Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “AMMONIUM COMPOUNDS”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 1,171 records · Page 65Linked to original sources

Pharmacokinetics of prifinium bromide in healthy volunteers.

The pharmacokinetics of prifinium bromide (Riabal), a specific antispasmodic agent, after oral (60 mg) and i.v. (7.5 mg) administration was studied in six healthy male volunteers. After i.v. administration, the drug was rapidly cleared from the serum. Individual serum levels were described by a bi-exponential equation and mean elimination half-life was 2.13 h. The volume of distribution at steady state was about 190% of body weight, and the total serum clearance and renal clearance were 12.5 and 5.80 ml/(min. kg), respectively. The drug reached maximum serum levels (6.76-14.3 ng/ml) within 2-3 h after administration of tablets: the apparent biologic half-life after oral dosing was 2.18 h. The oral bioavailability was low (3.4%), as expected for quaternary ammonium compounds, but the inter-individual variation of bioavailability was small.

Adult↗

Clinical pharmacokinetics of intramuscular thiazinamium methyl sulfate.

The disposition of the quaternary ammonium compound thiazinamium methyl sulfate is described after intramuscular injection in humans. The plasma concentration-time curves could be resolved into two exponential components, suggesting an open two-compartment model with absorption phase. Absorption was found to be extremely fast. Peak concentrations were always reached within 20 min, but in the majority of cases they were found to be between 6 and 10 min. Occasionally, the first sample (t = 3 min) proved to contain the highest concentration. Apparently the high solubility of the drug in the interstitial fluid is of prime importance for rapid absorption. Injection technique and the injection site seemed to be important for the final profile of the plasma concentration-time curve. Distribution was found to be very fast as well, with a half-life of approximately 20 min, and the apparent volume of distribution for the central compartment was about 40-60 l. Muscle activity and hence increased capillary blood flow during the distribution phase may result in a second peak in the plasma concentration-time curve. The distribution phase is followed by an elimination phase with a much longer half-life (mean value 375 min) and a volume of distribution of approximately 200-400 l. The total body clearance for thiazinamium methyl sulfate was found to be high (mean value about 800 ml/min), suggesting an active excretion process.

Adolescent↗

[Physiologic properties of nicotinic cholinoreceptor neurons of sympathetic ganglia].

The properties of nicotinic acetylcholine receptors (AChRs) of sympathetic neurons are described which determine their function--the generation of transmembrane current in response to the action of ACh. The stoichiometry of the relations between AChR and ACh, the relative potencies of different agonists and binding of alpha-bungarotoxin are determined and used for the characteristic of the recognition centre of the AChR. Two populations of AChRs, synaptic and extrasynaptic, are found different in their mean open channel lifetimes, but similar in their mean channel conductances. The bis-ammonium compounds, specific ganglion-blocking agents, exert two kinds of effects on the AChR: competitive and the noncompetitive (channel-blocking). The latter effect determines the specificity of the blockers.

Acetylcholine↗

Anticholinergic drugs in airways obstruction.

This paper reviews briefly the place of ipratropium bromide in the treatment of airways obstruction. Oxitropium bromide, a new quaternary ammonium compound derived from scopolamine was shown to be as effective a bronchodilator in a dose of 200 micrograms by inhalation as ipratropium bromide 80 micrograms in 20 patients with atopic asthma.

Asthma↗

[Hemodynamic effects in antagonism of neuromuscular blockage: atropine-pyridostigmine versus ipratropium bromide-pyridostigmine].

Antagonism of neuromuscular block using cholinesterase inhibitors and atropine is charged with several risks, which are at least partly caused by pharmacological characteristics of the anticholinergic drugs, e.g. short duration of action causing secondary bradycardia. Compared to atropine, ipratropium bromide, a new anticholinergic drug, is--due to its quarternary ammonium compound--characterized by longer duration of action. In contrast to atropine, this substance does not penetrate the blood-brain and placental barrier. Our present study was designed to compare the haemodynamic effects of both substances, using invasive monitoring, during antagonism of neuromuscular block with pyridostigmine. In contrast to atropine, ipratropium bromide induced a higher degree of initial tachycardia but did not allow secondary reduction of heart rate by rebound vagal stimulation. While cardiac output was almost constant, ipratropium bromide caused changes in stroke volume, which were due to alterations in heart rate. There were no clinically relevant changes of the other haemodynamic parameters. Cardiac arrhythmia were observed more often after administration of atropine and were of longer duration. In conclusion, ipratropium bromide is a useful alternative to atropine in patients with pre existing low heart rate and bradyarrhythmia.

Atropine↗

[Effect of ethylenediamine derivatives on Na+, K+-ATPase and K+-p-nitrophenyl phosphatase activity of brain enzyme preparations].

The activity of Na+, K+-ATPase preparations was studied as affected by ethonium and its analogs. Ethonium is found to be able of producing a strong inhibitory effect on the Na+, K+-ATPase and K+-n-nitrophenyl phospnatase activities (I50 = 2.5.10(-5) and 6.5.10(-5) M, respectively). The inhibition is irreversible under experimental conditions and is reduced when the concentration of protein and sodium ions in the incubation medium rises. A dependence is found between the inhibitory effect of the analogs and the length of their hydrocarbon radical (the inhibition maximum corresponds to bisquarternary ammonium compound with the hydrocarbon radical consisting of 10 links) and some kinetic characteristics of this effect are studied. It is supposed that the mechanism of the inhibitory effect is due to the ethonim binding by the hydrocarbon radical in the preparation hydrophobic zone, the electrostatic interaction being not excluded.

4-Nitrophenylphosphatase↗

A comparative study of two parasympatholytic bronchodilator agents: ipratropium bromide and diphemanil methylsulfate.

Ipratropium and diphemanil are synthetic quaternary ammonium compounds with antimuscarinic properties. By using in vitro measurements of tension changes in isolated guinea-pig trachealis muscle strips and in vivo measurements of lung mechanics changes in anesthetized, vagotomized cats, the two drugs were compared in terms of their relative bronchodilator potency, mode of action and apparent site of activity in the bronchial tree. Ipratropium and diphemanil were about equipotent in antagonizing airway smooth muscle contraction induced by the cholinergic agonists, methacholine (in vitro) and carbachol (in vivo). When noncholinergic stimulation was used to augment smooth muscle tone, i.e., hypertonic potassium in the isolated preparations and serotonin in the vagotomized animals, only diphemanil exhibited significant bronchodilator activity. Simultaneous measurements of pulmonary resistance and dynamic compliance were used to partition in vivo bronchodilator effects between large and small airways. The parasympatholytic bronchodilator effects of both drugs were distributed uniformly along the bronchial tree, whereas the direct spasmolytic action of diphemanil appeared to manifest itself preferentially on large airways.

Animals↗

[Bactericidal activity of various disinfectants with or without interfering protein substances].

Determination of bactericidal activity of 15 disinfectants by AFNOR standard NF T 72-151 (in distilled water) and AFNOR standard NF T 72-171 (in the presence of protein) provides practical guidelines for optimal use of the different available products. Inhibition by dirt is weak for products composed chiefly of phenol derivatives, while it is very strong for quaternary ammonium compounds as well as chlorine which therefore require prior cleansing of surfaces to be disinfected. Two strains (out of the five indicated by AFNOR standards), i.e. P. aeruginosa and M. smegmatis, are especially resistant when residual organic material is present. According to specific conditions of use, such as whether surfaces are clean or dirty, or whether a hospital or food factory is involved, appropriate AFNOR standards must be chosen to study the activity of disinfectants in various settings and on different strains.

Bacteria↗

Methenamine as an induced artifact during extraction of formaldehyde-preserved tissue.

The effect of different basic drug assay procedures on the formation of artifactual methenamine from formaldehyde preserved and nonpreserved tissue was studied. Trichloroacetic acid was compared with ammonium sulfate as a protein precipitant and sodium hydroxide was compared with ammonium hydroxide as a pH modifier. The assay of nonpreserved tissue failed to result in the detection of methenamine. However, when preserved tissue was assayed by procedures which utilized ammonium compounds, large quantities of methenamine were detected using TLC and GC/MS. Trace quantities of methenamine were detected in extracts of preserved autolyzed tissue which was assayed using nonammonium compounds.

Animals↗

Protection of day-old poults against Arizona hinshawii challenge by preincubation streptomycin egg treatment.

Poults were protected against challenge with Arizona hinshawii 7:1,7,8 inoculated into the yolk sac 30 hours post-hatching by preincubation streptomycin treatment of turkey eggs, administered by temperature-differential egg dipping in a solution composed of 250 ppm of a quaternary ammonium compound, 10 ppm of ethylenediaminetraacetate and streptomycin at 9 mg per ml. Mortalities at 17 hours and 22 days postchallenge were respectively 8% and 44% in poults from treated eggs vs 47% and 93% from untreated eggs. Liver isolation rates at 17 hours and 22 days postchallenge were respectively 0% and 16% in poults from treated eggs, vs 71% and 80% from untreated eggs.

Animals↗

Practical aspects of competitive exclusion for the control of Salmonella in turkeys.

In laboratory trials, a fourth-passage culture of adult chicken cecal contents was protective against challenge with Salmonella typhimurium in turkey poults raised on wood-shavings poultry litter. The culture was not protective against pre-treatment exposure to hatchery-introduced S. bredeney and was inhibited in poults that had received an antibiotic injection at the hatchery. The inhibitory effect of the hatchery antibiotic could be avoided if the cecal-culture treatment was delayed by 3 to 4 days after antibiotic injection. Under field conditions, there was a significant reduction in the salmonella contamination of turkeys and their environment when cecal culture was given to poults raised on wood-shavings litter sprayed with a quaternary ammonium compound. When used alone, both the cecal culture and the litter disinfectant were ineffective in preventing the establishment of S. heidelberg infection. Further studies are required to confirm the possibility of a synergistic effect between the two treatments. For the control of salmonella in turkeys, use of cecal cultures may be limited by the interference of antibiotics and by their failure to protect against pretreatment exposure to salmonella.

Animals↗

[Effect of decamethoxine, decamine and levorin on the content of cholesterol, phospholipids and triglycerides in albino rat liver].

It has been shown in experiments that intramuscular injection of guaternary ammonium compounds (decamethoxine and decamine) and levorin changed the content of cholesterol, phospholipids and triglycerides in the liver of white rats. Decamethoxine decreased the content of phospholipids and cholesterol and raised the concentration of triglycerides. Decamine decreased the level of phospholipids and raised the content of cholesterol and triglycerides, while levorin minimized the content of phospholipids, cholesterol and triglycerides.

Animals↗

Effect of inhaled diphemanil methylsulfate, a parasympatholytic agent, on histamine induced bronchoconstriction in asymptomatic asthmatics.

Parenterally administered diphemanil methylsulfate, a quarternary ammonium compound with both parasympatholytic and direct bronchial smooth muscle relaxing properties, has been found effective in the treatment of bronchial asthma. The present study was undertaken to test the effectiveness of inhaled diphemanil in preventing histamine induced bronchoconstriction in asymptomatic adult asthmatics. Twenty subjects, aged 19-40 years (average 25) were studied, each on three different days, observing an interval of at least 70 hours between testing. On day one, airway sensitivity to inhaled histamine was determined. On days two and three, histamine challenge was repeated 20 minutes after inhalation of either diphemanil (2 mg) or its vehicle in a double-blind crossover design. Airway sensitivity was assessed by determining cumulative log dose units of inhaled histamine required to provoke a 20% decline in FEV1 (log PD20 - FEV1). Diphemanil did not prevent histamine induced bronchoconstriction nor did it significantly affect log PD20 - FEV1 (p = 0.59). We conclude that a 2 mg dose of diphemanil, administered by oral inhalation 20 minutes before histamine challenge, is ineffective in protecting against induced bronchospasm in asymptomatic adult asthmatics.

Administration, Intranasal↗

[Elimination of organic cations from the eye].

Substances injected into the vitreous cavity leave the eye partly by diffusion into the flowing aqueous, but sometimes also by other mechanisms. To look for such other mechanisms removing organic cations from the rabbit eye, 5 labeled quaternary ammonium compounds were injected intravitreally, mixed with labeled sucrose. The latter leaves essentially by way of the aqueous only. After predetermined times had elapsed the rabbits were killed, and the radioactivity remaining in each eye was measured after combustion of the dried eye bulb. The anticholinergic drug Emepronium disappeared faster than sucrose but only after a delay of many hours. The main experiments were therefore concerned with the time interval 24-48 h after injection. The N- hexylhomologue of Emepronium ' Cetihex ' and the non-sedative antihistamine Aprobit were not eliminated faster than sucrose during this time interval. Since the molecular weights of these quaternaries are similar to that of sucrose and their free diffusion rate should be similar, the present experiments over a limited time interval have proved the existence of an elimination mechanism (besides aqueous flow) only for Emepronium. Tetramethylammonium and tetraethylammonium disappeared markedly faster than sucrose. Since there is no satisfactory way to take their much lower molecular weight into account, the question of a special system for these cations remains open.

Animals↗

[Glycopyrrolate (Robinul), a new anticholinergic substance].

Glycopyrrolate is a quaternary ammonium compound with indications for use similar to those for atropine. Because of the quaternary nature, it is poorly absorbed when taken orally and penetrates neither placental nor blood-brain barriers. When given by the parenteral route, the cardio-vagal blocking action of glycopyrrolate is twice that of atropine while inhibition of salivation is 5-6 times greater. The use of glycopyrrolate for premedication provides a therapeutic margin 2-3 times wider than that of atropine. Glycopyrrolate administered with neostigmine to antagonise the residual neuromuscular blockade of non-depolarising relaxants has advantages over atropine because the pharmacodynamic profile is more suited to that of neostigmine. The abrupt changes in cardiac rate, therefore, become minimal. If glycopyrrolate, 5 micrograms/kg-1, is injected intravenously just before the induction of anaesthesia, severe bradycardia is inhibited when repeated doses of succinylcholine are used. Although the alkalinising effect on gastric secretions has not been substantially verified, glycopyrrolate does provide long lasting bronchodilatation from its blocking action on smooth muscle. Only a few studies with glycopyrrolate in children have yet been published. However, it appears that this drug provides no real advantages over atropine when used in paediatric anaesthesia.

Anti-Arrhythmia Agents↗

[Interaction of frog brain cholinesterase with some reversible ammonium inhibitors].

The effects of some ammonium compounds diiodomethylate acetate (I), propionate (II), butyrate (III), valeriate (IV) N-hydroxyethylanabasine, tetramethylammonium, tetraethylammonium and acetylcholine amide analog derivatives (V-VIII) on acetylthiocholine hydrolysis by cholinesterase from frog brain, acetylcholinesterase from human erythrocytes and butyryl cholinesterase from horse blood serum were studied. Cholinesterase from frog brain possesses a lower sensitivity to the inhibitors than does the mammalian enzyme. Significant conformational changes of the inhibitor molecule, i. e. transition from trans-conformation (V) to the fixed gosh-conformation (VII), have no effect on the anticholinesterase activity of these compounds. A method for evaluation of effectivity of different types of the reversible inhibitors is proposed.

Animals↗

Effect of heat and selected chemical disinfectants upon infectivity of spores of Bacillus piliformis (Tyzzer's disease).

Spores of Bacillus piliformis of rabbit origin were harvested from the yolk sac of previously inoculated hen's eggs and subjected to various heat or chemical disinfectant treatments. Subsequently, spores were tested for infectivity in embryonated eggs inoculated via the yolk sac route, and others were treated with trypsin and then tested in embryonated eggs. The spores were not affected by the heat treatment of 60 degrees C but were rendered noninfective with treatments of 70 degrees C and 80 degrees C. Infectivity was not restored by treatment with trypsin. Infectivity was not lost when spores were treated with a phenolic germicidal detergent, ethanol or either of two quaternary ammonium compounds containing 9% or 17% benzalkonium chloride. A graded effect was observed with formaldehyde solution and an iodophor. Spores were rendered noninfective after treatment with peracetic acid (1.0%) and a wetting agent, sodium alkylarylsulfonate or sodium hypochlorite solution (0.3%) for 5 minutes, and infectivity was not restored by trypsin treatment. The probable means of transmission of Bacillus piliformis was discussed and sodium hypochlorite solution (0.3%) was recommended as a surface disinfectant in animal facilities as an aid to the prevention and control of Tyzzer's disease.

Animals↗

Glycopyrrolate-neostigmine and atropine-neostigmine mixtures affect postanesthetic arousal times differently.

Atropine-neostigmine and glycopyrrolate-neostigmine mixtures used in 54 premedicated patients for reversal of non-depolarizing neuromuscular blockade were compared for their effects on postanesthetic arousal times. Anesthesia was induced in all patients with thiopental and was maintained with N2O-O2. Atropine-neostigmine significantly delayed arousal for the first 30 minutes following cessation of anesthesia and reversal of neuromuscular blockade. The difference between the two mixtures following reversal of neuromuscular blockade is attributed to the fact that atropine is a tertiary amine that crosses the blood-brain barrier and delays arousal, whereas glycopyrrolate is a quaternary ammonium compound that does not cross this barrier.

Adult↗