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1950s - Spinner Flasks to Bioreactors
John A. Ryan, Ph.D.
McLimans' group developed the first "spinner flasks" in 1957.
Biotech companies, such as Genentech and Lonza, now routinely grow CHO and other
cell lines as suspension cultures in massive bioreactors as large as 20,000
liters to produce monoclonal antibodies and genetically engineered
protein-based drugs worth billions of dollars each year. The technology for
producing these products evolved rapidly in the 1950s, the work of those
researchers who contributed to this evolution are discussed below (1).
1953
The first successful suspension cultures, lymphoblastic MBIII cells, were grown
by Owens, Gey and Gey in 1953 (2). They used rapidly rotating (38 RPM) culture
tubes that were attached perpendicular to the axis of rotation of a roller drum
so that they tumbled end over end. This “tumble tube” approached allowed the
cells to grow in suspension at rates similar to attached cells.
1954
Earle and his group (3) extended these studies to L929 mouse cells growing them
in roller tubes (10+ RPM) to prove that normally attached cells could grow in
suspension. They then switched to growing them in small Erlenmeyer flasks on
rotary shakers (4).
The growth of cells in Erlenmeyer flasks on shaker platforms is still very
popular especially for insect cells and other cultures that require higher
levels of gas exchange. Both reusable glass and disposable plastic
Erlenmeyer flasks, with or without baffles for increased gas exchange,
and with a variety of cap and top styles are available
By 1960 commercially available magnetically driven spinner flasks with stir
bars were available.
1956
Cherry and Hull (5) used a magnetic stir bar suspended from a fishing swivel to
keep cells in suspension in a round bottom flask so that they could study the
effects of varying the medium, speed and seeding densities on cell growth.
1957
McLimans and his group (6) took the magnetic stir bar and attached it to a
sliding wire so that it could be raised a lowered to match the medium volume.
They added a side port for sampling and called it a “spinner flask”. This was
used to grow suspension cultures for HeLa and L cells in volumes up to 400mL.
Next they adapted this approach to work in commercially available 5L microbial
fermentors with baffles and spargers driven by an overhead impeller (7). This
showed that suspension cell culture could be successfully scaled up to grow at
levels that were commercially useful.
1967
None of the above techniques allowed for the growth of primary or
anchorage-dependent cell cultures in suspension since these cells must attach
to a substrate to multiply. This bottleneck was solved by van Wezel (8) who
used small (200-250µm diameter) solid particles, called microcarriers, as a
substrate for cell attachment. These particles were originally made from
Sephadex beads but have also been made from a variety of other materials
including polystyrene, glass and cross-linked collagen.
The use of these beads in culture required the use of more gentle stirring
techniques and by the 1980s spinner vessels were available with a variety of
stirring designs including magnetically driven paddles and ball and pendulums.
These new designs allowed stirring at much slower speeds reducing the damage
from bead-bead collsions and sheer effects. Today several biotherapeutic
protein drugs and vaccines are produced on cells grown in suspension on
microcarriers.
By using microcarrier beads, anchorage dependent cells could be grown in
suspension.
Paddles increased the performance of
glass spinner flasks in the 1980s allowing them to operate at slower
speeds with less damage to sensitive cells
Today
To meet the today’s demand for cell-based drugs, biotechnology and
pharmaceutical companies prefer to use large scale stirred tank bioreactors
with capacities from 1 liter to as high as 20,000 liters. In addition, other
technologies such as air lift fermentors and large bags placed on rocking
platforms are also used.
Suggested Readings
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Kuchler, R. and Merchant, D. (1958) Growth of tissue cells in suspension.
University of Michigan Medical Bulletin Vol. 24:200-212.
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Owens, O. et al. (1953) A new method for the cultivation of cells suspended in
agitated fluid medium. (Abstract) Proc. Am. Assoc. Can. Res. Vol.
1:141.
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Earle, W. R. et al. (1954) The growth of pure strain L cells in fluid-suspension
cultures. J. Nat. Cancer Inst. Vol. 14:1159-1171
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Earle, W. R. et al. (1954) Certain factors limiting the size of the tissue
culture and the development of massive cultures. Ann. New York Acad.
Sci. Vol. 58:1000-1011.
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Cherry, W. R. and Hull, R. N. (1956) Studies on the growth of mammalian cells in
agitated fluid medium. (Abstract TC 11) Anat. Rec. Vol. 124:483.
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McLimans, W. F. et al. (1957) The submerged culture of mammalian cells: The
spinner culture. J. Immunology, Vol.:79:428-433.
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McLimans, W. F. et al. (1957) The submerged culture of mammalian cells: The
five-liter fermentor. J.Bacteriology, Vol.:768-774.
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van Wezel, A. L. (1967) Growth of cell-strains and primary cells on
micro-carriers in homogeneous culture. Nature, Vol.216:64.
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