FATTY ACID ASSAY OF TWO SAMPLES BY HPLC WITH FLUORESCENCE DETECTION
FATTY ACID ASSAY OF TWO SAMPLES BY HPLC WITH FLUORESCENCE DETECTION
批准号:
7957551
负责人:
Parastoo Azadi
金额:
$0.22万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-02-01 至 2010-01-31
关键词:
AcetonitrilesAcidsAliquotBiological AssayChloroformComputer Retrieval of Information on Scientific Projects DatabaseDetectionEnoxaparin sodiumFatty AcidsFluorescenceFundingGrantHexanesHigh Pressure Liquid ChromatographyInjection of therapeutic agentInstitutionLipidsMethanolNitrogenParticle SizeProdigyResearchResearch PersonnelResourcesSamplingScanningSolutionsSourceStreamSystemTemperatureUnited States National Institutes of HealthWaterdetectorethyl acetatewater sampling
中文摘要
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英文摘要
This subproject is one of many research subprojects utilizing the
resources provided by a Center grant funded by NIH/NCRR. The subproject and
investigator (PI) may have received primary funding from another NIH source,
and thus could be represented in other CRISP entries. The institution listed is
for the Center, which is not necessarily the institution for the investigator.
Lipid Extraction
The Enoxaparin sodium solution (150 mg/mL) was divided into three 500-uL portions. Two of the portions were spiked with nonadecanoic acid (1 and 10 uL, respectively, of a 0.1 mg/mL solution). Three water samples were treated in exactly the same way.
1.85 mL chloroform-methanol (1:2) was added to each aliquot, and the mixtures were vortexed for 15 min. Then, 0.62 mL chloroform was added, and, after vortexing for another 5 min, 0.62 mL water. The mixtures were vortexed again for 5 min and centrifuged for 5 min. The organic layers of each sample were separated and dried down under a stream of nitrogen.
Lipid Saponification and Derivatization with 1-Pyrenyldiazomethane (PDAM)
Each sample was treated with 500 uL 1 M KOH in 50 % methanol for 30 min at 95 ¿C. After cooling, the samples were acidified with 2 M HCl and extracted with 1 mL chloroform-hexane (1:1). After vortexing 5 min, the organic layers were separated and dried down with a stream of nitrogen.
The samples were dissolved in 100 uL methanol and treated with 100 uL 1mg/mL PDAM in ethyl acetate for 90 min at room temperature.
HPLC with Fluorescence Detection
HPLC was carried out on an Agilent system using a 4.6x250 mm Phenomenex Prodigy C18 analytical column with 5um particle size.
Analytes were eluted by a linear gradient between water (A) and acetonitrile (B), starting at 90 % B (flow rate 1.0 mL/min), increasing to 100 % B (1.2 mL/min) over 40 min, then isocratic at 100 % B (1.2 mL/min) for 50 min.
Analytes were detected by a Waters 470 Scanning Fluorescence Detector (ex. 340 nm; em 395 nm). The injection volume was 5 uL.
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