Dielectric barrier discharge plasma pre-treatment to facilitate the acetylation process of corn starch under heating/cooling cycles.

The objective of the current work was to evaluate the impacts of dielectric barrier discharge plasma and repeated dry-heat treatments on the acetylation process of corn starch. The combined modification resulted in a higher substitution degree of acetate groups on starch chains compared to the acetylation treatment alone. This outcome was linked to the increase in surface area and structural organization level of granules achieved through the application of plasma and heating/cooling cycles, respectively. The successful esterification of starch structure was verified through FTIR (1710 cm-1) and 1H NMR (2 ppm). With the increase in plasma treatment duration up to 20 min, gelatinization enthalpy increased (10.81 J/g) due to the cross-linking reaction. Starch acetate produced through the combined treatment could find the application in the development of low-calorie food formulations due to its high resistant starch (70.5 g/100 g) and low viscosity (43 mPa s).

The cooperative effect of reduced graphene oxide and Triton X-114 on the electromembrane microextraction efficiency of Pramipexole as a model analyte in urine samples.

A new design of electromembrane microextraction coupled with high-performance liquid chromatography was developed for the determination of Pramipexole as a model analyte in urine samples. The presence of reduced graphene oxide in the membrane and Triton X-114 in the donor phase augments the extraction efficiency of Pramipexole by the proposed method. Dispersed reduced graphene oxide in the organic solvent was held in the pores of the fiber wall by capillary forces and sonication. It is possible that the immobilized reduced graphene oxide acts as a sorbent, affording an additional pathway for analyte transportation. Besides, the presence of Triton X-114 in the donor phase promotes effective migration of ionic analytes across the membrane. The parameters influencing the extraction procedure, such as type and concentration of surfactant, type of organic solvent, amount of reduced graphene oxide, sonication time, applied voltage, extraction time, ionic strength, pH of the donor and acceptor solutions, and stirring rate were optimized. The linear working ranges of the method for preconcentration- determination of Pramipexole in water and urine samples were found to be 0.13-1000 and 0.47-1000ngmL-1 with corresponding detection limits of 0.04 and 0.14ngmL-1, respectively. The proposed method allows achieving enrichment factors of 301 and 265 for preconcentration of the analyte in water and urine samples, respectively. The method was successfully applied for the determination of Pramipexole in the urine samples.