Research on solubilization used for micellar enhanced ultrafiltration

Micellar enhanced ultrafiltration （MEUF） is a new effective treatment technology for the filtration removal of organic pollutants through solubilization. The present paper is aimed to study the solubilization of organic compounds such as chlorobenzene （CB）, pyrene and phenol by anionic, cationic and mixed anionic-nonionic surfactants such as sodium dodecyl sulfate （SDS）, cetyltrimethylammonium bromide （CTMAB） and Tween-80 （TW80） and the mixed SDS-TW80 with a batch equilibrium method. This study enables us to supply deeper investigation for MEUF. The results showed that solubilization capacity was not obvious below the critical micellar concentration （CMC）. The apparent solubilities of organic compounds were linearly related to surfactant concentrations over their CMCs. Solubilization capacity by single surfactants follow the order of TW80 〉 CTMAB 〉 SDS. The results also proved that the solubilization of the organic contaminants by the mixed surfactants can significantly be enhanced compared with the single anionic surfactant SDS. Whereas the CMC can be decreased, the solubility can be increased as long as the mass ratio of nonionic surfactant increases. The solubility enhancement efficiency of the different organic compounds follow the order of phenol 〉 CB 〉 pyrene. In addition, the solubilization ratio appears to be positively relative to the intrinsic water solubility of the organic contaminants and negatively correlates to octanol-water coefficients （Kow） of organic compounds and the hydrophile-lypophile balance values （HLB） of the surfactants.

Simultaneous determination of Repaglinide and Irbesartan in biological plasmas using micellar enhanced excitation-emission matrix fluorescence coupled with ATLD method

A highly sensitive and selective 3D excitation-emission fluorescence method has been proposed to rapidly quantify the combined antidiabetics Repaglinide(Re) and Irbesartan(Ir) in rat and human plasmas with the aid of second-order calibration method based on alternating trilinear decomposition(ATLD) method. Re and Ir with weak fluorescence can be endowed with strong fluorescent property by changing the microenvironment in samples and improving the fluorescence quantum yield by using an appropriate micellar enhanced surfactant. The enhanced excitation-emission matrix fluorescence of Re and Ir can be accurately resolved and can simultaneously attain the optimal concentration even in the presence of a potentially strong intrinsic fluorescence from complex biological matrices, such as rat and human plasmas, by using the ATLD method, which completely exploits the "second-order advantage". The average recoveries of Re and Ir obtained from ATLD with the factor number of 3(N=3) were 101.0%±4.3% and 99.1%±4.1% for rat plasma and 100.5%±5.4% and 97.1%±3.6% for human plasma. Several statistical methods, including Student's t-test, figures of merit, and elliptical joint confidence region, have been utilized to evaluate the accuracy of the proposed method. Results show that the developed method can maintain second-order advantage in simultaneous determinations of the weak fluorescent analytes of interest in different biological plasma matrices.

O-(β-hydroxyethyl)rutosides determination by micellar flow injection(FI)-spectrofluorimetry

A simple,eco-friendly.sensitive and economic flow injection spectrofluorimetric method was developed for the determination of O-（β-hydroxyethyl）rutosidcs.The procedure was based on the use of an anionic surfactant such as sodium dodecyl sulfate to provide an appreciable O-（β-hydroxyethyl）rutosides fluorescence enhancement,increasing considerably the sensitivity of detection.All the variables affecting the fluorescence intensity were studied and optimized.The flow rate was 5 mL/min with detection at 450 nm（after excitation at 346 nm）.A linear correlation between drug amount and peak area was established for 0-（β-hydroxyethyl）rulosides in the range of 0.01-200 μg/mL with a detection limit of0.001 μg/mL（s/n = 3）.Validation processes were performed by recovering studies with satisfactory results.The new methodology can be employed for the routine analysis of 0-（P-hydroxyethyl）rutosides in bulks as well as in commercial formulations.