Wada D R, Drover D R, Lemmens H J
Department of Anesthesia, Stanford University School of Medicine, California, USA.
Clin Pharmacokinet. 1998 Jul;35(1):1-7. doi: 10.2165/00003088-199835010-00001.
An intravenous loading dose is given to rapidly achieve a desired drug concentration in the blood. A loading dose calculated with the volume of distribution (Vd) at steady state will result in high peak concentrations and possibly serious adverse effects. A loading dose based on the central compartment Vd (Vc) followed by a maintenance infusion may also miss the target drug concentration and cause serious adverse effects. The Vd can be viewed as a time-dependent variable that expands from the Vc immediately after injection, to eventually include the steady-state Vd. If the loading dose is calculated from a Vd determined after the time of peak effect (tmax), then the actual concentration will exceed the target concentration at the tmax. If a loading dose is calculated from a Vd before the peak effect occurs, the actual concentration will be insufficient to achieve the target concentration at tmax. A loading dose based on the Vd at the tmax will accurately achieve the concentration at the tmax without unexpected adverse effects. To determine the Vd at peak effect, it is necessary that an effect can be measured, the peak effect can be detected and the plasma concentrations are sampled frequently enough to quantify the plasma concentrations at the tmax. For drugs that attain an ultra-fast effect (1 to 2 minutes), arterial samples need to be measured. If the onset of effect is intermediate or slow, venous blood can be sampled as the arterial and venous concentrations may be similar at the tmax.
静脉注射负荷剂量是为了迅速在血液中达到所需的药物浓度。用稳态分布容积(Vd)计算的负荷剂量会导致高血药峰浓度,并可能产生严重的不良反应。基于中央室分布容积(Vc)给予负荷剂量后再进行维持输注,也可能达不到目标药物浓度并导致严重不良反应。分布容积可视为一个随时间变化的变量,在注射后立即从中央室分布容积(Vc)开始扩展,最终达到稳态分布容积。如果负荷剂量是根据效应峰值(tmax)出现后的分布容积计算得出的,那么在tmax时实际浓度将超过目标浓度。如果负荷剂量是根据效应峰值出现前的分布容积计算得出的,那么在tmax时实际浓度将不足以达到目标浓度。基于tmax时分布容积计算的负荷剂量将准确地在tmax时达到所需浓度,且不会产生意外的不良反应。为了确定效应峰值时的分布容积,必须能够测量效应、检测到效应峰值,并且血浆浓度采样频率要足够高,以便在tmax时对血浆浓度进行定量。对于起效极快(1至2分钟)的药物,需要测量动脉血样本。如果效应起效时间中等或较慢,静脉血可以作为采样对象,因为在tmax时动脉血和静脉血浓度可能相似。