Preclinical pharmacokinetics and general toxicology of iodixanol.

I F Heglund, A A Michelet, W F Blazak, K Furuhama, E Holtz
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引用次数: 55

Abstract

To document the safety of iodixanol and to assess its pharmacokinetic properties, extensive tests have been performed. Iodixanol was rapidly excreted, mainly via the kidneys, with a plasma half-life in rats and monkeys of 25 and 76 mins, respectively. The pharmacokinetic data were consistent with an extracelleular distribution of iodixanol. During the 24 hours post-dosing, the urinary excretion was from 72 to 100% in rats, and 78% in monkeys. Biliary excretion was 1.5% during the first 4 hours in rats. Fecal excretion was about 7% in rats and 0.8% in monkeys over the first 24 hours after injection. Approximately 0.5 and 1% of the dose was found in the kidneys of rats and monkeys, respectively, 24 hours after dosing. Acute toxicity of iodixanol in rats was low, with an LD(50) greater than 21 g I/kg. In mice the LD(50) was 21 g I/kg and the approximated median lethal dose (ADL(50)) was found to range from 15 to 21 g I/kg. A single dose of 1 and 3 g I/kg was well tolerated in monkeys. As for the other roentgen contrast media, a reversible, dose-related, vacuolation of the proximal tubules in the kidneys was seen in the acute and subacute studies in rats and monkeys. No relationship was seen between the vacuolation and kidney function. Local tolerance studies demonstrated a low irritation potential for iodixanol when injected by a variety of intravascular and extravascular routes. The reproductive capacity of male and female rats was unaffected by iodixanol when administered daily at doses up to 2 g I/kg/day. No teratogenic potential in rats and rabbits of iodixanol was observed. Further, no toxic effects on pups were seen when rats were dosed during the lactation period. Each of 4 standard genotoxicity tests was negative. No antigenic potential of iodixanol was observed when assessed by the passive cutaneous anaphylaxis test and the active systemic anaphylaxis test in guinea pigs. The intravascular tolerability of iodixanol is high, and therefore, iodixanol should be considered as a safe roentgen contrast medium for intravascular use.

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碘二醇的临床前药代动力学和一般毒理学。
为了证明碘沙醇的安全性并评估其药代动力学特性,已经进行了广泛的试验。碘沙醇主要通过肾脏迅速排出,大鼠和猴子的血浆半衰期分别为25分钟和76分钟。药代动力学数据与碘二醇的细胞外分布一致。在给药后的24小时内,大鼠的尿排泄率为72%至100%,猴子为78%。大鼠前4小时胆排泄量为1.5%。在注射后的前24小时内,大鼠和猴子的粪便排泄率分别为7%和0.8%。在给药24小时后,在大鼠和猴子的肾脏中分别发现约0.5%和1%的剂量。碘沙醇对大鼠急性毒性较低,LD(50) > 21 g I/kg。在小鼠中,LD(50)为21 g I/kg,估计中位致死剂量(ADL(50))在15 ~ 21 g I/kg之间。1和3g I/kg的单次剂量在猴子中耐受性良好。至于其他x线造影剂,在大鼠和猴子的急性和亚急性研究中,肾脏近端小管出现了可逆的、剂量相关的空泡化。空泡化与肾功能无明显关系。局部耐受性研究表明,当通过各种血管内和血管外途径注射碘沙醇时,其刺激潜力低。当每日给药剂量高达2g /kg/天时,雄性和雌性大鼠的生殖能力不受碘沙醇的影响。碘沙醇对大鼠和家兔无致畸作用。此外,当大鼠在哺乳期给药时,没有看到对幼崽的毒性作用。4项标准遗传毒性试验均为阴性。在豚鼠的被动皮肤过敏反应试验和主动全身过敏反应试验中,没有观察到碘沙醇的抗原性。碘沙醇的血管内耐受性高,因此,碘沙醇应被视为血管内使用的安全的x射线造影剂。
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