Transformation of bisphosphonates into insoluble material in human blood in vitro

被引:4
作者
Kautiainen, S
Luurila, S
Ylitalo, P
Ylitalo, R
机构
[1] Univ Tampere, Dept Pharmacol Sci, FIN-33101 Tampere, Finland
[2] Finn Medi Clin Trial Ctr, Tampere, Finland
来源
METHODS AND FINDINGS IN EXPERIMENTAL AND CLINICAL PHARMACOLOGY | 1998年 / 20卷 / 04期
关键词
bisphosphonates; protein binding; drug transformation;
D O I
10.1358/mf.1998.20.4.485682
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of the study was to Sind out whether bisphosphonates transform into insoluble material in human blood and serum in vitro. Samples of fresh blood and serum were incubated with various concentrations of C-14-labelled clodronate, etidronate, pamidronate and tiludronate for 2 h and 8 h at 37 degrees C. The presence of unfiltrable material in the plasma separated from the blood, and in the serum were studied with 1) 100, 300 and 1,000 kd (kilo Daltons) filter tubes centrifuged at 3,000 g for 60 min, and 2) high-speed centrifugation at 13,000 g for 30 min. The radioactivities in the ultrafiltrates and supernatants were compared to those in the native plasma or serum. All bisphosphonates transformed into unfiltrable material, which was separated from the samples with the 100 and 300 kd filters but not with the 1,000 kd filter. The material was not sedimented with the high-speed centrifugation. The lengthening of the incubation time from 2 h to 8 h increased the unfiltrable fraction, which generally was dependent an the drug concentration in the blood, too. However; the fraction of the unfiltrable material did not seem to increase with time when the drug was incubated with serum instead of blood. Since drug binding to plasma proteins is generally a very rapid process, some factors other than proteins only, e.g. cations or cation residues, present in the blood but not in the serum, should be involved iii transforming of bisphosphonates bisphosphonates into insoluble material in the blood. (C) 1998 Prous Science. All rights reserved.
引用
收藏
页码:289 / 295
页数:7
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