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S J Meier

Publications and source records attributed to S J Meier.

7 recordsLinked to original sources

Cell death from bursting bubbles: role of cell attachment to rising bubbles in sparged reactors.

Bursting bubbles are thought to be the dominant cause of cell death in sparged animal or insect cell cultures. Cells that die during the bubble burst can come from three sources: cells suspended near the bubble; cells trapped in the bubble lamella; and cells that attached to the rising bubble. This article examines cell attachment to rising bubbles using a model in which cell attachment depends on cell radius, bubble radius, and cell-bubble attachment time. For bubble columns over 1 m in height and without protective additives, the model predicts significant attachment for 0.5- to 3-mm radius bubbles, but no significant attachment in the presence of protective additives. For bubble columns over 10 cm in height, and without protective additives, the model predicts significant attachment for 50- to 100-micron radius bubbles, but not all protective additives prevent attachment for these bubbles. The model is consistent with three sets of published data and with our experimental results. Using hybridoma cells, serum-free medium with antifoam, and 1.60 +/- 0.05 mm (standard error) radius bubbles, we measured death rates consistent with cell attachment to rising bubbles, as predicted by the model. With 1.40 +/- 0.05 mm (SE) radius bubbles and either 0.1% w/v Pluronic-F68 or 0.1% w/v methylcellulose added to the medium, we measured death rates consistent with no significant cell attachment to rising bubbles, as predicted by the model.

Animals↗

Hepatocyte function in a hollow fiber bioreactor: a potential bioartificial liver.

We have developed a novel hepatocyte loaded hollow fiber bioreactor as a potential bioartificial liver. Freshly harvested rat hepatocytes were entrapped in a three-dimensional gel matrix within hollow fibers in a perfused bioreactor. Gel entrapment allowed cells to be cultured at high density while maintaining tissue-specific function. Hepatocyte function was evaluated in 10 bioreactors, each containing approximately 5 x 10(7) cells. Oxygen consumption averaged 0.32 pmole/cell/hr, albumin appearance averaged 0.60 pg/cell/hr, and lidocaine clearance (a measure of the P-450 activity) averaged 0.74 pg/cell/hr. Function persisted for the 7 days of the study. Electron microscopy at 7 days showed the distinctive ultrastructure of viable, differentiated hepatocytes: bile canaliculi, intercellular junctions, peroxisomes, abundant mitochondria, and glycogen granules. Maintenance of tissue specific function and ultrastructure suggests that this bioreactor configuration has potential as a device to support patients in liver failure, as well as to study hepatocytes in vitro.

Amino Acids↗

Hepatic resection of metastatic colorectal carcinoma: a ten-year experience.

Nineteen patients have undergone partial hepatectomy for metastatic colorectal carcinoma at UCLA during the past ten years, including five trisegmentectomies (TS), eight lobectomies (L), and six segmentectomies (SG), with only one (5.3%) mortality. Twelve lesions were solitary (S) and seven multiple (M). Mean survival is 27.4 months, with three patients surviving over five years and one nearly eight years. Better mean survival exists for S (33.2 months) compared with M (15.8 months) lesions; for lesser resections: SG (44.7 months), compared with L (24.3 months) and TS (11.0 months); and for those with delayed appearance of hepatic metastases: beyond two years (40.5 months), less than one year (24.8 months), and synchronous (23.1 months). Survival figures should improve, as none of the 12 surviving patients have evidence of recurrent disease and many have short follow-up. This experience defends aggressive surgical treatment of resectable colorectal carcinoma metastatic to liver, because systemic therapy is markedly less effective.

Adult↗

Evaluation of an automated coulometric back-titration analysis of bicarbonate.

The bicarbonate module of the Stat/Ion was assessed in a clinical laboratory setting. Within run precision was evaluated by doing replicate analyses of patients' sera. Day-to-day precision was studied by making daily replicate analyses of buffered serum controls. The values for bicarbonate on the Stat/Ion were compared to Skeggs' method for determining carbon dioxide content on the AutoAnalyzer I. It was also compared to the value calculated from the pH and carbon dioxide pressure values obtained on the IL313-03 Blood pH/Gas system. Bilirubin interference was studied.

Autoanalysis↗