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.
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.
The goal of this paper is the evaluation of fast two‐dimensional gas chromatography applied to bio‐oil samples. Bio‐oils are complex matrixes that usually are analyzed by conventional gas chromatography, involving long columns, long time of analysis due to slow heating rates, and consequently, high cost associated to time consumed. Fast gas chromatography techniques are based on the use of narrow capillary columns that allow the achievement high‐speed separations for complex samples, maintaining excellent resolution. Firstly, the two‐dimensional gas chromatography method was optimized varying the heating rate (10, 15 and 20°C min−1) and achieving the optimal separation at 15°C min−1. This method allies a good separation of bio‐oil constituents with shorter time analysis. The developed method and the traditional conventional two‐dimensional gas chromatography method (used in previous studies) were applied in the analysis of a mixture of 30 standard compounds. Despite coelutions of short retention time peaks (compounds with very similar physical‐chemical properties), the fast two‐dimensional gas chromatography method showed an increase in chromatographic signal and a noise reduction. Good results were also obtained in the real bio‐oil sample. Fast two‐dimensional gas chromatography maintained all the chromatographic information from conventional two‐dimensional gas chromatography, reducing drastically the total time of analysis.
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