ABSTRACT
OBJECTIVE@#To establish a method for directional screening of the cytotoxic components from the medicinal herb of Achnatherum inebrians by a combination of surface plasmon resonance (SPR) biosensor and chromatographic isolation technology.@*METHODS@#Under the guidance of bioactive assessment based on binding abilities between objects and the α-Mannosidase (α-Man) target, the active components from different solvents extracts, different polar extraction parts and fractions were screened orderly and directionally using SPR. Components with a high binding ability to α-Man can be precisely oriented in a narrower fractions range and are easy to isolate. Three human cancer cells were used to evaluate the cytotoxic activity of component with the highest affinity to α-Man.@*RESULTS@#Eight compounds were isolated and identificated from A. inebrians for the first time. Deoxyvasicinone possessed the highest affinity to α-Man among them. Moreover, deoxyvasicinone showed good effects on inhibited proliferation of human hepatoma cells HepG2 (IC50 = 5.7 μmol/L), human breast cancer cells MCF7 (IC50 = 7.21 μmol/L) and human lung cancer cells HCC827 (IC50 = 0.75 μmol/L), respectively. In particular, its inhibitory effect on HCC827 was stronger than the positive drug gefitinib (IC50 = 1.65 μmol/L).@*CONCLUSION@#A comprehensive strategy of directional screening potential cytotoxic components from herb based on biomolecular interaction and chromatography was established. Deoxyvasicinone as an effective anti-cancer component was initially isolated from A. inebrians. It is expected that this screening strategy could provide new perspectives for rapid screening and identification of active components from natural plants with the complex matrix.
ABSTRACT
Objective: To develop a new method for the determination of anti-oxidant activity of drugs by using the peroxidase activity of graphene nanoenzyme, and apply it for the determination of the anti-oxidant activity of the national medicine Achnatherum inebrians. Methods: The anti-oxidant activity of 18 batches of samples was measured after optimizing H2O2 concentration and reaction time. At the same time, the anti-oxidative activity was measured again using the DPPH method. The Bland-Altman and Passing-Bablok regression methods were used to compare the detection data of the two methods. Results: Using the nanoenzyme method, the inhibition rates of 18 batches of A. inebrians were between 37.28% and 71.58%, with an average of 50.87% and a median of 47.09%. Free radical scavenging rates of 18 batches of A. inebrians measured by the DPPH method were between 36.06% and 83.11%, with an average of 54.89% and a median of 50.83%. The statistical results showed that the measured values of nanoenzyme method and DPPH method were similar; There was a linear relationship between the two methods, and different methods can be transformed by Passing-Bablok regression method. Conclusion: The graphene nanoenzyme was successfully applied to the detection of anti-oxidant activity, and the anti-oxidant activity of A. inebrians was also found. The nanoenzyme method can avoid the problem of light sensitivity of the reagent, shorten the reaction time, reduce the amount of medicinal solution, and the results are consistent with the DPPH method, which is suitable for the determination of antioxidant activity.