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The protection of Nifedipin from photodegradation due to complex formation with β-cyclodextrin

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Nikolić V., Ilić D., Nikolić L., Stanković M., Cakić M., Stanojević L., Kapor A., Popsavin M.
Open Chemistry
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2010
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vol. 8
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issue 4
744-749
EN
The inclusion complex β-cyclodextrin:nifedipin was prepared in solid state by coprecipitation with 1:1 mol ratio. The structure of the obtained complex and nifedipin was characterized by use of X-ray diffraction (XR), infrared spectroscopy (FTIR), nuclear magnetic resonance (NMR), and differential scanning calorimetry (DSC) methods. The photodegradation of nifedipin and the β-cyclodextrin:nifedipin inclusion complex in solid state was monitored under natural daylight by infrared spectroscopy, whereby the free nifedipin degraded four to five times faster than the complexed nifedipin. The photodegradation products of both free and complexed nifedipin, formed during irradiation at 350 nm (with corresponding energy flux of 18 W m−2) were monitored by liquid chromatography during various time intervals. The speed of formation of nitroso- and nitro-phenyl derivatives by nifedipin irradiation was significantly higher than those of complexed nifedipin irradiation, which indicates its increased photostability in the inclusion complex. The effect on this property is significant because it contributes both to the improvement of the therapeutic effect of nifedipin and to the safer application thereof. [...]
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Determination of polyolefin additives by reversed-phase liquid chromatography

100%
Dopico-García M., Noguerol-Cal R., Castro-López M., Cela-Pérez M., Piñón-Giz E., López-Vilariño J., González-Rodríguez M.
Open Chemistry
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2012
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vol. 10
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issue 3
585-610
EN
This article examines the contribution of liquid chromatography to the study of polyolefin additives commonly used to obtain improved environmental resistance (antioxidants, ultraviolet light stabilizers, antistatics, and so on) and appearance enhancements (e.g. colorants). Several reversed-phase liquid chromatographic methods are summarized, and a detailed description of different detectors is provided. In addition, ways of applying these methods to analyse food contact materials and plastic toys are emphasized. Finally, the potential use of these methods is addressed which complies with European health safety regulations. [...]
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Analytical considerations on the use of a fruit-specific and representative matrix in pesticide residue analysis by LC-ESI-MS/MS

86%
Stachniuk A., Fornal E.
Open Chemistry
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2013
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vol. 11
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issue 7
1112-1131
EN
One of the quantification methods frequently applied to pesticide residue analysis in food by liquid chromatography - mass spectrometry (LC-MS) involves matrix-matched calibrations with a representative matrix used for all commodities belonging to one group. This approach, although very practical, is deemed to generate analytical errors. The effect of the application of a representative-matrix calibration curve on the pesticide quantification result was examined. Extractions of 56 pesticides from five soft fruits (strawberries, blackberries, raspberries, black currant and red currant) were carried out using QuEChERS method. Pesticide determinations were performed by LC-MS/MS in multiple reaction monitoring mode. Quantification difference functions and parameters were proposed and calculated. At the concentration of 0.05 mg kg−1 for ca. 90% of examined pesticides the quantification difference arising from the use of a representative matrix calibration curve (raspberries) instead of a specific fruit matrix calibration curve was below 20% for black and red currents, and below 30% and 35% in the case of strawberries and blackberries, respectively. The 25% difference limit was not exceeded for 51 pesticides in black and red currents, 46 pesticides in blackberries and 45 pesticides in strawberries. Quantification difference functions and parameters such as relative standard deviation of corrected process efficiencies were found to be helpful in data-driven decision-making on the applicability of a representative matrix; the former may be also used as a tool for data correction to ensure the reliability and accuracy of analyses. [...]
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