Studies on the reaction of fluorescamine with primary amines

Fluorescamine is a useful reagent for the fluorometric assay of primary amines. The extent of the reaction between fluorescamine and primary amines, as well as the fluorescence intensities of the resulting fluorophors depend on pH, solvent composition and reagent concentration. Optimum values for these variables further depend on the amine under study. The influence of these parameters on the fluorogenic reaction of representative amines, and on their fluorophoric derivatives has been investigated, and the results are reported here.     

Automatic Monitoring of primary amines in preparative column effluents with fluorescamine.

A system is presented for automatically monitoring primary amines in preparative column effluents by fluorescamine assay. A small portion of column effluent, containing nanograms of protein or picomoles of peptide, is diverted via a sampling valve into the detection system, while the remainder is recovered in a fraction collector.     

Determination of primary amines and protein by using fluorescamine in microorganism suspensions

The paper describes a fluorimetric technique for determining the overall amount of primary amines and protein using fluorescamine directly in suspensions of yeast and bacterial microorganisms. The optimal conditions are selected for the reaction. The technique is highly sensitive and has an advantage over biochemical methods when one has to make many assays of amine containing compounds in biological material. The technique can find wide application in industrial practice.     

Pyrazolidine derivatives: a comparative study of their effects on platelet aggregation.

Quantitative studies were carried out of the in vitro and ex vivo effects of phenylbutazone and 3-oxoalkyl substituted diphenyldioxopyrazolidines (kebuzone, tribuzone, benzopyrazone) on platelet aggregation. The specified pyrazolidine derivatives exhibited in vitro inhibitory effects on secondary platelet aggregation (induced by adrenaline and collagen), commensurable with the effects of sulfinpyrazone. The ex vivo efficacy was markedly influenced by the height of the drug level in blood and by differences in the elimination kinetics of the pyrazolidine derivatives in human organism. Inhibitory activities against primary aggregation (induced by ADP and thrombin) were found in vitro mainly in the phenyloxoalkyl derivative of diphenyldioxopyrazolidine (benzopyrazone) and its analogues. By substitution on the phenyl attached to its alkyl side chain (for example, by a halogen in the meta position), compounds were obtained which also possessed higher activities inhibiting secondary platelet aggregation.     

Chromatographic analysis of amino acids and primary amines with o-phthalaldehyde detection

The applicability of the o-phthalaldehyde reaction with fluorometric detection to the simultaneous chromatographic analysis of amines and nonprotein amino acids is demonstrated. The majority of the compounds tested could be quantitatively determined with high sensitivity. The method is particularly well suited for the analysis of β-amino acids. Amino compounds lacking an α-hydrogen atom are detected with lower sensitivity, due to a lower relative fluorescence. Secondary amino compounds are undetectable with this system.     

Pentafluorobenzoyl derivatives of doping agents : I. Extractive benzoylation and gas chromatography with electron-capture detection of primary and secondary amines

A sensitive and rapid method for the gas chromatographic (with electron-capture detection) confirmation of derivatizable sympathomimetic amines is described. Extractive derivatization with pentafluorobenzoyl chloride is performed on 2-ml urine or plasma samples. Especially for primary amines, the method appears to be very sensitive. Mass spectral data allowed confirmation of the monobenzoylation of all congeners.     

An electron microscope study of effects of various fixatives and thin-section enzyme treatments on a nuclear polyhedrosis virus

A comparison of fixatives and embedding media used in thin sectioning of polyhedra and isolated virions of the Pseudoplusia includens nuclear polyhedrosis virus demonstrated that best results are obtained with glutaraldehyde-OsO₄ fixation and epoxy embedding. Fixation was obtained with formaldehyde, acrolein-formaldehyde, or OsO₄ alone but the crystalline array of the polyhedral protein was not preserved. Glycol methacrylate embedding medium resulted in images of poor quality. Treatment of thin sections of polyhedra and virions with enzymes showed that the polyhedral membrane is resistant to digestion with proteases but the interiors of polyhedra were removed with pepsin, pronase, subtilisin, and a mixture of deoxyribonuclease and trypsin. Enzyme treatment of thin sections of virions resulted in removal of the nucleocapsid by all proteases tested except trypsin. A mixture of deoxyribonuclease and trypsin digested the nucleocapsid. The envelope of the virion resisted enzyme treatment.     

Biogenic amines and phenolics characterize the defensive secretion of saturniid caterpillars (Lepidoptera: Saturniidae): a comparative study

The morphology of the scoli of Eudia pavonia, Saturnia pyri and Eupackardia calleta last instar caterpilars has been clarified. Chemical and biochemical comparisons of scolus secretions and corresponding caterpillar haemolymphs indicate two differing defensive strategies: Eudia and Saturnia contain phenolic and related compounds, whereas Eupackardia additionally synthesizes biogenic amines (e.g. neurotransmitters) in considerable amounts. For most aromatic compounds from the caterpillars a theoretical biogenetic scheme is proposed. Deterrent effects of all secretions and most haemolymphs on particular predatory ants were ascertained.Abbrevations CI chemical ionisation - EI electronimpact ionisation - GC-MS gas chromatography-mass spectrometry - GS gland secretion - HL haemolymph - PMSF phenylmethylsulphonyl fluoride - SDS-PAGF sodium dodecyl sulphate-polyacrylamide gel electrophoresis - SEM scanning electron microscope     

The influence of the sleep-wake cycle on primary monosymptomatic nocturnal enuresis: a non-randomized comparative study

Backround: Enuresis implies severe stress in affected children, and impairs quality of life and sleep. Children with enuresis experience difficulties in their arousal from sleep, possibly associated with disturbances of the circadian rhythm. In this study, we aimed to evaluate the sleep–wake cycle and sleep disturbances in children with monosymptomatic enuresis nocturna (MEN). Method: The study comprised 70 children with MEN who were admitted to the pediatrics and urology outpatients department and 94 age-matched healthy controls. Parents completed “Strengths and Difficulties Questionnaire,” Children’s Sleep Habits Questionnaire (CSHQ), Children’s Chronotype Questionnaire scale. Results: Children with enuresis had significantly more sleep and psychological problem. Enuresis group reported higher bedtime resistance, parasomnias, breathing-related problems, and daytime sleepiness in CHSQ (p < 0.05). Although circadian preference did not differ statistically between the groups (p > 0.05), sleep duration on school days and awakening and mid-sleep points, both on scheduled and free days, were found to be significantly different in the enuretic group (p < 0.05). In logistic regression analysis, age, sleep period on scheduled days, sleep inertia on scheduled and free days were significant predictor for enuresis. Discussion: Children with enuresis were more likely to experience problematic sleep. This may reflect that enuretic children have impaired sleep–wake cycles, leading to dysregulation of daily functional changes of bladder capacity and related hormones such as ADH. These findings might imply a sleep–wake disturbance in enuresis.     

Screening of plant extracts for antioxidant activity: a comparative study on three testing methods

Three methods widely employed in the evaluation of antioxidant activity, namely 2,2'-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging method, static headspace gas chromatography (HS-GC) and beta-carotene bleaching test (BCBT), have been compared with regard to their application in the screening of plant extracts. The strengths and limitations of each method have been illustrated by testing a number of extracts, of differing polarity, from plants of the genus Sideritis, and two known antioxidants (butylated hydroxytoluene and rosmarinic acid). The sample polarity was important for the exhibited activity in the BCBT and HS-GC methods but not for the DPPH method. The complex composition of the extracts and partition phenomena affected their activity in each assay. The value of the BCBT method appears to be limited to less polar samples. Although slow, the HS-GC method is preferable for assessing the antioxidant inhibitory properties on the formation of unwanted secondary volatile products. Being rapid, simple and independent of sample polarity, the DPPH method is very convenient for the quick screening of many samples for radical scavenging activity.     

Genotoxic effects of ethylene oxide and propylene oxide: a comparative study

The two alkylating agents ethylene oxide (EO) and propylene oxide (PO) were compared for genotoxic effectiveness in various test systems. The study was undertaken partly to shed light on the difference between the compounds found after chronic exposure of monkeys (Lynch et al., 1984) where EO but not PO was able to induce SCE and chromosomal aberrations. In the present study EO was found to be 5–10 times more effective than PO with respect to gene conversion and reverse mutation in Saccharomyces cerevisiae D7 and sister-chromatid conversion in S. cerevisiae RS112. In contrast, the abilities of the two compounds to induce point mutation in S. typhimurium strains and SCE in human lymphocytes were approximately equal. One possible cause of EO being more effective than PO in certain respects, discussed on the basis of inference from earlier studies, is an expected difference in ability to cause strand breaks via alkylation of DNA-phosphate groups.     

Biochemical effects of the porphyrinogenic drug allylisopropylacetamide. A comparative study with phenobarbital

Successive administrations of allylisopropylacetamide, a potent porphyrinogenic drug, increase liver weight, microsomal protein and phospholipid contents. There is an increase in the rate of microsomal protein synthesis in vivo and in vitro. The drug decreases microsomal ribonuclease activity and increases NADPH-cytochrome c reductase activity. Phenobarbital, which has been reported to exhibit all these changes mentioned, is a weaker inducer of delta-aminolaevulinate synthetase and increases the rate of haem synthesis only after a considerable time-lag in fed female rats, when compared with the effects observed with allylisopropylacetamide. Again, phenobarbital does not share the property of allylisopropylacetamide in causing an initial decrease in cytochrome P-450 content. Haematin does not counteract most of the biochemical effects caused by allylisopropylacetamide, although it is quite effective in the case of phenobarbital. Haematin does not inhibit the uptake of [2-(14)C]allylisopropylacetamide by any of the liver subcellular fractions.     

LAMP for human African trypanosomiasis: a comparative study of detection formats

Loop-mediated isothermal amplification (LAMP) is at the forefront of the search for innovative diagnostics for human African trypanosomiasis (HAT). Several simple endpoint detection methods have been developed for LAMP and here we compare four of these: (i) visualization of turbidity; (ii) addition of hydroxynaphthol blue before incubation; (iii) addition of calcein with MnCl₂ before incubation and (iv) addition of Quant-iT PicoGreen after incubation. These four methods were applied to four LAMP assays for the detection of human African trypanosomiasis, including two Trypanozoon specific and two Trypanosoma brucei rhodesiense specific reactions using DNA extracted from cryo-preserved procyclic form T. b. rhodesiense. A multi-observer study was performed to assess inter-observer reliability of two of these methods: hydroxynapthol blue and calcein with MnCl₂, using DNA prepared from blood samples stored on Whatman FTA cards. Results showed that hydroxynaphthol blue was the best of the compared methods for easy, inexpensive, accurate and reliable interpretation of LAMP assays for HAT. Hydroxynapthol blue generates a violet to sky blue colour change that was easy to see and was consistently interpreted by independent observers. Visible turbidity detection is not possible for all currently available HAT LAMP reactions; Quant-iT PicoGreen is expensive and addition of calcein with MnCl₂ adversely affects reaction sensitivity and was unpopular with several observers.     

A latex agglutination test for the detection of Mycoplasma pneumoniae in respiratory exudates: a comparative study with a commercially available DNA-probe test.

We prepared polyclonal antibody specific to Mycoplasma pneumoniae. Using this antibody, we developed a latex agglutination test (LAT) for detecting the organism in respiratory exudates as rapid diagnosis of M. pneumoniae infection. Further, LAT was compared with DNA-probe test (DP) which was the only commercially available test for the rapid detection of the organism. In LAT, both M. pneumoniae and M. genitalium give positive agglutination, but the titer of M. genitalium was significantly lower than that of M. pneumoniae. The detection limit of LAT was 2 x 10(5) CFU/ml and that of DP was 5 x 10(4) CFU/ml in vitro. It was considered that target molecules in LAT were accumulated in the pharyngeal portion of the patients, because of their long half-life at 37 C. However, ribosomal RNA which was target molecule in DP was destroyed at 37 C much sooner, and the accumulation could not be expected. Actually, positive rate in LAT was higher than that in DP among clinical specimens in which M. pneumoniae was detected by culture method. The procedure of LAT is much easier and more rapid than that of DP in which radioactive isotope is required. LAT could be the choice of test for rapid diagnosis of M. pneumoniae infection.     

A comparative study of the effects of abscisic acid and new terpenoid abscisic acid analogues on plant physiological processes

The effects of new terpenoid abscisic acid analogues in comparison to abscisic acid (ABA) on some physiological and biochemical processes of various plant species have been investigated. The analogues exhibited ABA-like effects by inhibiting cell elongation and germination, and by promoting abscission, as well as the accumulation of proline and induction of stomatal closure coupled by a reduction in transpiration. In response to low temperature, the analogue-treated plants showed improved resistance to cold accompanied by a decrease in electrolyte leakage.     

A comparative study of the effects of abscisic acid and new terpenoid abscisic acid analogues on plant physiological processes

The effects of new terpenoid abscisic acid analogues in comparison to abscisic acid (ABA) on some physiological and biochemical processes of various plant species have been investigated. The analogues exhibited ABA-like effects by inhibiting cell elongation and germination, and by promoting abscission, as well as the accumulation of proline and induction of stomatal closure coupled by a reduction in transpiration. In response to low temperature, the analogue-treated plants showed improved resistance to cold accompanied by a decrease in electrolyte leakage.