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Fluconazole-d4 Sale

(Synonyms: 四氘代氟康唑,UK-49858-d4) 目录号 : GC47358

An internal standard for the quantification of fluconazole

Fluconazole-d4 Chemical Structure

Cas No.:1124197-58-5

规格 价格 库存 购买数量
500 μg
¥1,284.00
现货
1 mg
¥2,449.00
现货
5 mg
¥10,930.00
现货

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Sample solution is provided at 25 µL, 10mM.

产品文档

Quality Control & SDS

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产品描述

Fluconazole-d4 is intended for use as an internal standard for the quantification of fluconazole by GC- or LC-MS. Fluconazole is a triazole antifungal agent that is effective against most Candida strains.1 In vivo, fluconazole at 0.5-100 mg/kg demonstrates protective activity in various experimental animal models of systemic fungal diseases including aspergillosis, blastomycosis, candidiasis, coccidioidomycosis, cryptococcosis, and histoplasmosis.2

1.Herbrecht, R., Nivoix, Y., Fohrer, C., et al.Management of systemic fungal infections: Alternatives to itraconazoleJ. Antimicrob. Chemother.56(Suppl 1)i39-i48(2005) 2.Saag, M.S., and Dismukes, W.E.Azole antifungal agents: Emphasis on new triazolesAntimicrobial Agents and Chemotherapy32(1)1-8(1988)

Chemical Properties

Cas No. 1124197-58-5 SDF
别名 四氘代氟康唑,UK-49858-d4
Canonical SMILES FC1=CC(F)=C(C(C([2H])([2H])N2C=NC=N2)(O)C([2H])([2H])N3C=NC=N3)C=C1
分子式 C13H8D4F2N6O 分子量 310.3
溶解度 DMSO: Soluble,Ethanol: Soluble 储存条件 Store at -20°C
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储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
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溶解性数据

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1 mg 5 mg 10 mg
1 mM 3.2227 mL 16.1134 mL 32.2269 mL
5 mM 0.6445 mL 3.2227 mL 6.4454 mL
10 mM 0.3223 mL 1.6113 mL 3.2227 mL
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Research Update

A sensitive method for analyzing fluconazole in extremely small volumes of neonatal serum

J Pharm Health Care Sci 2020 Jul 1;6:14.PMID:32626595DOI:PMC7329421

Background: The need for a large volume of serum sample significantly reduces the feasibility of neonatal pharmacokinetic studies in daily practice, which must often rely on scavenged or opportunistic sampling. This problem is most apparent in preterm newborns, where ethical and practical considerations prohibit the collection of large sample volumes. Most of the fluconazole analysis assays published thus far required a minimum serum sample of 50 to 100 μL for a single assay. The purpose of the present study was to develop and validate a sensitive method requiring a smaller sample volume (10 μL) to satisfy clinically relevant research requirements. Methods: Following simple protein precipitation and centrifugation, the filtrated supernatant was injected into a liquid chromatography system and separated with a C18 reverse-phase column. Fluconazole and the internal standard (IS, Fluconazole-d4) were detected and quantified using tandem mass spectrometry. The method was validated with reference to the Food and Drug Administration's Guidance for Industry. Accuracy and precision were evaluated at six quality control concentration levels (ranging from 0.01 to 100 μg/mL). Results: Investigated calibration curves were linear in the 0.01-100 μg/mL range. Intra- and inter-day accuracy (- 7.7 to 7.4%) and precision (0.3 to 6.0%) were below 15%. The calculated limit of detection and the lower limit of quantification (LLOQ) was 0.0019 μg/mL and 0.0031 μg/mL, respectively. Fluconazole in the prepared samples was stable for at least 4 months at - 20 °C and - 80 °C. This method was applied to analyze 234 serum samples from ten neonates who received fosfluconazole, a water-soluble phosphate prodrug of fluconazole which converts to fluconazole in the body, as part of a pharmacokinetic study using daily scavenged laboratory samples. The median (range) concentration up to 72 h after fosfluconazole administration was 2.9 (0.02 to 26.8 μg/mL) μg/mL, which was within the range of the calibration curve. Conclusion: Fluconazole was able to be detected in an extremely small volume (10 μL) of serum from neonates receiving fosfluconazole. The method presented here can be used to quantify fluconazole concentrations for pharmacokinetic studies of the neonatal population by using scavenged samples.