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生物材料安全性评估新方法的评价

Evaluation of a new approach to the safety assessment of biomaterials.

作者信息

Benson W H, Stackhouse R A

出版信息

Drug Chem Toxicol. 1986;9(3-4):275-83. doi: 10.3109/01480548608998280.

Abstract

The effectiveness of a bacterial luminescence inhibition assay in assessing the toxicity of compounds which are released from biomaterials was evaluated. Luminescence from a strain of bacteria most closely resembling Photobacterium phosphoreum was measured. The concentration that inhibited luminescence by 50% (EC50) was determined for selected plasticizers, monomers and additives. The intraperitoneal (i.p.-ALD) and intravenous (i.v.-ALD) approximate lethal doses were determined using mice. By ranking the reference compounds toxic/non-toxic, a 37.5% agreement was obtained for the i.p.-ALD and i.v.-ALD toxicity data. While there was only a 12.5% agreement for the i.p. ALD and EC50 values, there was a 75% agreement between the i.v.-ALD and EC50 values. Although additional validation is required, these results provide preliminary indications that the bacterial luminescence inhibition assay is a promising alternative approach to the safety assessment of biomaterials.

摘要

评估了细菌发光抑制试验在评估生物材料释放的化合物毒性方面的有效性。测量了一种与费氏弧菌最相似的细菌菌株的发光情况。测定了选定增塑剂、单体和添加剂抑制发光50%的浓度(EC50)。使用小鼠确定腹腔内(i.p.-ALD)和静脉内(i.v.-ALD)近似致死剂量。通过对参考化合物的毒性/非毒性进行排名,腹腔内ALD和静脉内ALD毒性数据的一致性为37.5%。虽然腹腔内ALD和EC50值之间的一致性仅为12.5%,但静脉内ALD和EC50值之间的一致性为75%。尽管需要进一步验证,但这些结果提供了初步迹象,表明细菌发光抑制试验是生物材料安全评估的一种有前景的替代方法。

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