SPECIFICATIONA matrix for cell cultivation in vitroField of the inventionThe present invention relates to the in vitro cultivation and growth of various of living cells, and in particular to methods and devices for in vitro growth of mammalian tissue cells that require (in addition to sterile liquid nutrient media) attachment to a solid surface in order to effectively grow, metabolize nutrients, reproduce, and produce biologically active materials. Such tissue cells are called "anchorage dependent" cells. The provision of suitable surfaces to which such cells will attach themselves, is an essential requisite for their in vitro cultivation.
Background of the inventionTissue cell culture is therefore carried out on solid continuous surfaces. On laboratory scale these are in the form of petri-dishes, flat sided bottle or roller bottles. Recent improvements, applicable also to large scale culture have been the development of spheres of various sizes such as microbeads, as well as of ceramic blocks traversed by small rectangular channels. In all these devices the cells adhere and propgate on the available surface of a solid.
Cells will attach only to surfaces that have suitable surface compositions and an electrical surface charge.
Materials that have proved successful for this purpose are glass, ceramics, polyvinyl chloride, polystyrene, dextran, collagen, and certain other materials. Frequently the cell attachment surfaces of such materials are treated with 95% sulfuric acid, or preferably with a corona or oxygen plasma discharge to improve cell adherence. Under culturing conditions such as those described in (Kruse & Patterson Tissue Culture - Methods and Applications, Academic Press 1983), cells coming in contact with these surfaces will attach themselves to the surface, and reproduce until they cover the surfaces in a contiguous, confluent monolayer. On reaching confluence cell growth ceases. The phenomenon of cell growth cessation when a contiguous layer of cells is achieved is called "contact inhibition" and is a characteristic of non-cancerous cell growth on two dimensional surfaces.
The growth surfaces used at present for in vitro tissue culture suffer from certain serious shortcomings:a) They provide limited area per unit volume of nutrient medium supplied, so that the number of cells that can be grown per unit volume of nutrient medium is as much as three orders of magnitude smaller than the volumetric densities of cells in in vitro tissue.
b) They require high concentrations of inoculated cells in order to initiate cell growth. Typically cells are introduced to a fresh culture surface at a concentration and number which is 20-30% of the final number reached at confluence and it is usually impossible to inoculate with less then 10% of the number reached at confluence.
c) Cell growth of non-cancerous cells limited to monolayers;d) Cells tend to detach from their anchorage surface under conditions that include: monolayer saturation; high or low serum concentration; medium depletion, and particularly, viscous shear caused by stirring or perfusion of the culture medium. Cell growth and biosynthesis stop on cell detachment.
Though non cancerous cells are grown on two dimenisonal surfaces, it has long been known that normal cells will also grow in gels, and specifically those of collagen. One such gel is available commerically (trade name "Gelfoam", Upjohn, Kalmazoo). Gels have however a poor dimensional stablility and, due to their internal structure are unsuitable for growing cells to a reasonable density and especially not for systems with medium perfusion. They have therefore not found use for the large scale culture of cells. Their use in limited to laboratory studies of cell morphology, or studies of the "hystotypic" growth of primary cultures (e.g. Dougles et al., In Vitro, 16, 306-312 (1980)).
Also relevant to this invention is the fact that certain cells and particularly cancerous mammalian cells and altered forms of cells such as hybridomas can be grown freely suspended in culture medium or immobilized in small beads of porous gelled material such as carrageenan, agarose, collagen, gelatin and similar starch or proteinor polymer materials. Cells may be mixed into such gels prior to casting the gels into the form of small beads orparticles that will be suspended in nutrient medium. (Karkare, S.B., Phillips, P.G., Burke, D.H., and Dean Jr., R.C.
"Continuous Production of Monoclonal Antibodies by Immobilized Hybridoma Culture" A.C.S. Annual MeetingPhila. Pa, Aug 27, 1984, available from Verax Corp. Hanover, N.H.).
Alternatively, cells may be immobilized in microcapsules as described by Lim et al., Microencapsulation ofLiving Cells and Tissues; J. Pharm. Sci., 70, 4: 351-354, April 1981; Nilsson., Entrapment of Animal Cells forProduction of Monoclonal Antibodies and other Biochemicals, Nature 302, 629-630, 1973.
The invention herein described also relates to the cultivation of such non-anchorage dependent cells and othercells whose growth and harvesting may be facilitated by some form of immobilization as described above.
Summary of the inventionAccording to the present invention htere are provided:A matrix for use in cell cultivation in vitro providing a high-surface-area substrate the effective area of which is from 10 to about 100 times the area of same projected onto a plane surface, comprising a physiologicallyacceptable network of fibers having a porosity of from 40 to about 95% and a pores size of the order of 10 p to100 p, or an open-pore foamed structure with a pore size of from about 10 p ot 100 p, the overall height of thematrix being of the order of from 50 p to about 500 p; A matrix where the 3-dimensional structure is one of a non-woven fabric from round, flat, non-round, or hollow fibers or combination of such fibers of the order of from 0.5 pm to 50 pm diameter or width;;A matrix where the structure is composed of ribbon formed fibers of 2 um to 20 pm width which may be crimped, and where the ratio of width to thickness is 2:1 or more;A matrix for anchorage dependent cell attachment that has a high surface density by which is meant a high specific surface area, or surface area per unit of projected surface or, high surface area per unit volume of surrounding medium;A surface that increases the density of cells grown per unit volume of medium by at least one order of magnitude greater than that achievable in flat plate cultures;A high specific surface cell attachment matrix that may be disposed as a flat sheet;A matrix that may be disposed as a spiral sheet or as corrugated sheets.;A matrix that may be disposed as suspended cell carrier in a stirred culture tank reactor;A matrix that can be easily sampled for determining cells numbers;;A matrix that can be easily samples for microscopic examination;A matrix that protects cells from impact and viscous shear;A matrix that inhibits detachment of cells from said surface;A matrix that permits cell growth to be initiated at low inoculation densities, and consequently permits cell densities and number to increase by more than 10 fold, thus reducing the number of cultures that need to be started to achieve high production of cells and cell products;A matrix that permits cell growth in multiple layers and in a three dimensional matrix;A matrix that permits cells to grow in three dimensional non-planar forms;A matrix that allows rapid inward diffusion of materials such as nutrients, hormones, growth factors and serum components and outward diffusion of metabolic wastes and cell products;;A matrix for growing anchorage-dependent or non-anchorage dependent cells, said matrix providing high internal surface area and high internal volume with pores that are 1 to 20 times the volume of individual cells, said pores being within 100 micrometer of the exterior surface of the matrix so as to provide rapid diffusion throughout and into and out of the matrix;A matrix for entrapping cells that are not anchorage-dependent, that facilitates the harvesting of such cells in suspension culture;A matrix for protecting and growing non-anchorage dependent cells at high density while exposed to fluid nutrients that are moving at high velocities and that are under high shear;A matrix for entrapping or anchoring cells that has a near neutral buoyancy so that particles made of this matrix may be suspended in nutrient medium with minimal amounts of stirring;;A matrix for anchoring or entrapping cells that has a variable buoyancy controlled by the pressure imposed on the cell culture vessel, so as to permit moving the matrix up and down through the nutrient liquid by lowering or raising the pressure in the cell culture vessel;A process for producing tissue plasminogen activator at high concentrations and in large volumes of culture, while conserving serum and preventing dilution of cell products in excess medium, and means for carrying our such process.
These and other objectives will became apparent from the following detailed disclosure.
General description of the inventionAccording to the invention there is provided a growth matrix that substantially increases the available attachment surface for the adherence of the cultivated cells: the increase is by a factor of from 10 to 30 times, calculated on the projection of the base on which structures of the invention are supported. Such an increase by a factor of 10 to 30 times, is per unit layer, and if a plurality of such layers, separated by spacers or the like, is used, the factor of 10 to 30 times applies per each such structure.When the matrix is used in sheet form, preferably non-woven fiber sheets, or sheets of open-pore framed polymers, the preferred thickness of the sheet is about 50 to 250 pom, there being provided adequate porosity for cell entrance, entrance of nutrients and for removal of waste products from the sheet said pores having an effective diameter of 10 pm to 100 vim. Such sheets can be be prepared from fibers of various thicknesses, the preferred fiber thickness or fiber diameter range being from 0.5 um to 20 pm, still more preferred being in the range of 10 pm to 15 pm diameter.
A plurality of such sheets can be used, stacked above each other, and in such case suitable spacing means are resorted to. A porous spacer of from 150 um to about a millimeter generally gives satisfactory results.
The structures of the invention may be supported by, or even better bonded to, a porous support sheet or screen providing for dimensional stability and physical strength.
Such matrix sheets may also be cut, punched, or shredded to provide particles with projected area of the order of about 0.2 mm2 to about 10 mm2, with the same order of thickness (about 50 to 250 pom), said particles being particularly useful in suspension of fluidized culture.
The present invention relates also to devices or matrices for entrapping and growing non-anchorage dependent cells in open encapsulation, providing a protected micro-environment for growth of cells and facilitating cell harvest.
To produce large quantities of non-anchorage dependent cells, the cells are usually grown in suspension in a nutrient liquid medium that is stirred to ensure that each cell is adequately bathed in nutrients, and that metabolic wastes are carried away from the cell. A certain fraction of the cells is destroyed by impact with the impeller or by high shear. Harvesting cells from conventional suspension culture requires special supplemental equipment such as centrifuges or micro-porous filters. Also cell concentration per cubic centimeter of nutrient liquid is relatively low.
One method of simplifying the harvesting of such cells and increasing their density involves encapsulating the cells in permeable microcapsules as described by the preciously cited works of Lim and Nilsson. These microcapsules are larger and denser than the cells they entrap. Consequently they are easily separated from the nutrient medium by settling or by filtration. The microcapsules have certain disadvantages:- they are costly and delicate to produce;- at high density growth, cells at the center of the capsule frequently die;- capsules may burst prematurely losing their content cells.
- each new inoculation requires a fresh encapsulation procedure.
The present invention pertains to the provision of forms of materials that provide improved surfaces and morphologies for cell attachment and/or entrapment during in vitro culture, said improved surfaces and morphologies overcoming the shortcomings of currently used attachment surfaces, as well as providing new capabilities for improved culture of other cells not requiring an anchorage surface.
Porous sheets as cell growth matricesWe have found that certain forms and composition of fibers and certain high porosity membranes provide highly effective supports for culturing cells and particularly anchorage dependent cells; particularly when said fibers are arranged in flat, highly porous, non-woven sheets, or mats, having an appearance like filter or tissue paper, or of thin porous felt. Said non-woven sheets can be made by any of the wide variety of well known techniques for making non-woven fabrics, papers, or felts, which include spin-bonding, thermal bonding, calendering, needling, etc., techniques. The sheets should preferably be free of glue or adhesive coatings not specifically used to promote cell adhesion to the fiber surfaces.
The fibers used to form the non-woven fiber sheets may be in the form of continuous filaments, staple filaments, hollow filaments, pulp, or floc, or combinations of such forms, and are preferably disposed in the sheet in a highly disordered, random-like, intertangled, manner; the axes of the fibers forming an open, multi-dimensional array. The porosity of the sheet should range from 40 to 95% with a preferred porosity of 60-80%. Preferred pore-size is between 10 and about 100 pom.
The individual fibers should have deniers (weight in grams of 9000 meters of fiber) of between 0.05 and 5 denier per filament (dpf) with a preferred weight of 1.0 to 1.5 dpf. Fiber cross-section may be round or not, with a preferred cross-section being that of a ribbon, that may in addition have a crimp imposed along its axis. Fiber width may range from 0.5 to 50 micrometers, but a preferred width is 10 to 15 micrometers. When hollow filaments are incorporated in the non-woven sheet, they may have single or multiple lumens and their denier will generally be greater than solid cross-section fiber, ranging as high as 50 denier per filament.
High porosity membranes suitable for this application must have a sponge-like structure and porosity, and pore dimensions similar to the non-woven fiber mats; that is 40 to 95% porosity and pore size between 10 and 80 micrometers. Pores must be opened and have high tortuosity. The polymer matrix should be continuous and can have any composition that promotes cell adhesion. Examples of polymers suitable for porous membrane growth are cellulose, cellulose acetate, polyethylene, polyesters, polyfluorochloroethylenes, polyvinylchlorides, polystyrenes, polysulfones, fiber glass, etc.
The thickness of the non-woven fiber sheet or porous membrane is an important parameter. Under proper culture conditions many cells inoculated on these sheets grow within the thickness of the sheet, rather than on the top surfaces of the sheet. Cells proliferate among the fibers of the sheet in three dimensions, rather than in two dimensions as in conventional tissue culture bottles, flasks, petri dishes and on microcarrier beads. Cells may attach themselves to more than one fiber (Figure 1) and cell growth thus takes place in the internal volume of the fiber matrix. The cells form a multilayered tissue-like structure whose thickness is that of the non-woven fiber sheet.To ensure adequate diffusion of nutirents and products to and from the interior of the cell aggregate and to prevent necrosis of cells in the interior of this dense structure, the sheet must be between about 25 and 250 vim thick. A preferred thickness is 100-150 pm. An ideal sheet thickness is approximately equal to the spacing of capillaries that occurs in vivo in the particular kind of tissue being cultured.
The non-woven porous growth matrix sheets may be used alone or they can be thermally bonded to rigid support materials that help the sheets retain their shape, or prevent the sheets from settling into dense contact with each other when used in a close packed array. A particularly useful configuration is to thermally laminate the growth matrix sheet to coarse (1 mm mesh) polypropylene screen (Figure 2). This also allows adjustment of the net density of the matrix so that it can be neutrally buoyant when used in a suspension culture.
The growth matrix sheets and the support and separator sheets may be provided with means to distribute liquid medium uniformly to all parts of a stack of such sheets and with means to promote the flow of medium parallel to the plane of each matrix sheet. Such means may be integral baffles or channelling orifices as shown by 20, and 21, in Figure 4a.
Growth matrix sheets can be used in many ways:- as liners on bottoms of petri dishes or on the inside surfaces of roller bottles, increasing growth surface area by more than one order of magnitude;- as spiral sheets inside roller bottles (Figure 3);- as in Figures 6 and 7, as sheets (11) laminated or layered external to and between flattened tubes (13) of permeable or microporous polymers wherein each alternate flattened tube serves as a conduit, the one for liquid nutrient medium (14), the other for gases (15) such as oxygen, air, CO2 and water vapor, the entire assembly being wound into a spiral as shown in Figure 6, or placed in a laminated interleaved stack (Figure 8) and immersed in a closed sterile container (16) Figure 7, filled with nutrient medium (17) and inoculated with cells for cultivation.Gases and nutrient medium are pumped through the flattened permeable tubes in a pulsatile fashion so that cells growing on the porous or non-woven fiber matrix sheet (11) are bathed in gently surging fluid that is never depleted of oxygen or nutrients and in which wastes do not accumulate through stagnation.
Four connections (Figures 6, 7, (18), generally running through the cover (19) of the assembly serve to introduce and remove gases, and nutrient medium to and from the flattened tubes (13). Probes for monitoring culture parameters such as PO2 (10), pH (11) and glucose concentration (12) may be placed in the growth medium (17) external to the flattened spiral tubes and used to control the nutrient (14) flow rate and composition, as well as the gas (15) CO2 and oxygen content. Polypropylene screens or similar spacers (12) are placed inside each flatted tube and between tubes to maintain minimum separation distances between each layer of the spiral or stack.Access to the cell growth matrix (11) and external or immersion growth medium (17) is made through ports (20) that may also be used to perfuse or remove the immersion medium, or for product collection, or for change of medium, or to samples cells.
- as packing in columns that are continuously perfused with medium, (Figure 4);- as microcarriers in suspension cultures replacing such materials as modified dextran beads. (Reference "Microcarrier Cell Culture" Pharmacia Chemicals, Uppsala, Sweden (1981)).
When used as microcarriers or as column packing the growth matrix is advantageously laminated to polyproplyene screen (as previously mentioned (Figure 2) that are then cut into small discs, squares, rings cruciforms, or corrugated and folded shapes, to give desired hydrodynamic characteristics to the packing or suspension material.
Alternatively the growth matrix material when used as microcarriers in suspension culture can be cut from fibrous non-woven sheets composed of mixtures of fibers whose density and relative proportions give the sheet a near neutral buoyancy. As an example, circular microdiscs having a diameter of 2 millimeters were stamped from a non-woven sheet composed of a ramdomly oriented mixture of 20 weight percent polyethylene terephthalate fibers and 80% fibers of polypropyline. Because the polyethylene terephthalate fibers had a specific gravity of 1.33 and the polypropylene fibers a specific gravity of 0.92, the composite non-woven fabric had a density of 1.002, so that microdiscs stamped from this sheet were kept suspended in liquid medium when stirred at much lower speeds then are required to maintain in suspension discs composed of solid polyethylene terephthalate fibers only.
Near neutral buoyancy microdiscs were also made by combining in suitable proportions hollow filament polymer fibers having gas filled lumens, with solid, low denier per filament polymer fibers (Figures 2a, 2b). The advantage of microcarriers bearing entrapped gas bubbles is that their buoyancy can be controlled. Because the volume of the entrapped gas increases or decreases as the external pressure on the suspension culture is decreased or increased, the microdiscs are made periodically to float and sink in the nutrient liquid without using an agitator or stirrer. This produces a very gentle washing action and is particularly effective for bringing nutrients to the surface of growing cells and removing metabolic wastes, with cell types that tend to become dislodged from attachment surfaces when stirred.It also eliminates the need for agitators and stirrers, simplifying and reducing the cost of large culture vessels.
A major advantage of this invention is the application of porous matrix cell attachment surfaces to microcarrier tissue cell "suspension culture" (Microcarrier suspension tissue cell culture procedures are described in "Microcarrier Cell Culture," Pharmacia Fine Chemicals, Uppsala, Sweden, (1981); and in the article "Large ScaleProduction of Tissue Cells" Scientific American Jan (1983)). For suspension culture application the porous sheet is cut into small pieces, each having a projected surface of between about 1 to 100 square millimeters, with a preferred projected area of about one to 20 square millimeters. The shape of said small pieces may take many forms, with a disc or circular form being preferred.The porous matrix cell attachment sheet material may be thermally bonded to materials such as polypropylene screening having a 1 mm or finer mesh, in order to strengthen the porous matrix material and also in order to increase its buoyancy as described previously. It is particularly advantageous to punch such discs using a heated die so that the fibers at the circumferential edge of the dsic are thermally bonded or partially fused to each other.
We have discovered on theorectical grounds and verified through experiments that such porous matrix microcarriers require substantially lower concentrations of inoculum (cells introduced at the start of a culture) to initiate successful cell growth. For example in a typical suspension culture of microcarriers (modified dextran beads), the inoculum contains 30% of the number of cells that are harvested at the end of the culture(Fleiscschaker, p. 117, Ph.D. Thesis, June 1982, M.I.T. Dept. of Nutrition and Food Science). We have discovered that when polyester fiber porous matrix microcarriers having a total attachment surface area equal to that of the modified dextran microbeads are used, the inoculum cell content need only be less than about 5% of the final number of cells harvested. This reduction in inoculum size is an immense advantage in large scaleproduction of tissue cells and cell products, in that production from a single culture can be increased by a factor of approximately 6 to 10, and contamination and reseeding problems are diminished.
The effectiveness of fiber or porous matrix microcarriers with low concentrations of cell inocula is not obvious, and is an important discovery. The explanation for this superior effectiveness is as follows:In a microcarrier suspension culture, for confluent cell growth to occur on an individual microcarrier particle, a minimum number of inoculum cells must collide with and fix themselves to that microcarrier particle. This minimum number of cells will depend to some extent on the cell type, however a typical number is 7 cells per microcarrier particle. (Fleiscschaker, J., pg 171, Ph.D Thesis June 1982, M.I.T. Dept., of Nutrition (FoodSceince).Because the collisions between microcarrier particles and inoculum cells are purely random processes, the fraction of microcarrier particles (fj) experiencing collisions with any number (i) of cells can be estimated by the Poisson Distribution (Equation I): fj = A(ei (i) ) (I) where i r the number of inoculant cells colliding with a microcarrier particle r average number of inoculum per microcarrier particle, or, inoculum cells per milliliter/microcarrierparticles per milliliterIf "n" collisions are required to initiate confluent growth, it follows that the fraction (P), of microcarriers experiencing confluent growth will be one minus the fraction of microcarriers having fewer than n collisions.
P= 1 En-1 (f) (II)when n = 7, and 105 cells/ml are inoculated on a normal concentration of 3 x 104 microcarrier bead particles per milliliter, 15 then 2, in equation I, is equal to 3.3 cells/microcarrier particle. From equation (I), the fractions of particles experiencing zero to six collisions are found to be: f,=.O; f, =.12; f,=.20; f, = .22; f,=.18; f,=.12; f,= 0.7; consequently equation (II) becomes: P=1-(f0+f1+f2+f3+f4+f5+f6) = 0.05 meaning that only one particle in 20 will have 7 or more collisions, and experience confluent cell growth. This culture will therefore fail. Such is in fact the general experience when attempting to inoculate conventional microcarrier cultures at these dilute cell concentrations and conditions (Fleiscschaker ibid. pg. 117).
This statistical reasoning explains the striking superiority of porous or fiber matrix microcarriers. Typically such carriers are 2.0 mm diameter microdiscs stamped from a 150 urn thick non-woven sheet composed of 10 urn diameter polyester fibers. The sheet presents an area for cell attachment of more than 3000 cm2/gram of sheet material. A concentration of 50 such microdiscs per milliliter of culture solution furnishes the same cell attachment area as 3 x 104 conventional microcarrier beads per milliliter. At 105 cells/ml inoculant concentration the average number of inoculant cells per microdisc, (2), is now 105/50, or 2000 cells/per microdisc (in contrast to 3.3 cells per microbead).
The collision frequency of a microdisc with these 2000 cells is magnitudes higher than that of a dextran microcarrier bead with its 3.3 cells. In fact insertion of 2 = 2000 in equation (I) shows that disc particles having fewer than even 100 cell collisions are vanishingly rare. Consequently at the same inoculant concentration and surface anchorage area, the probability of a microdisc experiencing more than 100 cell collisions is given by equation II as P is approximately equal to one. Therefore all the microdisc carriers are bombarded with cells and their growth surface reaches saturation on exposure to dilute inocula. Experimentally, 1% inoculation has succeeded in producing confluent growth.
This effect cannot be reproduced with microbeads or non-porous carriers because reducing the number of microbeads reduces the surface available for cell attachment hence microbead suspension culture is limited to a heavy inoculum.
Examples 1. Material to be used for cells culture matrices were first passed through a discharge from a plasma torch andwashed with methanol. The materials were sterilized under a UV light then immersed in a solution of 100 lig/ml poly-D-lysine, and rinsed with sterile water. Cell culture was carried out at 37"C, in an atmosphere of5% CO2 in air.
2. Unwoven sheets of polyester (0.15 mm nominal thickness, 15 urn fibers) or polypropylene (0.15 mm nominalthickness, 12 urn fibers) were cut into 30 mm diameter circles, and laid on the bottom of 30 mm petri dishes.
The same size tissue culture dishes were used as controls. Human dipolid fibroblasts (lung) (1.5 x 105 cells)were seeded in each plate with 2.5 ml of DMEM (Dulbeco modified Eagle's medium) + 10% serum and theprogress of the cultures was examined microscopically. It was observed (Figure 1) that the cells formed amulti-layered, tissue like structure. The culture was continued until the cells appeared as a congruent mass,whereupon the number of cells in each plate was determined by measuring the amount of DNA. The results(Table 1) show that 7-10 times more cells were obtained in the polymer matrix than on an equal projectedarea of a regular culture dish.
TABLE IMatrix No. cells/Cm 2 Level of confluencyas observed by microscopePolypropylene 4 x 105 70%Polyester 6 x 105 60%Nunc TC. dish 4 x 104 100%Sheets of non-woven fabric were cut into 21 x 34 cm rectangles, which were attached as 'lines' to the inside of 850 cm2 corning roller bottles. Uncoated roller bottles were used as controls. The fabric lined bottles wereeach seeded with 1) 0.3 x 107, 2)1 x 107 and 3)1.5 x 107 cells. The uncoated bottles were seeded with1.5 x 107 cells each. All bottles were then half-filled with medium, and cultures were carried out on a rotatingBelleo Roller apparatus 0.5/rev/min. Medium was replaced with fresh medium at 2 day intervals.Theuncoated bottle reached confluence, as judged by microscopic examination after 3 days and contained a cellcount of 5.7 x 107 cells. The 'lined' bottles were cultured for an additional 5 days. DNA determinationsshowed that 3-5 x 108 cells were obtained in each fabric lined bottle, irrespective of the amount seeded.
4. Sheets 200 cm long and 21 cm wide of non-woven fabric were laminated to a polypropylene screen (1 mmopening, 0.6 mm thick). The laminate was rolled into a spiral and placed within a roller bottle against the innersurface to form a spiral lining 7 layers deep. The roller bottles were seeded each with 1.5 x 107 cells, and halffilled with medium. The progress of culture was followed by removing periodically a piece of the liner, and thegrowth medium was replaced periodically (based on analysis of glucose and lactic acid) to avoid nutrientexhaustion. The cell proliferated with an average doubling time of 1.2 days and reached after 12 daysapproximately 4 x 109 cells per bottle.
5. Cell culture on non-woven fabrics in a flow-through reactor were tested in a laboratory scale assemblydepicted in Figure 5. Polypropylene or polyester support matrix was introduced into the reactor chamber(Figure 5) in wither of the following forms. i) Stacked circles of a laminate of the unwoven fabric andpolypropylene screens. Round holes, 3 mm diameter, were punched (1 or 5 holes per circle) in each circle toallow medium flow (Figure 4). ii) A rectangle of laminate was rolled into a tight spiral which fitted snugly intothe reactor chamber (Figure 4).
The cells were seeded into the reactor with enough growth medium to cover the matrix. The reactor wasclosed and the reservoir was filled with medium. After 4 hours of static incubation, medium circulation wasstarted. Pump speed was adjusted to give an initial medium residence time of 25 mins, and as the cellsproliferated pumping rate was increased to decrease residence time to about 1 min. The reactor chamber wassampled periodically, by taking out a piece of support, and determining DNA. After 8 days of culture the celldensity in the reactor chamber reached 2 x 106 cells/ml with stacked circles and nearly 7 x 106 cells/ml withthe spiral.
6. Flocks of fibers of rayon (18 urn thick, 0.5 - 2 mm long), nylon (15 urn 0.5 - 1.5 mm) and acrylic (10 - 20u x0.2 -1 mm) were treated as in Example 1. One tenth g. of each was layered on the bottem of 50 mm petridishes, seeded with cells and covered with 3 ml of DMEM + 10% serum. The number of cells that attached tothe fiber layer was determined after 24 hours. The attachment efficiency was 15-20% on the acrylic fibers, 35%on the rayon, and nearly 60% on the nylon fibers. A control with a regular tissue culture dish gave 70%attachment efficiency.
7. Sheets of non-woven fabric (400 cm2) were cut into small squares (approximately 3 x 3 mm) and loadedinto Techne 200 ml culture vessel with 100 ml of medium. Bottles were seeded with 1 x 106, 5 X 106 and 1.5 X 107 cells each. Stirring was 30 rpm, and for the first 4 hours the stirrer was on for 30 min and off for 5 min.
After that stirring was continuous. On the third day after seeding 70 ml of medium were replaced with freshmedium and thereafter 35 ml were replaced daily. Cell counts were carried our daily by DNA determination.
Cell attachment determined 24 hours after seeding was on the average 67% (56-81%) independent ofseeding density. The runs were continued for 4 days after seeding and cell doubling time was on the averageabout 32 hours. Final cell counts indicated that the cells in each bottle had increased approximately 10 times,and that the rate of increase was insensitive to low concentration of inoculum.
8. Two millimeter diameter microdiscs were punched from a non-woven fiber sheet composed of 1.5 devices perfilament polyester fibers and 15 devices per filament hollow polypropylene fibers, using a heated die thatthermally bonded the edges of the discs in the manner shown in Figure 2a giving the disc a doubly convex orlens-like appearance. The discs were then treated as in Example 1, and placed into Techne 200 ml stirredculture bottles at a concentration of 50 particles per ml in 100 ml of medium. IMR-90 human lung fibroblastcells were inoculated at a concentration of 105 cells/ml.
Stirring was intermittent and then continuous as in Example 7. Medium was replaced as in Example 7. After 8days, cells were counted and were found to have a concentration of 4 x 106 cells per milliliter, proving that aninoculation of 2.5% of final concentration was feasible.
9. A spiral laminated structure comprised of two flattened, one-inch-wide, cellulose dialysis tubes (13); to stripsof surface treated non-woven polyester fabric (11) (1 Oum fiber diameter); and four strips of polypropylenespacer screening (12) (0.6 um diameter monofilament, 1 mm opening) was assembled in the form shown inFigure 6 where, each flattened tube (13) had within itself a strip of spacer screening (12), and was bound onits external flat surfaces by a strip of non-woven fiber-grwoth matrix (11) and spacer screen (12). The entireassembly was placed in a sterile container (16) and imersed in growth medium (17) as shown in Figure 7.
The dialyses tubes were each 50 cm long. Nutritional medium without serum was pumped through oneflattened tube at a linear flow rate of about 1 cm per second. A sterile mixture of air and 5% CO2 was pumpedthrough the other flattened permeable spiral tube. By suitable means the discharge flow from the gas tube wasrestricted at two minute intervals so as to cause the spiral tube carrying the gas to periodically swell andcontract so as to cause a gentle, reversible, periodic displacement of the growth medium in which the spiral isimmersed.
The laminated spiral assembly of fiber growth matrix, spacers, and tube, was immersed in 100 ml of DMEMgrowth medium containing 10% serum. Hybridomas were inoculated into the serum containing growth medium at a density of 1.5 x 105 cells/ml. After nine days the cell concentration in the immersion medium had grown to above 107 cells/ml. The circulating medium contained no serum. The immersion growth medium contained serum and was perfused at a rate that replaced the serum once every 24 hours. After nine days, when full growth had been attained the immersion growth medium was changed to a production immersion medium that contained no serum. The perfusion rate was continued with removal of mono-clonal antibody from the immersion medium. The concentration of monoclonal antibody remained stable for 6 weeks at which time the experiment was stopped, although it could have continued.
The spiral assembly separated the growth medium, nutrient medium and gas channels, allowing each to be perfused separately which mass-transfer diffusive contact was maintained among the channels. Serum was conserved and antibody titer was maintained at an optimal level.
LEGENDS TO THE FIGURESFigures 1 A & B Fibroblasts grown on polyester sheets.
Discs of polyester sheets were cut to fit into 30 mm petri dish. Cells were seeded and allowed toproliferate for (A) 4 days (B) 12 days. The cells were then fixed and stained with gimza stain formicroscopic obervation.
Figure 2 Matrix sheet (1) laminated to polypropylene screen (2).
Figure 2A Doubly convex suspension culture fibrous microdisc comprised of randomly oriented filamentsof variety of polymers some of which are capable of thermal bonding, and some of which arehollow and open ended entrapping air or gas bubbles whose size and buoyancy is determined byexternal pressure in the suspension culture vessel. The thermally bonded edge-formed by stmping through a heated die or punch.
Figure 2B Hollow fiber showing gas bubbles trapped in lumen.
Figure 3 Spiral sheets of matrix inside roller bottle.
Matrix sheets (1), Polyproylene screen (2)Figure 4 Matrix sheets as packing in column.
A-circular -B. Spiral. Matrix sheets (1), Polypropylene screen (2).
Figure 5 Laboratory scale reactor with medium perfusion.
Figure 6 Spiral assembly of growth matrix and flatten ed permeable tubes carrying nutrient medium andair. Cell growth occurs in the matrix laminated ourside the flattened tubes.
Figure 7 Laminated spiral assembly as in Figure 6, shown inserted in sterile contained containingimmersion growth medium, said container having suitable connections for perfusing all fluidchannels.
Figure 7a Cross-section of laminated spiral assembly of Figure 6 and 7.
Figure 8 Laminated stack of growth matrix sheets interleaved with flattened medium and gas tubes, andseparator screens.