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鼻腔药物纤毛抑制作用的分类。

Classification of cilio-inhibiting effects of nasal drugs.

作者信息

Merkus P, Romeijn S G, Verhoef J C, Merkus F W, Schouwenburg P F

机构信息

Department of Otorhinolaryngology & Head and Neck Surgery, Academic Medical Center, Amsterdam, The Netherlands.

出版信息

Laryngoscope. 2001 Apr;111(4 Pt 1):595-602. doi: 10.1097/00005537-200104000-00008.

Abstract

OBJECTIVE/HYPOTHESIS: Nasal drug formulations are widely used for a local therapeutic effect, but are also used for systemic drug delivery. In the development of new nasal drugs, the toxic effects on the mucociliary clearance and therefore on the ciliated tissue is of importance. In this study, the effect of nasal drugs and their excipients on the ciliary beat frequency (CBF) is investigated.

STUDY DESIGN

Experimental, in vitro.

METHODS

CBF is measured by a photograph-electric registration method. Excised ciliated chicken trachea tissue is incubated for 15 minutes in the formulation, followed by a reversibility test. To estimate the ciliostatic potential, a classification is given of all tested formulations. According to the CBF, after 60 minutes every drug or excipient could be classified as follows: cilio-friendly: after 60 minutes the CBF has regained 75% or more of its initial frequency; cilio-inhibiting: after 60 minutes the CBF has regained between 25% and 75% of its initial frequency; or ciliostatic: after 60 minutes the CBF has regained 25% or less of its initial frequency.

RESULTS

Most formulations used are cilio-friendly or cilio-inhibiting. Only some are ciliostatic. Preservatives have a major role in the cilio-inhibiting effect of the drug. Also, other additives can contribute to the toxicity profile of nasal drug formulations.

CONCLUSION

This classification of the cilio-inhibiting potential of nasal drug formulations is a valuable tool in the design of safe nasal drugs. The number of animal studies in vivo can be reduced substantially by using this in vitro screening technique. This study demonstrates that the effect on ciliary movement of most drug formulations is due to the preservatives and/or additives and mostly not to the drug itself.

摘要

目的/假设:鼻腔药物制剂广泛用于局部治疗效果,但也用于全身给药。在新型鼻腔药物的研发中,对黏液纤毛清除功能以及由此对纤毛组织产生的毒性作用至关重要。本研究调查了鼻腔药物及其辅料对纤毛摆动频率(CBF)的影响。

研究设计

体外实验。

方法

采用光电记录法测量CBF。将切除的鸡气管纤毛组织在制剂中孵育15分钟,随后进行可逆性测试。为评估纤毛抑制潜力,对所有测试制剂进行分类。根据CBF,60分钟后每种药物或辅料可分类如下:纤毛友好型:60分钟后CBF恢复至初始频率的75%或更高;纤毛抑制型:60分钟后CBF恢复至初始频率的25%至75%;或纤毛静止型:60分钟后CBF恢复至初始频率的25%或更低。

结果

大多数使用的制剂为纤毛友好型或纤毛抑制型。只有一些是纤毛静止型。防腐剂在药物的纤毛抑制作用中起主要作用。此外,其他添加剂也会影响鼻腔药物制剂的毒性特征。

结论

这种鼻腔药物制剂纤毛抑制潜力的分类是设计安全鼻腔药物的有价值工具。通过使用这种体外筛选技术,可大幅减少体内动物研究的数量。本研究表明,大多数药物制剂对纤毛运动的影响是由于防腐剂和/或添加剂,而大多不是药物本身。

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