Su K S, Campanale K M, Gries C L
J Pharm Sci. 1984 Sep;73(9):1251-4. doi: 10.1002/jps.2600730915.
The blood levels of the [14C]clofilium ion in rats after various routes of administration of clofilium tosylate were compared. The results indicate that the blood levels after nasal administration were not statistically different from levels after intravenous administration (p greater than 0.05). Administration by the oral route resulted in considerably lower blood levels. Nasal administration of clofilium tosylate appeared to be superior to oral administration. Histological examinations of nasal mucosa were conducted. At the lower concentration, mild necrosis was observed, and large areas of mucosa were unaffected. However, necrosis of large areas of mucosa occurred after exposure to the higher concentration. Levels of radioactivity in heart, liver, lung, and kidney tissue, as a function of time, were also studied. Unlike the blood levels after nasal administration, the levels of radioactivity were persistent in heart tissue. The data suggest that the [14C]clofilium ion and/or metabolite concentrate in the heart and that blood levels of radioactivity may not be an accurate index of cardiac levels or biological response.
比较了大鼠经不同途径给予甲苯磺酸氯非铵后[¹⁴C]氯非铵离子的血药浓度。结果表明,经鼻给药后的血药浓度与静脉给药后的血药浓度无统计学差异(p>0.05)。口服给药导致血药浓度显著降低。甲苯磺酸氯非铵经鼻给药似乎优于口服给药。对鼻黏膜进行了组织学检查。在较低浓度下,观察到轻度坏死,大片黏膜未受影响。然而,暴露于较高浓度后,大片黏膜发生坏死。还研究了心脏、肝脏、肺和肾脏组织中的放射性水平随时间的变化。与经鼻给药后的血药浓度不同,心脏组织中的放射性水平持续存在。数据表明,[¹⁴C]氯非铵离子和/或代谢物在心脏中浓缩,放射性血药浓度可能不是心脏浓度或生物学反应的准确指标。