Future Trends

HPLC will continue to be one of the most important laboratory separation techniques for analytical and preparative purposes. Biotechnology and the life sciences is where HPLC will be a crucial procedure. Biotechnology companies will use HPLC to continue to prove to the government that their products are nontoxic, pure, and active. Fast and microbore columns will be important in the analytical and mass-scale preparative applications for biologicals and heterologously expressed gene products. Affinity and immunoaffinity techniques will be utilized more frequently for the production of biotechnological pharmaceuticals because of the need for ultrapurification in order to remove all unwanted material from the host cell. HPLC will continue to be the mainstay in purification and separation of proteins, peptides, and nucleotides. Smaller analytical columns will be needed to map the human genome. The need for more accurate and higher capacity chiral separation columns will be needed by the pharmaceutical companies in order to optimize efficiency in mass-production of "active" enantiomeric compounds.Specialization in detection and identification methods will increase in importance. This would involve the monitoring of environmental pollutants, using special chelate packing to detect metal contaminants in water, developing fast separations to monitor fermentation, and developing rapid methods in the identification of viruses and bacteria. HPLC-MS will be important in forensic medicine and athletic governing boards. Use of HPLC-MS will allow certain analyses and evidence to stand up in court. HPLC alone or in combination with other methods can monitor for drugs in athletes.Silica was the resin/support of the 1980's; possibly, organic resins will take flight in years to come since they are unreactive, they operate at a wide range of pH's, reproducibility is favorable, they can be stereoselective, and they can be used with SEC (Knox, 1989).Polytyptic chromatography will increase in popularity as should lasers because of their increased selectivity and sensitivity. The light- scattering detectors may well replace the RI detectors in the future. Multiple detectors per system is a possiblity and computer-generated optimization of HPLC conditions will increase and keep pace with the computer literacy movement. Use of robots may be near; one important function could be to handle and load hazardous sample such as AIDS samples, viral/bacterial samples, radioisotopes, or environmental contaminants. All information in this section, with the one referenced exception, mostly reflects the information and opinion received from the following article: Brown, P.R. Analytical Chemistry, 1990, Vol. 62, pp. 995-1008. Knox, J.H. and Kauer, B.; High Performance Liquid Chromatography; Brown. P.R. and Hartwick, R.A. Eds.; Wiley Interscience: New York, 1989, Chapter 4. Return to Theory of Operation Menu Return to Users Guide PageExit to the University of Kentucky College of Pharmacy