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Printable Handouts
Navigable Slide Index
- Introduction
- Introduction to monolithic silica
- Chromatographic base materials
- HPLC method development
- Sample: HPLC column selection
- Selection of column
- Manufacturing process of Chromolith®
- Bi-modual pore structure
- Chromolith® HPLC column modifications
- Particulate vs. Monolithic HPLC columns
- Chromolith® HPLC columns
- Chromolith® stability and reproducibility
- Column material selection
- Advantages of monolithic HPLC columns
- Monolithic columns (silica based)
- Enabling speed
- Optimal flow rate
- 9 x faster at the same performance
- Longer columns = higher resolution
- Maximising plate count per column (1)
- Maximising plate count per column (2)
- Various eluent options
- Chromolith®: performance vs. HR
- Sample preparation and analysis time
- Paraben in sun-lotion
- Cost and lifetime calculation
- Limiting the carry over effect
- Column robustness and lifetime
- Increase speed – safe time
- Chromolith® guard columns and holder
- 2D separation: HILIC & RP MS
- 2D separation: 1st dimension - HILIC
- 2D separation: 2nd dimension - RP MS
- Pharma applications
- Pharmacopoeia: up-to-date information
- Benefits in pharmaceutical applications
- Esomeprazole magnesium (API assay)
- Determination of matrix-rich samples
- API assay: alternative HPLC procedure
- Esomeprazole magnesium – dissolution
- Alternative column method conversion
- Spironalactone USP monograph
- Summary
- Thank you
- Disclaimer
Topics Covered
- Monolithic silica
- Particulate columns
- HPLC
- UHPLC
- Mass spectrometry
- Chromatography
- Chromolith
- Multidimensional separation
- Alternative HPLC methodology
Links
Categories:
External Links
Talk Citation
Machtejevas, E. (2021, August 29). Advantages of using monolithic silica gel columns in the pharma industry 1 [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 22, 2024, from https://doi.org/10.69645/ZVEI8219.Export Citation (RIS)
Publication History
Financial Disclosures
- Dr. Machtejevas is an employee of Merck KGaA, all used material belongs to Merck KGaA, however, material is presented from scientific point of view, with no commercial goal intended.
Advantages of using monolithic silica gel columns in the pharma industry 1
Published on August 29, 2021
61 min
A selection of talks on Methods
Transcript
Please wait while the transcript is being prepared...
0:00
Hello, I'm Egidijius Machtejevas,
I'm the Lead Expert in Chromatography Products at Merck.
Today I would like to talk about the advantages of
using monolithic silica gel columns in the pharma industry.
I would also like to mention that this is part 1.
In part 1, I will talk about small molecular weight compounds,
and in part 2, I will focus on the larger molecular weight compound separations.
0:34
First I will start by introducing you to the world of monolithic silica.
0:41
Talking about chromatographic base materials, we have several different options.
We could use fully porous silica particles,
we could use fused-core superficially porous particles,
there are also fully porous polymeric particles, and also monolithic silicas.
All these different materials have certain strengths, and some weaknesses too.
For example, fully porous silicon materials have the best loadability.
Fused-core type of materials have the highest efficiency possible on the market.
In this presentation, I will focus on monolithic silica.
I will show in the slides to come, why monolithic silica can supply
certain advantages, and how best to benefit from using monolithic silica columns.
1:34
In HPLC method development, there are several important parts.
First of all we have to define our separation goals,
we need to know why we're separating and what the separation should look like.
Then of course, there is a lot of focus around the sample.
Sample is a key element, we have to know all the sample components,
impurities, concentration levels, sizes and so on.
I'll go more into details in my next slides.
Then if we are free to choose any instrument we could select one or another instrument.
It could be HPLC, it could be UHPLC, it depends which one you prefer, or what advantages you would like to get.
Then we select the column-based material, column modification,
we go to conditions, and the circle is closed.
We can verify how this aligns with our separation goals.
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