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[强心苷及其代谢产物——组织提取物中的回收问题。纳克范围内可见物质斑点的分离(作者译)]

[Cardiac glycosides and metabolites--problems of recovery in tissue extracts. Separation of visible substance spots in the nanogram range (author's transl)].

作者信息

Aderjan R, Doster S, Petri H, Schmidt G

出版信息

Z Rechtsmed. 1979 Aug;83(3):201-7. doi: 10.1007/BF02333322.

DOI:10.1007/BF02333322
PMID:494819
Abstract

The recovery measurements in rat tissues performed via i.p. injected radioactive digoxin derivates (3H-digoxin, 125J-digoxin derivative) showed that approximately 50% of the total glycoside content will be extracted. Thus, an addition of digoxin standards to drug-free tissues may lead to false negative determinations. By comparison of the radioactivity before and after extraction the following results were obtained: Recovery from tissues 3H-digoxin 50% 125J-digoxin 40% from serum 3H-digoxin 60% added to drug free tissue homogenates 3H-digoxin 85% After i.p. application of 15 mg/kg of beta-methyldigoxin to BD9 (Berlin)-rats the resulting tissue concentrations were extracted by Amberlite XAD-2. beta-Methyldigoxin and its metabolites digoxin and digoxinbisdigitoxide could be separated and distinguished from artifacts by fluorescence detection on HPTLC-plates with a detection limit of 60 ng/spot. Concentration determined by radioimmunoassay are in satisfactory agreement with HPTLC results.

摘要

通过腹腔注射放射性地高辛衍生物(3H-地高辛、125I-地高辛衍生物)对大鼠组织进行的回收率测量表明,约50%的总糖苷含量会被提取出来。因此,向无药物组织中添加地高辛标准品可能会导致假阴性测定。通过比较提取前后的放射性,得到以下结果:组织中3H-地高辛的回收率为50%,125I-地高辛为40%;血清中3H-地高辛的回收率为60%;添加到无药物组织匀浆中的3H-地高辛回收率为85%。对BD9(柏林)大鼠腹腔注射15mg/kg的β-甲基地高辛后,用Amberlite XAD-2提取所得的组织浓度。β-甲基地高辛及其代谢产物地高辛和地高辛双洋地黄毒苷可通过在高效薄层层析板上进行荧光检测与假象分离并区分,检测限为60ng/斑点。放射免疫测定法测定的浓度与高效薄层层析结果吻合良好。

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1
[Cardiac glycosides and metabolites--problems of recovery in tissue extracts. Separation of visible substance spots in the nanogram range (author's transl)].[强心苷及其代谢产物——组织提取物中的回收问题。纳克范围内可见物质斑点的分离(作者译)]
Z Rechtsmed. 1979 Aug;83(3):201-7. doi: 10.1007/BF02333322.
2
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Klin Wochenschr. 1978 May 15;56(10):497-502. doi: 10.1007/BF01492862.
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Concentration of digoxin, methyldigoxin, digitoxin and ouabain in the myocardium of the dog following coronary occulsion.冠状动脉闭塞后犬心肌中地高辛、甲基地高辛、洋地黄毒苷和哇巴因的浓度。
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Identification and estimation of endogenous digoxin in biological fluids and tissues by TLC and HPLC.通过薄层色谱法(TLC)和高效液相色谱法(HPLC)对生物体液和组织中的内源性地高辛进行鉴定和测定。
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引用本文的文献

1
Interactions of amiodarone with digoxin in rats.胺碘酮与地高辛在大鼠体内的相互作用。
Br J Pharmacol. 1987 Nov;92(3):553-9. doi: 10.1111/j.1476-5381.1987.tb11356.x.

本文引用的文献

1
A fluorometric determination of myocardial digoxin at autopsy, with identification of digitalis leaf, digitoxin, and gitoxin.尸检时心肌地高辛的荧光测定法,同时鉴定洋地黄叶、洋地黄毒苷和吉他洛苷。
Am J Clin Pathol. 1969 Mar;51(3):347-57. doi: 10.1093/ajcp/51.3.347.
2
Determination of therapeutic and toxic serum digoxin concentrations by radioimmunoassay.采用放射免疫分析法测定治疗性和中毒性血清地高辛浓度。
N Engl J Med. 1969 Nov 27;281(22):1212-6. doi: 10.1056/NEJM196911272812203.
3
Interpretation of post mortem serum levels of cardiac glycosides after suspected overdosage.
疑似用药过量后尸检血清强心苷水平的解读
Acta Pharmacol Toxicol (Copenh). 1974 Nov;35(5):386-94. doi: 10.1111/j.1600-0773.1974.tb00759.x.
4
Tissue concentrations of digoxin in an autopsy material.尸检材料中地高辛的组织浓度。
Acta Pharmacol Toxicol (Copenh). 1974 May;34(5):385-90. doi: 10.1111/j.1600-0773.1974.tb03534.x.
5
A radioimmunoassay for digoxin in serum, urine and myocardial tissue.血清、尿液及心肌组织中地高辛的放射免疫测定法。
Acta Pharmacol Toxicol (Copenh). 1974 Mar;34(3):198-204. doi: 10.1111/j.1600-0773.1974.tb03498.x.
6
[Determination of glycoside concentrations in human tissue by means of radioimmunoassay (author's transl)].用放射免疫测定法测定人体组织中的糖苷浓度(作者译)
Klin Wochenschr. 1977 Jan 1;55(1):23-30. doi: 10.1007/BF01469780.
7
[Suicide with beta-methyldigoxin (author's transl)].β-甲基地高辛自杀(作者译)
Dtsch Med Wochenschr. 1978 Nov 17;103(46):1841-4. doi: 10.1055/s-0028-1129354.
8
Investigation of cardiac glycoside levels in human post mortem blood and tissues determined by a special radioimmunoassay procedure.通过一种特殊的放射免疫分析程序对人死后血液和组织中的强心苷水平进行调查。
Arch Toxicol. 1979 Jun 8;42(2):107-14. doi: 10.1007/BF00316490.