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7683b auto injector

Manufactured by Agilent Technologies
Sourced in United States

The 7683B auto-injector is a laboratory instrument designed to automate the process of injecting samples into a gas chromatograph. It is capable of performing precise and consistent sample introductions, improving the reliability and reproducibility of analytical results.

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3 protocols using 7683b auto injector

1

Quantification of Limonene in Polymer Films

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The limonene loading content in the films was determined using GC-MS (Agilent-Technologies 6890N network gas chromatographic system combined with Agilent-Technologies 5973 inert XL mass selective detector and Agilent-Technologies 7683B auto-injector, Little Falls, CA, USA). The films were cut into a 50 mm2 area and their weights were recorded. They were then cut into small pieces. Limonene was extracted from the films by soaking them in 5 mL ethanol for 24 h. The extracted solution was diluted to 100 µg/mL (theoretical concentration was calculated by the weight of each film). Each sample was analyzed in triplicate. Limonene content was determined from the standard curve of limonene in absolute ethanol, which was linear with a high correlation coefficient (r2 = 0.9988). The following regression equation was obtained: y = 169867x − 397775, where y is the peak area and x is the concentration of limonene (mg/L). The limonene loading was calculated using the following equation:
Limonene loading content (%)=Aq (g)C (%ww) × W (g) × 100
where Aq is the actual quantity of limonene present in the film (g), C is the concentration of limonene (%w/w), and W is the film weight (g).
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2

Multi-dimensional GC-MS Analysis of Compounds

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The GC×GC instrument used was a Pegasus 4D from Leco Corporation (St. Joseph, USA) equipped with a time-of-flight mass spectrometer. A split/splitless injector and 7683B auto injector (Agilent Technologies, Little Falls, USA) was used on this system. The first dimension column was a 30 m × 0.25 mm ID, 0.25 μm df StabilWax column (Restek, Bellefonte, USA) and in the second dimension a 1.5 m × 0.1 mm ID, 0.1 μm df RTXi-5 column (Restek, Bellefonte, USA) was used. Helium was used as a carrier gas at a constant flow rate of 1.2 mL/min. A split ratio of 200:1 and injection volume of 0.5 μL was used for all analysis. The first oven was programmed from 40 °C (2.0 min) to 255 °C at 2 °C/min. The secondary oven and modulator followed the first temperature program but started at 60 °C and 70 °C, respectively. TOF-MS spectra were collected between 35 and 500 m/z at 100 spectra/s.
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3

Quantification of Short-Chain Fatty Acids in Cecal Content

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Samples of cecal contents preserved in 0.1% trifluoroacetic acid (1:1, vol/vol) and immediately frozen in liquid nitrogen and stored at -80°C were used for the analysis of SCFA. The analysis was performed using an Agilent 7890A gas chromatography system coupled with a flame ionization detector and a 7683B autoinjector (Agilent Technologies, Santa Clara, CA). The SCFA were separated using an SGE BP21 capillary column (30 m × 0.53 mm; film thickness = 0.5; SGE Analytical Science, Melbourne, Australia). Helium was supplied as the carrier gas at flow rate of 5 mL/min. The initial oven temperature was 85°C, raised to 180°C at 6°C/min, and held for 5 min. The temperature of the flame ionization detector and injection port were 290 and 250°C, respectively. Samples (0.5 μL of clear supernatant) were injected in a split mode with a ratio of 10:1. The content of the individual compounds was measured using external standards of acetic, propionic, butyric, valeric, isovaleric, and lactic acid (Sigma-Aldrich, Saint Louis, MO).
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