ГОСТ ISO 10993-11—2011
Библиография
1 Общая литература
[1] U.S-УЕРА РВ 86/108958 and 89/124077
[2] U.S./FDA Toxicological principles for the safety assessment of direct food additives. 1982
[3] U.S. Code of Federal Regulation 1500.40: Method of Testing Toxic Substances
[4] United States Pharmacopoeia 26: Biological Reactivity Tests. In Vivo; The National Formulary 21. Rockvile. MD;
Pharmacopoeial Convention. 2003. pp. 2028-2032
[5] ASTM F619-03. Standard Practice for Extraction of Medical Plastics
[6] SN 119800:1990. Biological Evaluation of Dental Materials
[7] European Pharmacopoeia 4th Edition. 2002
[8] MHLW Notification No. 0213001(2003.02.13): Principles for Biological Safety Evaluation of Medical Devices
[9] HALLE. W. (2003) The Registry of Cytotoxicity: Toxicity testing in cell cultures to predict acute toxicity (LD^) and to
reduce animal testing. ATLA 31:89-98
2 Библиография по объему доз
[10] HULL. R.M. Guideline limit volumes for dosing animals in the preclinical stage of safety evaluation. Human and
Environmental Toxicology. 1995. 14. pp. 305-307
[11] DERELANKO. M.J. and HOLUNGER. M.A. CRC Handbook of Toxicology. CRC Press. NY. 2nd edition. 2001. p. 98
[12] DIEHL. K.-H. et al. Agood practice guide to the administration of substances and removal of blood, including routes
and volumes. J. Applied Toxicology. 21. 2001. pp. 15-23
[13] MORTON. D. et al. Effects of infusion rates in rats receiving repeated large volumes of intravenous saline solution.
Laboratory Animal Sciences, 47. 1997, pp. 656-659
[14] RICHMOND. J.D. Dose limit volumes: The United Kingdom view — past and present. Presented at the Humane
Society of the United States — Refinement in Toxicology Testing: Dosing Data: Volume and Frequency. March 14.
1999. New Orleans. LA
[15] MORTON, D.B. et al. Refining procedures for the administration of substances. Report of the BVAAWF/FRAME/
RSPCA/UFAW Joint Working Group on Refinement. Laboratory Animals. 35. 2001. pp. 1-41
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