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Gcms qp2010 plus gas chromatograph mass spectrometer

Manufactured by Shimadzu
Sourced in Japan

The GCMS-QP2010 Plus is a high-performance gas chromatograph/mass spectrometer (GC/MS) system designed for accurate and sensitive analysis of a wide range of samples. It combines a high-speed gas chromatograph with a quadrupole mass spectrometer, enabling efficient separation, detection, and identification of chemical compounds.

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5 protocols using gcms qp2010 plus gas chromatograph mass spectrometer

1

GC-MS Analysis of Seaweed Essential Oil

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GC–MS analysis was performed to determine the chemical composition of SEO. SEO was subjected to GC–MS analyses using a Shimadzu, Tokyo, Japan, GCMS-QP-2010 Plus Gas Chromatograph Mass Spectrometer. The column was kept at 50 °C for 2 min after injection before being programmed at 5 °C/min to 210 °C and then at 10 °C/min to 280 °C. With a split ratio of 1:115, the injection volume was 1.0 l of pure essential oil. The carrier gas was helium, and the flow rate was maintained at 1.0 (mL/min). The temperature of the injector was 260 °C, and the temperature of the ion source was 220 °C. The compounds were recognized by contrasting the retention times and retention indices of the chromatographic peaks with those of authentic reference standards that were subjected to the exact same conditions during the chromatographic analysis. The National Institute of Standards and Technology (NIST) MS spectral database (version 2005) was used to search the mass spectrum database and to compare the MS fragmentation pattern with those of pure compounds.
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2

Erythrocyte Fatty Acid Profiling

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Erythrocytes were separated from the plasma by centrifugation (3000 rpm, 1500 ×g, for 10 min) and washed with an equal volume of saline. These erythrocytes resuspended with saline were stored in a freshly 0.01% butylated hydroxyl toluene- (BHT-) treated Eppendorf vials at −80°C. The fatty acids composition was determined using the method by Lepage and Roy [19 (link)]; erythrocyte's membranes were extracted from aliquots of 200 μL of erythrocyte suspensions and the fatty acids converted to methyl esters by reaction with acetyl chloride for 60 min at 100°C. Methyl ester fatty acids (FAME) were separated and analyzed by gas chromatography performed on a Shimadzu GCMS-QP2010 Plus gas chromatograph/mass spectrometer (Shimadzu, Kyoto, Japan) and peaks were identified through mass spectra and by comparing with respect to a reference FAME mixture (GLC-744 Nu-Chek Prep. Inc., Elysian MN, USA) the elution pattern and relative retention times of FAME. The O3Ix was calculated as erythrocyte (EPA + DHA)/(total fatty acids) × 100% (percentage molar of total fatty acids) [11 (link)].
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3

Comprehensive GCMS Analysis of MOEO Composition

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Gas Chromatography–Mass Spectrometry (GCMS) analysis was performed to determine the composition of MOEO using GCMS-QP-2010 Plus Gas chromatograph Mass Spectrometer, Shimadzu, Japan. Sample size and GCMS conditions such as oven temperature, ramp rate, split ratio, the flow rate of Helium, and temperature of the ion source and injector were used as reported in our previous study [31 (link)]. The analysis was performed by similarity searches in the National Institute of Standards and Technology (NIST) mass spectra database with the obtained pure mass spectrum of each component.
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4

GCMS Analysis of Spearmint Essential Oil

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Gas Chromatography Mass Spectrometry (GCMS) analysis of spearmint essential oil (SEO) was performed using a GCMS-QP-2010 Plus Gas chromatograph Mass Spectrometer (Shimadzu, Japan). After injecting the sample, the oven was maintained at a temperature of 50 °C (2 min) and later programmed to 210 °C (ramp rate: 3 °C/min). Further increase in temperature (280 °C) was achieved by increasing the ramp to 6 °C/min. 1 µL of the sample (SEO) was injected (split ratio = 1:115). Helium was utilized at a consistent flow rate (1.0 mL/min) as the carrier gas. The temperatures of the ion source and injector were set at 220 and 260 °C, respectively. The compounds were identified by comparing the retention indices and retention times (RT) of the chromatographic peaks with the reference standards run under identical conditions. Peak enrichment was also performed on co-injection with authentic reference compounds. The comparison of the MS fragmentation pattern with those of pure compounds and mass spectrum database search was performed using the National Institute of Standards and Technology (NIST) MS spectral database (version 2005).
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5

Fatty Acid Profiling in Erythrocyte Membranes

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Analysis of the fatty acid profile in the erythrocyte membrane was analyzed as follows: 10-mL blood samples were taken from the antecubital vein 10 min before the physical tests in tubes with tripotassium EDTA (ethylenediamine tetraacetic acid) washed with isotonic saline and purged with nitrogen gas and centrifuged at 2000 rpm for 30 min at 4 °C. The supernatant was collected and frozen at −80 °C and the cell phase (erythrocytes) was frozen at −80 °C for fatty acid analysis. Erythrocyte lipids were determined as methyl esters after methylation reaction, using the method of Lepage and Roy [31 (link)]. GC analysis was performed on a Shimadzu GCMS-QP2010 Plus gas chromatograph/mass spectrometer (Shimadzu, Kyoto, Japan). Fatty acid methyl esters (FAMEs) were identified through mass spectrometry and through comparison of the elution pattern and relative retention times of FAMEs with the reference FAME mixture (GLC-744 Nu-Chek Prep. Inc., Elysian, MN, USA). The results were expressed in relative amounts (percentage molar of total fatty acids) [32 (link)]. The fatty acid methyl esters are analyzed by capillary gas chromatography with an ionized flame detector [33 (link)].
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