Literature DB >> 11006

The processing of human bone marrow for cryopreservation and reinfusion.

R S Weiner, J S Tobias, R A Yankee.   

Abstract

Bone marrow was aspirated from 22 patients with solid tumors. A median of 1.2 x 10(10) net bone marrow cells were obtained during a 1 hour 45 minute operative procedure. Three methods were used to concentrate the bone marrow for cryopreservation. The greatest concentration of mononuclear cells was obtained by the Haemonetics pheresis procedure. Bone marrow was cryopreserved in 10 % DMSO in volumes ranging from 150 to 700 ml. The thawed marrow was further processed to remove both DMSO and free hemoglobin prior to reinfusion. Cell clumping was observed in the first 6 of the 10 marrows thawed. Acidification of the thawed marrow to pH 6.65 was found to retard cell clumping. The immediate recovery of cells frozen was 66 % with a viability of 50 %. The mean number of viable mononuclear bone marrow cells per kilogram available for reinfusion was therefore 5.5 x 10(7).

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Year:  1976        PMID: 11006

Source DB:  PubMed          Journal:  Biomedicine        ISSN: 0300-0893


  5 in total

1.  Intensive chemotherapy with autologous bone marrow rescue for recurrent malignant gliomas.

Authors:  K Nomura; T Watanabe; O Nakamura; M Ohira; S Shibui; K Takakura; Y Miki
Journal:  Neurosurg Rev       Date:  1984       Impact factor: 3.042

2.  Bone marrow processing and cryopreservation.

Authors:  D C Linch; L J Knott; K G Patterson; D A Cowan; P G Harper
Journal:  J Clin Pathol       Date:  1982-02       Impact factor: 3.411

3.  Effect of acyclovir and interferon on human hematopoietic progenitor cells.

Authors:  L M Parker; J M Lipton; N Binder; E L Crawford; M Kudisch; M J Levin
Journal:  Antimicrob Agents Chemother       Date:  1982-01       Impact factor: 5.191

4.  Cryoprotection of human bone marrow committed stem cells (CFU-c) by dextran, glycerol and dimethyl sulfoxide.

Authors:  R Odavic; J Blom; E A Beck; U Bucher
Journal:  Experientia       Date:  1980-09-15

5.  Cryopreservation of equine mesenchymal stem cells in 95% autologous serum and 5% DMSO does not alter post-thaw growth or morphology in vitro compared to fetal bovine serum or allogeneic serum at 20 or 95% and DMSO at 10 or 5.

Authors:  Alexis Mitchell; Kristen A Rivas; Roger Smith; Ashlee E Watts
Journal:  Stem Cell Res Ther       Date:  2015-11-26       Impact factor: 6.832

  5 in total

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