3r s applied to in vivo biological activity of recombinant human erythropoietin assay

Ana Paula Arévalo, Tatiana Basika, Sergio Ancheta, Karen Perelmuter, Alejandro Ricciardi, Mariela Bollati-Fogolín, Martina Crispo
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Abstract

An enhanced protocol for the evaluation of in vivo biological activity of recombinant human erythropoietin (rhEPO) assay in mice is described, following European Pharmacopoeia ( Ph. Eur. ) version 10.0 guideline and optimized by applying the principles of Replacement, Reduction and Refinement (3Rs) in animal experimentation. In Laboratory Animal Science, one of the main principles is to optimize the experimental protocols in order to achieve the best results with the lowest number of animals and refine the procedures to avoid unnecessary suffering. The main objective of this protocol is to comply with international guidelines for rhEPO evaluation, applying refinement on procedures and reduction in animal use. Some of the features included in this protocol are the increase in number of rhEPO batches tested simultaneously against an international standard, leading to a substantial reduction in the number of animal’s used, and refinement on animal handling techniques for subcutaneous drug administration and blood withdrawal. The implemented improvements were validated by reticulocyte estimation to ensure compliance with international criteria established for this trial and institutional quality management system.
应用于重组人红细胞生成素体内生物活性测定
根据欧洲药典(Ph. Eur.),描述了一种用于评估小鼠体内重组人红细胞生成素(rhEPO)测定生物活性的增强方案。10.0版指南,并通过在动物实验中应用替换、减少和改进(3Rs)原则进行优化。在实验动物科学中,主要原则之一是优化实验方案,以便以最少的动物数量获得最佳结果,并改进程序以避免不必要的痛苦。本方案的主要目标是遵守rhEPO评估的国际准则,改进程序并减少动物使用。该方案中包括的一些特点是增加了根据国际标准同时检测rhEPO批次的数量,从而大大减少了动物使用的数量,并改进了皮下给药和抽血的动物处理技术。通过网织红细胞评估验证了实施的改进,以确保符合为该试验和机构质量管理体系建立的国际标准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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