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药物吸附对氯美噻唑和利多卡因药代动力学研究的影响。

The influence of drug sorption on pharmacokinetic studies of chlormethiazole and lignocaine.

作者信息

Upton R N, Mather L E, Runciman W B

出版信息

J Pharm Pharmacol. 1987 Jun;39(6):485-7. doi: 10.1111/j.2042-7158.1987.tb03427.x.

Abstract

The influence of drug sorption on the measurement of dose and blood concentrations during pharmacokinetic studies of chlormethiazole and lignocaine in a chronically catheterized sheep preparation has been examined. There was no sorption to soda glass tubes, borosilicate glass volumetric flasks or soda glass microlitre syringes but minor sorption to polypropylene syringes, polypropylene pipette tips and rubber bottle stoppers after 240 min contact. During infusions through administration sets including either polyvinyl chloride or polyethylene catheters, no significant loss of lignocaine occurred, but only 41.7-63.9% of the chlormethiazole dose was delivered. No significant decreases in either drug occurred from blood sampled through an intravascular catheter and stopcock system. There was negligible degradation of the samples over 4 h. Sorption of chlormethiazole or lignocaine to the laboratory equipment used was not a significant source of error but polyvinyl chloride infusion catheters could result in significant reductions in chlormethiazole dose.

摘要

研究了在长期插管绵羊制剂中进行氯美噻唑和利多卡因药代动力学研究时,药物吸附对剂量测量和血药浓度的影响。苏打玻璃管、硼硅酸盐玻璃容量瓶或苏打玻璃微升注射器未出现吸附现象,但接触240分钟后,聚丙烯注射器、聚丙烯移液器吸头和橡胶瓶塞有轻微吸附。在通过包括聚氯乙烯或聚乙烯导管的给药装置进行输注期间,利多卡因未出现显著损失,但氯美噻唑剂量仅输送了41.7%-63.9%。通过血管内导管和旋塞系统采集的血样中,两种药物均未出现显著减少。4小时内样品降解可忽略不计。氯美噻唑或利多卡因对所用实验室设备的吸附不是误差的重要来源,但聚氯乙烯输注导管可能导致氯美噻唑剂量显著降低。

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