
Chromatography Stationary Phase & Purification Media

Chromatography Stationary Phase & Purification Media
Mechotech supplies a complete range of chromatography stationary phases — the silica and polymeric media that do the actual separating inside a purification column. Every grade is built from perfectly spherical, monodisperse particles with a tightly controlled pore size, so packed beds are uniform, mechanically stable and highly reproducible from lot to lot. Particle sizes of 3, 5, 7, 10, 20 and 50 µm span high-resolution analytical-prep work through robust, high-throughput process purification. The portfolio covers normal-phase, reverse-phase (RPC), ion-exchange (IEX), hydrophobic-interaction (HIC), affinity, Protein A and chiral chemistries for peptide, protein, API and natural-product purification.
A Mechotech stationary phase starts from a spherical base bead — high-purity silica or a rigid polymeric backbone — whose narrow particle-size distribution and defined pore structure give low back-pressure, sharp peaks and predictable scale-up. Reverse-phase grades carry bonded alkyl chemistries for peptide and small-molecule separations; ion-exchange grades offer strong and weak cation- and anion-exchange functionalities; HIC grades resolve by surface hydrophobicity under high-salt conditions; and affinity grades, including Protein A media, capture target biomolecules with high selectivity. Chiral separations are supported with both mobilised and immobilised chiral selectors for resolving enantiomers. Media are supplied loose for self-packing or pre-qualified for Mechotech's preparative columns, so the same chemistry can be carried from method development straight through to production without changing selectivity.
Technical Specifications
| Media Type | Monodisperse silica and polymeric stationary phase |
|---|---|
| Particle Shape | Perfectly spherical, uniform (monodisperse) |
| Particle Sizes | 3, 5, 7, 10, 20 and 50 µm |
| Pore Structure | Controlled, defined pore size (configurable) |
| Base Matrix | High-purity silica or rigid polymeric backbone |
| Separation Modes | Normal phase, RPC, IEX, HIC, affinity, Protein A, chiral |
| Ion-Exchange Types | Strong / weak cation and anion exchange |
| Chiral Selectors | Mobilised and immobilised |
| Chemical Stability | Withstands clean-in-place and sanitisation cycles |
| Supply Form | Loose media or pre-qualified for Mechotech columns |
| Reusability | Regenerable for many cycles |
| Applications | Peptide, protein, API and natural-product purification |
Plant Capacities
| Media / Mode | Particle Size | Typical Use |
|---|---|---|
| Reverse Phase (RPC) silica | 3 / 5 / 7 µm | High-resolution peptide & small-molecule prep |
| Reverse Phase (RPC) silica | 10 / 20 µm | Process-scale peptide & API purification |
| Normal Phase silica | 5 / 10 µm | Natural-product & lipophilic compound separation |
| Ion Exchange (IEX) polymeric | 10 / 20 / 50 µm | Protein, peptide & charged-molecule capture |
| Hydrophobic Interaction (HIC) | 10 / 20 µm | Protein polishing under high-salt conditions |
| Affinity | 20 / 50 µm | Selective capture of tagged biomolecules |
| Protein A affinity | 20 / 50 µm | Antibody & Fc-fusion protein capture |
| Chiral (mobilised / immobilised) | 5 / 10 µm | Enantiomer resolution for pharmaceuticals |
Representative media grades; each chemistry is offered across particle sizes and controlled pore sizes and can be supplied loose or pre-qualified for Mechotech columns. Selectivity, capacity and particle size are matched to the target molecule and scale — custom grades on request.
Manufacturing Process
Mode & Chemistry Selection
The target molecule and the impurity profile set the separation mode — reverse-phase, ion-exchange, HIC, affinity, Protein A or chiral — and therefore the base media chemistry.
Particle & Pore Selection
Particle size (3, 5, 7, 10, 20 or 50 µm) and controlled pore size are chosen to balance resolution, back-pressure and loading for the required scale.
Slurry & Conditioning
The media is slurried in a compatible solvent or buffer and conditioned so particles are fully wetted and evenly dispersed before packing.
Column Packing
The monodisperse, spherical particles pack into a dense, uniform, low-void bed — ideal for dynamic-axial-compression columns and highly reproducible between packs.
Equilibration & Loading
The bed is equilibrated to the starting mobile phase, then sample is loaded so target and impurities begin to partition on the stationary phase.
Elution & Fractionation
A gradient or step elution separates the components; sharp, symmetrical peaks from the uniform particles give clean fractions and high recovery.
Cleaning-in-Place & Sanitisation
The rigid spherical base withstands aggressive clean-in-place and sanitisation cycles, restoring the bed between batches without loss of performance.
Regeneration & Reuse
The media is regenerated and re-equilibrated for the next cycle; its mechanical and chemical stability supports many reuse cycles across a campaign.
Applications
- Preparative and process purification of synthetic and recombinant peptides
- Protein, enzyme and monoclonal-antibody capture and polishing
- Protein A affinity capture of antibodies and Fc-fusion proteins
- Small-molecule API and intermediate purification
- Chiral resolution of pharmaceutical enantiomers
- Desalting, buffer exchange and impurity removal
- Isolation of natural-product actives, alkaloids and glycosides
- Nutraceutical, food and cosmetic ingredient purification
Key Features
Monodisperse Spherical Particles
Perfectly spherical, uniform particles form even, low-void beds that give sharp peaks, low back-pressure and reproducible results lot to lot.
Controlled Pore Size
A defined pore structure matched to the target molecule maximises usable surface area, binding capacity and mass transfer.
Full Range of Modes
Normal-phase, reverse-phase, ion-exchange, HIC, affinity, Protein A and chiral chemistries cover peptide, protein, API and natural-product work.
Silica & Polymeric Backbones
High-purity silica for efficiency and resolution, or rigid polymeric bases for wide-pH stability and demanding clean-in-place regimes.
Particle Sizes 3–50 µm
Fine 3–7 µm grades for high-resolution prep and coarser 10–50 µm grades for robust, high-throughput process purification.
Seamless Scale-Up
The same chemistry is available across particle sizes and pre-qualified for Mechotech columns, so methods scale without changing selectivity.
Frequently Asked Questions
What is a chromatography stationary phase?
Why does monodisperse, spherical particle shape matter?
Which particle size should I choose?
What separation modes are available?
Silica or polymeric — which base should I use?
Can the media be cleaned and reused?
Can I buy media pre-qualified for your columns?
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