ABSTRACT
The eigensolution of nonaxisymmetric entry flow of a Newtonian viscous fluid with very small Reynolds number in a semiinfinite rigid circular pipe is obtained. Leading eigenvalues are computed for steady flow and two periodic cases. The result shows that the entry length for nonaxisymmetric flows should be longer than the entry length for axisymmetric flows.
Subject(s)
Lung/physiology , Mathematics , Models, Biological , Animals , Humans , Lung/anatomy & histology , ViscositySubject(s)
Aerosols/analysis , Biomedical Engineering , Lung/analysis , Respiration , Diffusion , Gravitation , Humans , Mathematics , Motion , Particle Size , Time FactorsSubject(s)
Anesthesia, Inhalation/methods , Halothane/blood , Models, Biological , Computers, Analog , Drug Administration Schedule , Halothane/administration & dosage , Halothane/metabolism , Humans , Kinetics , Lung/physiology , Nitrous Oxide/administration & dosage , Pharmacology , Pulmonary Alveoli/metabolism , Respiratory Dead Space , Tissue DistributionABSTRACT
It is appropriate to consider dose-regulated or quantitative closed-circuit anesthesia in terms of uptake of inhalation anesthetics from a reservoir bag which is never allowed to fill completely. The method which the authors have used routinely for 8 years requires reduction of the dose as a function of the inverse square root of elapsed anaesthesia time. Nitrogen does not accumulate because there is an inevitable loss of 20 to 100 ml/min between cuff and trachea. A simpler method, which has been well received, is that of "minimal flow" anesthesia (Virtue) with a constant fresh gas flow of 300 ml/min O2 and 200 ml/min N2O. "Low-flow" techniques typically entail use of 500 ml each of O2 and N2O per min.
Subject(s)
Anesthesia, Inhalation/instrumentation , Anesthetics/blood , Humans , Mathematics , Methods , Nitrogen , Respiration, Artificial , Time FactorsABSTRACT
The problem of whether the initiation of bacterial protein synthesis involves the obligatory formation of a 30S initiation complex intermediate was examined in a model system with N-acetylphenylalanyl-tRNA as initiator 5RNA nad poly(uridylic acid) as mRNA. The time courses of the formation of the 30S and 70S initiation complex with Escherichia coli ribosomes were measured simultaneously by stopping the reaction with dextran sulfate and differentiating the N-acetylphenylalanyl-tRNA bound to 30S ribosomal subunits from that bound to 70S ribosomes with RNase I, which hydrolyzes N-acetylphenylalanyl-tRNA bound to 30S subunits but not that bound to 70S ribosomes. A maximum in the 30S complex concentration was observed within the first 10-15 sec of the reaction, whereas 70S complex formed formed more slowly with a slight initial time lag. When an analog computer was programmed with rate constants determined separately for the formation of the 30S initiation complex from preformed 30S complex, kinetic curves very similar to the empirical curves were obtained for the entire time course of the reaction. The results show clearly that formation of the 70S complex obeys the kinetic laws for consecutive reactions, and the 30S complex is, therefore, an obligatory intermediate in the initiation of polyphenylalanine synthesis in the model system.