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使用铝或微晶酪氨酸基佐剂进行变应原免疫治疗后大鼠体内铝的分析。

Analysis of aluminium in rat following administration of allergen immunotherapy using either aluminium or microcrystalline-tyrosine-based adjuvants.

作者信息

McDougall Stuart A, Heath Matthew D, Kramer Matthias F, Skinner Murray A

机构信息

ARCINOVA, Willowburn Avenue, Alnwick, Northumberland, NE66 2JH, UK.

Allergy Therapeutics plc, Dominion Way, Worthing, BN14 8SA, UK.

出版信息

Bioanalysis. 2016 Mar;8(6):547-56. doi: 10.4155/bio.16.10. Epub 2016 Feb 26.

Abstract

BACKGROUND

Investigation into the absorption, distribution and elimination of aluminium in rat after subcutaneous aluminium adjuvant formulation administration using ICP-MS is described.

METHOD & RESULTS: Assays were verified under the principles of a tiered approach. There was no evidence of systemic exposure of aluminium, in brain or in kidney. Extensive and persistent retention of aluminium at the dose site was observed for at least 180 days after administration.

CONCLUSION

This is the first published work that has quantified aluminium adjuvant retention based on the quantity of aluminium delivered in a typical allergy immunotherapy course. The results indicate that the repeated administration of aluminium-containing adjuvants will likely contribute directly and significantly to an individual's body burden of aluminium.

摘要

背景

描述了使用电感耦合等离子体质谱法(ICP-MS)对皮下注射铝佐剂制剂后大鼠体内铝的吸收、分布和消除情况进行的研究。

方法与结果

按照分层方法的原则对测定进行了验证。没有证据表明铝在脑或肾中有全身暴露。给药后至少180天观察到铝在给药部位广泛且持续滞留。

结论

这是首次发表的基于典型过敏免疫治疗疗程中铝的给药量对铝佐剂滞留进行量化的研究。结果表明,含铝佐剂的重复给药可能会直接且显著地增加个体体内的铝负荷。

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