The aim of this study was to investigate the influence of ethylenediaminetetraacetic acid （EDTA） irrigation on demineralization rate of dentine located in the apical third of root canal walls. Teeth were divided int...The aim of this study was to investigate the influence of ethylenediaminetetraacetic acid （EDTA） irrigation on demineralization rate of dentine located in the apical third of root canal walls. Teeth were divided into A and B two groups. In group A, all of the teeth was irrigated with EDTA and NaOCI （sodium hypochlorite）, followed by cutting the apical third into slices longitudinally to examine the influence of EDTA on different portions of apical third of root canal. In group B, the apical third of a tooth was firstly cut into slices longitudinally, followed by coating the root canal walls with EDTA to in-situ observe the demineralization of dentine with different time. It was found that the influence of EDTA on root-canal was gradually increased from the apical to the upper end of the apical third for group A. In addition, the demineralization rate of dentine was remarkable in the first 25 min for group B. The diffusion of EDTA into root dentine would lead to potential damage to the dentine. Furthermore, demineralization rate curve was calculated.展开更多
Objective: Increasing the emergence of Metallo-β-lactamase (MBL) producing gram-negative bacteria and their dexterous horizontal transmission demands rapid and accurate detection. This study was conducted to determin...Objective: Increasing the emergence of Metallo-β-lactamase (MBL) producing gram-negative bacteria and their dexterous horizontal transmission demands rapid and accurate detection. This study was conducted to determine a suitable method to promptly detect MBL-producing gram-negative bacteria. Methods: A total of 103 gram-negative bacteria were identified from various clinical samples at a tertiary care hospital in Dhaka city. MBL producers were detected by two phenotypic methods, the Disk Potentiation Test (DPT) and the Double Disk Synergy Test (DDST) based on β-lactam chelator combinations where EDTA/SMA has been used as an inhibitor and Imipenem, Ceftazidime as substrates. Results: 103 isolates which were identified as Escherichia coli spp, Klebsiella spp, Pseudomonas spp, Acinetobacter spp, Proteus spp, Providencia spp were found to be multidrug-resistant in antibiogram test. Isolates showed complete resistance (100%) to Imipenem, Meropenem, and Amoxiclav. The highest carbapenem-resistant etiological agents were Acinetobacter spp 40 (38.8%) followed by Pseudomonas spp 27 (26.2%), Klebsiella spp 26 (25.2%), Escherichia coli 8 (7.8%), Proteus spp 1 (1%) and Providencia spp 1 (1%). DPT method detected significantly (p = 0.000009) a higher number of MBL-producers (Imipenem with 0.5 M EDTA n = 61, 59.2% & Ceftazidime with 0.5 M EDTA n = 56, 54.4%) compared to the DDST method (Imipenem -0.5 M EDTA n = 43, 41.7%, Imipenem – SMA n = 38, 36.9% & Ceftazidime -0.5 M EDTA n = 15, 14.6%). Conclusion: Pieces of evidence suggest that DPT is a more sensitive method than DDST and could be recommended for identifying MBL-producing bacteria in Bangladeshi hospitals for the proper management of patients, to reduce time constraints and treatment costs.展开更多
基金the financial support of the project from the Foundation of the Education Department of Liaoning Province(Grant No.L2013285)Science and Technology Planning Project of Shenyang City(Grant No.F11262-9-16)
文摘The aim of this study was to investigate the influence of ethylenediaminetetraacetic acid （EDTA） irrigation on demineralization rate of dentine located in the apical third of root canal walls. Teeth were divided into A and B two groups. In group A, all of the teeth was irrigated with EDTA and NaOCI （sodium hypochlorite）, followed by cutting the apical third into slices longitudinally to examine the influence of EDTA on different portions of apical third of root canal. In group B, the apical third of a tooth was firstly cut into slices longitudinally, followed by coating the root canal walls with EDTA to in-situ observe the demineralization of dentine with different time. It was found that the influence of EDTA on root-canal was gradually increased from the apical to the upper end of the apical third for group A. In addition, the demineralization rate of dentine was remarkable in the first 25 min for group B. The diffusion of EDTA into root dentine would lead to potential damage to the dentine. Furthermore, demineralization rate curve was calculated.
文摘Objective: Increasing the emergence of Metallo-β-lactamase (MBL) producing gram-negative bacteria and their dexterous horizontal transmission demands rapid and accurate detection. This study was conducted to determine a suitable method to promptly detect MBL-producing gram-negative bacteria. Methods: A total of 103 gram-negative bacteria were identified from various clinical samples at a tertiary care hospital in Dhaka city. MBL producers were detected by two phenotypic methods, the Disk Potentiation Test (DPT) and the Double Disk Synergy Test (DDST) based on β-lactam chelator combinations where EDTA/SMA has been used as an inhibitor and Imipenem, Ceftazidime as substrates. Results: 103 isolates which were identified as Escherichia coli spp, Klebsiella spp, Pseudomonas spp, Acinetobacter spp, Proteus spp, Providencia spp were found to be multidrug-resistant in antibiogram test. Isolates showed complete resistance (100%) to Imipenem, Meropenem, and Amoxiclav. The highest carbapenem-resistant etiological agents were Acinetobacter spp 40 (38.8%) followed by Pseudomonas spp 27 (26.2%), Klebsiella spp 26 (25.2%), Escherichia coli 8 (7.8%), Proteus spp 1 (1%) and Providencia spp 1 (1%). DPT method detected significantly (p = 0.000009) a higher number of MBL-producers (Imipenem with 0.5 M EDTA n = 61, 59.2% & Ceftazidime with 0.5 M EDTA n = 56, 54.4%) compared to the DDST method (Imipenem -0.5 M EDTA n = 43, 41.7%, Imipenem – SMA n = 38, 36.9% & Ceftazidime -0.5 M EDTA n = 15, 14.6%). Conclusion: Pieces of evidence suggest that DPT is a more sensitive method than DDST and could be recommended for identifying MBL-producing bacteria in Bangladeshi hospitals for the proper management of patients, to reduce time constraints and treatment costs.
基金This work was supported by Collaborative Innovation Center of Suzhou Nano Science and Technology,the National Basic Research Program of China (No.2014CB932700),National Natural Science Foundation of China (Nos.21573206,51371164,and 51132007),Strategic Priority Research Program B of the CAS (No.XDB01020000),Hefei Science Center CAS (No.2015HSC-UP016),and Fundamental Research Funds for the Central Universities.
