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Digoxin-d3 Sale

(Synonyms: 12β-Hydroxydigitoxin-d3) 目录号 : GC47223

An internal standard for the quantification of digoxin

Digoxin-d3 Chemical Structure

Cas No.:127299-95-0

规格 价格 库存 购买数量
500 μg
¥994.00
现货
1 mg
¥1,781.00
现货
5 mg
¥7,950.00
现货

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Sample solution is provided at 25 µL, 10mM.

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产品描述

Digoxin-d3 is intended for use as an internal standard for the quantification of digoxin by GC- or LC-MS. Digoxin is a cardiac glycoside and metabolite of digitoxin that binds to and inhibits the Na+/K+-ATPase in cardiac tissues in an ATP- and Mg2+-dependent manner.1 This inhibition results in loss of the transmembrane Na+ gradient, which decreases activity of the Na+/Ca2+ exchanger, increasing intracellular Ca2+ levels, inotropy, and cardiac force.2 It increases activity of mitochondrial ATPase and actomyosin ATPase in rat hearts, which is directly correlated with increased myofibrillar contractile strength.3 In vivo, digoxin also decreases right atrial pressure and increases cardiac output in a canine model of congestive heart failure produced by pulmonary artery constriction.4 Formulations containing digoxin have been used to treat atrial fibrillation.5

1.Matsui, H., and Schwartz, A.Mechanism of cardiac glycoside inhibition of the (Na+-K+)-dependent ATPase from cardiac tissueBiochim. Biophys. Acta.151(3)655-663(1968) 2.Neves, C.H., Tibana, R.A., Prestes, J., et al.Digoxin induces cardiac hypertrophy without negative effects on cardiac function and physical performance in trained normotensive ratsInt. J. Sports Med.38(4)263-269(2017) 3.Hamrick, M.E., and Fritz, P.J.Enzymatic adaptation: Molecular basis for cardiac glycoside action• 1. Increase in rat heart actomyosin and mitochondrial ATPase specific activities following digoxin injectionBiochem. Biophys. Res. Commun.22(5)540-546(1966) 4.Davis, J.O., Howell, D.S., and Hyatt, R.E.Effects of acute and chronic digoxin administration in dogs with right-sided congestive heart failure produced by pulmonary artery constrictionCirc. Res.3(3)259-263(1955) 5.Kotecha, D., Calvert, M., Deeks, J.J., et al.A review of rate control in atrial fibrillation, and the rationale and protocol for the RATE-AF trialBMJ Open7(7)e015099(2017)

Chemical Properties

Cas No. 127299-95-0 SDF
别名 12β-Hydroxydigitoxin-d3
Canonical SMILES C[C@@]12[C@@](CC[C@]3([H])[C@]2([H])C[C@@H](O)[C@@]4(C)[C@]3(O)CC[C@@H]4C(C([2H])([2H])O5)=C([2H])C5=O)([H])C[C@@H](O[C@]6([H])O[C@H](C)[C@@H](O[C@@]7([H])C[C@H](O)[C@H](O[C@]8([H])O[C@H](C)[C@@H](O)[C@@H](O)C8)[C@@H](C)O7)[C@@H](O)C6)CC1
分子式 C41H61D3O14 分子量 784
溶解度 DMSO: Soluble,Methanol: Heated 储存条件 Store at -20°C
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1 mg 5 mg 10 mg
1 mM 1.2755 mL 6.3776 mL 12.7551 mL
5 mM 0.2551 mL 1.2755 mL 2.551 mL
10 mM 0.1276 mL 0.6378 mL 1.2755 mL
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Research Update

Therapeutic monitoring of serum digoxin for patients with heart failure using a rapid LC-MS/MS method

Clin Biochem 2010 Feb;43(3):307-13.PMID:19833118DOI:10.1016/j.clinbiochem.2009.09.025.

Objective: Here we develop a liquid chromatography tandem mass spectrometry (LC-MS/MS) method for the determination of digoxin in serum. Design and methods: The serum samples were extracted with methyl tert-butyl ether using an isotope-labeled Digoxin-d3 as internal standard. The analyte was separated on a reverse phase Capcell C18 column and detected in positive electrospray ionization multiple reaction monitoring mass spectrometry. Results: The chromatographic analysis was carried out within 3 min, but the complete analysis took longer because of the liquid-liquid extraction. The lower limit of quantification was 0.1 ng/mL for digoxin. The intra- and inter-batch precisions were less than 12%, and the bias ranged from -9.1% to 10.7%. The external quality assessment (EQA) results obtained with the LC-MS/MS method were comparable to target values. Subsequently, this method has been applied to the therapeutic monitoring of digoxin in a clinical setting. Conclusion: In this study, we have developed a rapid and reliable LC-MS/MS method for the therapeutic monitoring of digoxin in human serum.

Method validation of a survey of thevetia cardiac glycosides in serum samples

Forensic Sci Int 2012 Feb 10;215(1-3):146-51.PMID:21376490DOI:10.1016/j.forsciint.2011.02.013.

A sensitive and specific liquid chromatography tandem mass spectrometry (HPLC-ESI(+)-MS/MS) procedure was developed and validated for the identification and quantification of thevetin B and further cardiac glycosides in human serum. The seeds of Yellow Oleander (Thevetia peruviana) contain cardiac glycosides that can cause serious intoxication. A mixture of six thevetia glycosides was extracted from these seeds and characterized. Thevetin B, isolated and efficiently purified from that mixture, is the main component and can be used as evidence. Solid phase extraction (SPE) proved to be an effective sample preparation method. Digoxin-d3 was used as the internal standard. Although ion suppression occurs, the limit of detection (LOD) is 0.27 ng/ml serum for thevetin B. Recovery is higher than 94%, and accuracy and precision were proficient. Method refinement was carried out with regard to developing a general screening method for cardiac glycosides. The assay is linear over the range of 0.5-8 ng/ml serum. Finally, the method was applied to a case of thevetia seed ingestion.