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Shim pack gist hp c18 column

Manufactured by Shimadzu
Sourced in Japan

The Shim-pack GIST-HP C18 column is a high-performance liquid chromatography (HPLC) column designed for the separation and analysis of a wide range of organic compounds. It features a bonded C18 stationary phase, which provides efficient and reproducible chromatographic separations. The column is suitable for various applications, including pharmaceutical, environmental, and food analysis, where the need for reliable and accurate separation of analytes is essential.

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4 protocols using shim pack gist hp c18 column

1

Evaluating QAMS Method Robustness

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For further investigation on the robustness of QAMS method, the mixed standard solution should be analyzed under different condition. The RCFs and RTT of the other target peaks to IRS were calculated in different flow rates, column temperatures, and columns using the AVG method and assessed by relative standard deviation (RSD, less than 5%) [39 (link)]. The flow rate was set at 0.3/0.4/0.5 mL/min with temperature maintained at 30/35/40°C, respectively. Waters ACQUITY UPLC® BEH C18 column (2.1 × 50 mm, 1.7 μm), Waters ACQUITY UPLC® BEH C18 column (2.1 × 100 mm, 1.7 μm), SHIMADZU Shim-pack GIST C18-HP column (50 mm × 2.1 mm, 3 μm), SHIMADZU Shim-pack GIST C18-HP column (100 mm × 2.1 mm, 3 μm), and SHIMADZU Shim-pack GIST C18-HP column (150 mm × 2.1 mm, 3 μm) were used to study the effect of different columns.
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2

Umami Compound Isolation via RP-HPLC

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The most intense umami fraction obtained through GFC was further subjected to an RP-HPLC system (CBM-20A, Shimadzu, Japan) according to Kong et al. (2019) [14 (link)], with some modifications. The fraction (50 mg/mL, 0.2 mL) was loaded onto a Shim-pack GIST-HP C18 column (150 mm × 10 mm, 3 μm, Shimadzu, Japan). The mobile phase was ultrapure water containing 0.05% (v/v) TFA (A) and CAN containing 0.05% (v/v) TFA (B). The gradient elution was set as 0–15 min, 90–50% A; 15–25 min, 50–10% A; 25–40 min, 10–90% A, at a flow rate of 1 mL/min. The detector wavelength was monitored at 214 nm. The resulting fractions were collected and lyophilized for further evaluation.
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3

HPLC Determination of Tyrosine and Phenylalanine

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Tyrosine and phenylalanine were determined by the HPLC method.
Pre-column derivatization.
The pre-column derivatization using o-phthalaldehyde was carried out according to the previously developed method [45 (link)]. To achieve that, 70 μL of extracts or given standard solutions were mixed with 10 μL of o-phthalaldehyde (OPA) reagent at 25 °C for exactly 120 s, following which the mixture was immediately analyzed by HPLC.
The separation by HPLC was performed according to the previously designed method [46 (link)], using a Shim-pack GIST-HP C18 column (internal diameter 150 × 3 mm, particle size 5 μm) (Shimadzu, Kyoto, Japan). Comparing the amino acids retention time and UV spectrum with those of amino acids’ standards (tyrosine and phenylalanine, respectively) confirmed their chromatographic peaks.
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4

Quantification and Characterization of HGA via UPLC-MS/MS

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The qualitative and quantitative analyses of HGA were determined on a UPLC-MS/MS 8045 system (Shimadzu, Kyoto, Japan), which equipped with a triple quadrupole mass spectrometer using positive ionization mode and coupled with a UPLC equipped with a Shimadzu Shim-pack GIST-HP C18 column (2.1× 100 mm, 3 μm). Mobile phase A consisted of 0.1% formic acid and 10 mmoL/L ammonium acetate in HPLC-grade water, mobile phase B composed of HPLCgrade methanol. The ow rate was 0.3 mL/min and the elution gradient was programmed as follows: 0 min, 22% B; 1 min, 22% B; 3 min, 25% B; 6 min, 30% B; 8 min, 60% B; 13 min, 80% B; and nally, the initial conditions were held for 3 min to re-equilibrate the column. In addition, the instrument parameters were set as follows: sheath gas ow was 3 L/min, aux gas ow was 10 L/min and heated gas ow was 10 L/min. The temperature of ion transfer tube, DL and heating block were 300, 250 and 400 °C, respectively. Multiple-reaction monitoring (MRM) was used to obtain the quantitative and qualitative data. The quantitation ion of HGA was based on the transition m/z 142.10 → 74.05, with regard to the conformation ion, was on the grounds of the transition m/z 142.10 → 96.05. The collision energies (CE) of HGA were11.0 V.
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