Baxter Healthcare, 25212 W. Illinois Rt. 120, WG2-1S, Round Lake, IL 60073, USA.
J Med Toxicol. 2010 Sep;6(3):331-6. doi: 10.1007/s13181-010-0025-6.
Previously, it was observed that a nanosuspension formulation of itraconazole was more efficacious and yet less acutely toxic in rats as compared with the conventional solution formulation, SPORANOX (itraconazole) Injection. The present study compares the two formulations with respect to specifically myocardial contractility in conscious dogs. Motivation for doing so is highlighted by the black-box warning in the package insert for SPORANOX (itraconazole) Injection, which warns of negative inotropic effects. Conscious dogs, instrumented with a high-fidelity pressure transducer in the left ventricle, were placed in a sling for dosing and cardiac monitoring. Test and control articles were administered intravenously via a peripheral vein, and left ventricular parameters were measured continuously through 60 min from the start of dosing. As expected, SPORANOX (itraconazole) Injection caused a significant reduction in myocardial contractility as determined by the contractility index. In contrast, the itraconazole nanosuspension administered at twice the dose and at twice the rate of infusion did not result in significant changes in myocardial contractility. A novel formulation technology applied to itraconazole completely prevented the negative inotropic effect observed in conscious dogs as compared with SPORANOX (itraconazole) Injection.
先前有研究观察到,与传统的注射用溶液制剂(商品名:斯泊沙星,通用名:伊曲康唑)相比,伊曲康唑纳米混悬剂在大鼠体内更有效,且毒性更小。本研究旨在比较两种制剂对清醒犬心肌收缩力的影响。斯泊沙星注射液的说明书中有黑框警告,提示其具有负性变力作用,因此我们选择进行此项研究。将装有高保真压力传感器的左心室的清醒犬用吊带固定,用于给药和心脏监测。通过外周静脉静脉内给予受试和对照制剂,并从给药开始后连续测量 60 分钟的左心室参数。正如预期的那样,斯泊沙星注射液导致心肌收缩力明显下降,通过收缩力指数来确定。相比之下,以两倍剂量和两倍输注率给予的伊曲康唑纳米混悬剂并未导致心肌收缩力发生显著变化。与斯泊沙星注射液相比,应用于伊曲康唑的新型制剂技术完全预防了在清醒犬中观察到的负性变力作用。