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MB Sample ID: SA079877

Local Sample ID:FFS108B
Subject ID:SU001216
Subject Type:Human
Subject Species:Homo sapiens
Taxonomy ID:9606
Age Or Age Range:19 - 26 yr
Weight Or Weight Range:50.6 - 94.1 kg
Height Or Height Range:1.6 - 1.85 m
Gender:Male and female
Human Smoking Status:Non-smoker
Human Exclusion Criteria:Subjects with anemia, diabetes, thyroid disease, MetS, cancer, previous cardiovascular events or other disease diagnoses were excluded. Subjects were also excluded if they had extreme dietary or exercise patterns, or were taking prescription medications or other supplements known to alter lipoprotein metabolism such as isoflavones.

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Subject:

Subject ID:SU001216
Subject Type:Human
Subject Species:Homo sapiens
Taxonomy ID:9606
Age Or Age Range:19 - 26 yr
Weight Or Weight Range:50.6 - 94.1 kg
Height Or Height Range:1.6 - 1.85 m
Gender:Male and female
Human Smoking Status:Non-smoker
Human Exclusion Criteria:Subjects with anemia, diabetes, thyroid disease, MetS, cancer, previous cardiovascular events or other disease diagnoses were excluded. Subjects were also excluded if they had extreme dietary or exercise patterns, or were taking prescription medications or other supplements known to alter lipoprotein metabolism such as isoflavones.

Factors:

Local Sample IDMB Sample IDFactor Level IDLevel ValueFactor Name
FFS108BSA079877FL012242FFTreatment
FFS108BSA079877FL012242PostTimepoint

Collection:

Collection ID:CO001210
Collection Summary:HDL fractions were isolated from plasma using a 2-step sequential density-based ultracentrifugation method
Sample Type:Blood (plasma)
Storage Conditions:-80℃

Treatment:

Treatment ID:TR001231
Treatment Summary:Each subject was given either a fast food or a Mediterranean for 4 days in randomized order.

Sample Preparation:

Sampleprep ID:SP001224
Sampleprep Summary:Lipids were extracted using methanol-MTBE method.
Sampleprep Protocol Filename:zivkovic_protocol.pdf

Combined analysis:

Analysis ID AN001899
Analysis type MS
Chromatography type Reversed phase
Chromatography system Waters Acquity
Column Waters Acquity CSH C18 (100 x 2.1mm,1.7um)
MS Type ESI
MS instrument type QTOF
MS instrument name Agilent 6550 QTOF
Ion Mode NEGATIVE
Units ug/ml

Chromatography:

Chromatography ID:CH001375
Methods Filename:zivkovic_protocol.pdf
Instrument Name:Waters Acquity
Column Name:Waters Acquity CSH C18 (100 x 2.1mm,1.7um)
Column Temperature:65°C
Flow Gradient:0 min 15% (B), 0–2 min 30% (B), 2–2.5 min 48% (B), 2.5–11 min 82% (B), 11–11.5 min 99% (B), 11.5–12 min 99% (B), 12–12.1 min 15% (B), 12.1–15 min 15% (B)
Flow Rate:0.6 mL/min
Injection Temperature:4°C
Solvent A:40% water/60% acetonitrile; 0.1% formic acid; 10 mM ammonium formate
Solvent B:90% isopropanol/10% acetonitrile; 0.1% formic acid; 10 mM ammonium formate
Chromatography Type:Reversed phase

MS:

MS ID:MS001755
Analysis ID:AN001899
Instrument Name:Agilent 6550 QTOF
Instrument Type:QTOF
MS Type:ESI
MS Comments:Data are analyzed in a four-stage process. First, raw data are processed in an untargeted (qualitative) manner by Agilent’s software MassHunter Qual to find peaks in up to 300 chromatograms. Peak features are then imported into MassProfilerProfessional for peak alignments to seek which peaks are present in multiple chromatograms, using exclusion criteria by the minimum percentage of chromatograms in which these peaks are positively detected. We usually use 30% as minimum criterion. In a tedious manual process, these peaks are then collated and constrained into a MassHunter quantification method on the accurate mass precursor ion level, using the MS/MS information and the LipidBlast library to identify lipids with manual confirmation of adduct ions and spectral scoring accuracy. MassHunter enables back-filling of quantifications for peaks that were missed in the primary peak finding process, hence yielding data sets without missing values.
Ion Mode:NEGATIVE
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