1.Ultrasonic microbubbles for glioma-targeted drug delivery.
Lijuan CHEN ; Cuitao LU ; Yingzheng ZHAO ; Lina DU ; Yiguang JIN
Acta Pharmaceutica Sinica 2015;50(1):99-103
		                        		
		                        			
		                        			Ultrasonic microbubbles were used to open blood-brain barriers (BBB) with a reversed and limited behavior feature in the study, which could improve the brain-targeted delivery of anti-tumor drugs. The glioma rat model was prepared. Low-frequency ultrasound was combined with microbubbles to affect the permeability of BBB compared with the permeability of independently administered Evans blue (EB) crossing BBB. Time point and length of ultrasound were investigated whether they affect the permeability of BBB and the damage of brain tissue. The effect of the growth time of glioma on BBB permeability was explored. Only glioma had a very little impact on BBB permeability. However, ultrasonic microbubbles opened the BBB with the features of temporary, limited and reversed behavior and improved EB and magnetic resonance imaging contrast agent penetrating BBB. A length of 30 s ultrasound is appropriate for opening BBB and no damage of brain tissue. Drugs should be injected before ultrasound so that they enter into brain as BBB opening. Ultrasonic microbubbles can open BBB effectively and safely, which improve drugs penetrating BBB under proper time point and length.
		                        		
		                        		
		                        		
		                        	
2.Anti-tumor activity of extracts from cultured cells of Taxus chinensis on cancer cell lines SMMC-7721 and HEp-2
Cuitao LU ; Xingguo MEI ; Wei GONG ; Yan LIU ;
Chinese Pharmacological Bulletin 2003;0(07):-
		                        		
		                        			
		                        			AIM  To analyze the toxicity and inhibitory mechanism of extracts from cultured cells (F  4 cell line) of   Taxus chinensis   on cancer cell lines SMMC  7721 and HEp  2. METHODS  MTT assay for cell viability and flow cytometry for cell cycle analysis. RESULTS  IC    50   of SMMC  7721 and HEp  2 were   0  161 4   g DCW?L    -1   and   0  275 6   g DCW?L    -1   respectively,tumor cells in G  2~M stage all increased with higher concentration and longer incubation of extracts from   Taxus chinensis   cells. CONCLUSION  Extracts from cultured cells of   Taxus chinensis   could have cytotoxic effect on SMMC  7721 and HEp  2 and could induce apoptosis of both two cancer cells.
		                        		
		                        		
		                        		
		                        	
3.Multi-index test applied in orthogonal design
Yingzheng ZHAO ; Cuitao LU ; Xingguo MEI ;
Journal of Medical Postgraduates 2003;0(07):-
		                        		
		                        			
		                        			Objective:To optimize the overall desirability of orthogonal design sith multi  index evaluations.  Methods:Four multi  index evaluations were applied to optimize the overall desirability of an orthogonal design,and their results wer analyzed.  Results:According to the optimum conditions,there was no difference among the four multi  index evaluations.  Conclusion:multi  index test can be used to represent the most desirable variables in experimental design.
		                        		
		                        		
		                        		
		                        	
4.Extract from cultured cells of Taxus chinensis on proliferation inhibition and apoptosis induction of tumor cells
Cuitao LU ; Yingzheng ZHAO ; Xingguo MEI ;
Chinese Traditional and Herbal Drugs 1994;0(11):-
		                        		
		                        			
		                        			Object  To study the inhibitory effect and mechanism of extract from cultured cell of Taxus chinensis (Pilg.) Rehd. on hepatocarcinoma cell line SMMC  7721. Methods  Trypan blue stain assay was used to determine tumor cell growth curve, flow cytometry and Giemsa staining were used to analyze cell cycle and cell apoptosis. Results  Inhibitory effect happened on tumor cell line SMMC  7721, G  2/M stage of tumor cells increased with the addition of T. chinensis cell extract by carrene and apoptosis happened. Conclusion  The extracts from cultured cell of T. chinensis have inhibitory effect on SMMC  7721 cells and can further induce cell apoptosis.
		                        		
		                        		
		                        		
		                        	
            
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