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[Seminar Materials Released] Basics of Ion Chromatography

Recommended for those who will be involved in ion chromatography and those who want to relearn the basics!

We are pleased to announce the release of the slide materials from the seminar program "Basics of Ion Chromatography," which was popular at the Dionex IC Technology Seminar 2019 - Basic Course on Chromatography! This seminar focuses on understanding and acquiring essential foundational knowledge related to analysis, such as the principles and theories of ion exchange separation and the basic components of the equipment, making it suitable for beginners in ion chromatography.

  • Analytical Equipment and Devices

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Basics of Ion Chromatography: The Flow Rate of the Eluent Affecting Separation

A clear explanation of the basics of ion chromatography! Let's understand how changes in the flow rate of the eluent affect separation.

Ion exchange separation occurs due to the competition between the measurement ions and the eluent ions on the ion exchange sites. One of the factors that affects this ion exchange separation is the change in the flow rate of the eluent. I will explain the differences in the chromatograms obtained by varying the flow rate of the eluent and the points to be cautious about.

  • Analytical Equipment and Devices

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Basics of Ion Chromatography: Temperature Affecting Separation

A clear explanation of the basics of ion chromatography! Let's understand the impact of changes in column temperature on separation.

Ion exchange separation occurs due to the competition between the measurement ions and the eluent ions on the ion exchange sites. One of the factors that affects this ion exchange separation is the change in column temperature. When the column temperature is altered, the retention time of the measurement ions changes due to variations in separation equilibrium, diffusion rates, degree of dissociation, and the viscosity of the eluent. The impact of temperature varies depending on the type of measurement ions and also changes with different columns and eluents. This factor of temperature will be explained.

  • Analytical Equipment and Devices

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[Analysis Case] Risk Assessment of Nitrosamines in Pharmaceuticals

[Introduction to Ion Chromatography Cases] Measurement of Nitrite and Amines

N-nitrosodimethylamine (NDMA) is an organic compound represented by the chemical formula (CH3)2NNO. NDMA is a known carcinogen found in some fermented foods. The measurement of nitrite ions can be performed using wet chemical analysis, but a representative method in instrumental analysis is ion chromatography (IC). In IC, separation is achieved using an ion exchange column, and detection is carried out using conductivity detection, electrochemical detection, UV detection, or mass spectrometry. Methods using IC typically require little to no sample pretreatment for many pharmaceutical samples, and derivatization of the target components is also unnecessary.

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Basics of Ion Chromatography: Hydrophobicity Affecting Separation

A clear explanation of the basics of ion chromatography! Let's understand the impact of hydrophobic interactions on separation.

Ion exchange separation occurs due to the competition between the measured ions and the eluent ions on the ion exchange sites. One factor that affects this ion exchange separation is hydrophobic interaction. I will explain this factor of hydrophobicity.

  • Analytical Equipment and Devices

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Basics of Ion Chromatography: The Concentration and Types of Eluents Affecting Separation

A clear explanation of the basics of ion chromatography! Let's understand the concentration and types of elution solutions.

Ion exchange separation occurs due to the competition between the measurement ions and the eluent ions on the ion exchange sites. This explains the concentration and types of eluent that affect this ion exchange separation.

  • Analytical Equipment and Devices

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Basics of Ion Chromatography: Principles of Ion Exchange Separation

A clear explanation of the basics of ion chromatography! Let's understand ion exchange separation.

Ion exchange separation is the fundamental mechanism of separation in ion chromatography, where ionic components repeatedly adsorb and desorb between the ion exchange sites and the electrolyte solution. This principle and its characteristics will be explained.

  • Analytical Equipment and Devices

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Transfer of the analysis method for chlorhexidine impurities.

We will explain the key points for successfully transferring HPLC analysis methods using the results of rigorous analytical comparisons!

Transferring liquid chromatography (LC) methods between instruments is a challenging task that many analytical laboratories frequently face. The success of this method transfer depends on many factors, making it important to reduce the differences between the systems being transferred and the robustness of the method being transferred. This application note presents a smooth transfer from the Thermo Scientific UltiMate 3000 HPLC system to the Thermo Scientific Vanquish Core HPLC system using an HPLC method from the European Pharmacopoeia.

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  • Analytical Equipment and Devices

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[Case Study] Analysis of Tocopherols α, β, γ, and δ using 2D-LC

Vitamin E (alpha, beta, gamma, delta tocopherols) in vegetable oils can be separated and quantified without the influence of interfering components using single-loop heart-cut 2D-LC.

This document introduces a method for the high-precision separation and quantification of four types of tocopherols contained in vegetable oils using the single-loop heart-cut 2D-LC method. Under the separation conditions of a reverse-phase system using a general ODS column, the separation of β-tocopherol and γ-tocopherol is difficult; however, the 2D-LC method allows for easy separation. In the first dimension, tocopherols and interfering components in the sample are separated, and in the second dimension, the four types of tocopherols (α, β, γ, δ) are separated. The repeatability of the standard samples achieved a high reproducibility with RSD < 0.1%. Additionally, measurements conducted on multiple vegetable oils showed that quantification was possible without the influence of interfering peaks. The single-loop heart-cut 2D-LC method is the simplest technique among 2D-LC methods, making it applicable for routine analysis and a useful tool for food analysis involving samples with a high content of matrix components. 【Features】 ■ High-precision separation achieved with the single-loop heart-cut 2D-LC method ■ Separation of β-tocopherol and γ-tocopherol, which is difficult in reverse-phase systems ■ Effective separation of interfering substances in food ■ High reproducibility with repeatability of RSD < 0.1%

  • Analytical Equipment and Devices

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[Case Study] Simultaneous Analysis of Vitamins A, D, and E using 2D-LC

Simplifying the preprocessing with the single loop heart cut 2D-LC method significantly reduces analysis time. It enables the highly sensitive detection of vitamins A, D, E, and their isomers.

This technical document introduces a rapid and quantitative analytical method for the simultaneous detection of seven types of vitamins (vitamin A, vitamin D2, vitamin D3, and four types of vitamin E isomers) in infant formula using a conventional HPLC system with a diode array detector and a fluorescence detector, following offline solid-phase extraction (SPE) and two-dimensional liquid chromatography (2D-LC) analysis. By changing the traditional liquid-liquid extraction method to solid-phase extraction, the time required for sample preparation was reduced from 3 hours to 1 hour. Additionally, by simplifying the sample preparation and optimizing the separation conditions, the influence of the matrix was reduced, allowing for the detection of target substances with higher sensitivity. ■ Simplified sample preparation through two-dimensional liquid chromatography (2D-LC) analysis ■ Simultaneous separation analysis of vitamins A, D, E, and their isomers ■ Developed a method with higher recovery rates and sensitivity than liquid-liquid extraction ■ Simplified the preprocessing process and reduced analysis time by 2.5 times ■ Reduced the influence of the matrix and provided reliable data

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  • Analytical Equipment and Devices

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