De Muynck C, De Vroe C, Remon J P, Colardyn F
Laboratory of Pharmaceutical Technology, State University of Gent, Belgium.
J Clin Pharm Ther. 1988 Oct;13(5):335-40. doi: 10.1111/j.1365-2710.1988.tb00202.x.
The binding of diazepam, digoxin, dopamine and fentanyl to different 0.2 microns end-line filters was investigated under simulated infusion conditions. All the drugs were diluted in either 5% dextrose or 0.9% NaCl infusion fluid. For digoxin and diazepam a marked reduction in the amount of drug delivered to the patient in the first 20-60 min of infusion is observed. For dopamine, the drug loss was less pronounced and no fentanyl was absorbed to the filters during the infusion experiment.
在模拟输注条件下,研究了地西泮、地高辛、多巴胺和芬太尼与不同的0.2微米终端滤器的结合情况。所有药物均在5%葡萄糖或0.9%氯化钠输注液中稀释。对于地高辛和地西泮,在输注的最初20 - 60分钟内观察到输送给患者的药量显著减少。对于多巴胺,药物损失不太明显,且在输注实验过程中没有芬太尼被滤器吸附。