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Related Concept Videos

Sample Preparation for Analysis: Overview01:21

Sample Preparation for Analysis: Overview

Sample preparation is an essential step in the analytical process. It involves preparing a sample so that it can be analyzed accurately. The goal is to extract the analyte, the substance you want to measure, from the sample while removing any components that may interfere with the analysis. Sample preparation techniques vary depending on the physical state of the sample.
Bulk or large solid samples are typically reduced in size using grinding, crushing, or milling techniques to increase the...
High-Performance Liquid Chromatography: Introduction01:11

High-Performance Liquid Chromatography: Introduction

High-performance liquid chromatography(HPLC), formerly referred to as High-pressure liquid chromatography, is a powerful technique used to separate, identify, and quantify components in complex mixtures. The term "high pressure" refers to using high pressure to push the liquid mobile phase through the tightly packed columns.
In HPLC, two phases play a critical role in the separation process:
Affinity Chromatography01:03

Affinity Chromatography

Affinity chromatography is a powerful technique extensively utilized for separating and purifying specific biomolecules from complex mixtures. It capitalizes on the highly selective binding between an analyte and its counterpart, such as antibody-antigen interactions. The counterpart is immobilized on the stationary phase, forming an affinity column. The stationary phase typically consists of solid support, such as agarose or porous glass beads, immobilizing the affinity ligand. The mobile...
Analyte Adsorption and Distribution01:09

Analyte Adsorption and Distribution

In certain chromatographic separations, solutes transfer between the mobile phase and the stationary phase via sorption, which typically refers to the process of adsorption. For many chromatographic systems, the sorption process often depends on the polarity of the compounds—an expression of the overall dipole moment within the molecule. During the separation process, there is competition between the solute and solvent for adsorption to the stationary phase. Highly polar compounds and solvents...
Optimizing Chromatographic Separations01:15

Optimizing Chromatographic Separations

Optimizing chromatographic separations is crucial for obtaining clean separations in a minimum amount of time. Optimization is required for several factors, including kinetic effects related to band broadening, plate height, capacity factor, and separation factor.
Band broadening refers to spreading solute bands as they travel through the column. This broadening can impact resolution. Plate height (H) represents the length required for one theoretical plate. A lower plate height corresponds to...
Chromatography: Introduction01:10

Chromatography: Introduction

Chromatography is a technique used to separate compounds based on differences of partitioning between two phases, the stationary phase and the mobile phase.
The phase in which the compounds linger or on which the compounds adsorb is called the stationary phase, whereas the mobile phase is the solvent that carries the solutes to be analyzed. In traditional column chromatography, the mixture flows through the stationary phase, and the compounds partition between the stationary and mobile phases...

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Related Experiment Video

Updated: Jun 20, 2026

Multi-step Preparation Technique to Recover Multiple Metabolite Compound Classes for In-depth and Informative Metabolomic Analysis
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Separation and sample pre-treatment in bioanalysis using monolithic phases: A review.

Kenneth C Saunders1, Ashraf Ghanem, Wei Boon Hon

  • 1Pfizer Global Research and Development, Sandwich, UK.

Analytica Chimica Acta
|September 30, 2009
PubMed
Summary

Monolithic phases offer innovative solutions for bioanalytical assays in drug discovery. This review explores their application, challenges, and future potential in quantitative bioanalysis.

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Area of Science:

  • Analytical Chemistry
  • Pharmaceutical Science
  • Biotechnology

Background:

  • The pharmaceutical industry increasingly relies on advanced bioanalytical assays for drug discovery and development.
  • Quantitative bioanalysis in biological matrices presents challenges in sensitivity, speed, and specificity, especially for low-concentration analytes.
  • Complex techniques like HPLC column switching and microfluidics are employed, necessitating robust analytical technologies.

Purpose of the Study:

  • To provide an overview of monolithic phase applications in bioanalysis.
  • To discuss the challenges and technical hurdles in developing sensitive and high-throughput bioanalytical assays.
  • To highlight the synthesis, use, and applicability of monolithic phases, particularly polymer-based ones.

Main Methods:

  • Review of scientific literature on monolithic phases in bioanalytical settings.
  • Analysis of current bioanalytical techniques and approaches utilizing monolithic materials.
  • Exploration of emerging technologies and future possibilities for monolithic phase implementation.

Main Results:

  • Monolithic phases represent a successful emerging technology for overcoming bioanalytical challenges.
  • Polymer-based monolithic phases show significant promise and applicability in quantitative bioanalysis.
  • Current bioanalytical techniques are being adapted and advanced through the use of monolithic materials.

Conclusions:

  • Monolithic phases offer a viable and effective technology for enhancing quantitative bioanalysis in drug discovery.
  • Further research and development in monolithic phase technology will expand their role in high-throughput bioanalytical applications.
  • The application of monolithic phases is crucial for achieving the required sensitivity, speed, and specificity in modern bioanalytical studies.