Recognition and reward deservedly come to those biomedical scientists who succeed in groundbreaking research to discover new
proteins, pathways, techniques or mechanisms. There are a host of awards and honors from professional societies, trade organizations,
national charities focused on diseases, and the ultimate in prestigious awards, the Nobel Prizes. Yet what is the practical
value of such discoveries unless they are applied and developed to bring new medicines to the world?
As bioprocessors, we are appliers of those discoveries, the developers who put into practice the discoveries of research and
turn them into new biopharmaceutical products. We are the "D" of "R&D" —the ones who apply what research has discovered to
create something useful. We look both ways, to research and manufacturing, to bridge these worlds with processes that are
both robust and scalable.
Michiel E. Ultee, PhD
Our work covers all aspects of biopharmaceuticals, from the earliest cell cultures to the finished vials of product. Research
often presents us with low-titer cultures, sometimes with untenable ingredients like serum, and purification processes based
on nonscalable techniques, such as affinity tags, dialysis, or precipitation. Processing is understandably minimal in research,
given the focus on key properties of the molecule of interest rather than residual impurities or minor variants. Similarly,
analytics, beyond those assessing the activity of the protein, are often limited as well.
What research does do is suggest a new potential therapeutic, a new approach to a disease or condition, and hence new hope
for patients. Yet none of these admirable concepts can be realized until that discovery is developed into a safe and effective
new biopharmaceutical. This is where we come into the picture.
Our upstream developers push titers with new cell lines, media and feeds, applying expert knowledge to bioreactor parameters
to render the cells both prolific and productive. Our downstream scientists apply advanced chromatographic and filtration
methods to yield "squeaky clean" proteins with only ppm levels of impurities, yet with reasonable recoveries. Our analytical
biochemists analyze these trace impurities and apply sophisticated instrumentation to assess the multitude of molecular properties
of the typically complex glycoproteins that we are developing.
Finally, formulation is an essential component of any biopharmaceutical. Stability is not a given, even for well-behaved proteins.
We need to ensure that the chemical "neighborhood" in which we place a protein is one where it will both retain its activities
and properties and not develop any new ones.
It is ironic that Alfred Nobel, himself a formulator and developer, chose to honor basic rather than applied research with
his scientific prizes. In his own work, the key discovery, nitroglycerine, had been discovered more than twenty years before
Nobel began working with it. There was just no safe way to handle it. His genius was in developing an effective, robust and
scalable formulation that would allow this potent explosive to be safely and practically used. If basic research is our "Nitro,"
then bioprocessing should be considered the "Dynamite" of biopharmaceuticals.
Michiel E. Ultee, PhD, chief scientific officer, Laureate Biopharmaceutical Services, Princeton, NJ, Michiel.Ultee@LBioS.com