Prep- and Industrial Process Chromatography is about producing compounds at highest throughput, yield and purity at lowest costs !
If you know what you want - we offer plant & equipment :
How to start in successful large scale chromatography?
Prep and process chromatography is about producing pure compounds at highest possible yield and purity at lowest possible cost. Every additional gram of compound is additional income but sometimes also additional risks. Many process specialists had to sign confidentiality agreements with their employers and affright to take risks, procrastination is the result. Many chemist prefer re-crystallization or distillation over chromatography as purification method. Biochemist, Biotechnologist, Food technologist know that they have almost no choice of alternative molecular purification / separation processes than chromatography.
Chromatography is still a young process industry that is continuously being advanced with new materials and process methods. Competition in the market is driving the industry towards specialised niche products with smaller but high value added markets. Many new molecules used as API or exipients are highly active and produced in small quantities, many do not crystallize and thus demand for high yielding low cost methods is growing.
Prep & Production scale Chromatography is used to extract, separate and purify molecules in
- Fine chemical production
- Manufacture of pharmaceutical compound
- Food processing
We are a network of independent and highly innovative chromatography pioneers. All of us have built through the years our own process technologies, unique particles, plants, equipment and software tools. Pooling our skills and knowledge we move production scale chromatography into new era. We are determined to systematically evolve liquid chromatography as the most competitive of all purification methods. With our accumulated skills we help you to manufacture the most competitive compounds! Dont hesitate to contact us for help. Nevertheless we have to ask some fundamental question to understand the basics of your status quo. It is common practice to sign mutual confidential disclosure agreements.
The field of Prep and Process Scale Chromatography is wide. There are simply no turn key solution available. To narrow the choices for solutions a number of questions require to be answered.
What kind of compounds to be purified / separated?
- Organic Synthetic Compounds (MW<2000) (Heterocycles, Vitamins, Organometallics, Hormones, Pesticides,)
- Natural Products (MW <2000) (Saccarides, Lipides, Phospholipides, Isoprenoids, Steroids, Alkaloids, Flavenoids, Terpenes, Polyphenols, Saponins, Proanthocyanidins, Tannins etc from a wide range of matrixes)
- Amino Acids, Peptides, Oligonucleotides
- Large scale racemate purification
- Inorganics Separation (Cations and Anions, Metals, Nobel Metals, Acids, Alkalis, Industrial Waste,Hydrometallurgical- refining, leachages, extracts, precipitants )
- Protein, Biomarkers and Biotherapeutic Proteins, (Enzymes, Membrane Proteins, Recombinant Proteins, Antibodies, extracts from mammalian Tissue, Erythrocytes, Yeast, Bacteria)
What is you sample preparation method? Please describe.
Sample separation and purification method do you want to use? Please describe.
Every process can be looked at from three perspectives. It is important to write down and to quantify the various anticipations.
Is a description of origin of sample (E.g. Sap from a plant XYZ that growth in A, Animal feed named ABC from company X or slurry from a chemical process A, retentate of a membrane process in a communal waste water treatment plant, piece of tissue from a biopsy from Z etc. ) and a description of how the sample was harvested or synthesized and prepared prior separation / purification / modification process.
The project encompasses either purification / separation / fractionation / alteration or all of those processes. It requires a precise description of process steps to be undertaken. Important is to write down the anticipated quantification of the output results.
People with low job security and no expertise avoid formulating such parameters. They often go out into internet forums and lend up with with many different opinion
Every output has to go through downstream processes. This requires a description of what should happen with the sample, what downstream processes the sample will be exposed too, what upper / lower level of purity , throughput and target cost should be achieved. In a commercial environment the ultimate arbiter of success is productivity.
From which level do we start ?
Please supply start up data such as analytical chromatograms. Make-up of liquid extract, Bio-broth, chemical raw material analysis etc
Factors of Success
Most processes comprise of a number of steps and involve a number of persons with different perspectives and skills. Frustration and money can be saved by gathering the process responsible people to invest time to go through the Upstream, Project and Downstream perspective. It is important that everybody understands the requirements and commits to it.
Sample preparation is often over or under designed, conducted by unskilled labour, badly communicated or simply not given the respect it deserves. Sample preparation means for everybody something different! We have to simply consider it as a process step within a chain of many sequential or parallel processes. In this chain we have to look back in time, upstream and to learn what happened to the sample before it reached us. Sample preparation is important. All participants have to know from to what state the sample has to be converted and which which method (physical separation, pulverisation, dissolution, filtration, membrane filtration, solvent extraction, soxhlet extraction, distillation, adsorption, precipitation, centrifuging, chelating, masking, reacting etc. (If you need help please dont hesitate to contact us!)
People often assume that everybody knows what will and should happen in the following process stage or they dont care. In some industries people simply don’t talk to each others because they consider this as not their territory or concern. They work toward a specification and think that will suffice. Many specifications are not complete or ambivalent. Discussing the downstream process people may also trigger new ideas how to handle the project best. Furthermore it is also improving relationships and responsibilities between the parties.
The bottom line in chromatography cost efficiency and effectiveness (Yield, throughput and purity) and they are influenced by the following factors:
There is quite a difference in cost whether or not you are using organic solvent or water and this in turn is dependent on what infrastructure is available. Some companies do have infrastructures to recycles solvents but some don’t. Some chromatography separation materials don’t use as much solvent as others. Please ask us for advice at the start of your project. Compatibility of target molecules with water or solvents is an important aspect. Availability of solvent is another important issue and so is purity of solvents.
Sometimes it may be necessary to design your plant according to ATEX regulations! The cost difference between ATEX or not ATEX conform plants is substantial. Let us know we may have intelligent solutions to get around ATEX costs!
Process selection commences with definition of:
- Anticipated Business volume (mg, g, kg or tons per day / week or month output). Sales and marketing people should normally provide such information. Often they dont know and keep quiet. The Japanese taught us to design processes that break even with satisfying local demand. Every additional export can be done at fixed cost. This enables to build up a very competitive global market.
Type /chemistry of molecules / particles to be processed (This is important for assessing availability of raw materials and environmental cost and precautions)
Level of purity to be achieved. (We dont over or under design the process. Regulatory authorities and clients define this dimension. It is often possible to increase market share with more pure compounds for similar costs)
Envisaged process life
Envisaged process cost and maintenance costs
Envisaged capital requirements and form of financing the capital investment
In which industrial sector are you working. Some industries operate with low cost high trough put conditions others deals in highly differentiated speciality products e.g.
- 1 to 20 g/8h
- 20 to 100 g/ 8h
- 100 to 500 g / 8 h
- 500 to 1000 g / 8 h
- 1 Kg to 10 Kg/ 8 h
- 10 to 100 Kg / 8 h
- 100 to 1000 Kg/ 8 h
- > 1 T / 8 h
Who is responsible for process validation
- Pharma Research & Development (FDA, Local regulations)
- Generic API Production (EMEA, FDA , Local regulations)
- Fine chemical Production (Environmental regulations)
- Food & Cosmetic Industry (Food regulation )
- Others (No governing regulation)
Everybody wants to possess the very best plants/ components. Unfortunately everybody has a different perception of what he considers to be the best. Please check yourself
- Plant – supplier
- Component supplier
- We prefer to buy branded turn-key plants from the largest supply companies.
- We buy from suppliers that show us plant-/component configurations which result in low cost final products. (This may include high investment but low running costs and process licensing)
- We buy what we are told to buy.
- We get a number of quotations and select the cheapest one.
- We buy branded components and plant that we bought before.
- We procure the latest and most automated technology.
- We buy components and develop in-house our own plants
- Chromatography (LC, Flash, MPLC, HPLC)
Solid Phase Extraction ,
Expanded Bed Adsorption
Chemical Synthesis (Heterogeneous Catalysts, SPPS, SPOS, Scavenging etc.)
- Flash/MPLC/Membrane Purity (for intermediates, industrial grade raw materials)
- 99 % Purity (HPLC, SMB)
- Patient injectable quality (Enantiomer pure, selective solvents)
Separation materials to be used
A large cost component is the separation material. Low cost materials may not be the best solution particularly if costly materials are being lost in the separation process.
Process chromatographers tend to look for materials with large surface area because they take higher loadings. The basis for a large surface area is small pore diameters. Make sure that the pore diameter correlates with the molecular weight of the samples. Type of surface structure and ligand density has also a dramatic influence on available surface area
Process configuration and equipment selection
In process chromatography there are many different processes available - some unique and protected by intellectual proprietary rights and many are commodities that can be utilised by everybody. Make sure that you are using processes that provide sufficient “freedom to move” so as to avoid patent infringement. It is much more advisable to check-out the “freedom to operate” issue long before you invest large amount of money in process development. We are in contact with some “process developers” that have IPR protected processes. Process developers protect their processes because they use combination of factors that lead to better yield, better resolution or to faster processing. It is advisable to sign a CDA and to evaluate the process for its claimed benefits. Process developers have invested large sums and time in developing and protecting their processes so it is only logical that they demand a small royalty payment. Never ignore IPR because it is much cheaper to pay an agreed royalty than a fine for patent violation.
Large enterprises mistrust small enterprises or only for a short time. They rather buy from large suppliers and commodity equipment. The history books are full of purchases that finally led to non competitive products. Many small companies have highly innovative process equipment and some dont even try to collaborate with large life science enterprises from bad experiences.
The list of process configuration is endless here just a few:
- Batch (Every batch a different sample )
- Single columns chromatography (Flash, MPLC, HPLC, Expanded Bed Purification, new experimental processes)
- Parallel column chromatography
Continuous column processes
- Touching band
- Sample overload mode
- Displacement mode
- Flip-flop process
- Column Recycling
- SMB (Simulated Moving Bed)
- SSR (Steady State Recycling) and Varicol®
- Fauquet Process etc
Please let us know if you are interested in some of above processes we can help you with the appropriate IPR and contact persons and of course to provide some of the relevant components and software
Column Loading Capacity:
Being able to get enough from the column in a given period of time is one of the most important factors in prep chromatography. What are our yield and cost objectives? You should ant to know how long it takes to get to satisfy your objectives with regards to sample quantity. Sometime solvents are chosen that are not optimal and load ability is decrease or intra column crystallisation occur. One has to find appropriate diluent solvents to match the mobile phase. Every column has its own load capacity. Please enquire with us.
Cost per sample:
If the column cost is very high as in the case of chiral materials all parameters have to be looked at including costs of time, solvents used column replacement costs etc. . . . You will realize this is a very important criterion in prep chromatography since there are large differences in yield and costs.
Cost of solvents.
Cost of solvent varies from type and purity of solvents used and from country to country. There a re large differences in solvent usage between the different chromatography materials and methods.
- Runtime, ml / minute – some column have reduced run times.
- Equilibration time, ml / minute – some columns use very small quantities of solvents for column equilibration. Please enquire.
- Cost of disposal, total volume – use less, dispose of less.
Less equilibration time, more runtime per day – Due to time saving in equilibration time. There are columns that require only 1 column volume to equilibrate and they are columns that use 20 column volume for equilibration
There are columns that last up to 10 times longer than ordinary columns.
Column cleaning procedures
Column live can be extended if they are serviced properly. This can be done quickly and hysteresis effects avoided. Its cost has to be included.
Many different surface chemistries.
Some columns allow running a number of modalities (RP, HILIC, ANP etc.) This enables diverse use of solvents to improve solubility range for the column / sample match or to reduce conditioning time.
Some compounds require extreme conditions (low / high pH, Temp etc) that may lead to accelerated column degradation. In reverse extreme conditions may also hydrolyze, modify compounds or lead to in-column crystallisation. Change process or columns chemistry!
Availability of bulk materials
Some suppliers manufacture only small quantities of separation materials for analytical applications. In the past 10 years we have seen a departure from in-house packed to professionally packed columns. Column packing is not trivial – particularly new type B, C and hybrid materials are much more sensitive to be packed. The market is today very price and quality competitive and so it makes sense to let the material manufacturer pack your column.
Cost of Hardware / Systems
Technical people often avoid talking about costs, - its complex and based on many variables. They rather fish around for low cost suppliers because they dont understand that cost is part of the productivity equation. In large enterprises technical people often look for performance properties of a particular process component and then submit a capital expenditure form to the finance department together with a debate about importance and benefits of the proposed acquisition. The finance department either approve or disapproves the acquisition. In smaller enterprises new equipment /plant acquisition is often debated between general , finance an technical management. Size of investment and productivity gains are important issues. It often helps technical people to get some overall cost related data and demands from their superiors. That includes
Costs & Budgets anticipation
- What is the cost of raw materials?
- What is the anticipated maximum / minimum cost for the process or cost of producing compound X ?
- What is the capital expenditure budget for the procurement of plant / Equipment ?
- Is there a budget for consumables (Solvents, Columns, Materials etc.)?
- Is there an anticipated sales price for the final compound?
The productivity of purification / separation depends largely on process configurations and consumables used and to a lesser degree on plant / component costs. Location is another issue. In some countries government supports investment in new technologies with special grants or taxation benefits. Depreciation rulings also vary from country to country, from province to province. There are a number of patented processes that result in high productivity. With high cost compounds yield is an important issue. Paying small amounts of royalties may be very profitable particularly if the purification / separation technology can be made part of the compound IPR so as to extend the patent life for a few years. Patent life is between 20 and 25 years. Towards the end of patent life the largest profits are made. Extending patent life is thus very attractive. Unfortunately external influencers in large multinational enterprises such as investors and finance analysts have a huge influence on management behaviour and career lifetime. They all think in short term dimensions when investment gains are minimal. The situation if often quite different in small privately owned enterprises
Environmental and Safety Cost Issues
Many processes use large quantities of solvents (organic and aqueous) that may cause environmental problems. Environmental and safety cost may have a huge impact on overall costs and productivity. In purification / separation organic solvents are very popular as mobile phases. To avoid unexpected surprised you should prose the following questions:
- Do we have earthed solvent storage tanks?
- What solvents will be use?.
- What are the cost of solvents?
- Do the supplied pants / components have to be EX-Protected?
- Could some operations be done outside the Ex-Protected area?
- Do we dispose off or recycle the spend organic solvent?.
- Are solvent reduction strategies of interest?.
There are also questions for water based system users
- Do your raw materials come directly from a sterile bio process?
- Can you legally discard the spent eluent into the waste water system without post process treatment?
- Would you have to incinerate the spent eluent?
Branded chromatography systems:
Large pharmaceutical manufacturing companies prefer branded equipment from the large system suppliers. They assume that large system suppliers are here to stay and will offer better service. History has shown that this is not the case because large companies grow by acquiring smaller technology suppliers and their competitors.
After the acquisition is completed they often have to pay for the acquisition and this is traditionally done by streamlining the product range and releasing the competent technical people.
Small privately owned companies do lots of custom based development work. This way they advance the industry. Some also manufacture for large system manufacturer branded products. Privately owned speciality engineering and manufacturing enterprises such as ours are generally very stable suppliers particularly those that supply reliable quality products. To survive small speciality product manufacturer are forced to offer very competitive pricing and functional products. Our clients are primarily small and expanding companies and research institution with limited budgets.
Small companies have much to lose and so many use conservative designs or over design their products. Large enterprises have large overheads and are under pressure to maximize their income some manufacturers cut down on raw material cost on their products (low cost steel, thin steel for housing and base plates). Our components are heavier and sturdier and run for many years without maintenance. Our components and systems are being used not only in chromatography but also in heavy engineering environment such as in oil exploration. Prep Chromatography systems are working horses. They have to be designed conservatively and have to be mechanically robust.
Turn-key system vs. evolving system
There are two kinds of end-users those who prefer turn-key systems and those who want to evolve a system. Turnkey systems can’t be altered and fine tuned very much. The client has to know precisely what he needs. In turbulent times chromatographers often have to modify or extend their processes.