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11.
12.
LAURENT MICLO EMMANUEL PERRIN ALAIN DRIOU MICHEL MELLET GUY LINDEN 《Chemical biology & drug design》1995,46(2):186-192
A method for the simultaneous determination of the ratios of the three aromatic amino-acid residues in peptides was set up in acidic conditions. Binary and ternary mixtures of these amino acids were prepared, and first- and second-derivative spectra then calculated from their 0.1 nm resolution spectra between 240 and 320 nm. Certain spectral bands were chosen to differentiate tyrosine from tryptophan on the first-derivative spectra, and phenylalanine from tyrosine and tryptophan on the second-derivative spectra. Variation of the amplitude of the chosen bands was shown to be a linear function of the ratio of the aromatic amino acids in the mixture. This technique was validated with peptides whose sequence was known. The difference between theoretical and experimentally determined ratios was lower than 10%. Since the results are obtained as ratios, neither the concentration nor the nature of the peptide has to be known. The feasibility of application using a photodiode array detector with high resolution in reversed-phase high-performance liquid chromatography is discussed. © Munksgaard 1995. 相似文献
13.
荧光分析法测定血清中微量硒 总被引:1,自引:0,他引:1
为测定血清中微量硒,较低温度消化后,用2,3-二氨基萘为试剂,以荧光法测定,取得了满意的结果。方法简便快速,结果稳定准确。血清中加入标准硒,8次测定的回收率为96.6%~102.4%,平均值±标准差为99.6±1.8%。 相似文献
14.
O. N. Tatarinova T. N. Lukyanova M. A. Zaitseva K. Yu. Veremeev V. A. Karpov A. N. Chuvilin D. D. Petrunin G. E. Pozmogova 《Bulletin of experimental biology and medicine》2008,145(3):312-316
Analysis of the use of real-time PCR with fluorescent registration of results for gene diagnosis of infectious diseases showed
that the sensitivity and reliability of quantitative evaluation of DNA targets directly depended on the method of purification
of oligonucleotide probes. Chromatographic behavior of synthetic probes carrying various fluorophores and fluorescence quenchers
was analyzed. Approaches to optimization of purification methods are proposed enabling elimination of previously undetectable
admixtures. The importance of these studies is explained by the need in extending the armory of methods for the development
and production of diagnosticums for detection of infectious and hereditary diseases, identification of genetically modified
organisms, and for a wide spectrum of research in molecular biology and medicine.
__________
Translated from Byulleten’ Eksperimental’noi Biologii i Meditsiny, Vol. 145, No. 3, pp. 280–284, March, 2008 相似文献
15.
Hsiao-Chuan Lin Jang-Jih Lu Lee-Chung Lin Cheng-Mao Ho Kao-Pin Hwang Yu-Ching Liu Chao-Jung Chen 《Journal of microbiology, immunology, and infection》2019,52(1):81-89
Background
Group B Streptococcus (GBS) is an important invasive pathogen in neonates, pregnant women and the elderly. Serotype VI GBS, which has been rarely reported globally, has emerged as a significant pathogen in Asia. However, traditional serologic latex agglutination (LA) methods may fail to type isolates that lack of or low expression of CPS.Methods
A total of 104 GBS strains were analyzed by MALDI-TOF MS. Multiplex PCR and multilocus sequence typing (MLST) were also performed to confirm their strains. The protein markers were purified with gel electrophoresis and LC-column, followed by identification with nanoLC–MS/MS analysis.Results
Protein peak of 6251-Da was appeared in most (20/24, 92%) serotypes VI (94% ST-1 or single locus variant of ST-1), and protein peak of 6891-Da was appeared in most serotypes III (15/18, 83%) and Ib (19/23, 83%) strains. The protein peak of 6251-Da and 6891-Da were identified as CsbD family protein and UPF0337 protein gbs0600, respectively.Conclusions
The protein peak of 6251 Da may play a role of emergence of ST-1 clone, serotype VI GBS in central Taiwan and could be useful in rapid identifying invasive serotype VI from III isolates, which is hardly achieved by LA. 相似文献16.
Chun Chang John Lipian Dennis A. Barnes Larry Seger Cheryl Burns Brian Bennett Laura Bonney Larry F. Rhodes George M. Benedikt Robert Lattimer Shyhchang S. Huang Victor W. Day 《Macromolecular chemistry and physics.》2005,206(19):1988-2000
Summary: Homopolymers of a bis‐trifluorocarbinol substituted norbornene ( 1 ) (α,α‐bis(trifluoromethyl)bicyclo[2.2.1]hept‐5‐ene‐2‐ethanol or HFANB) and copolymers of 1 with t‐butyl ester of 5‐carboxylic acid ( 2 , t‐BuEsNB) were produced using palladium catalysts and olefinic chain transfer agents such as 1‐hexene and ethylene to control molecular weight. However, these low‐molecular‐weight polymers exhibited relatively low optical transparencies at 193 nm. In fact, the opacity (measured as optical densities in absorbance units per micron) of thin films of these homo‐ and co‐polymers was inversely proportional to their molecular weight. This relationship is consistent with an end group contribution to the film opacity. Spectroscopic analysis of these polymers by 1H NMR and MALDI‐TOF MS confirmed that 1‐hexene and ethylene chain transfer agents generated olefin‐terminated vinyl addition polymers. The olefinic end group contribution to optical density can be eliminated by appropriate chemical modification. Both epoxidation and hydrogenation of the polymer olefinic end groups generated very low optical density materials, independent of molecular weight, that are suitable as 193‐nm photoresist binder resins.
17.
Martina Adler Frank Rittig Stefan Becker Harald Pasch 《Macromolecular chemistry and physics.》2005,206(22):2269-2277
Summary: The chromatographic analysis of hydrophilic copolymers is complicated due to the fact that in most cases aqueous eluents must be used. In aqueous eluents different polar and ionic effects may disturb the selective interactions between the macromolecules and the stationary phase making it impossible to separate such copolymers with regard to chemical composition. Therefore, 2D chromatography combining a separation according to composition with a separation according to molar mass has been applied mostly to polymers that are soluble in organic solvents. The present contribution describes experimental approaches to analyze such hydrophilic copolymers by 2D‐chromatography. For a model polymer system resulting from the copolymerization of methacrylic acid and a poly(ethylene glycol) macromonomer, it is shown that different analytical techniques including SEC, LC‐CC, MALDI‐TOF MS and 2D chromatography can be used to analyze the different parameters of molecular heterogeneity of such copolymers.
18.
Peter S. Lee Richard M. Schreck Bradley A. Hare James J. McGrath 《Annals of biomedical engineering》1994,22(1):120-125
Tunable diode laser spectrometry was used to measure breath carbon monoxide (CO) concentrations in nonsmoking subjects. Corresponding
blood carboxyhemoglobin (COHb) saturations between physiological levels and levels after 1 and 8 hours exposure to 9 ppm CO,
the maximum permissible concentration in the air under federal regulations, were also determined. A good linear correlation
between breath CO and blood COHb saturation for low levels representing ambient conditions was established, with a correlation
coefficient better than 0.999 for the means and 0.945 for the individual data points. Similar studies on the other compounds
of concern are also possible using tunable diode laser spectrometry, requiring only a breath sample and with no sample preparation.
This technique will facilitate fast, noninvasive environmental health effect and biomedical studies. 相似文献
19.
Olof Beck Kym F. Faull David B. Repke 《Naunyn-Schmiedeberg's archives of pharmacology》1986,333(3):307-312
Summary Racemic methtryptoline (1-methyltetrahydro--carboline) and 5-hydroxymethtryptoline-9-carboxylic acid (6-hydroxy-1-methyltetrahydro--carboline-1-carboxylic acid) were administered intraperitoneally to rats and the components of their urine was subsequently investigated by chiral gas chromatography-mass spectrometry. Methtryptoline rapidly became hydroxylated in the 5- and 6-position and excreted in urine. There was about a ninefold predominance of the S(–) enantiomer over the other in the 5-hydroxylated species, while the 6-hydroxylation produced a small excess of the R(+) enantiomer. About 75% of the injected dose of methtryptoline was recovered in the urine as 5- and 6-hydroxylated compounds during the first 24 h period, demonstrating that hydroxylation represents the major metabolic pathway. Treatment with 6-hydroxymethtryptoline-9-carboxylic acid led to a fivefold increase in the urinary excretion of 5-hydroxymethtryptoline during the first 24 h period with a predominance of the S(–)-enantiomer, indicating a much smaller conversion rate than from methtryptoline. It was concluded that hydroxylation of methtryptoline is a likely pathway for the natural formation of 5-hydroxymethtryptoline. 相似文献
20.
Alberti MB Pinzauti S Moneti G Agati G Giannellini V Coran SA Vincieri FF 《Journal of pharmaceutical and biomedical analysis》1984,2(3-4):409-415
The medicinally important quaternary ammonium salts benzyldimethyltetradecylammonium chloride (BDTA), cetylpyridinium chloride and benzethonium chloride, all afford, under fast atom bombardment (FAB) mass spectrometric conditions, abundant and persistent [M---Cl]+ species usefully amenable to quantitative analysis with the aid of thioglycerol as a liquid FAB matrix. The use of BDTA as an internal standard allowed a direct, precise and accurate determination of cetylpyridinium and benzethonium chlorides, either as pure samples or in dosage forms, in the concentration range 0.05–2 mg/ml. 相似文献