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Shim pack giss c18 column

Manufactured by Shimadzu
Sourced in Japan

The Shim Pack GISS C18 column is a reversed-phase high-performance liquid chromatography (HPLC) column with a C18 stationary phase. It is designed for the separation and analysis of a wide range of organic compounds.

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4 protocols using shim pack giss c18 column

1

HPLC-ESI-MS/MS Compound Identification

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The mass spectrometer (Shimadzu) with electrospray ionization mode (ESI) coupled to the HPLC Prominence (Shimadzu) was applied to record all mass spectra. The compounds were separated on a 50 × 2.1 mm i.d., 1.9 μm Shim Pack GISS C18 column (Shimadzu) thermostated at 40 °C. Samples were dosed in a volume of 2 μL and the flow rate was 0.2 mL/min. The separation of the analytes was performed in the same gradient systems as in the case of LC-DAD-ESI-MS/MS. The parameters of LCMS-IT-TOF spectrometer were set as follows: curved desolvation line (CDL) and heat block temperature was 230 °C, the nebulizing gas flow rate was 1.5 L/min, and capillary voltage was 4.5 kV. Positive ion mode with the mass range within 100–2000 Da was applied for recording all mass spectra. The collision energy was in the range of 12–50% independence on the structure of the compounds. The Formula Predictor within LCMS Solution software was used for the elaboration of results obtained in high-resolution mass spectrometry experiments (HRMS). Only an empirical formula with a mass error below 5 ppm was considered.
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2

Gradient Chromatography for Analyte Separation

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Gradient Chromatography was performed on a Nexera LC-2040C (Shimadzu, Japan) with Shim-pack GISS C18 column (150 mm × 2.1 mm i.d, 1.9 µm) (Shimadzu, Japan) protected by a Shim-pack GISS C18 guard column (10 mm × 2.1 mm i.d, 1.9 µm) (Shimadzu, Japan).

ZX3 Advanced Vortex mixer (F20230176, Alfa medical Westbury, China)

Mechanical Shaker (Heidolph, Germany)

Z 36 HK Super High Speed Refrigerated Centrifuge (Hermle Labortechnik, Germany)

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3

Mass Spectrometry Analysis of Compounds

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The mass spectrometer (Shimadzu) with electrospray ionization method (ESI) was applied to record all mass spectra. It was coupled to the HPLC Prominence (Shimadzu). Compounds were separated on a 50 mm × 2.1 mm i.d., 1.9 μm Shim Pack GISS C18 column (Shimadzu) thermostated at 40 °C. Samples were dosed in a volume of 2 μL and the flow rate was 0.2 mL/min. The separation of the analytes was performed in the same gradient systems as in the case of LC-DAD-ESI-MS/MS. Parameters of LCMS-IT-TOF spectrometer were set as follows: curved desolvation line (CDL) and heat block temperature 230 °C, nebulizing gas flow rate 1.5 L/min and capillary voltage 4.5 kV. Positive ion mode with mass range within 100–2000 Da was applied for recording all mass spectra. Collision energy was in the range of 12–50% depending on the structure of compounds. The Formula Predictor within the LCMS Solution software was used for elaboration of results obtained in high resolution mass spectrometry experiments (HRMS). Only empirical formula with a mass error below 5 ppm were taken into account.
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4

UHPLC Analysis of Herbal Compounds

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The solution of BYHWD (0.1 ml) was added into 10 ml 50% methanol and filtered by 0.22 μM membrane. The six standards of amygdalin, hydroxysafflor yellow A, paeoniflorin, calycosin glycoside, formononetin, and calycosin were dissolved in methanol at concentration of 1 mg/ml, 300 μg/ml, 300 μg/ml, 5 μg/ml, 50 μg/ml, and 25 μg/ml, respectively. Chromatographic analysis was performed by ultra high-performance liquid chromatography (UHPLC, Shimadzu, Japan). Chromatographic separation was operated on a Shim-pack GISS-C18 column (2.1 × 100 mm, 1.9 μm, Shimadzu) at 30°C. Formic acid aqueous solution and acetonitrile were used for gradient elution: 0-10 min, 5%-10% acetonitrile; 10-13 min, 10%-15% acetonitrile, 13-25 min, 15%-25% acetonitrile, and 25-43 min, 25%-55% acetonitrile. The sample volume was 2 μL and the flow velocity was 0.3 mL/min. The detection wavelength was 264 nm.
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