Wolff R K, Dorato M A
Toxicology Research Laboratories, Lilly Research Laboratories, A Division of Eli Lilly and Company, Greenfield, IN 46140.
Crit Rev Toxicol. 1993;23(4):343-69. doi: 10.3109/10408449309104076.
This paper reviews technical issues related to the toxicologic testing of inhaled pharmaceuticals. Although there are commonalities between approaches to general and inhalation toxicity testing, there also are specific challenges in the toxicity testing of inhaled pharmaceuticals. A major issue is that of dose; inhaled dose is more difficult to determine than intravenous or oral doses. Also, it is harder to relate dose in laboratory animals to that in man for inhalation exposure than for other routes of administration. Additionally, in the case of inhaled pharmaceuticals, people generally inhale through the mouth, whereas most laboratory animals inhale primarily through the nose. This presents significant challenges in exposure methodology and technology that often need innovative approaches involving alteration to particle size of the agent or dosing procedure. Because the respiratory tract is the site of deposition, local respiratory toxicity and possible damage to lung cells need to be assessed. Systemic toxicity also needs to be evaluated and may be an issue in some cases. Special studies on pulmonary function, mucociliary clearance, or immune response may be needed, depending on the nature of the inhaled pharmaceutical. This review explores the main issues involved in toxicity testing of inhaled pharmaceuticals, the approaches that have been used, and the current and future challenges.
本文综述了与吸入性药物毒理学检测相关的技术问题。尽管一般毒性检测方法与吸入毒性检测方法存在共性,但吸入性药物的毒性检测也面临着特殊挑战。一个主要问题是剂量问题;吸入剂量比静脉注射或口服剂量更难确定。此外,与其他给药途径相比,将实验动物的吸入暴露剂量与人体剂量相关联更为困难。另外,对于吸入性药物,人通常通过口腔吸入,而大多数实验动物主要通过鼻腔吸入。这在暴露方法和技术方面带来了重大挑战,通常需要采用创新方法,包括改变药物颗粒大小或给药程序。由于呼吸道是药物沉积的部位,因此需要评估局部呼吸道毒性以及对肺细胞可能造成的损害。还需要评估全身毒性,在某些情况下这可能是一个问题。根据吸入性药物的性质,可能需要进行关于肺功能、黏液纤毛清除或免疫反应的专项研究。本综述探讨了吸入性药物毒性检测中涉及的主要问题、已采用的方法以及当前和未来面临的挑战。