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Related Concept Videos

Gas Chromatography: Types of Columns and Stationary Phases01:17

Gas Chromatography: Types of Columns and Stationary Phases

Gas chromatography (GC) relies on stationary phases to separate and analyze components in a sample. There are two main types of stationary phases: liquid and solid. Liquid stationary phases are non-volatile, thermally stable, and chemically inert liquids coated onto the column. Solid stationary phases are particles of adsorbent material, such as silica gel or molecular sieves.
For an analyte to remain on the column for a sufficient amount of time, it must exhibit some level of compatibility (or...
Ion-Exchange Chromatography01:09

Ion-Exchange Chromatography

Ion-exchange chromatography, or IEC, is a technique for separating ions based on their affinity for the stationary phase. The stationary phase is a cross-linked polymer resin with covalently attached ionic functional groups. The functional groups can be either positively charged (cation exchangers) or negatively charged (anion exchangers). A cation exchanger consists of a polymeric anion and active cations, while an anion exchanger is a polymeric cation with active anions. The choice of...
Types Of Column Chromatography01:29

Types Of Column Chromatography

The stability and compatibility of column material with samples are crucial for efficient purification in chromatographic techniques. Various operating parameters such as pH, temperature, or solvent affect the packing of the column material, thereby determining the purification efficiency. The choice of column material also plays an essential role in deciding the operating parameters and can be modified based on the proteins that need to be purified.
Gel Filtration Chromatography
When the...
Principles Of Column Chromatography01:13

Principles Of Column Chromatography

The chromatography technique was first invented in 1901 by Michael S. Tswett, a Russian botanist, to separate plant pigments using organic solvents. Further, in 1941, Archer John Porter Martin and R. L. M. Synge modified the technique by packing silica gel into a column. A mixture of amino acids was then separated on the packed column using chloroform and water mixture as the mobile phase. This was the first report on column chromatography. At present, column chromatography is a widely used...
Pharmaceutical Alternatives: Polymorphic Form-Related and Particle Size-Related Therapeutic Nonequivalence01:27

Pharmaceutical Alternatives: Polymorphic Form-Related and Particle Size-Related Therapeutic Nonequivalence

Changes in polymorphic forms can significantly influence the bioavailability of poorly soluble drugs. Although the FDA defines pharmaceutical equivalence based on having the same active ingredient, dosage form, and route of administration, it does not automatically disqualify products with different polymorphic forms. This means two products with different polymorphs can still be deemed pharmaceutically equivalent. However, polymorphic differences can affect properties like wettability,...
Ion Exchange01:17

Ion Exchange

Ion exchange chromatography separates charged molecules from a solution by reversibly exchanging them with mobile, or 'active', ions associated with the oppositely charged stationary phase. This method can be used to separate ions, soften and deionize water, and purify solutions. The polymers comprising the ion-exchange column are high-molecular-weight and chemically stable polymers, crosslinked to be porous and essentially insoluble. They are also functionalized with either acidic or basic...

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Simple In-House Ultra-High Performance Capillary Column Manufacturing with the FlashPack Approach
13:36

Simple In-House Ultra-High Performance Capillary Column Manufacturing with the FlashPack Approach

Published on: December 4, 2021

Pharmaceutical applications on columns packed with sub-2 microm particles.

Rossana Russo1, Davy Guillarme, Dao T-T Nguyen

  • 1Laboratory of Phytoanalysis, Dipartimento di Scienza e Tecnologia del Farmaco, Turin University, Via P. Giuria 9-10125 Turin, Italy.

Journal of Chromatographic Science
|March 13, 2008
PubMed
Summary

Ultra-fast liquid chromatography using sub-2-micrometer particles offers enhanced separation power and faster analysis. These stable columns provide significant reductions in analysis time for pharmaceutical applications.

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Preparation and Characterization of Individual and Multi-drug Loaded Physically Entrapped Polymeric Micelles
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Last Updated: Jul 6, 2026

Simple In-House Ultra-High Performance Capillary Column Manufacturing with the FlashPack Approach
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Published on: December 4, 2021

Preparation and Characterization of Individual and Multi-drug Loaded Physically Entrapped Polymeric Micelles
07:32

Preparation and Characterization of Individual and Multi-drug Loaded Physically Entrapped Polymeric Micelles

Published on: August 28, 2015

Area of Science:

  • Analytical Chemistry
  • Chromatography

Background:

  • Growing interest in fast liquid chromatography (FLC).
  • Sub-2-micrometer particle size is a key strategy for improving separation power and analysis speed.

Purpose of the Study:

  • To evaluate the chromatographic performance and stability of sub-2-micrometer particle columns.
  • To demonstrate the potential for ultra-fast or highly efficient separations in pharmaceutical applications.

Main Methods:

  • Utilized plate-height curves to assess chromatographic performance.
  • Conducted system suitability experiments to evaluate column stability.
  • Tested columns under pressure conditions ranging from 200 to 800 bar.
  • Applied columns in both isocratic and gradient modes for pharmaceutical analyses.

Main Results:

  • Columns demonstrated stable performance over 1700 injections, maintaining retention, efficiency, and pressure.
  • Achieved 5- to 10-fold reduction in analysis time in isocratic mode with minimal impact on efficiency and resolution.
  • Reduced run times by up to 30-fold using shorter columns (30 mm).
  • Improved separation of pharmaceutical compounds and impurities in gradient mode using 100 mm columns, enhancing peak capacity and resolution.

Conclusions:

  • Sub-2-micrometer particle columns are stable and effective for fast and ultra-fast liquid chromatography.
  • These columns offer significant advantages in reducing analysis time and improving separation efficiency for pharmaceutical applications.