期刊文献+

穿心莲内酯增强产生物被膜铜绿假单胞菌对左氧氟沙星敏感性的实验研究 被引量:6

Study on andrographolide to enhance the Pseudomonas aeruginosa 's sensitiveness of Levofloxacin
原文传递
导出
摘要 目的考察穿心莲内酯提高产生物被膜(BF)铜绿假单胞菌对左氧氟沙星的敏感性。方法采用琼脂倍比稀释法体外药物敏感性实验,考察穿心莲内酯与左氧氟沙星不同配比的22个样品对160株临床上近期分离的BF阳性铜绿假单胞菌的MIC值,并采用概率单位分析法,评价不同配比受试药物的抗菌活性;构建体外BF的渗透模型,观察穿心莲内酯在300、30、3μg·mL-1剂量下对BF渗透性的影响。结果左氧氟沙星配比穿心莲内酯在1:0.001~1:0.01时,药物的Emax和ED50虽然有一定的波动,但总体趋势上表现出Emax高于和ED50低于单用左氧氟沙星;穿心莲内酯在受试剂量下均可以提高铜绿假单胞菌BF模型对左氧氟沙星的渗透性,在模型构建后的2、4、6、8、10、24h时药物的渗透量显著升高。结论穿心莲内酯在一定剂量范围内有提高左氧氟沙星对产BF铜绿假单胞菌抗菌活性的作用,并且这一作用与药物提高BF的渗透性有关。 OBJECTIVE Study of andrographolide enhancing the sensitiveness of Levofloxacin on Pseudomonas aeruginosa producing biofilm (BF). METHODS Using experiments recommended and agar dilution method about the drug sensitivity in vitro, we investi- gate the influence of 22 samples of different andrographolide/Levatloxacin ratio on MIC of 160 BF - positive Pseudomonas aeruginosa after clinical separation using probit analysis ; In vitro BF infiltration model was established. Effeetes of 300,30,3 μg. mL - 1 androgra- pholide on the permeability of BF. RESULTS In vitro drug sensitivity resuhs showed that when the ration of Levofloxacin thtoan andrographolide was in 1 : 0. 001 -1 : 0.01 ,there were certain fluctuations in E and ED50 ,but the overall trend showed a higher E and lower ED50 than Levofloxaein used alone; Andrographolide could improve the permeability of Pseudomonas aeruginosa' s BF, the peruleability of Levofloxacin significantly increased in 2, 4, 6, 8, 10, 24 h after infiltration. CONCLUSION The results of drugin vitro sensitivity experiments suggest andrographolide can improve the antibacterial activity of Levofloxacin at dose within a certain related, which was related to increasing the permeability of Levofloxacin.
出处 《华西药学杂志》 CAS CSCD 北大核心 2014年第2期128-131,共4页 West China Journal of Pharmaceutical Sciences
基金 成都中医药大学自然科学基金面上项目(批准号:ZRMS201238)
关键词 左氧氟沙星 穿心莲内酯 BF 铜绿假单胞菌 敏感性 Levofloxacin Andrographolide BF Pseudomonas aeruginosa Drug sensitivity
  • 相关文献

参考文献8

  • 1I,isa S,Jane S. hffection control in cystic fibrosia[ J ]. Clin Micro- biol Rev ,2004,17 ( 1 ) :57 - 71. 被引量:1
  • 2谢轶,杨维青,贾文祥,程曦,曾蔚,杜艳,李学如,张再容.铜绿假单胞菌耐药性在生物被膜形成过程中的变化[J].中华微生物学和免疫学杂志,2005,25(4):314-318. 被引量:19
  • 3Stepanovic S, Vukovic D, l)akic, l,et al. A mortified microtiter- plate lest tbr quantifi('ation Df staphylococcal biofilm formation [ J ]. J Microbiol Methods ,2000,40 ( 2 ) : 175 - 179. 被引量:1
  • 4陈思敏,王平,曾南.抗菌药物体外敏感性实验的结果分析方法研究[J].成邯医学院学报,2012,7(4):579-581. 被引量:1
  • 5官妍,王宁,汪长中,刘志芳,章九云,石晶金.穿心莲内酯等中药有效成分对表皮葡萄球菌生物膜渗透性的比较[J].中国微生态学杂志,2012,24(1):9-12. 被引量:13
  • 6Chandrasekaran CV, Gupta A, Agarwal A. Effect of an extract of Androgrpbis pniculttta leaves on inflanunato17 and allergic mediators in t,itro [ J ]. J Ethnopharmacol, 2010, 129:203 - 207. 被引量:1
  • 7郭威,周莹,叶露,等.穿心莲内酯抑制铜绿假单胞菌外排泵MexAB-OprM的作用[J].中团医院药学杂志.2010,30(16):1343-1346. 被引量:1
  • 8Calabrese E J, B 1 ain R. The occurren'e of hormetie dose responses in the toxicologicalliterature, the honuesis database: An overview [ J ]. Toxicol Appl Pharmaco1,2005 ,202 :289 - 301. 被引量:1

二级参考文献23

  • 1张良,黄云超,奚廷斐(审校者).表皮葡萄球菌生物膜形成与生物材料感染[J].生物医学工程与临床,2006,10(3):194-196. 被引量:12
  • 2CHANG C H,LIN C C,YANG J J,et al. Anti-inflammatory effects of emodin f tom ventilago leiocarpa [ J ]. Am J Chin Med, 1996,24 ( 2 ) : 139-142. 被引量:1
  • 3Chalfie MY, Tu G, Euskirchen WW, et al. Green fluorescent protein as a marker for gene expression. Science, 1994, 263(5148): 802-805. 被引量:1
  • 4James DB, Ching-Tsan H. Recombinant plasmid retention and expression in bacterial biofilm cultures. Water Science and Technology, 1995, 31(2): 105-115. 被引量:1
  • 5Barnard FM, Maxell A. Interaction between DNA gyrase and quinolones: effects of alanine mutation at gyrA subunit residues Ser83 and Asp87. Antimicrob Agents Chemother, 2001, 45(7): 1994-2000. 被引量:1
  • 6Xian-Zhi L, Nikaido H. Efflux-mediated drug resistance in bacteria. Drugs, 2004, 64 (1): 1-31. 被引量:1
  • 7Rodney MD. Biofilm: microbial life on surfaces. Emerg Infect Dis, 2002, 8(9): 881-890. 被引量:1
  • 8Sauer K, Camper AK, Ehrlich GD, et al. Pseudomonas aeruginosa displays multiple phenotypes during development as a biofilm. J Bacteriol, 2002, 184(4): 1140-1154. 被引量:1
  • 9Cachia PJ, Hodges RS. Synthetic peptide vaccine and antibody therapeutic development: prevention and treatment of Pseudomonas aeruginosa. Biopolymers, 2003, 71(2): 141-168. 被引量:1
  • 10Lisa S, Jane S. Infection control in cystic fibrosis. Clin Microbiol Rev, 2004, 17(1): 57-71. 被引量:1

共引文献30

同被引文献123

引证文献6

二级引证文献52

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部