1973
DOI: 10.1016/0041-008x(73)90088-4
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Distribution and retention of fluorocarbon in mice and dogs after injection or liquid ventilation

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1976
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Cited by 45 publications
(16 citation statements)
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“…The biodistribution of PFC to other organs is a function of tissue perfusion, tissue-blood partition coefficients, lipid concentration and compartmental volume [54,56]. In the current studies, the concentration of PFC was both time-and tissue-dependent; tissue levels of PFC increased from 24 to 72 h. Additionally, the PFC concentrations correlated with the tissue-specific lipid concentrations ( fig.…”
Section: Discussionmentioning
confidence: 63%
“…The biodistribution of PFC to other organs is a function of tissue perfusion, tissue-blood partition coefficients, lipid concentration and compartmental volume [54,56]. In the current studies, the concentration of PFC was both time-and tissue-dependent; tissue levels of PFC increased from 24 to 72 h. Additionally, the PFC concentrations correlated with the tissue-specific lipid concentrations ( fig.…”
Section: Discussionmentioning
confidence: 63%
“…The effect of fluorocarbon liquid ventilation on pulmonary gas exchange (10,17), surfaceactive properties (15), function (10,21,24,27), and structure (19) has been studied previously. In addition, in order to pave the way for clinical applications, long term experiments have been conducted looking for residual fluorocarbon as well as morphologic, biochemical, and/or histologic evidence of toxicity after ventilation with fluorocarbon liquid (I I, 16).…”
mentioning
confidence: 99%
“…One might question whether this form of ventilation mav have a long-term deleterious effect on the developing newbornHlung, but Ge cannot directly address these issues. It is noteworthy that long-term experiments in adult dogs (6,8,11) indicated scant morphologic, biochemical, and/or histologic evidence of toxicity after ventilation with fluorocarbon liquid. ' FRC, functional residual capacity.…”
Section: Discussionmentioning
confidence: 99%