Kerchner J, Colaluca D M, Juhl R P
Am J Hosp Pharm. 1980 Oct;37(10):1323-5.
Insulin availability following the addition of whole blood to insulin infusions was evaluated. Solutions of 0.45% sodium chloride containing insulin (50) units/liter) and tracer amounts of 125I-labeled insulin were prepared and added to plastic or glass intravenous containers. Blood (5 ml) was added to the containers at the same time as the insulin or one hour after insulin. The cumulative amount of insulin delivered from these solutions over six hours was compared with that of insulin solutions containing no blood. When no blood was added to the insulin infusions, cumulative insulin delivery after two hours was 68% from the plastic containers and 76% from the glass bottles. The corresponding values for blood added simultaneously with insulin or one hour after insulin, ranged between 93% and 98%. The addition of whole blood to these low-dose insulin intravenous infusions was found to be effective in minimizing insulin adsorption onto the components of the infusion system. The method described does not expose the patient to the risks associated with receiving exogenous human serum albumin and also involves less expense.
评估了向胰岛素输注液中添加全血后胰岛素的可得性。制备了含胰岛素(50单位/升)和微量125I标记胰岛素的0.45%氯化钠溶液,并添加到塑料或玻璃静脉输液容器中。在加入胰岛素的同时或加入胰岛素一小时后,向容器中加入5毫升血液。将这些溶液在六小时内输送的胰岛素累积量与不含血液的胰岛素溶液的累积量进行比较。当未向胰岛素输注液中添加血液时,两小时后塑料容器中胰岛素的累积输送量为68%,玻璃瓶中为76%。与胰岛素同时添加或在胰岛素添加一小时后添加血液的相应值在93%至98%之间。发现向这些低剂量胰岛素静脉输注液中添加全血可有效减少胰岛素在输液系统组件上的吸附。所述方法不会使患者面临接受外源性人血清白蛋白相关的风险,且成本较低。