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Comparative pharmacokinetics and insulin action for three rapid-acting insulin analogs injected subcutaneously with and without hyaluronidase

机译:皮下注射透明质酸酶和不注射透明质酸酶的三种速效胰岛素类似物的比较药代动力学和胰岛素作用

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OBJECTIVE-To compare the pharmacokinetics and glucodynamics of three rapid-acting insulin analogs (aspart, glulisine, and lispro) injected subcutaneously with or without recombinant human hyaluronidase (rHuPH20). RESEARCH DESIGN AND METHODS-This double-blind six-way crossover euglycemic glucose clamp study was conducted in 14 healthy volunteers. Each analog was injected subcu-taneously (0.15 units/kg) with or without rHuPH20. RESULTS-The commercial formulations had comparable insulin time-exposure and time-action profiles as follows: 50% exposure at 123-131 min and 50% total glucose infused at 183- 186 min. With rHuPH20, the analogs had faster yet still comparable profiles: 50% exposure at 71-79 min and 50% glucose infused at 127-140 min. The accelerated absorption with rHuPH20 led to twice the exposure in the first hour and half the exposure beyond 2 h, which resulted in 13-to 25-min faster onset and 40- to 49-min shorter mean duration of insulin action. CONCLUSIONS- Coinjection of rHuPH20 with rapid-acting analogs accelerated insulin exposure, producing an ultra-rapid time-action profile with a faster onset and shorter duration of insulin action.
机译:目的-比较皮下注射或不注射重组人透明质酸酶(rHuPH20)的三种速效胰岛素类似物(天冬氨酸,谷氨酸和赖脯胰岛素)的药代动力学和糖动力学。研究设计和方法-该双盲六向交叉正常血糖葡萄糖钳夹研究在14位健康志愿者中进行。每种仿制药物分别注射(0.15单位/千克)有或没有rHuPH20。结果-该商业制剂具有可比较的胰岛素时间暴露和时间作用曲线,如下:在123-131分钟时50%暴露,在183-186分钟时50%总葡萄糖注入。使用rHuPH20,这些类似物具有更快但仍可比较的特性:71-79分钟时暴露50%,而127-140分钟时注入50%葡萄糖。 rHuPH20的加速吸收在头一个小时内暴露两次,而在2小时后暴露一半,导致胰岛素作用的起效时间缩短13至25分钟,平均作用时间缩短40至49分钟。结论:rHuPH20与速效类似物的共同注射可加速胰岛素的暴露,产生超快的时间作用谱,起效更快,作用时间更短。

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