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A modified matrix perfusion–microcarrier bead cell culture system. I. Adaptation of the matrix perfusion system for growth of human foreskin fibroblasts
Author(s) -
Strand Janie M.,
Quarles John M.,
McConnell Stewart
Publication year - 1984
Publication title -
biotechnology and bioengineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.136
H-Index - 189
eISSN - 1097-0290
pISSN - 0006-3592
DOI - 10.1002/bit.260260515
Subject(s) - microcarrier , foreskin , perfusion , matrix (chemical analysis) , cell culture , fibroblast , biomedical engineering , membrane , extracellular matrix , materials science , chemistry , cell , biophysics , microbiology and biotechnology , chromatography , biology , biochemistry , medicine , genetics
Two strains of human foreskin fibroblast cells were incapable of sustained growth in a matrix perfusion culture system, possibly because of their inability to attach to the fiber surfaces. Addition of microcarrier beads to the extracapillary space allowed attaining high cell densities in excess of 10 7 cells per culture unit. Microcarrier beads were tested in hollow fiber culture devices containing membranes of 10 4 or 10 5 D nominal porosities. Best results were obtained when initial cell densities of at least (2–3) × 10 6 cells were used in units with 10 5 D pore size membranes and DEAE–Sephadex or polyacryl‐amide microcarrier beads in the extracapillary space. This extension of the matrix perfusion system should be useful for growing other anchorage dependent cells while retaining the advantages of perfusion culture.