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Surfactants are amphiphilic compounds having hydrophilic and hydrophobic moieties in their structure. They can be of synthetic or of microbial origin, obtained respectively from chemical synthesis or from microorganisms' activity. A new generation of ecofriendly surfactant molecules or biobased surfactants is increasingly growing, attributed to their versatility of applications. Surfactants can be used as drug delivery systems for a range of molecules given their capacity to create micelles which can promote the encapsulation of bioactives of pharmaceutical interest; besides, these assemblies can also show antimicrobial properties. The advantages of biosurfactants include their high biodegradability profile, low risk of toxicity, production from renewable sources, functionality under extreme pH and temperature conditions, and long-term physicochemical stability. The application potential of these types of polymers is related to their properties enabling them to be processed by emulsification, separation, solubilization, surface (interfacial) tension, and adsorption for the production of a range of drug delivery systems. Biosurfactants have been employed as a drug delivery system to improve the bioavailability of a good number of drugs that exhibit low aqueous solubility. The great potential of these molecules is related to their auto assembly and emulsification capacity. Biosurfactants produced from bacteria are of particular interest due to their antibacterial, antifungal, and antiviral properties with therapeutic and biomedical potential. In this review, we discuss recent advances and perspectives of biosurfactants with antimicrobial properties and how they can be used as structures to develop semisolid hydrogels for drug delivery, in environmental bioremediation, in biotechnology for the reduction of production costs and also their ecotoxicological impact as pesticide alternative.

Comprehensive two-dimensional gas chromatography coupled with time-of-flight mass spectrometry (GC × GC/TOFMS) is used to characterize complex bio-oil samples because of the high peak capacity associated with the high acquisition rate and mass spectra deconvolution capability of TOFMS. A recent application of fast GC × GC for this type of analysis improved sample throughput while achieving the same peak capacity without the use of cryogenic liquids. This work evaluates the effect of the TOFMS data acquisition rate on the quality of the analytical information obtained by GC × GC/TOFMS. In the analysis of coconut fiber bio-oil under fast GC × GC/TOFMS conditions, use of high data acquisition rates (200-300 Hz) increases the number of identifiable peaks by more than 50% compared with that achieved at the conventional rate of 100 Hz. The acquisition rate can affect the peak capacity by a factor of 3 or more. This is the first study to demonstrate the importance of optimizing the data acquisition rate, a parameter that has previously been neglected in the literature, in GC × GC/TOFMS development., (Copyright © 2020 Elsevier B.V. All rights reserved.)

Silica gel containing silver ions was prepared and characterized. Silica was organofunctionalized with 3-mercaptopropyl group by using grafting reaction followed by silver ions adsorption (silver covalently bonded to mercaptopropyl silca gel, Ag-MPSG). The organofunctionalization and silver coordination were observed by transmission infrared spectroscopy and elemental analyses (CHN and EDS). The textural characteristics were studied by N 2 adsorption-desorption isotherms. Additionally, optical properties were studied by diffuse reflectance spectroscopy. The Ag-MPSG material was employed as stationary phase for the first time for fractionation of a heavy gas oil sample resulting in a fraction that is richer in polycyclic aromatic sulfur heterocycles (PASH). The fractions were analyzed by comprehensive two-dimensional gas chromatography with time-of-flight mass spectrometric detector and Ag-MPSG material provided similar fractionation performance when compared to conventional material [palladium covalently bonded to mercaptopropyl silca gel, Pd(II)-MPSG] usually employed for the same purpose and as the cost of silver is less than the one of palladium, the cost of the fractionation phase was reduced., (Copyright © 2016 Elsevier B.V. All rights reserved.)

The present research is based on the development and use of a flow-modulation (FM) comprehensive two-dimensional gas chromatography-quadrupole mass spectrometry (GC×GC-qMS) method for the determination of recently-highlighted (by the Scientific Committee on Consumer Safety) fragrance allergens (54) in cosmetics. FM GC×GC-qMS conditions were finely tuned to generate flow conditions (≈7 mL min(-1)) compatible with the qMS system used. Six-point calibration curves, over the range 1, 5, 10, 20, 50, 100 mg L(-1), were constructed for the 54 target allergens, with satisfactory linearity observed in all cases. Absolute quantification was performed by using extracted ions; target analyte identification was performed through measurement of ion ratios (qualifier/quantifier), full-scan MS database matching and the use of linear retention indices. Additional analytical figures of merit subjected to measurement were intra-day repeatability, accuracy at the 25 and 5 mg L(-1) levels, and limits of detection and quantification. The number of data points per peak, along with mass spectral skewing, was also subjected to evaluation. Finally, the FM GC×GC-qMS method was used not only for the quantification of target allergens in five commercial perfumes, but also for general qualitative profiling., (Copyright © 2015 Elsevier B.V. All rights reserved.)

The selection of ester-producing yeasts is difficult because these molecules evaporate quickly, are extremely unstable and may be missed during analytical manipulation. We propose an easy, fast and efficient headspace-SPME method for screening of ester-producing yeasts directly at the extraction vials (in situ HS-SPME)., (Copyright © 2014 Elsevier B.V. All rights reserved.)

The microalgae Desmodesmus subspicatus (Chlorophyta) was cultivated in a tubular photobioreactor using effluent from the wastewater treatment plant of the University of Santa Cruz do Sul, Brazil to demonstrate the reactor's operation. The algae's ability to remove nutrients from wastewater and the oleaginous potential of the algae's biomass were also evaluated. Total phosphorus and ammonia nitrogen were measured. The photobioreactor consisted of a system of three acrylic tubes, a reservoir, connections and a CO2 supply. The gas supply was semicontinuous with CO2 added from a cylinder. The culture's growth was estimated from cell numbers counted on a daily basis. Lipid content in the biomass was analysed using gas chromatography. A maximum cell density of 9.11 x 10(6) cellsmL-1 and a dry weight of 234.00 mg L-1 were obtained during cultivation without CO2, and these values rose to 42.48 x 10(6) cells mL-1 and 1277.44 mg L-1, respectively, when CO2 was added to the cultivation. Differences in the quality of the effluent and the presence of CO2 did not result in different lipid profiles. The presence ofpalmitic acid and oleic acid was notable. The average extracted oil content was 18% and 12% for cultivation with and without the input of CO2, respectively.