Biomedical Research Center, University Hospital, Hradec Kralove, Czech Republic.
Toxicol Lett. 2013 Jul 4;220(2):167-71. doi: 10.1016/j.toxlet.2013.04.013. Epub 2013 Apr 25.
Pigs were administered intramuscularly molar equivalents of HI-6 salts (HI-6 dichloride 10.71 mg/kg and HI-6 DMS 13.59 mg/kg) either with or without hyaluronidase (60 U/kg). Hyaluronidase is supposed to increase tissue permeability and diminishes discomfort caused by the intramuscular injection. Doses of HI-6 salts corresponded with standard HI-6 dichloride dose in one autoinjector (500 mg) and were recalculated for 1 kg of body weight. According to the results, both HI-6 salts applied in combination with hyaluronidase had increased tissue absorption and improved pharmacokinetic profile. The Cmax was significantly higher in case of HI-6 DMS plus hyaluronidase (29.6 ± 2.98 μg/ml) administration increase compared to HI-6 DMS (23.8 ± 3.04 μg/ml) and HI-6 dichloride (19.0 ± 0.93 μg/ml); both without hyaluronidase. Bioavailability calculated as AUCtotal (HI-6 DMS with hyaluronidase, 4,119 ± 647 min μg/ml) was also significantly higher compared to HI-6 DMS (2,259 ± 329 min μg/ml) and HI-6 dichloride (1,969 ± 254 min μg/ml); both without hyaluronidase. The results suggest that administration of HI-6 salt with higher solubility is the first step in the improvement of application strategy, but use some substances with spreading effect (hyaluronidase) may also leads to better absorption and better bioavailability. Improved bioavailability could to go hand in hand with increased effectiveness of therapy without the need of multiple autoinjector applications.
猪肌肉内给予等摩尔当量的 HI-6 盐(HI-6 二盐酸盐 10.71mg/kg 和 HI-6 DMS 13.59mg/kg),同时或不同时给予透明质酸酶(60U/kg)。透明质酸酶据推测可以增加组织通透性,并减轻肌肉内注射引起的不适。HI-6 盐的剂量与一个自动注射器中的标准 HI-6 二盐酸盐剂量(500mg)相对应,并根据 1kg 体重重新计算。根据结果,HI-6 盐与透明质酸酶联合应用均增加了组织吸收并改善了药代动力学特征。与 HI-6 DMS(23.8±3.04μg/ml)和 HI-6 二盐酸盐(19.0±0.93μg/ml)相比,HI-6 DMS 加透明质酸酶给药后 Cmax 显著升高(29.6±2.98μg/ml);两者均无透明质酸酶。作为 AUCtotal(HI-6 DMS 加透明质酸酶,4119±647minμg/ml)计算的生物利用度也显著高于 HI-6 DMS(2259±329minμg/ml)和 HI-6 二盐酸盐(1969±254minμg/ml);两者均无透明质酸酶。结果表明,给予溶解度更高的 HI-6 盐是改进应用策略的第一步,但使用一些具有扩散作用的物质(透明质酸酶)也可能导致更好的吸收和更好的生物利用度。改善的生物利用度可能与治疗效果的提高同时出现,而无需多次应用自动注射器。