Response to nutrient variation on lipid productivity in green microalgae captured using second derivative FTIR and Raman spectroscopy

Two green microalgae species Monoraphidium contortum (M. contortum) and Chlamydomonas sp. that were identified to accumulate lipids were subjected to four different nutrient treatments (NP1-NP4), ranging in nitrate (0.05–5 mM N) and phosphate (2.8–264 μM P) concentrations, at a fixed N:P ratio of ∼18. The effect of nutrient variation on lipid productivity in the species was investigated using second derivative (SD) FTIR and Raman spectroscopy of algal biomass. SD spectral analysis revealed high production of lipid in the form of hydrocarbons (CH) (3000–2800 cm−1), triacylglycerides (TAGs)(∼1740 cm−1), saturated (SFA)(∼1440 cm−1), and unsaturated fatty acids (UFA)(∼3010 cm−1) for the nutrient deplete condition (NP1) in both species. Changes in signals attributed to lipids in proportion to other biochemical components were consistent with physiological changes expected from nutrient depletion. Relative signal intensities for lipids showed a significant increase in NP1, in particular, CH, TAGs in relation to protein signals (in SD-FTIR), and SFA, UFA in relation to carotenoid signals (in SD-Raman). PCA performed on the negative spectral values of the SD-FTIR and SD-Raman data for the four NP treatments enabled discrimination not only between the species but also between the NP treatments and the timing of harvest. M. contortum was found to contain a relatively higher proportion of CH, TAGs, SFA, and UFA compared to Chlamydomonas sp. Peak areas from the negative SD spectra, informed by PCA analysis, enabled capturing quantifiable changes in a manner that is consistent with known microalgal physiology. SD-FTIR and SD-Raman spectroscopy have been shown to possess superior potential to capture relevant microalgal physiological changes

Influence of Silver Nanoparticles on 2,3-Bis(Chloromethyl)Anthracene-1,4,9,10-Tetraone

International audienceSize effect of silver nano particles on the photophysical properties of 2,3-bis(chloromethyl)anthracene-1,4,9,10-tetraone (BCMAT) have been investigated using optical absorption and fluorescence emission techniques. Silver NPs of different sizes have been prepared by two different methods. Quenching of fluorescence of BCMAT has been found to increase with decrease in the size of the silver NPs. Stern-Volmer quenching constants have also been calculated

Characterization of new cocrystals by raman spectroscopy, powder X-ray diffraction, differential scanning calorimetry, and transmission raman spectroscopy

Cocrystals have been increasingly recognized as an attractive alternative delivery form for solids of drug products. In this work, salicylic acid was employed as a cocrystal former with the nicotinic acid, dl-phenylalanine, and 6-hydroxynicotinic acid (6HNA). Also, 3,4-dihydroxybenzoic acid with oxalic acid was studied. The cocrystals in all cases were prepared by slow evaporation from ethanol followed by characterization using Raman spectroscopy, powder X-ray diffraction, transmission Raman spectroscopy (TRS), and differential scanning calorimetry. Full understanding of the effects of formation on the vibrational modes of motion was obtained by the complete assignment of the spectra of the starting materials and of the cocrystal components. The results show that all the cocrystals, prepared in a 1:1 molar ratio, possess unique thermal, spectroscopic, and X-ray diffraction properties. Raman and TRS spectra showed that the vibrational modes of the cocrystal were different from those of the starting materials, suggesting that Raman spectroscopy and TRS are effective tools to evaluate cocrystal formation through interaction of their components. In addition, we have used a synthetic standard containing a 1:1:1 mixture of KNO 3 and raw material for which each sample was analyzed at seven random positions, with each point sampled twice. We have done the same with all cocrystals (1:1 KNO 3 and cocrystal), the ratios confirming that the cocrystal components (were in a 1:1 molar ratio). © 2010 American Chemical Society