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Biomedical subjects

L Prins

Publications and source records attributed to L Prins.

6 recordsLinked to original sources
PubMed1991

The entire nucleotide sequence of foxtail mosaic virus RNA.

The nucleotide sequence of the RNA genome of foxtail mosaic virus (FMV), a member of the potexvirus family, is 6151 nucleotides long, exclusive of a poly(A) tail. The RNA contains five principal open reading frames (ORFs), designated from the 5' terminus as encoding proteins with Mr values of 152.3K (ORF1), 26.4K (ORF2) which overlaps an 11.3K (ORF3) product, 5.8K (ORF4) which overlaps a 28.8K readthrough protein (ORF5A) which leads into the coat protein cistron of 23.7K (ORF5). The sizes and composition of the proteins encoded by the ORFs are generally similar to those found in other potexviruses; the least similar is the coat protein which nonetheless retains apparently critical consensus regions. The 5' terminus of the previously reported 0.9 kb subgenomic (sg) RNA was determined by S1 nuclease mapping and shown to begin with the sequence GAAGA, 43 nucleotides upstream from the first nucleotide of the coat protein initiation codon. The positions of the 5' end of this sgRNA and of that deduced from the nucleotide sequence for a 1.9 kb sgRNA are entirely consistent with the previously published sizes of these sgRNAs.

Amino Acid Sequence↗
PubMed1990

Disposition and metabolic profiling of the penetration enhancer Azone. I. In vitro studies: urinary profiles of hamster, rat, monkey, and man.

Chain-labeled 14C-Azone was intravenously administered to hamster, monkey, and rat, to compare its metabolic profile with that obtained previously in humans after dermal application. Azone-derived radioactivity was excreted predominantly in the urine for both hamster and monkey, which is similar to the disposition in humans. Metabolic profiling in urine revealed extensive systemic metabolism to occur in all species studied. The main fraction of the metabolites was most polar in man, followed by rat, monkey, and hamster. Traces of the parent compound were detectable only in hamster urine. Although some of the polar major human metabolites were also present in rat urine, the animals were unsuitable for collecting metabolites of Azone observed in humans. In rats, complete cleavage of the dodecyl side chain was ruled out by administering Azone that had been labeled at two distinct positions of the molecule. Additionally, oral administration of Azone to rats resulted in the same metabolic profile as intravenous administration, indicating that gastrointestinal metabolism does not occur or is similar to systemic metabolism.

Animals↗
PubMed1980

Hypoxic gas mixtures delivered by anaesthetic machines equipped with a downstream oxygen flowmeter.

The oxygen concentration of fresh gas mixtures delivered to a Bain circuit by a Boyle's anaesthetic machine equipped with leaking oxygen flowmeters was measured at the common gas outlet during free flow and during controlled ventilation of a model lung. The results demonstrate that, despite satisfactory oxygen and nitrous oxide rotameter settings, such a machine can deliver hypoxic fresh gas mixtures irrespective of whether the leaking flowmeter is mounted downstream or upstream. This selective loss of oxygen increases with the size of the leak and increases with the back pressure on the flowmeter assembly during controlled ventilation. A downstream position of the oxygen flowmeter should not be regarded as foolproof. Continuous monitoring of the oxygen concentration of fresh gas mixtures with an in-line oxygen analyzer is recommended.

Anesthesiology↗
PubMed1980

An evaluation of gas density dependence of anaesthetic vaporizers.

Four commonly used vaporizers were studied for the effect of carrier gas density on vaporizer output. Vapour concentrations from a halothane Cyprane (Fluotec) Mark 2 increased in relation to the density of carrier gas, whereas the concentrations delivered by an enflurane Ohio vaporizer decreased. The halothane Cyprane (Fluotec) Mark 3 and enflurane Cyprane vaporizers were largely independent of density. Of clinical importance, nitrous oxide/oxygen (75/25), compared with oxygen alone, increased the vapour concentration outputs of the halothane Mark 2 up to 30% and decreased the outputs of the enflurane Ohio unit up to 20%.

Anesthesia, Inhalation↗