ABSTRACT
This paper assesses the financing gap faced by innovative start-ups in the European Union (EU) when they reach the scaling-up stage of their development. It draws on data collected through a seminar involving 117 experts representing start-ups and scale-ups, financial actors, academia, and EU policymakers and aimed at investigating the causes, consequences, and policy solutions of the scale-up gap in the EU. Besides highlighting supply-side deficiencies, the seminar also emphasised weaknesses in both the demand side of the scale-up gap and the EU ecosystem for high-growth entrepreneurship. The paper offers policy recommendations, highlighting the need for policy solutions involving private actors and specifically targeting scale-ups. The paper also calls for more robust research on measuring the scale-up financing gap and its economic impact to improve the policy response.
ABSTRACT
A liquid chromatography-mass spectrometry (LC-MS) method was developed for the determination of five macrolides in natural water samples, using kitasamycin as surrogate. The macrolides were extracted from water samples using Oasis HLB cartridges. Pre-concentration factors up to 250 were obtained. Separation was carried out in an end-capped silica-based C18 column and mobile phases consisting of water/acetonitrile mixtures containing ammonium acetate. Detection was performed by mass spectrometry with a single quadrupole and a triple quadrupole using an electrospray interface. The quality parameters obtained with these two approaches were compared. The detection limits of the whole process were about 1 ng l(-1). The recoveries from 250 ml of water samples spiked at 25-125 ng l(-1) level were in the range 85-115%, except for azithromycin levels, which were around 70%. Erythromycin-H2O, clarithromycin and azithromyzin were found, at the sub ng l(-1) level, in the studied rivers.
Subject(s)
Anti-Bacterial Agents/analysis , Chromatography, High Pressure Liquid/methods , Spectrometry, Mass, Electrospray Ionization/methods , Water Pollutants, Chemical/analysisABSTRACT
A liquid chromatography-mass spectrometry method is proposed for the determination of seven macrolides authorised in the EU as veterinary drugs for food-producing animals. Sample treatment involves extraction of the analytes with a water-methanol mixture containing metaphosphoric acid and clean-up by SPE with a cation-exchange cartridge. Separation was carried out in an end-capped silica-based C18 column and mobile phases consisting of water/acetonitrile mixtures containing trifluoroacetic acid. A gradient elution, from 28 to 40% acetonitrile was used. Detection was performed by mass spectrometry with electrospray ionisation in the positive mode. Several parameters affecting the mass spectra were studied. The protonated molecular ion was selected for quantitation purposes under selected ion monitoring mode. Detection limits were in the range 1-20 microg l(-1). Recoveries ranged between 56 and 93% with RSD lower than 12%. The method has been successfully applied for multiresidue determination of seven macrolides below the MRLs established by the European Union.
Subject(s)
Anti-Bacterial Agents/analysis , Chromatography, Liquid/methods , Drug Residues/analysis , Muscles/chemistry , Spectrometry, Mass, Electrospray Ionization/methods , Animals , Chickens , Macrolides , Reproducibility of Results , Sensitivity and SpecificityABSTRACT
Liquid chromatography coupled to electrospray-mass spectrometry (LC-ES-MS) with positive ion detection was evaluated for the determination of tributyltin and triphenyltin in water samples using tripropyltin as internal standard. The separation was performed in the isocratic mode on a silica-based C18 column with a mobile phase containing 0.02% trifluoroacetic acid in acetonitrile-water (50:50, v/v). The optimum LC-ES-MS conditions were established and quantification was performed on the basis of the [M]+ ions. Limits of detection for standard solutions were 100 and 200 pg Sn injected for triphenyltin and tributyltin, respectively, and good reproducibility was observed. Solid-phase extraction was carried out on C18 cartridges to preconcentrate the analytes from natural water samples, with recoveries ranging from 80 to 110%. Limits of detection for SPE-LC-ES-MS were in the range of low ng l(-1), which demonstrates the suitability of the method for environmental samples.
Subject(s)
Chromatography, Liquid/methods , Organotin Compounds/analysis , Spectrometry, Mass, Electrospray Ionization/methods , Water Pollutants, Chemical/analysis , Reference Standards , Sensitivity and SpecificityABSTRACT
The features of the Dumas combustion method (CM) and those of the Kjeldahl method (KM) were compared as they apply to total nitrogen determination in animal feed. Both methods achieved similar repeatability (S.D., 0.11-0.38 from Kjeldahl and 0.15-0.36 from combustion) and similar intra-laboratory reproducibility (S.D., 0.11-0.39 from Kjeldahl and 0.15-0.37 from combustion). R.S.D. is always below 2%. These results show that the CM is suitable for the analysis of protein content in animal feed (5-75% protein content). The CM is recommended owing to its shorter analysis time, its cost and its environmental suitability.
