1.Cost-effectiveness Analysis of Therapeutic schemes for Peptic Ulcer With Helicobacteria Pylori
China Pharmacy 1991;0(05):-
OBJECTIVE:To evaluate the economic effectiveness of different pharmacotherapeutic schemes for the same disease Three therapeutic schemes(including A,B and C schemes)for peptic ulcer with Helicobacteria pylori were compared METHODS:The schemes were evaluated with pharmacoeconomic cost-effectiveness analysis RESULTS:The results showed that B was the best scheme from either cost-effectiveness analysis(C/E)or increasing costeffectiveness analysis(?C/?E) CONCLUSION:Pharmacoeconomics is very important in optimizing therapeutic scheme,guiding rational drug use and in_creasing economic effectiveness
2.Cost- effectiveness Analysis of Therapeutic schemes for Peptic Ulcer With Helicobacteria Pylori
Qinyun ZHENG ; Yanle QI ; Guanyang LIN
China Pharmacy 2001;12(5):282-283
OBJECTIVE: To evaluate the economic effectiveness of different pharmacotherapeutic schemes for the same disease Three therapeutic schemes( including A, B and C schemes) for peptic ulcer with Helicobacteria pylori were compared METHODS: The schemes were evaluated with pharmacoeconomic cost- effectiveness analysis RESULTS: The results showed that B was the best scheme from either cost- effectiveness analysis( C/E) or increasing costeffectiveness analysis( Δ C/Δ E) CONCLUSION: Pharmacoeconomics is very important in optimizing therapeutic scheme, guiding rational drug use and in_ creasing economic effectiveness
3.Protein expression and preparation of polyclonal antibody of AD-004 and study on its expression in the adrenal and testis
Jie QIAO ; Cuixia ZHENG ; Xia CHEN ; Xuesong LI ; Shengxian LI ; Qinyun MA ; Shuangxia ZHAO ; Guoyue YUAN ; Mingdao CHEN
Chinese Journal of Endocrinology and Metabolism 1986;0(04):-
Objective To prepare rabbit antibody against mouse AD-004 by AD-004 expressed in the prokaryotic expression system and to identify its distribution in the testis and adrenal. Methods The full-length cDNA of mouse AD-004 was cloned into PET28 plasmid, and the protein was induced in E. coli BL21 bacteria by adding IPTC and then purified by Ni2+ -NTA column. The purified protein was used as an immunogen to prepare polyclonal antibody ( pAb) of AD-004. The specificity of the antibody was detected by Western blotting. Immunohistochemical staining was performed in the mouse adrenal and testis via pAb of AD-004. Results Hisfused AD-004 was expressed efficiently in the prokaryotic system. Western blot analysis showed that the polyclonal antibody was duly bound to purified AD-004 with high specificity and sensitivity. AD-004 could be abundantly identified in the adrenal medulla and mainly expressed in the Leydig cells of testis. Conclusion The mouse protein of AD-004 is obtained from the prokaryotic expression system. The rabbit anti-AD-004 antibody has been prepared successfully. AD-004 protein is mainly localized in the interstitium of testis, suggesting that AD-004 may play a role in the synthesis of sex-steroid hormone.