A novel approach to estimate in vitro antibacterial potency of Chinese medicine using a concentration-killing curve method
文献类型: 外文期刊
作者: Liu, YQ 1 ; Zhang, YZ 2 ; Sun, CY 2 ; Gao, PJ 2 ;
作者机构: 1.Shandong Univ, State Key Lab Microbial Technol, Jinan 250100, Peoples R China
2.Shandong Univ, State Key Lab Microbial Technol, Jinan 250100, Peoples R China; Shandong Acad Agr Sci, Inst Anim Sci & Vet Med, Jinan 250100, Peoples R China
关键词: Radix et rhizoma rhei;Cortex phellodendri;Rhizoma coptidis;antibacterial potency;concentration-killing curve;BC50
期刊名称:AMERICAN JOURNAL OF CHINESE MEDICINE ( 影响因子:4.667; 五年影响因子:4.135 )
ISSN: 0192-415X
年卷期: 2005 年 33 卷 4 期
页码:
收录情况: SCI
摘要: The antibacterial pharmacodynamics against E. coli of Chinese medicine (CM) Rhizoma coptidis (Coptis Root) and its formula Sanhuang, and the control antibiotics enoxacin, were analyzed by a concentration-killing curve (CKC) approach, and the novel parameters BC50 and r for antibacterial potency were proposed. Using the agar plate method, about 400 cells of E. coli were evenly inoculated into LB agar plates containing a series of different concentrations of CM or antibiotic, and after a 24 hour incubation at 37 degrees C, all the viable colonies were enumerated. This resulted in a sigmoid concentration-killing curve that could be closely fitted (R-2 > 0.9) with the function: N = N0/1 = e(r(x-BC50)), in which N-0, BC50 and r represent meaningfully inoculums size, median bactericidal concentration, and bactericidal intensity, respectively. N modeled the survival of colony-forming units on each plate (CFU/plate) in a concentration series x of the drug. The CKC was symmetrical about its single inflexion (BC50, N-0/2). Therefore theoretically, 2BC(50) can replace MBC (minimum bactericidal concentration). BC1 = BC50 + 1n(N-0-1)/r, the drug concentration at r which only one colony survived, was the least critical value of ABC in CKC. The parameters 2BC(50) and BC1 agreed more closely with the definition of MBC, and were little affected by either the biochemical basis of the antibacterial or the inoculum's size (200-400 CFU/plate), and were determined by a multi-point curve. As a result, these were more accurate, reproducible and practical as metrics than was the endpoint of ABC. The two-dimensional CKC, involving BC50 and r, captures the intrinsic dynamics of the antibacterial effect of CM/strain versus concentration, and it is consistent with the Logistic equation of the bacterial growth curve in the format. This verified approach has considerable value as a tool for the accurate and proper administration of CM. The CKC of CM, different from that of antibiotics, is likely to be the resultant force of each ingredient in certain CM, which provides a clue to solve the problem of antibiotic resistance.
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