Alternatives to animal testing

Animal testing

Main articles
Animal testing
Alternatives to animal testing
Testing on: invertebrates
frogs · primates
rabbits · rodents
Animal testing regulations
History of animal testing
History of model organisms
IACUC
Laboratory animal sources
Pain and suffering in lab animals
Testing cosmetics on animals
Toxicology testing
Vivisection

Issues
Biomedical research
Animal rights · Animal welfare
Animals (Scientific Procedures)
Great ape research ban
International trade in primates

Cases
Brown Dog affair
Cambridge University primates
Pit of despair
Silver Spring monkeys
UCR 1985 laboratory raid
Unnecessary Fuss

Companies
Jackson Laboratory
Charles River Laboratories, Inc.
Covance · Harlan
Huntingdon Life Sciences
UK lab animal suppliers
Nafovanny · Shamrock

Groups/campaigns
AALAS · AAAS · ALF
Americans for Medical Progress
Boyd Group · BUAV
Dr Hadwen Trust
Foundation for Biomedical
Research
 · FRAME
National Anti-Vivisection Society
New England Anti-Vivisection Society
PETA · Physicians Committee
for Responsible Medicine

Primate Freedom Project
Pro-Test
SPEAK · SHAC
Speaking of Research
Understanding Animal Research

Writers/activists
Tipu Aziz · Michael Balls
Neal Barnard · Colin Blakemore
Simon Festing · Gill Langley
Ingrid Newkirk · Bernard Rollin
Jerry Vlasak · Syed Ziaur Rahman

Categories
Animal testing · Animal rights
Animal welfare

Related templates
Template:Animal rights

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

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.

Types

Cell culture and tissue engineering

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 fetal cows are sacrificed each year to obtain the world's supply of fetal bovine serum, used to grow cultured cells.[8]

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[9] and EpiSkin[10] and SkinEthic RHE model[11] 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).[12] 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.[13]

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.[14]

Skin absorption

Several tissue culture methods which measure the rate of chemical absorption by the skin have been approved by the OECD.

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.[15] Although originally derived from a mouse embryo, the 3T3 cell line was developed in 1962.

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. 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.[16]

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.[17]

Computer simulation

Crash test dummies have been used to replace live animals in impact testing.
See also: in silico

Examples of computer simulations available include models of asthma,[18] 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.[19] Prior to this, live pigs were used as test subjects for crash testing.[20]

Other non-animal simulators have been developed for military use to mimic battlefield induced traumas. TraumaMan[21] and the Combat Trauma Patient Simulator can be used to simulate hemorrhaging, fractures, amputations and burns. Previously, animals were intentionally subjected to various traumas to provide military training. TraumaMan is also now used for training medical students.[22]

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.[23] In 2007, US researchers using the world's fastest computer at the time, BlueGene L, modeled half a mouse's brain for just 10 seconds. However, due to limitations in computing power, the simulation could only be run at 1/10th the speed of an actual mouse brain.[24] 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."[24]

For pharmacology and toxicology, physiologically based pharmacokinetic models are much used for in vitro to in vivo extrapolation of alternative testing.

Medical imaging

Further information: Medical imaging and Microdosing

Medical imaging is able to demonstrate to researchers both how drugs are metabolized by use of microdosing, and the detailed condition of organ tissue.[25]

Microfluidic Chip

Further information: microfluidics and Lab-on-a-chip

Microfluidic chip, which is just 2 cm wide, have engraved into a series of small chambers, each containing a sample of tissue from different parts of the body. A substitute of blood flows through micro-channels where the compartments of chips linked by. When injected, 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.[26]

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.[27]

Fungal model for mammalian drug metabolism

Fungi like Cunninghamella elegans can be used as a microbial model of mammalian drug metabolism[28][29][30][31] thereby reducing the need for laboratory animals.[32]

Future alternatives

Organs on a chip

Main article: Organ-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".[33] 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",[34] 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[35] ) 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".[36] 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.[37] This is also the field where until now only two alternative tests exist worldwide: One guideline, OECD TG 236,[38] and one guidance (OECD series on testing and assessment 126)[39] are so far available.

Euroecotox[40] 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 fulfill this growing need by providing a focal point for dialogue and collaboration.[41] Humane Society International is part of the consortium.

Scientific congresses

The European Society for Alternatives to Animal Testing (EUSAAT)[42] 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.[43]

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).[44]

Industry and corporate initiatives

Legislation

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 28 EU Member States (MS),[48] repealing Directive 86/609/EEC.[49] 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.[50] Purposes of this Directive are to provide scope (via Articles 1 & 3), harmonise the current EU understanding of what defines an animal (Article 1.3), map resources, identify competent people and authorities (Articles 47.5 & 48), establish a common framework, and promote collaboration of the Member States with the EC to promote animal welfare in the EU as a European value in Article 13 of the Treaty of the Functioning of the EU (TFEU).

Animal welfare is not an EU policy area per se as it is for agriculture, fisheries, research, etc., but rather that "In formulating and implementing the Union's agriculture, fisheries, transport, internal markets, research, technological development, and space policies, the Union and the Member States shall, since animals are sentient beings, pay full regard to the welfare of animals, while respecting the legislative or administrative provisions and customs of the Member States relating in particular to religious rites, cultural traditions and regional heritage". Therefore, no legal action can be taken by the EC when animal welfare is not respected; one must refer a complaint directly to the Member States. However, promotion and use of alternative test methods and 3Rs are written elsewhere within EU legislation (e.g. REACH, Cosmetics, PPP, Biocides ...). EU agencies (ECHA, EMA, EFSA) also contribute to the protection of laboratory animals used for scientific purposes.

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, Commission announced the creation of NETVAL [51] (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.[52] Currently there are 13 test facilities in 9 Member States: Germany (3), The Netherlands (2), Spain (2), Belgium (1), Czech Republic (1), Finland (1), France (1), Italy (1) and Sweden (1).[51]

Any EU laboratory is allowed to apply as long as they follow the eligibility criteria listed by the EC, such as sufficient scientific staff, adequate equipment and GLP/or ISO certificates.[53]

EU cosmetic regulation

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.[54]

EU chemical policy: REACH

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.[55] 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.

EU test methods regulation

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".[56] 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 Regulation for Food Additives, Food Enzymes, and Food Flavourings

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.[57]

Within the EU animal welfare law (2010/63/EU), the principles of the 3Rs are invoked whenever toxicological test methods are necessary.[58]

Animal welfare and animal rights organizations

Europe

Austria

France

Germany

Italy

Monaco

United Kingdom

United States

Joint

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

Australia

India

Japan

South Korea

South America

Brazil

North America

Canada

United States of America

Europe

Austria

Finland

France

Germany

Norway

Romania

United Kingdom

International

ICATM

International Cooperation on Alternative Test Methods (ICATM): On April 27, 2009 the U.S., 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.[107]

OECD

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.[111] 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.[112] NGOs are represented at the technical level at the OECD, under the ICOPA International Council on Animal Protection in OECD program.[113]

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.[111]

See also

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. doi:10.1038/nature03193. PMID 15602551.
  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
  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., Jürgen Frank, Helmut App, Harald Schöffl, Walter Pfaller and Gerhard Gstraunthaler. 2010 Serum-free Cell Culture: The Serum-free Media Interactive Online Database. Altex 27:53–62.
  9. "EpiDermTM Tissue Model". MatTek Corporation. Retrieved 7 July 2015.
  10. "L'Oréal cutaneous tissue engineering platform". Invitroskin. 2007-04-30. Retrieved 2014-02-26.
  11. "News - Congress - Workshops - SkinEthic Laboratories - SkinEthic Reconstructed Human Epidermis RHE validated in Europe". Skinethic.com. 2008-12-19. Retrieved 2014-02-26.
  12. "Alternatives In Testing". Neaves Humane Science is Superior Science. Retrieved 7 July 2015.
  13. "Test No. 439: In Vitro Skin Irritation - Books - OECD iLibrary". OECD I-Library. Retrieved 24 Apr 2014.
  14. 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. doi:10.1080/10915810305094. PMID 12745991. INIST:14763182.
  15. "Background - 3T3 Neutral Red Uptake Phototoxicity Assay - MB Research Labs". 3t3nru.mbresearchlabs.com. Retrieved 24 Apr 2014.
  16. "The use of reconstructed human epidermis for skin absorption testing: Results of the validation study". PubMed.gov. Retrieved 7 July 2015.
  17. Guthrie, Catharine (2008-03-27). "Putting Immunity in a Test Tube". TIME. Retrieved 2009-12-22.
  18. "Asthma". entelos.com. Archived from the original on 2005-04-15. Retrieved 2007-10-05. (from internet archive)
  19. "Using test dummy experiments to investigate pediatric injury risk in simulated short-distance falls". PubMed.gov. Retrieved 7 July 2015.
  20. "I was a human crash-test dummy - Salon.com". Archive.salon.com. 1999-11-19. Retrieved 2014-02-26.
  21. "About the TraumaMan System | Simulab Corporation". Simulab.com. Retrieved 2014-02-26.
  22. "TraumaMan Offers Lifelike Practice for Med Students". NPR. Retrieved 2014-02-26.
  23. "Game of Hearts". Portfolio.com. 2008-07-16. Retrieved 2014-02-26.
  24. 1 2 "Technology | Mouse brain simulated on computer". BBC News. 2007-04-27. Retrieved 2014-02-26.
  25. "alternatives to animal testing". Peta
  26. Robert C. R. Wootton, and Andrew J. Demello. "Microfluidics: Analog-to-digital Drug Screening." Nature 483.7387 (2012): 43. Web.
  27. Prot, Jean, and Eric Leclerc. "The Current Status of Alternatives to Animal Testing and Predictive Toxicology Methods Using Liver Microfluidic Biochips." Annals of Biomedical Engineering 40.6 (2012): 1228-243. Web.
  28. 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.
  29. Joanna D. Moody, Donglu Zhang, Thomas M. Heinze and Carl E. Cerniglia (2000). "Transformation of amoxapine by Cunninghamella elegans". Applied and Environmental Microbiology 66 (8): 3646–3649. doi:10.1128/AEM.66.8.3646-3649.2000. PMC 92200. PMID 10919836.
  30. 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.
  31. Hezari, M.; Davis, P. J. (1993). "Microbial models of mammalian metabolism. Furosemide glucoside formation using the fungus Cunninghamella elegans". Drug metabolism and disposition: the biological fate of chemicals 21 (2): 259–267. PMID 8097695.
  32. 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.
  33. "Lung-on-a-chip". Hansjorg Wyss Institute for Biologically Inspired Engineering. Retrieved 27 January 2014.
  34. Committee on Toxicity Testing and Assessment of Environmental Agents, National Research Council (2007). "Toxicity testing in the 21st century: A vision and a strategy". Retrieved August 12, 2013.
  35. "The Human Toxome Project". The Human Toxome Project. Retrieved 27 January 2014.
  36. "SEURAT-1 - Towards the Replacement of in vivo Repeated Dose Systemic Toxicity Testing". Seurat-1.eu. Retrieved 2014-02-26.
  37. "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.
  38. 20 February 2015. "Comparing the LAL Method with the Pyrogen Test on Rabbits". Wako Pyrostar. Retrieved 6 March 2015.
  39. "SHORT GUIDANCE ON THE THRESHOLD APPROACH FOR ACUTE FISH TOXICITY". Organisation for Economic Co-operation and Development (OECD). Retrieved 27 January 2014.
  40. "euroecotox.eu". euroecotox.eu. Retrieved 2014-01-27.
  41. "Home| AXLR8". Axlr8.eu. 2012-10-10. Retrieved 2014-01-27.
  42. "Home". Eusaat.org. Retrieved 2014-01-27.
  43. "World Congress flyer" (PDF). ALTEX. ALTEX.
  44. "COLAMA 2012". Uff.br. Retrieved 2014-01-27.
  45. "Cosmetics Europe - Alternative Methods". Cosmeticseurope.eu. 2011-08-25. Retrieved 2014-02-26.
  46. "Developing alternative approaches to animal testing | Sustainable living | Unilever Global". Unilever.com. 2013-07-17. Retrieved 2014-01-27.
  47. "Alternative Methods in Use - BASF - The Chemical Company - Corporate Website". BASF. Retrieved 2014-02-26.
  48. The European Parliament and the Council of the European Union (2010). Directive 2010/63/EU "Directive 2010/63/EU of the European Parliament and of the Council" Check |url= value (help). Retrieved August 12, 2013.
  49. "EUR-Lex - 31986L0609 - EN - EUR-Lex". Eur Lex. 11 Apr 2014. Retrieved 24 Apr 2014.
  50. "Animals used for scientific purposes - Environment - European Commission". European Commission. 11 Apr 2014. Retrieved 24 Apr 2014.
  51. 1 2 "EURL ECVAM's" (PDF). Ihcp.jrc.ec.europa.eu. Retrieved 2014-02-26.
  52. "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.
  53. "EURL ECVAM's" (PDF). Ihcp.jrc.ec.europa.eu. Retrieved 2014-02-26.
  54. "Regulation (EC) No 1223/2009 of the European Parliament and of the Council". Eur-lex.europa.eu. Retrieved 2014-02-26.
  55. European Parliament and the Council of the European Union (2006). "Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH)". Retrieved August 11, 2013.
  56. 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.
  57. "Regulations: No 1331/2008". Eur-lex.europa.eu. Retrieved 2014-02-26.
  58. "Guidance for Submission for Food Additive Evaluations" (PDF). European Food Safety Authority. 16 Aug 2012. Retrieved 23 Apr 2014.
  59. "Animal Testing | What We Do". Eurogroup For Animals. Retrieved 2014-02-26.
  60. "Medical research on animals: facts and fiction". Vier-pfoten.org. 2012-11-13. Retrieved 2014-01-27.
  61. "Antidote Europe". Antidote Europe. Retrieved 2014-02-26.
  62. "Tierschutzbund". Tierschutzbund.de. Retrieved 2014-02-26.
  63. "LAV - Diritti agli animali - LAV". Lav.it. Retrieved 2014-02-26.
  64. "R&D on Alternative Methods to Animal Experimentation". AlexandraProject.org. Retrieved 24 Apr 2014.
  65. "About US". Buav.org. Retrieved 2014-01-27.
  66. "NEAVS". Neavs.org. Retrieved 2014-02-26.
  67. "Advancing Humane Science : Humane Society International". Hsi.org. Retrieved 2014-02-26.
  68. "Home". PETA.org.uk. 2012-01-10. Retrieved 2014-01-27.
  69. "stopvivisezione.net". stopvivisezione.net. Retrieved 2014-02-26.
  70. "Welcome". Go Cruelty Free. Retrieved 2014-02-26.
  71. "End Animal Testing : Humane Society International". Hsi.org. Retrieved 2014-02-26.
  72. "About the £250,000 Lush Prize". Lushprize.org. Retrieved 2014-02-26.
  73. "Enterprise and Industry - European Commission". Ec.europa.eu. 2011-01-01. Retrieved 2014-01-27.
  74. "Alternatives Research Grants | Alternatives Research & Development Foundation (ARDF)". Ardf-online.org. Retrieved 2014-01-27.
  75. "3Rs Prize 2013". NC3Rs. 2013-12-11. Retrieved 2014-01-27.
  76. 1 2 "About Us | AFAAR". Alternativestoanimalresearch.org. Retrieved 2014-01-27.
  77. "IIVS". Iivs.org. Retrieved 2014-02-26.
  78. NORINA
  79. "Norecopa". norecopa.no. Retrieved 2014-11-12.
  80. "Welcome". InterNICHE. Retrieved 2014-02-25.
  81. "Mission statement :: Tierschutz macht Schule". Tierschutzmachtschule.at. Retrieved 2014-02-25.
  82. "Cell Culture Technology". XCellR8. Retrieved 2014-02-25.
  83. "MAWA Trust". MAWA Trust. Retrieved 2014-02-25.
  84. 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)
  85. Akbarsha, MA; Pereira, Shiranee (Nov–Dec 2010). "Mahatma Gandhi-Doerenkamp Center for Alternatives to Use of Animals in Life Science Education". Pharmacol Pharmacother 1 (2): 108–10. doi:10.4103/0976-500X.72353. PMC 3043344. PMID 21350619. Archived from the original on July 13, 2011.
  86. "JaCVAM". Jacvam.jp. Retrieved 2014-02-26.
  87. "International Cooperation > KoCVAM". Nifds.go.kr. Retrieved 2014-02-26.
  88. "BRA : Brazilian Center for Validation of Alternative Methods established" (PDF). Altex.ch. Retrieved 2014-02-26.
  89. 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. PMID 19154096.
  90. "Three Rs". Ccac.ca. Retrieved 2014-02-26.
  91. "Framework for International Cooperation on Alternative Test Methods (ICATM) - Consumer and Personal Care Products - Health Canada". Hc-sc.gc.ca. Retrieved 2014-02-25.
  92. "NTP Interagency Center for the Evaluation of Alternative Toxicological Methods - National Toxicology Program". Iccvam.niehs.nih.gov. Retrieved 2014-02-26.
  93. "Center for Alternatives to Animal Testing - Johns Hopkins Bloomberg School of Public Health". Caat.jhsph.edu. Retrieved 2014-02-26.
  94. 1 2 "European Union Reference Laboratory for alternatives to animal testing (EURL ECVAM) — Institute for Health and Consumer Protection – (JRC-IHCP), European Commission". Ihcp.jrc.ec.europa.eu. 2014-01-24. Retrieved 2014-02-26.
  95. "Home page". Evcam Database Service on Alternative methods to Animal Experimentation).
  96. "Review of REACH - Chemicals - Enterprise and Industry". Ec.europa.eu. 2013-06-28. Retrieved 2014-02-25.
  97. "European Partnership for Alternatives Approaches to Animal Testing - European Commission". Ec.europa.eu. 2014-02-20. Retrieved 2014-02-26.
  98. "ecopa - european consensus-platform for alternatives". Ecopa.eu. Retrieved 2014-02-26.
  99. "Zentrum für Ersatz- und Ergänzungsmethoden zu Tierversuchen". zet. Retrieved 2014-02-26.
  100. "FICAM front page". Ficam.fi. 2012-09-26. Retrieved 2014-06-02.
  101. "FRANCOPA: Accueil". Francopa.fr. Retrieved 2014-02-25.
  102. "ZEBET database on alternatives to animal experiments on the Internet (AnimAlt-ZEBET)". BfR. 2004-09-30. Retrieved 2014-02-26.
  103. "Mission". BfR. Retrieved 2014-02-26.
  104. "Norwegian consensus platform for the replacement, reduction and refinement of animal experiments". Retrieved 2014-11-12.
  105. "Fund for the Replacement of Animals in Medical Experiments". Frame.org.uk. Retrieved 2014-02-26.
  106. "NC3RS". Nc3rs.org.uk. Retrieved 2014-02-26.
  107. NIH. "Reducing the Number of Animals in Research Testing" (PDF). Archived from the original (PDF) on June 27, 2013. Retrieved 24 Apr 2014.
  108. "Official web site". ICH. Retrieved 2014-02-26.
  109. "Testing of chemicals". OECD. Retrieved 2014-02-26.
  110. "International Cooperation on Cosmetic Regulation (ICCR)". Fda.gov. Retrieved 2014-02-26.
  111. 1 2 "Testing of chemicals". OECD. Retrieved 2014-02-25.
  112. "Members and partners". OECD. Retrieved 2014-02-25.
  113. "Welcome to ICAPO". Icapo.org. Retrieved 2014-02-25.

External links

Wikiversity has learning materials about Alternatives to animal testing
This article is issued from Wikipedia - version of the Monday, April 25, 2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.