Migration of phenolic active ingredients in Danshen Dizhuye during ultrafiltration of hollow fiber membrane / 中国中药杂志

Study the suitability of organic film for salvianolic acid in the ultrafiltration process of Danshen Dizhuye. UPLC was used to analyze the migration of nine phenolic active ingredients in Danshen Dizhuye during ultrafiltration of PES hollow fiber membrane and PS hollow fiber membrane. The structural composition of multi-components was analyzed by three different batches of Danshen Dizhuye before and after ultrafiltration of the two membranes. The results showed that 9 phenolic active ingredients in Danshen Dizhuye did not change significantly after ultrafiltration through PES membrane. However, after ultrafiltration through PS membrane, the content of sodium danshensu, protocatechualdehyde, caffeic acid, 3-hydroxy-4-methoxycinnamic acid and rosmarinic acid in Danshen Dizhuye did not change significantly, while salvianolic acid D, salvianolic acid B and lithospermic acid decreased by about 20%, and the content of salvianolic acid A decreased significantly. The final content in equilibrium was only about 20% of the original solution. Therefore, an in-depth study on the migration particularity of salvianolic acid A in ultrafiltration membrane was the focuse. The results showed that the loss of salvianolic acid A was caused by both membranes during ultrafiltration, and salvianolic acid A was lost more in PS membrane. When the membrane was washed and regenerated, it was found that salvianolic acid A was detected in the ethanol washing solution, but not in the washing liquid, indicating that the loss of salvianolic acid A during the ultrafiltration was mainly adsorptive action. The results suggested that the migration of phenolic active ingredients in Danshen Dizhuye during the membrane ultrafiltration process did not completely follow the molecular weight passing rule of the membrane pore size. At the same time, it may be affected by factors, such as the structure of the membrane material, and the interaction between the membrane structure and the structure of components, and exhibit different migration behaviors during the ultrafiltration of the membrane.

Kinetics of addition of aromatic amines on trans-3- [P-Substituted phenyl] -1- Phenyl-Prop-2-En-1-Ones

The reactions of a series of trans-3-[p-substituted phenyl]-1-phenyl- prop-2-en-1-ones Ia-e with p-anisidine and p-nitroaniline IIa,b were studied in methanol, and their reaction rates were measured. The reaction followed a second order kinetics. In addition, the activation parameters delta H* and delta S* for the reactions of both amines were calculated and led to the conclusion of a cyclic multistep mechanism for that amine. Michael addition reaction involving one molecule from each of olefin and amine used. The nucleophilic attack of the aromatic amines IIa,b on olefines Ia-e obeyed Hamett equation