $3B per year), time-consuming, low-throughput and often provide results of limited predictive value for human health effects. The low-throughput of current toxicity testing approaches (which are largely the same for industrial chemicals, pesticides and drugs) has led to a backlog of more than 80,000 chemicals to which humans are potentially exposed whose potential toxicity remains largely unknown. In 2007, the National Research Council (NRC) released the report "Toxicity Testing in the 21st Century: A Vision and a Strategy", [38] that charted a long-range strategic plan for transforming toxicity testing. The major components of the plan include the use of predictive, high-throughput cell-based assays (of human origin) to evaluate perturbations in key toxicity pathways, and to conduct targeted testing against those pathways. This approach will greatly accelerate our ability to test the vast "storehouses" of chemical compounds using a rational, risk-based approach to chemical prioritization, and provide test results that are hopefully far more predictive of human toxicity than current methods. Although a number of toxicity pathways have already been identified, most are only partially known and no common annotation exists. Mapping the entirety of these pathways (i.e. the Human Toxome [39] ) will be a large-scale effort, perhaps on the order of the Human Genome Project.

Research initiatives

SEURAT-1

SEURAT-1 is a long-term strategic target for "Safety Evaluation Ultimately Replacing Animal Testing". [40] It is called "SEURAT-1" to indicate that more steps have to be taken before the final goal will be reached. SEURAT-1 will develop knowledge and technology building blocks required for the development of solutions for the replacement of current repeated dose systemic toxicity testing in vivo used for the assessment of human safety. SEURAT-1 is composed of six research projects, which started on January 1, 2011 and will run for five years. These projects will closely cooperate with a common goal and combine the research efforts of over 70 European universities, public research institutes and companies. The collaboration between these six research projects, the dissemination of results, the cooperation with other international research teams, and the continuous updating on research priorities will be facilitated by the coordination and support action project "COACH".

SEURAT-1 was developed through the Framework Programme 7 (FP7) research initiative and was created through a call for proposals by the European Commission (EC) that was published in June 2009. The Cosmetics Europe industry offered to match the EC's funds to make a total of EUR 50 million available to try to fill current gaps in scientific knowledge and accelerate the development of non-animal test methods.

Euroecotox

Laboratory animals are not restricted to rats, mice, dogs, and rabbits, but also include fish, frogs and birds. Research into alternatives to replace these species is often neglected, although fish are the third most widely used laboratory animal used for scientific purposes in the EU. [41] This is also the field where until now only two alternative tests exist worldwide: One guideline, OECD TG 236, [42] and one guidance (OECD series on testing and assessment 126) [43] are so far available.

Euroecotox [44] is a European network for alternative testing strategies in ecotoxicology. It was funded by the Seventh Framework Programme (FP7) of the European Commission Environment Programme. The main objectives of the Euroecotox network are: To contribute to the advancement of alternative methods of ecotoxicity testing in Europe. To promote the validation and regulatory acceptance of new alternative ecotoxicity methods. To facilitate the networking of research groups working in the field of alternative ecotoxicology. To provide a gathering point for all stakeholders involved in the development, validation, regulatory acceptance and final use of alternative ecotoxicity testing strategies. To act as the one voice for alternative ecotoxicity testing in Europe.

AXLR8

AXLR8 is a coordination action funded by the European Commission Directorate General for Research & Innovation under the 7 Framework Programme 7 (FP7) Health Theme. The European Commission is currently funding a number of research consortia to develop new 3Rs (replacement, reduction and refinement) test methods and strategies as potential alternatives to the use of animals in safety testing. Monitoring of these 3Rs activities at pan-European, national, and international levels is vital to facilitate swift progress. AXLR8 aims to fulfil this growing need by providing a focal point for dialogue and collaboration. [45] Humane Society International is part of the consortium.

Regulation

European Union

EU Directive 2010/63/EU

On January 1, 2013, EU Directive 2010/63/EU "on the protection of animals used for scientific purposes" entered into force for the EU member states (MS), [46] repealing Directive 86/609/EEC. [47] Because it is a directive, it allows member states certain flexibility in transposition of national rules. The status of the implementation of the new directive in the EU is described by the EC General Environment Directorate. [48]

Article 1.3: The new EU directive applies to the following animals: (a) live non-human vertebrate animals, including: (i) independently feeding larval forms; and (ii) foetal forms of mammals from the last third of their normal development; (b) live cephalopods.
Article 4: The directive refers directly to the 3Rs: [6] "Principle of replacement, reduction and refinement".
Article 47-2: Member states shall assist the commission in identifying and nominating suitable specialised and qualified laboratories to carry out such validation studies.

In July 2013, the commission announced the creation of NETVAL [49] (European Union Network of Laboratories for the Validation of Alternative Methods). EU-NETVAL's primary role is to provide support for EURL ECVAM validation projects, including aspects of training and dissemination, and the identification of methods that have a potential to reduce, refine or replace animals used for scientific purposes. [50] Currently there are thirteen test facilities in nine member states: Germany (3), the Netherlands (2), Spain (2), Belgium (1), Czech Republic (1), Finland (1), France (1), Italy (1) and Sweden (1). [49]

Other regulations

The Cosmetics Directive provides the regulatory framework for the phasing out of animal testing for cosmetics purposes. It establishes prohibitions against (a) testing finished cosmetic products and cosmetic ingredients on animals (testing ban), and (b) marketing in the EU finished cosmetic products and ingredients included in cosmetic products which were tested on animals for cosmetics purposes (marketing ban). The same provisions are contained in Cosmetics Regulation EU 1223/2009, which replaces the Cosmetics Directive as of July 11, 2013. [51]

In 2007, EU legislation on the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH EC 1907/2006) came into force, relating to chemicals and their safe use. [52] The aim of REACH is to improve the protection of human health and the environment through the better and earlier identification of the intrinsic properties of chemical substances. It promotes the use of alternative methods for animal testing, but does not oblige the test performer to do so; "Article 25.1 - In order to avoid animal testing, testing on vertebrate animals for the purposes of this Regulation shall be undertaken only as a last resort. It is also necessary to take measures limiting duplication of other tests."

In parallel to the adoption of REACH, the EC published standardised and accepted methods for testing hazardous properties of chemicals. These were written into the "Test Methods Regulation". [53] All the alternative test methods among the in vivo studies are included in PART B; "The European Union is committed to promoting the development and validation of alternative techniques which can provide the same level of information as current animal tests, but which use fewer animals, cause less suffering or avoid the use of animals completely. Such methods, as they become available, must be considered wherever possible for hazard characterisation and consequent classification and labeling for intrinsic hazards and chemical safety assessment."

EU philosophy on food additives, food enzymes, and food flavourings and ingredients intended for human consumption is that none should be put on the market unless they are included on a published Community list of authorised substances, in accordance with the conditions laid down in relevant food law. This approach is intended to bring food producers into compliance with the provisions of Regulation (EC) 1334/2008 that pertain to the safety of food flavourings. As part of the approval process, the EC will require full disclosure of study data, safety issues, and toxicological findings for all such additives. [54]

Within the EU animal welfare law (2010/63/EU), the principles of the 3Rs are invoked whenever toxicological test methods are necessary. [55]

Organizations and programs

Scientific congresses

The European Society for Alternatives to Animal Testing (EUSAAT) [56] organises an annual conference in Linz (Austria) for

  1. Dissemination and validation of alternative methods to animal testing
  2. Promotion of research in the field of the 3Rs
  3. Reduction of the use of animals for tests in the field of education and continuing education
  4. Reduction of suffering and stress of laboratory animals by better breeding, keeping, test planning and other accompanying measures
  5. Experts' guidance and referees' opinion for public and private organizations, companies, universities
  6. Suitable information for the public and the media

The World Congress on Alternatives and Animal Use in the Life Sciences takes place every three years. The next conference (10th) will be held in September 2017 in Seattle. [57]

The 1st Latino-Americano Congress on Alternative to Animal Testing took place in 2012. Colama (I Congresso Latino-Americano De Metodos Alternativos Ao Uso De Animais No Ensino, Pesquisa E Industria). [58]

The Johns Hopkins University Center for Alternatives to Animal Testing (CAAT) co-organizes an annual symposium on the 3Rs with the USDA's Animal Welfare Information Center (AWIC) and NIH's Office of Laboratory Animal Welfare. [59] Previously known as the Social Housing Symposium, the symposium has occurred annually (except for 2015) since 2013 with past symposia archived on video on the AWIC website. [60] Videos of the most recent symposium, "7th Annual 3Rs Symposium: Practical Solutions and Success Stories", held in June 2020, may also be found on the AWIC website. [61]

Industry and corporate initiatives

Animal welfare and animal rights organizations

Public campaigns and awards

Education and training

Institutes and national or international organizations

Institutes and organizations that research or fund alternatives to animal testing include:

Asia - Oceania

  • Medical Advances Without Animals Trust (Australia) [91]
  • Alternatives to Animal Experimentation Laboratory, Department of Pharmacology, Jawaharlal Nehru Medical College, Aligarh Muslim University, Aligarh (India). [92]
  • Mahatma Gandhi-Doerenkamp Center for Alternatives to Use of Animals in Life Science, Bharathidasan university, Trichy, Tamil Nadu, India Education [93]
  • Japanese Center for the Validation of Alternative Methods (JACVAM), since 2005 [94]
  • The Korean Center for the Validation of Alternative Methods (KOCVAM), since 2009 [95]

South America

  • BraCVAM as the Brazilian Center for the Validation of Alternatives Methods. It was established in 2011. [96] [97]

North America

Europe

  • The European Commission's role in promoting the development, validation and uptake of alternative approaches to animal testing started in 1991, with the launch of ECVAM (European Centre for the Validation of Alternative Methods), hosted by the Joint Research Centre. As from 2011, ECVAM became known as the EU Reference Laboratory for Alternatives to Animal Testing (EURL ECVAM). EURL ECVAM hosts an online database of toxicological, non-animal alternative test methods DB-ALM. [102]
  • Under the Framework Programmes 6 and 7, the EC funded a significant number of large integrated research projects aiming to develop alternatives to animal testing for about EUR 330 million based on the Review of REACH from February 2013 (the European Chemical Program). [103]
  • The European Partnership for Alternative Approaches to Animal Testing (EPAA) as a liaison between the EC and industries. [104]
  • The European Consensus Platform for Alternatives (ECOPA) coordinates efforts amongst EU member states. [105]
  • Zentrum fuer Ersatz (Austria) [106]
  • Finnish Center for Alternative Methods (FICAM), since 2008 [107]
  • FRANCOPA is the French platform dedicated to development, validation, and dissemination of alternative methods in animal testing. It was created on November 16, 2007. [108]
  • The Italian Centro 3R was created in 2017. It is an interuniversity center dedicated to the promotion of the 3Rs in teaching and research.
  • Zentralstelle zur Erfassung und Bewertung von Ersatz- und Ergänzungsmethoden (ZEBET) (Germany), since 1989 [109] [110]
  • Norecopa is the Norwegian consensus platform for the replacement, reduction and refinement of animal experiments. It was founded on October 10, 2007. [111]
  • Romanian Center for Alternative Test Methods (ROCAM) promotes the application of alternative methods in industry and their acceptance by regulators in Romania and also the development of new methods and approaches. ROCAM was established in June 2015 with the main goal to support and promote the 3Rs principles in Romania and regionally.
  • Dr Hadwen Trust (United Kingdom)
  • Fund for the Replacement of Animals in Medical Experiments (United Kingdom) [112]
  • National Centre for the Replacement, Refinement and Reduction of Animals in Research (NC3Rs) (United Kingdom), since 2004 [113]

International

  • International Cooperation on Alternative Test Methods (ICATM): On April 27, 2009, the United States, Canada, Japan and EU signed a memorandum of cooperation that could reduce the number of animals required for consumer product safety testing worldwide. The agreement will yield globally coordinated scientific recommendations on alternative toxicity testing methods that should speed their adoption in each of these countries, thus reducing the number of animals needed for product safety testing. [114]
International Cooperation on Alternative Test Methods (ICATM)
Legend :
ICH: The International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use
OECD: The Organisation for Economic Co-operation and Development has a Test Guideline program that deals with chemicals.
ICCR: The International Cooperation on Cosmetics Regulation (ICCR) is an international group of cosmetic regulatory authorities from the United States (FDA), Japan (Ministry of Health, Labour, and Welfare), the EU (EC, DG Enterprise), and Canada (Health Canada). This multilateral framework maintains the highest level of global consumer protection, while minimizing barriers to international trade. International Cooperation on Alternative Test Methods (ICATM).jpg
International Cooperation on Alternative Test Methods (ICATM)
Legend :
ICH: The International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use
OECD: The Organisation for Economic Co-operation and Development has a Test Guideline program that deals with chemicals.
ICCR: The International Cooperation on Cosmetics Regulation (ICCR) is an international group of cosmetic regulatory authorities from the United States (FDA), Japan (Ministry of Health, Labour, and Welfare), the EU (EC, DG Enterprise), and Canada (Health Canada). This multilateral framework maintains the highest level of global consumer protection, while minimizing barriers to international trade.
  • The OECD (Organisation for Economic Co-operation and Development) is a forum for discussion where governments express their points of view, share their experiences, and search for common ground, as opposed to a supranational organization. [118] OECD is a forum where alternative test methods also undergo validation and are therereafter accepted for regulatory purposes in more than 35 member countries worldwide. [119] NGOs are represented at the technical level at the OECD, under the ICOPA International Council on Animal Protection in OECD program. [120] The testing of chemicals is labor-intensive and expensive. Often the same chemical is tested in several countries simultaneously, which means that redundant animal tests are performed. To relieve some of this burden, the OECD Council adopted a decision in 1981, stating that data generated in a member country, in accordance with OECD Test Guidelines and Principles of Good Laboratory Practice (GLP), shall be accepted in other member countries for assessment purposes and other uses relating to the protection of human health and the environment. This principle is referred to using the acronym MAD, for the Mutual Acceptance of Data. [118]

See also

Related Research Articles

<i>In vitro</i> Latin term meaning outside a natural biological environment

In vitro studies are performed with microorganisms, cells, or biological molecules outside their normal biological context. Colloquially called "test-tube experiments", these studies in biology and its subdisciplines are traditionally done in labware such as test tubes, flasks, Petri dishes, and microtiter plates. Studies conducted using components of an organism that have been isolated from their usual biological surroundings permit a more detailed or more convenient analysis than can be done with whole organisms; however, results obtained from in vitro experiments may not fully or accurately predict the effects on a whole organism. In contrast to in vitro experiments, in vivo studies are those conducted in living organisms, including humans, known as clinical trials, and whole plants.

<span class="mw-page-title-main">Toxicology</span> Study of substances harmful to living organisms

Toxicology is a scientific discipline, overlapping with biology, chemistry, pharmacology, and medicine, that involves the study of the adverse effects of chemical substances on living organisms and the practice of diagnosing and treating exposures to toxins and toxicants. The relationship between dose and its effects on the exposed organism is of high significance in toxicology. Factors that influence chemical toxicity include the dosage, duration of exposure, route of exposure, species, age, sex, and environment. Toxicologists are experts on poisons and poisoning. There is a movement for evidence-based toxicology as part of the larger movement towards evidence-based practices. Toxicology is currently contributing to the field of cancer research, since some toxins can be used as drugs for killing tumor cells. One prime example of this is ribosome-inactivating proteins, tested in the treatment of leukemia.

<span class="mw-page-title-main">Animal testing</span> Use of nonhuman animals in experiments

Animal testing, also known as animal experimentation, animal research, and in vivo testing, is the use of non-human animals in experiments that seek to control the variables that affect the behavior or biological system under study. This approach can be contrasted with field studies in which animals are observed in their natural environments or habitats. Experimental research with animals is usually conducted in universities, medical schools, pharmaceutical companies, defense establishments, and commercial facilities that provide animal-testing services to the industry. The focus of animal testing varies on a continuum from pure research, focusing on developing fundamental knowledge of an organism, to applied research, which may focus on answering some questions of great practical importance, such as finding a cure for a disease. Examples of applied research include testing disease treatments, breeding, defense research, and toxicology, including cosmetics testing. In education, animal testing is sometimes a component of biology or psychology courses. The practice is regulated to varying degrees in different countries.

The Draize test is an acute toxicity test devised in 1944 by Food and Drug Administration (FDA) toxicologists John H. Draize and Jacob M. Spines. Initially used for testing cosmetics, the procedure involves applying 0.5 mL or 0.5 g of a test substance to the eye or skin of a restrained, conscious animal, and then leaving it for set amount of time before rinsing it out and recording its effects. The animals are observed for up to 14 days for signs of erythema and edema in the skin test, and redness, swelling, discharge, ulceration, hemorrhaging, cloudiness, or blindness in the tested eye. The test subject is commonly an albino rabbit, though other species are used too, including dogs. The animals are euthanized after testing if the test renders irreversible damage to the eye or skin. Animals may be re-used for testing purposes if the product tested causes no permanent damage. Animals are typically reused after a "wash out" period during which all traces of the tested product are allowed to disperse from the test site.

In vitro toxicity testing is the scientific analysis of the toxic effects of chemical substances on cultured bacteria or mammalian cells. In vitro testing methods are employed primarily to identify potentially hazardous chemicals and/or to confirm the lack of certain toxic properties in the early stages of the development of potentially useful new substances such as therapeutic drugs, agricultural chemicals and food additives.

<span class="mw-page-title-main">Cruelty-free</span>

In the animal rights movement, cruelty-free is a label for products or activities that do not harm or kill animals anywhere in the world. Products tested on animals or made from animals are not considered cruelty-free, since these tests are often painful and cause the suffering and death of millions of animals every year.

In toxicology, the lethal dose (LD) is an indication of the lethal toxicity of a given substance or type of radiation. Because resistance varies from one individual to another, the "lethal dose" represents a dose at which a given percentage of subjects will die. The lethal concentration is a lethal dose measurement used for gases or particulates. The LD may be based on the standard person concept, a theoretical individual that has perfectly "normal" characteristics, and thus not apply to all sub-populations.

<span class="mw-page-title-main">Center for Alternatives to Animal Testing</span>

The Johns Hopkins University Center for Alternatives to Animal Testing (CAAT) has worked with scientists, since 1981, to find new methods to replace the use of laboratory animals in experiments, reduce the number of animals tested, and refine necessary tests to eliminate pain and distress. CAAT is an academic, science-based center affiliated with the Johns Hopkins Bloomberg School of Public Health.

The fixed-dose procedure (FDP), proposed in 1992 by the British Toxicology Society, is a method to assess a substance's acute oral toxicity.

Michael Balls is a British zoologist and professor emeritus of medical cell biology at the University of Nottingham. He is best known for his work on laboratory animal welfare and alternatives to animal testing.

<span class="mw-page-title-main">Testing cosmetics on animals</span> Form of animal testing

Cosmetic testing on animals is a type of animal testing used to test the safety and hypoallergenic properties of cosmetic products for use by humans.

<span class="mw-page-title-main">Toxicology testing</span> Biochemical process

Toxicology testing, also known as safety assessment, or toxicity testing, is the process of determining the degree to which a substance of interest negatively impacts the normal biological functions of an organism, given a certain exposure duration, route of exposure, and substance concentration.

Fund for the Replacement of Animals in Medical Experiments (FRAME) is a charity based in Nottingham, UK. FRAME funds and promotes alternatives to animal testing.

<span class="mw-page-title-main">European Partnership for Alternative Approaches to Animal Testing</span>

The European Partnership for Alternative Approaches to Animal Testing (EPAA) promotes the application of the 3Rs principles in meeting regulatory requirements for products such as pharmaceuticals, chemicals, soaps, detergents and cosmetics. The EPAA covers research and development, as well as the use of 3Rs approaches in regulatory compliance and communication and dissemination.

The New England Anti-Vivisection Society (NEAVS) is a national, registered 501(c)(3) nonprofit organization "dedicated to ending the use of animals in research, testing, and science education" and replacing them with "modern alternatives that are ethically, humanely, and scientifically superior."

<span class="mw-page-title-main">Three Rs (animal research)</span> Principles for ethical use of animals in science

The Three Rs (3Rs) are guiding principles for more ethical use of animals in product testing and scientific research. They were first described by W. M. S. Russell and R. L. Burch in 1959. The 3Rs are:

  1. Replacement:methods which avoid or replace the use of animals in research
  2. Reduction: use of methods that enable researchers to obtain comparable levels of information from fewer animals, or to obtain more information from the same number of animals.
  3. Refinement: use of methods that alleviate or minimize potential pain, suffering or distress, and enhance animal welfare for the animals used.
<span class="mw-page-title-main">Federal Institute for Risk Assessment</span>

The German Federal Institute for Risk Assessment, abbreviated BfR, is a body under public law of the German federal government with full legal capacity. The institute comes under the portfolio of the Federal Ministry of Food and Agriculture and has the task of providing scientific advice to the federal government on issues relating to food safety, product safety, chemical safety, contaminants in the food chain, animal protection and consumer health protection. Further technical supervision is performed by the Federal Ministry for the Environment, Nature Conservation, Building and Nuclear Safety and the Federal Ministry of Transport.

<span class="mw-page-title-main">Directive 2010/63/EU</span> European Union legislation

Directive 2010/63/EU is the European Union (EU) legislation "on the protection of animals used for scientific purposes" and is one of the most stringent ethical and welfare standards worldwide.

<span class="mw-page-title-main">Uwe Marx</span>

Uwe Marx is a German physician and biotechnologist, and one of the world’s leading researchers in the fields of organ-on-a-chip technology and antibody production.

Björn Ekwall was a Swedish cell toxicologist, known for his pioneering work in in vitro toxicology.

References

  1. R E Hester R M Harrison et al. Alternatives To Animal Testing (Issues in Environmental Science and Technology) Royal Society of Chemistry; 1 edition (June 7, 2006) ISBN   978-0-85404-211-1
  2. Lipinski, Christopher; Hopkins, A (16 December 2004). "Navigating chemical space for biology and medicine". Nature. 432 (7019): 855–61. Bibcode:2004Natur.432..855L. doi:10.1038/nature03193. PMID   15602551. S2CID   4416216.
  3. Malcolm Rowland (February 2006). "Microdosing and the 3Rs". National Center for the Replacement, Refinement, and Reduction of Animals in Research ( NC3Rs ). Archived from the original on 28 September 2007. Retrieved 2007-09-22.
  4. "Alternatives?". Speaking of Research. 2009-07-31. Retrieved 2014-02-26.
  5. FRAME (2005). "Human microdosing reduces the number of animals required for pre-clinical pharmaceutical research". Alternatives to Laboratory Animals. 33 (439).
  6. 1 2 Russell, W.M.S. and Burch, R.L., (1959). The Principles of Humane Experimental Technique, Methuen, London. ISBN   0-900767-78-2 Archived 2011-09-27 at the Wayback Machine Digital text Archived 2022-12-01 at the Wayback Machine available for free on the website of the Center for Alternatives to Animal Testing.
  7. "Special section: Monoclonal antibodies". Johns Hopkins Bloomberg School of Public Health. Archived from the original on 2007-08-20. Retrieved 2007-09-20.
  8. Brunner D.; Frank Jürgen; App Helmut; Schöffl Harald; Pfaller Walter; Gstraunthaler Gerhard (2010). "Serum-free Cell Culture: The Serum-free Media Interactive Online Database". Altex. 27 (1): 53–62. doi: 10.14573/altex.2010.1.53 . PMID   20390239.
  9. Doke, Sonali K.; Dhawale, Shashikant C. (July 2015). "Alternatives to animal testing: A review". Saudi Pharmaceutical Journal. 23, 3: 223-229 (3): 223–229. doi:10.1016/j.jsps.2013.11.002. PMC   4475840 . PMID   26106269.
  10. "EpiDermTM Tissue Model". MatTek Corporation. Retrieved 7 July 2015.
  11. "L'Oréal cutaneous tissue engineering platform". Invitroskin. 2007-04-30. Archived from the original on 2012-03-15. Retrieved 2014-02-26.
  12. "News - Congress - Workshops - SkinEthic Laboratories - SkinEthic Reconstructed Human Epidermis RHE validated in Europe". Skinethic.com. 2008-12-19. Retrieved 2014-02-26.
  13. "Alternatives In Testing". Neaves Humane Science is Superior Science. Archived from the original on 8 July 2015. Retrieved 7 July 2015.
  14. OECD (26 June 2020). Test No. 439: In Vitro Skin Irritation: Reconstructed Human Epidermis Test Method (PDF). OECD Guidelines for the Testing of Chemicals, Section 4. OECD. doi:10.1787/9789264242845-en. ISBN   9789264242845. S2CID   243117943 . Retrieved 12 March 2021.
  15. Stobbe JL, Drake KD, Maier KJ (2003). "Comparison of in vivo (Draize method) and in vitro (Corrositex assay) dermal corrosion values for selected industrial chemicals". International Journal of Toxicology. 22 (2): 99–107. CiteSeerX   10.1.1.816.8092 . doi:10.1080/10915810305094. PMID   12745991. S2CID   8901737. INIST   14763182.
  16. Khan, Firdos Alam (September 20, 2011). Biotechnology Fundamentals. CRC Press. ISBN   9781439820094 via Google Books.
  17. "Background - 3T3 Neutral Red Uptake Phototoxicity Assay - MB Research Labs". 3t3nru.mbresearchlabs.com. Retrieved 24 Apr 2014.
  18. "NIH3T3 General Information". NIH 3T3 Cell Line. Retrieved 12 March 2021.
  19. Kristian Björnstad; Anders Helander; Peter Hultén; Olof Beck (2009). "Bioanalytical investigation of asarone in connection with Acorus calamus oil intoxications". Journal of Analytical Toxicology . 33 (9): 604–609. doi: 10.1093/jat/33.9.604 . PMID   20040135.
  20. Joanna D. Moody; Donglu Zhang; Thomas M. Heinze; Carl E. Cerniglia (2000). "Transformation of amoxapine by Cunninghamella elegans". Applied and Environmental Microbiology . 66 (8): 3646–3649. Bibcode:2000ApEnM..66.3646M. doi:10.1128/AEM.66.8.3646-3649.2000. PMC   92200 . PMID   10919836.
  21. A. Jaworski; L. Sedlaczek; J. Dlugoński; Ewa Zajaczkowska (1985). "Inducible nature of the steroid 11-hydroxylases in spores of Cunninghamella elegans (Lendner)". Journal of Basic Microbiology . 25 (7): 423–427. doi:10.1002/jobm.3620250703. S2CID   85744435.
  22. Hezari, M.; Davis, P. J. (1993). "Microbial models of mammalian metabolism. Furosemide glucoside formation using the fungus Cunninghamella elegans". Drug Metabolism and Disposition. 21 (2): 259–267. PMID   8097695.
  23. Sharma, KK; Mehta, T; Joshi, V; Mehta, N; Rathor, AK; Mediratta, KD; Sharma, PK (2011). "Substitute of animals in drug research: An approach towards fulfillment of 4R's". Indian Journal of Pharmaceutical Sciences. 73 (1): 1–6. doi: 10.4103/0250-474X.89750 . PMC   3224398 . PMID   22131615.
  24. Hogberg, Helena (June 4, 2020). "Mini-brain Organoids". Animal Welfare Information Center. Center for Alternatives to Animal Testing, Johns Hopkins University. Retrieved December 17, 2020.
  25. Khan, Firdos Alam (September 20, 2011). Biotechnology Fundamentals. CRC Press. ISBN   9781439820094 via Google Books.
  26. Schäfer-Korting M, Bock U, Diembeck W, Düsing HJ, Gamer A, Haltner-Ukomadu E, Hoffmann C, Kaca M, Kamp H, Kersen S, Kietzmann M, Korting HC, Krächter HU, Lehr CM, Liebsch M, Mehling A, Müller-Goymann C, Netzlaff F, Niedorf F, Rübbelke MK, Schäfer U, Schmidt E, Schreiber S, Spielmann H, Vuia A, Weimer M (2008). "The use of reconstructed human epidermis for skin absorption testing: Results of the validation study". Altern Lab Anim. 36 (2): 161–87. doi: 10.1177/026119290803600207 . PMID   18522484. S2CID   19259027.
  27. Guthrie, Catharine (2008-03-27). "Putting Immunity in a Test Tube". Time. Archived from the original on March 30, 2008. Retrieved 2009-12-22.
  28. "alternatives to animal testing". Peta. 2010-06-21.{{cite journal}}: Cite journal requires |journal= (help)
  29. "Asthma". entelos.com. Archived from the original on 2005-04-15. Retrieved 2007-10-05. (from Internet Archive)
  30. Bertocci GE, Pierce MC, Deemer E, Aguel F, Janosky JE, Vogeley E (2003). "Using test dummy experiments to investigate pediatric injury risk in simulated short-distance falls". Arch Pediatr Adolesc Med. 157 (5): 480–6. doi: 10.1001/archpedi.157.5.480 . PMID   12742885.
  31. "I was a human crash-test dummy - Salon.com". Archive.salon.com. 1999-11-19. Archived from the original on 2014-02-26. Retrieved 2014-02-26.
  32. "Game of Hearts". Portfolio.com. 2008-07-16. Retrieved 2014-02-26.
  33. 1 2 "Technology | Mouse brain simulated on computer". BBC News. 2007-04-27. Retrieved 2014-02-26.
  34. Wootton Robert C. R., Demello Andrew J. (2012). "Microfluidics: Analog-to-digital Drug Screening". Nature. 483 (7387): 43–44. Bibcode:2012Natur.483...43W. doi:10.1038/483043a. PMID   22382977. S2CID   205070310.
  35. 1 2 Rachid Jellali. "Liver and kidney cells cultures in a new perfluoropolyether biochip".{{cite journal}}: Cite journal requires |journal= (help)
  36. Prot Jean, Leclerc Eric (2012). "The Current Status of Alternatives to Animal Testing and Predictive Toxicology Methods Using Liver Microfluidic Biochips". Annals of Biomedical Engineering. 40 (6): 1228–243. doi:10.1007/s10439-011-0480-5. PMID   22160577. S2CID   6568516.
  37. "Lung-on-a-chip". Hansjorg Wyss Institute for Biologically Inspired Engineering. Archived from the original on 2014-02-02. Retrieved 27 January 2014.
  38. Committee on Toxicity Testing and Assessment of Environmental Agents, National Research Council (2007). Toxicity testing in the 21st century: A vision and a strategy. doi:10.17226/11970. ISBN   978-0-309-15173-3 . Retrieved August 12, 2013.
  39. "The Human Toxome Project". The Human Toxome Project. Archived from the original on 2014-02-02. Retrieved 27 January 2014.
  40. "SEURAT-1 - Towards the Replacement of in vivo Repeated Dose Systemic Toxicity Testing". Seurat-1.eu. Retrieved 2014-02-26.
  41. "Sixth Report from the Commission to the Council and the European Parliament on the Statistics on the number of animals used for experimental and other scientific purposes in the member states of the European Union COM(2010) 511/final 2" (PDF). European Commission. 2010. Retrieved August 20, 2013.
  42. 20 February 2015. "Comparing the LAL Method with the Pyrogen Test on Rabbits". Wako Pyrostar. Retrieved 6 March 2015.{{cite web}}: CS1 maint: numeric names: authors list (link)
  43. "Short Guidance On the Threshold Approach for Acute Fish Toxicity". Organisation for Economic Co-operation and Development (OECD). Retrieved 27 January 2014.
  44. "euroecotox.eu". euroecotox.eu. Archived from the original on 2014-01-01. Retrieved 2014-01-27.
  45. "Home| AXLR8". Axlr8.eu. 2012-10-10. Archived from the original on 2014-02-02. Retrieved 2014-01-27.
  46. The European Parliament and the Council of the European Union (2010). "Directive 2010/63/EU of the European Parliament and of the Council" . Retrieved August 12, 2013.
  47. "EUR-Lex - 31986L0609 - EN - EUR-Lex". Eur Lex. 11 Apr 2014. Retrieved 24 Apr 2014.
  48. "Animals used for scientific purposes - Environment - European Commission". European Commission. 11 Apr 2014. Retrieved 24 Apr 2014.
  49. 1 2 "EURL ECVAM's" (PDF). Ihcp.jrc.ec.europa.eu. Retrieved 2014-02-26.
  50. "EU-NETVAL (European Union Network of Laboratories for the Validation of Alternative Methods) — Institute for Health and Consumer Protection – (JRC-IHCP), European Commission". Ihcp.jrc.ec.europa.eu. 2014-01-20. Retrieved 2014-01-27.
  51. "Regulation (EC) No 1223/2009 of the European Parliament and of the Council". Eur-lex.europa.eu. Retrieved 2014-02-26.
  52. European Parliament and the Council of the European Union (2006). "Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH)" . Retrieved August 11, 2013.
  53. European Union (31 May 2008). "Acts adopted under the EC Treaty/Euratom Treaty whose publication is obligatory". Official Journal of the European Union. Retrieved 24 Apr 2014.
  54. "Regulations: No 1331/2008". Eur-lex.europa.eu. Retrieved 2014-02-26.
  55. "Guidance for Submission for Food Additive Evaluations". EFSA Journal. European Food Safety Authority. 10 (7). 16 Aug 2012. doi: 10.2903/j.efsa.2012.2760 .
  56. "Home". Eusaat.org. Retrieved 2014-01-27.
  57. "World Congress flyer" (PDF). ALTEX.
  58. "COLAMA 2012". Uff.br. Archived from the original on 2014-02-02. Retrieved 2014-01-27.
  59. "CAAT Workshops". Johns Hopkins University Center for Alternatives to Animal Testing. Retrieved December 8, 2020.
  60. "Social Housing: Selected Presentations: Symposiums on Social Housing of Laboratory Animals". Animal Welfare Information Center, National Agricultural Library. Retrieved December 8, 2020.
  61. "7th Annual 3Rs Symposium: Practical Solutions and Success Stories". Animal Welfare Information Center, National Agricultural Library. Retrieved December 8, 2020.
  62. "Cosmetics Europe - Alternative Methods". Cosmeticseurope.eu. 2011-08-25. Retrieved 2014-02-26.
  63. "Developing alternative approaches to animal testing | Sustainable living | Unilever Global". Unilever.com. 2013-07-17. Archived from the original on 2014-02-01. Retrieved 2014-01-27.
  64. "Alternative Methods in Use - BASF - The Chemical Company - Corporate Website". BASF. Archived from the original on 2013-08-19. Retrieved 2014-02-26.
  65. "Animal Testing | What We Do". Eurogroup For Animals. Archived from the original on 2014-03-25. Retrieved 2014-02-26.
  66. "Medical research on animals: facts and fiction". Vier-pfoten.org. 2012-11-13. Archived from the original on 2013-12-03. Retrieved 2014-01-27.
  67. "Antidote Europe". Antidote Europe. Archived from the original on 2014-02-07. Retrieved 2014-02-26.
  68. "Tierschutzbund". Tierschutzbund.de. Retrieved 2014-02-26.
  69. "LAV - Diritti agli animali - LAV". Lav.it. Retrieved 2014-02-26.
  70. "R&D on Alternative Methods to Animal Experimentation". AlexandraProject.org. Retrieved 24 Apr 2014.
  71. "About US". Buav.org. Archived from the original on 2014-02-08. Retrieved 2014-01-27.
  72. "NEAVS". Neavs.org. Archived from the original on 2014-02-23. Retrieved 2014-02-26.
  73. "Advancing Humane Science : Humane Society International". Hsi.org. Retrieved 2014-02-26.
  74. "Home". PETA.org.uk. 2012-01-10. Retrieved 2014-01-27.
  75. "stopvivisezione.net". stopvivisezione.net. Retrieved 2014-02-26.
  76. "Welcome". Go Cruelty Free. Archived from the original on 2007-06-06. Retrieved 2014-02-26.
  77. "Be Cruelty-Free Campaign". Humane Society International. Retrieved 2019-10-30.
  78. "End Animal Testing : Humane Society International". Hsi.org. Retrieved 2014-02-26.
  79. "About the £250,000 Lush Prize". Lushprize.org. Retrieved 2014-02-26.
  80. "Enterprise and Industry - European Commission". Ec.europa.eu. 2011-01-01. Retrieved 2014-01-27.
  81. "Alternatives Research Grants | Alternatives Research & Development Foundation (ARDF)". Ardf-online.org. Retrieved 2014-01-27.
  82. "3Rs Prize 2013". NC3Rs. 2013-12-11. Archived from the original on 2013-12-03. Retrieved 2014-01-27.
  83. 1 2 "About Us | AFAAR". Alternativestoanimalresearch.org. Retrieved 2014-01-27.
  84. "IIVS". Iivs.org. Retrieved 2014-02-26.
  85. "NORINA database". norecopa.no.
  86. "Norecopa". norecopa.no. Archived from the original on 2016-03-24. Retrieved 2014-11-12.
  87. "Welcome". InterNICHE. Retrieved 2014-02-25.
  88. "Mission statement :: Tierschutz macht Schule". Tierschutzmachtschule.at. Archived from the original on 2013-12-03. Retrieved 2014-02-25.
  89. "Cell Culture Technology". XCellR8. Retrieved 2014-02-25.
  90. "AWIC Workshops & Trainings". Animal Welfare Information Center, National Agricultural Library. Retrieved December 8, 2020.
  91. "MAWA Trust". MAWA Trust. Retrieved 2014-02-25.
  92. A Guide to the Alternatives of Animal Experimentation (2009; revised edition 2010). Eds. Syed Ziaur Rahman and Mohd Tariq Salman, Ibn Sina Academy of Medieval Medicine and Sciences, Aligarh, India ( ISBN   978-81-906070-4-9)
  93. Akbarsha, MA; Pereira, Shiranee (Nov–Dec 2010). "Mahatma Gandhi-Doerenkamp Center for Alternatives to Use of Animals in Life Science Education". Journal of Pharmacology and Pharmacotherapeutics. 1 (2): 108–10. doi: 10.4103/0976-500X.72353 . PMC   3043344 . PMID   21350619.
  94. "JaCVAM". Jacvam.jp. Archived from the original on 2014-03-02. Retrieved 2014-02-26.
  95. "International Cooperation > KoCVAM". Nifds.go.kr. Archived from the original on 2014-04-13. Retrieved 2014-02-26.
  96. "BRA : Brazilian Center for Validation of Alternative Methods established" (PDF). Altex.ch. Retrieved 2014-02-26.
  97. Presgrave OA (December 2008). "The need for the establishment of a Brazilian Centre for the Validation of Alternative Methods (BraCVAM)". Alternatives to Laboratory Animals. 36 (6): 705–8. doi: 10.1177/026119290803600613 . PMID   19154096. S2CID   29946117.
  98. "Three Rs". Ccac.ca. Archived from the original on 2013-12-11. Retrieved 2014-02-26.
  99. "Framework for International Cooperation on Alternative Test Methods (ICATM) - Consumer and Personal Care Products - Health Canada". Hc-sc.gc.ca. Archived from the original on 2014-02-08. Retrieved 2014-02-25.
  100. "NTP Interagency Center for the Evaluation of Alternative Toxicological Methods - National Toxicology Program". Iccvam.niehs.nih.gov. Archived from the original on 2013-12-09. Retrieved 2014-02-26.
  101. "Center for Alternatives to Animal Testing - Johns Hopkins Bloomberg School of Public Health". Caat.jhsph.edu. Retrieved 2014-02-26.
  102. "Home page". Evcam Database Service on Alternative methods to Animal Experimentation. Archived from the original on 2006-12-06. Retrieved 2018-10-13.
  103. "Review of REACH - Chemicals - Enterprise and Industry". Ec.europa.eu. 2013-06-28. Retrieved 2014-02-25.
  104. "European Partnership for Alternatives Approaches to Animal Testing - European Commission". Ec.europa.eu. 2014-02-20. Archived from the original on 2013-11-01. Retrieved 2014-02-26.
  105. "ecopa - european consensus-platform for alternatives". Ecopa.eu. Retrieved 2014-02-26.
  106. "Zentrum für Ersatz- und Ergänzungsmethoden zu Tierversuchen". zet. Archived from the original on 2014-03-02. Retrieved 2014-02-26.
  107. "FICAM front page". Ficam.fi. 2012-09-26. Archived from the original on 2014-09-01. Retrieved 2014-06-02.
  108. "FRANCOPA: Accueil". Francopa.fr. Retrieved 2014-02-25.
  109. "ZEBET database on alternatives to animal experiments on the Internet (AnimAlt-ZEBET)". BfR. 2004-09-30. Retrieved 2014-02-26.
  110. "Mission". BfR. Retrieved 2014-02-26.
  111. "Norwegian consensus platform for the replacement, reduction and refinement of animal experiments" . Retrieved 2014-11-12.
  112. "Fund for the Replacement of Animals in Medical Experiments". Frame.org.uk. Retrieved 2014-02-26.
  113. "NC3RS". Nc3rs.org.uk. Retrieved 2014-02-26.
  114. NIH. "Reducing the Number of Animals in Research Testing" (PDF). Archived from the original (PDF) on June 27, 2013. Retrieved 24 Apr 2014.
  115. "Official web site". ICH. Retrieved 2014-02-26.
  116. "Testing of chemicals". OECD. Retrieved 2014-02-26.
  117. "International Cooperation on Cosmetic Regulation (ICCR)". Fda.gov. Retrieved 2014-02-26.
  118. 1 2 "Testing of chemicals". OECD. Retrieved 2014-02-25.
  119. "Members and partners". OECD. Retrieved 2014-02-25.
  120. "Welcome to ICAPO". Icapo.org. Retrieved 2014-02-25.