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21.
Priyanka Trivedi Jonnala Kotesh Kumar Arvind Singh Negi Karuna Shanker 《Biomedical chromatography : BMC》2011,25(6):697-706
Extraction and pre‐concentration of a bioactive marker compound, phenyl‐1,3,5‐heptatriyne from Bidens pilosa, prior to HPLC has been demonstrated using both organic and ecofriendly solvents. Non‐ionic surfactants, viz. Triton X‐100, Triton X‐114 and Genapol X‐80, were used for extraction. No back‐extraction or liquid chromatographic steps were required to remove the target phytochemical from the surfactant‐rich extractant phase. The optimized cloud point extraction procedure has been shown to be a potentially useful methodology for the preconcentration of the target analyte, with a preconcentration factor of 4–99. Moreover, the method is simple, sensitive, rapid and consumes lesser solvent than traditional methods. An isocratic chromatographic separation and quantitation was accomplished on a C18 column with acetonitrile–acidified aqueous as mobile phase at a flow rate of 1.0 mL/min, UV detection at 254 nm and specificity with photo diode‐array detector (PDA) and MS. Under the optimum experimental conditions recovery was satisfactory (99.18–100.33%) without interference from the surfactant. The method seems to be reliable with intraday precision and interday precision below 2.0%. Good linearity was obtained in the working range from 7.5 to 30 µg/mL with correlation coefficient >0.99. The limits of detection and quantitation were 1.84 and 6.13 µg/mL, respectively. The method was validated following international guidelines and successfully applied for quantitative assays of cytotoxic compound phenyl‐1,3,5‐heptatriyne in Bidens pilosa. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
22.
Priyanka G. Mandhane 《Tetrahedron letters》2010,51(23):3138-939
An environmentally benign aqueous Biginelli protocol for the synthesis of substituted 3,4-dihydropyrimidin-2(1H)-ones using thiamine hydrochloride as a catalyst has been achieved. These ultrasound-assisted reactions proceed efficiently in water in the absence of organic solvent. Utilization of ultrasound irradiation, simple reaction conditions, isolation, and purification makes this manipulation very interesting from an economic and environmental perspective. 相似文献
23.
Matthew Curtis Mikael A. Minier Priyanka Chitranshi O. David Sparkman Patrick R. Jones Liang Xue 《Journal of the American Society for Mass Spectrometry》2010,21(8):1371-1381
Direct analysis in real time (DART) mass spectrometry is a recently developed innovative technology, which has shown broad
applications for fast and convenient analysis of complex samples. Due to the ease of sample preparation, we have recently
initiated an investigation of the feasibility of detecting nucleotides and nucleosides using the DART-AccuTOF instrument,
which we will refer to as the DART mass spectrometer. Our experimental results reveal that the ions representing the intact
molecules of nucleotides are not detectable in either positive-ion or negative-ion mode. Instead, all four natural nucleotides
fragment in the DART ion source, and a common fragment ion, [C5H5O]+ (1), is observed, which is probably formed via multiple-elimination reactions. Interestingly, 1 can form adducts with nucleobases
in different molar ratios in the DART ion source. In contrast to nucleotides, the ions representing the intact molecules of
nucleosides are detected in both positive-ion and negative-ion mode using DART mass spectrometry. Surprisingly, the fragmentation
pattern of nucleosides is different from that of nucleotides in the DART ion source. In the cases of nucleosides (under positive-ion
conditions), the production of 1 is not observed, indicating that the phosphate group plays an important role for the multiple
eliminations observed in the spectra of nucleotides. The in-source reactions described in the present work show the complexity
of the conditions in the DART ion source, and we hope that our results illustrate a better understanding about DART mass spectrometry. 相似文献
24.
Santanu Pyne Priyanka Sarkar Samita Basu Gobinda Prasad Sahoo Dipak Kumar Bhui Harekrishna Bar Ajay Misra 《Journal of nanoparticle research》2011,13(4):1759-1767
Synthesis of core @ shell (Au @ Ag) nanoparticle with varying silver composition has been carried out in aqueous poly vinyl
alcohol (PVA) matrix. Core gold nanoparticle (~15 nm) has been synthesized through seed-mediated growth process. Synthesis
of silver shell with increasing thickness (~1–5 nm) has been done by reducing Ag+ over the gold sol in the presence of mild reducing ascorbic acid. Characterization of Au @ Ag nanoparticles has been done
by UV–Vis, High resolution transmission electron microscope (HRTEM) and energy dispersive X-ray (EDX) spectroscopic study.
The blue shift of surface plasmon resonance (SPR) band with increasing mole fraction of silver has been interpreted due to
dampening of core, i.e. Au SPR by Ag. The dependence of nonlinear optical response of spherical core @ shell nanoparticles
has been investigated as a function of relative composition of each metal. Simulation of SPR extinction spectra based on quasi-static
theory is done. A comparison of our experimental and the simulated extinction spectra using quasi-static theory of nanoshell
suggests that our synthesized bimetallic particles have core @ shell structure rather than bimetallic alloy particles. 相似文献
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26.
Reactions of 2‐isopropoxy‐1, 3, 2‐ benzodioxaborole with equivalent amounts of Schiff base ligands having two hydroxyl groups ( 1a–3a ) yield mononuclear derivatives with one residual hydroxy group. The reactions of these mononuclear derivatives with hexamethyldisilazane in a 2:1 ratio yield heterodinuclear derivatives. All these newly synthesized derivatives have been characterized by elemental analyses and molecular weight measurements. Tentative structures have been proposed on the basis of IR and NMR (1H, 13C, 11B,29Si)spectral data and Fab‐mass studies. Schiff bases and their corresponding mono‐ and heterodinuclear derivatives of boron have also been screened for antifungal activities. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
27.
Imprinted silica nanoparticles coated with N‐propylsilylmorpholine‐4‐carboxamide for the determination of m‐cresol in synthetic and real samples
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Manisha Ghai Priyanka Narula Varinder Kaur Raghubir Singh 《Journal of separation science》2015,38(19):3442-3449
m‐Cresol‐imprinted silica nanoparticles coated with N‐propylsilylmorpholine‐4‐carboxamide have been developed that contain specific pockets for the selective uptake of m‐cresol. Silica nanoparticles were synthesized by a sol–gel process followed by functionalization of their surface with N‐propylsilylmorpholine‐4‐carboxamide. The formation of m‐cresol‐imprinted silica nanoparticles was confirmed by UV‐Vis spectrophotometry, infrared spectroscopy, thermogravimetric analysis, scanning electron microscopy and transmission electron microscopy. Electron microscopic studies revealed the formation of monodispersed imprinted silica nanoparticles with spherical shape and an average size of 83 nm. The developed nanoparticles were filled in a syringe and used for the extraction of m‐cresol from aqueous samples followed by quantification using high‐performance liquid chromatography with diode array detection. Various adsorption experiments showed that developed m‐cresol‐imprinted silica nanoparticles exhibited a high adsorption capacity and selectivity and offered a fast kinetics for rebinding m‐cresol. The chromatographic quantification was achieved using mobile phase consisting of acetonitrile/water (70:30 v/v) at an isocratic flow rate of 1.0 mL/min using a reversed‐phase C18 column and detection at λmax = 275 nm. The limits of detection and quantification were 1.86 and 22.32 ng/mL, respectively, for the developed method. The percent recoveries ranged from 96.66–103.33% in the spiked samples. This combination of this nanotechnique with molecular imprinting was proved as a reliable, sensitive and selective method for determining the target from synthetic and real samples. 相似文献
28.
Patil Priyanka T. Warekar Poojali P. Patil Kirti T. Jamale Dattatraya K. Kolekar Govind B. Anbhule Prashant V. 《Research on Chemical Intermediates》2017,43(7):4103-4114
Research on Chemical Intermediates - A convenient and new method has been developed for the synthesis of highly substituted dihydro-2H-dipyrimido[1,2-a,4,5-d]pyrimidine-2,4(3H)-dione derivatives by... 相似文献
29.
Fungal isolates (Aspergillus wentii 1, A. wentii 2, Penicillium citrinum, Penicillium granulatum) were selected to study their in vitro antioxidant potential by various assay procedures. Czapek–Dox’s medium was selected
for the growth of fungi as it supported the best antioxidant activity based on their EC50 values, P. citrinum was the best followed by P. granulatum, A. wentii 1, and A. wentii 2. The chromatographic analyses showed several compounds possessing antioxidant activity in the fungal extracts. Two such
compounds were partially purified from P. citrinum which demonstrated potent antioxidant activity, equally effective or better than some of the standard antioxidants. 相似文献
30.
Yadav RA Rani P Kumar M Singh R Singh P Singh NP 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2011,84(1):6-21
IR and spectra of the L-ascorbic acid (L-AA) also known as vitamin C have been recorded in the region 4000-50 cm(-1). In order to make vibrational assignments of the observed IR and Raman bands computations were carried out by employing the RHF and DFT methods to calculate the molecular geometries and harmonic vibrational frequencies along with other related parameters for the neutral L-AA and its singly charged anionic (L-AA(-)) and cationic (L-AA(+)) species. Significant changes have been found for different characteristics of a number of vibrational modes. The four ν(O-H) modes of the L-AA molecule are found in the order ν(O(9)-H(10))>ν(O(19)-H(20))>ν(O(7)-H(8))>ν(O(14)-H(15)) which could be due to complexity of hydrogen bonding in the lactone ring and the side chain. The CO stretching wavenumber (ν(46)) decreases by 151 cm(-1) in going from the neutral to the anionic species whereas it increases by 151 cm(-1) in going from the anionic to the cationic species. The anionic radicals have less kinetic stabilities and high chemical reactivity as compared to the neutral molecule. It is found that the cationic radical of L-AA is kinetically least stable and chemically most reactive as compared to its neutral and anionic species. 相似文献