Couple of days ago I wrote about September Discussion group organized by CASSS International separation science society. As I promised I made notes and I would like to share them with you now.

Although I expected slightly different format of meeting (selection of few topics and their detailed discussion with the attendants) I was able to find some new ideas and directions in current and future analytical chemistry.

The speakers (Robert Stevenson, Tom Jupille, and David Sparkman) presented their views about new directions in analytical chemistry, liquid chromatography, and mass spectrometry.

Robert Stevenson – New technologies in analytical chemistry

Robert Stevenson started with the importance of semantic technologies and data processing and control. With emerging techniques more and more data is acquired and analyzed. In comparison to “regular” database with x and y coordinates, semantic analysis allows to add another flexible and dynamic dimension(s) using RDF framework.

Next, he focused on high content analysis – relatively young technique (6 – 7 years) connected mainly with fluorescence microscopy and further data analysis. Using this technique human stem cells can be tested and thus testing on animals avoided. The drawback is large data output and higher prize ($0.25/well and in usual experiment 10⁵ to 10⁷ wells is analyzed).

Software enabled microscopy was a last part of Robert Stevenson’s talk. With this approach correction of optical imperfection is done using software. Using this approach, fluorescent photo-activated localization microscopy enables imaging of DNA strains during the cell division. Unbelievable.

Tom Jupille – High performance liquid chromatography

Tom Jupille summarized history of liquid chromatography separation, which started in 1905 by Michael Tswett. There was not any giant step in the instrumental development during first fifty years. Columns in 1955 looked almost the same as those used by M. Tswett and used gravity as driving force for the mobile phase (although they were much bigger).

Oppositely, next 50 years changed the instrumentation completely. New techniques such as HPLC were introduced thanks to rapid development of a high quality engineering and computers technology. Then, instrumentation in 2005 looked like self-standing, robust, machines controlled with a PC producing hundreds and thousands results every day.

And 2055? Miniaturization and Black-boxes. Tom Jupille compared the evolution of chromatographic system to personal computers. Nowadays, only small group of people knows how computers work. Majority of people uses computers in their daily life but has no clue about bits, RAM or binary system.

HPLC systems

The same applies for chromatographic instruments. In the future, people are going to use LC system and they may not even notice using one. For them, it will be the only way how to reach a result– composition of the sample, level of compound of interest, sample preparation for further analysis and so on.

My (footnote) heretical question: is liquid chromatography sample preparation technique for mass spectrometry?

Future of HPLC instrument began with introduction of Dionex ICS 5000, which is a system with minimal extracolumn volumes and flexible and modular approach. In this I agree with Tom Jupille and his “As instruments evolve, they became appliances” statement. We as method development crowd should provide end-customer with required technology/instrument/column. And end-customer does not need to know value of efficiency at minimum of van Deemter curve.

Column development

The general trend in column development is reduction of particle size. From tens of micrometer on the beginning of HPLC history to current highly efficient sub 2 μm particles. The advent of ultra high pressure liquid chromatography (UPLC) is closely related to pressure issue of HPLC columns packed with small particles (high pressure is a prize for speed and efficiency).

The question is is there always need for very high efficient columns. No. We need resolution and selectivity (as Peter Schoenmakers mentioned during HPLC 2010 and Tom Jupille during his talk).

Another issue related to HPLC columns packed with very small particles is contribution of extracolumn volumes to a separation (I already mentioned it a bit). By reducing extracolumn volume you can very easily improve separation power of your HPLC system with very low or no additional cost. However, the sub 2 μm superficially porous particles are probably going to be future packing material.

Monoliths, on the other hand, have efficiency as 3 μm particles with back-pressure of particles with 10 – 15 μm. According Tom Jupille, they are not going to dominate over other separation materials mainly because of patent issues.

From my point of view, I see room for monoliths in special application using stationary phases tailored for certain separation problem with desired selectivity (as well as efficiency and back pressure). Another advantage of monoliths is easy preparation in special format of separation devices (lab on chip).

I believe that 2nd generation of organic polymer monoliths (hypercrosslinked materials) may contribute significantly as a new family of stationary phases. I call them superficially porous monoliths.

David Sparkman – Mass spectrometry as a separation technique

I had an opportunity to share a table with a last speaker – David Sparkman. He likes the Czech Republic, which he visited during an international conference a few years ago.
David Sparkman said that mass spectrometry can be considered as a separation tool since the beginning of this technique. Main improvement of MS detection is attributed to development of MS/MS detection in 1978 . Surprisingly, in 1990s the GC-MS technique almost disappeared.

Nowadays, the main driving forces in development of mass spectrometry instrumentation focus on tandem quadrupole arrangement and/or ion mobility mass spectrometry. In later case, the ions are separated not only using MS, but also according their different mobilities based on size, charge and so on.

During his talk David Sparkman described later development in the field of mass spectrometry instrumentation. He started with Waters Xero TQ with quadrupole – collision cell – quadrupole arrangement, which improve signal to noise ration and allows analysis of femtograms of sample.

AB/Sciex developed Triple TOF, which is NOT instrument with three time-of-flight analyzers, but it looks like the analysis is done using three TOF systems. Triple TOF uses 40 GHz time to digital detector which allows very high sensitivity and detection.

QIT (Thermo, I believe) is quadrupole – ion trap mass spectrometer with dual cell arrangement (low and high pressure) and shows very high resolution.

Because of time, David Sparkman only quickly mentioned other producers, such as Bruker and his maXis, Shimadzu with LCMS 8030 system or Agilent 6490 using jet-stream technology.

From chromatographic point of view, the most important characteristics for mass spectrometry are robustness, repeatability and reproducibility of chromatographic separation for subsequent analysis with mass spectrometry.

“If you do LC and don’t know MS you may be out in the cold” David Sparkman

Conclusion

During the discussion I have asked about the sample preparation. With decrease in time of anlysis (seconds, minutes) the importance of fast and robust sample preparation increases. If your analysis is 5 minutes, you don’t want to prepare your sample for one hour. According the panelist this topic needs special attention, however because of time they did not elaborate on this topic further.

I am glad to be here in Bay Area and attend such meetings. I believe that in the future CASSS Discussion groups can be webcasted on the internet (live or for download). Since then you need to trust me ;-)

I would be more than happy to discuss your opinion about future of analytical chemistry (and separation techniques in particular). Please feel free to comment on this article. If you prefer more open communication, you can use chromatographer.com facebook page.

In May, I announced that CASSS organizes a discussion group about consulting.

Today, I would like to mention next discussion group focused on New directions/developments in Separation Science.

The meeting is taking place on September 15th, 2010 in Woodfin Suites in Emeryville, CA at 6 pm.

Personally, I am looking forward to attending this meeting. The topic as well as a list of panelist (see below) are very interesting. It will be nice to hear opinions about new directions in separation science from people with different background and experience.

I have to admit that my knowledge, interest, and predictions focus mainly on liquid chromatography (and monoliths, of course;)  so I am very curious about other topics, such as sample preparation, miniaturization and/or new materials in separations, which are possibly going to be part of the discussion too (I don’t know, just guessing;)

The information from CASSS website

Today’s sophisticated separation and analytical instruments and techniques bear scant resemblance to the “absorption analysis” technique reported by M.S. Tswett in 1903.  But that same drive for innovation and improvement is alive and well in 2010.

Join us for a lively discussion on the latest trends and technical innovations presented at the Pittcon, ASMS and HPLC conferences this year.  Question our expert panelists on where the trends might be taking the industry - and what to watch out for.

One thing is constant in this field … change.  From mergers and acquisitions to plenty of new products – stay abreast of the trends that will affect you most.

Invited panlists

• Tom Jupille, LC Resources
• O. David Sparkman, University of the Pacific, Stockton
• Robert Stevenson, R. Stevenson Consulting

Registration starts at 5:30 p.m., dinner at 6:00 p.m., and Panel discussion at 7:00 p.m.

The prize for registration before Wednesday, September 8 is $35 for Discussion only and $49 for Discussion and Dinner. On-site registration are not eligible for dinner. More info on CASSS website.

Future post

I will try to remember (ie. make notes of;) discussed topics and possible conclusions and bring them to you here on chromatographer.com soon after the meeting. Keep in touch.

PS: if you would like to be informed about new posts, you might consider subscribtion to RSS chanel or email newsletter.

I have to admit that this information is mainly interested for chromatographers located in California (especially Bay Area). The CASSS (An International Separation Science Society) organizes the Discussion group focused on the Keys to Successful Consulting.

Maybe you dont know it yet. Maybe your future job is a consulting.

Following information are from a Discussion group website:

If you’re serious about becoming a consultant (or even if you daydream about telling your boss to “take this job and shove it”), this course is a required investment in your future. While most scientists and engineers have traditionally sought full-time, long-term employment in industry, academia and government, many have found rewarding, flexible and dynamic careers as full- or part-time consultants.

This Workshop will be taught by Bob Stevenson, a successful consultant with a 20-year track record, “Keys to Consulting Success” takes you through the entire start up process. Consulting is a business – and successful businesses require serious commitment and planning. If you’re considering a consulting career or want to improve your existing business, join us for Keys to Consulting Success.

For complete meeting details and registration please visit: Discussion group website at www.casss.org

PS: Registration does close this Friday (May 28th).

Dr. J. Kirkland during the award talk

Yesterday, I had a great opportunity to participate in Discussion group organized by the An International Separation Science Society (CASSS). The main topic was the Scientific Achievements Award for one of the founders of modern HPLC – Dr. Jack Kirkland.

Jack Kirkland is the inventor of superficially porous particle stationary phases. These particles have solid core covered with small layer of porous nanoparticles. Maybe you know them as Poroshell or Halo columns. Columns packed with these particles show extremely strong separation power for different kinds of applications. In the past, I had a opportunity to compare various types of chromatographic stationary phases (including totally porous, non-porous, superficially porous particles and monolithic stationary phases) and I have to confirm their strengths.

In his very inspiriting presentation Dr. Kirkland mentioned not only history of development but also current state of the art and possible future steps for superficially porous particles as stationary phases. Do you know, that the size of the Halo particles (2.7 μm) is chosen according the theory calculations (the highest achievable efficiency for certain conditions) as well as because of the end frits in the column (the holes in the frits are 2 μm wide so the particles with 2.7 μm i.d. can’t go through them therefore same frits as for 5 μm i.d. particles can be used)?

One of the most important message in the presentation was that in chromatography the separation is always a compromise. Either you are looking for high throughput (then your choice will be probably UPLC or monoliths) or you are looking for the best selectivity and peak capacity (and you are going to choose porous particles). I know, this paragraph is very schematic conclusion, however it is usually like this. You have to always choose what you want and what is your goal in separation and to separate.

I was also happy to meet another founder of the (high performance) liquid chromatography: Dr. Lloyd R. Snyder.