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Chen-Fu Lin

Publications and source records attributed to Chen-Fu Lin.

3 recordsLinked to original sources

In vitro activities of various piperacillin and sulbactam combinations against bacterial pathogens isolated from Intensive Care Units in Taiwan: SMART 2004 programme data.

We investigated the in vitro activity of various piperacillin and sulbactam combinations against Gram-negative bacterial isolates from Intensive Care Units (ICUs) in Taiwan. Antimicrobial susceptibility testing of 1030 bacterial isolates recovered from ICUs of nine major teaching hospitals was performed using the agar dilution method. Sulbactam was added to piperacillin either at a fixed sulbactam concentration of 4 mg/L and 8 mg/L or at a piperacillin:sulbactam ratio of 2:1 and 4:1. Piperacillin/sulbactam at a ratio of 2:1 or a fixed 8 mg/L concentration of sulbactam had better activities against Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis and Serratia marcescens than other piperacillin/sulbactam formulations. For Pseudomonas aeruginosa, piperacillin/sulbactam (2:1 or 4:1 ratios) had MIC(90) values (minimum inhibitory concentration for 90% of the organisms) of 64 mg/L (>90% susceptibility) compared with 64 mg/L for cefoperazone/sulbactam (68% susceptibility) and 128 mg/L for piperacillin/tazobactam (82% susceptibility). For Acinetobacter baumannii, both piperacillin/sulbactam (either 2:1 ratio or a fixed 8 mg/L sulbactam) and cefoperazone/sulbactam were the most potent agents. Adding sulbactam to piperacillin resulted in increased susceptibility rates among piperacillin-resistant P. aeruginosa (53-57% in either 2:1 or 4:1 ratios) and A. baumannii (38-46% in either 2:1 ratio or a fixed 8 mg/L concentration of sulbactam) isolates. Results of susceptibility tests with piperacillin/sulbactam are dependent on the method used. Piperacillin/sulbactam combinations possessed better in vitro activities than piperacillin alone or piperacillin/tazobactam against P. aeruginosa and A. baumannii.

Bacteria↗

Microfluidic pH-sensing chips integrated with pneumatic fluid-control devices.

This paper presents a microfluidic chip capable of performing precise continuous pH measurements in an automatic mode. The chip is fabricated using micro-electro-mechanical-systems (MEMS)-based techniques and incorporates polydimethylsiloxane (PDMS) microstructures, pH-sensing electrodes and pneumatic fluid-control devices. Through its enhanced microchannel design and use of pneumatic fluid-control devices, the microfluidic chip reduces the dead volume of the sample and increases the pumping rate. The maximum pumping rate of the developed micro-pump is 28 microL/min at an air pressure of 10 psi and a driving frequency of 10 Hz. The total sample volume consumed in each sensing operation is just 0.515 microL. As a result, the developed chip reduces the sample volume compared to conventional large-scale pH-sensing systems. The microfluidic chip employs the electrochemical sensing method to conduct precise pH level measurements. The sensing electrodes are fabricated by sputtering a layer of SiO(2)-LiO(2)-BaO-TiO(2)-La(2)O(3) (SLBTLO) onto platinum (Pt) electrodes and the pH value of the sample is evaluated by measuring the potential difference between the sensing electrodes and a reference electrode. Additionally, the integration of the microfluidic chip with a pneumatic fluid-control device facilitates automatic sample injection and a continuous sensing operation. The developed system provides a valuable tool with which to examine pH values in a wide range of biomedical and industrial applications.

Electrochemistry↗

Comparison of animal models with soft tissue infection by different bacilli.

In clinical medicine improved diagnostic methods for the detection of infection are needed. A good infectious animal model is very important for the development of a new diagnostic method or drug. The purpose of this study was to establish a good animal model with soft tissue infection. Twenty-four SD rats were divided into four groups (6 in each group). Various bacilli including Staphylococcus aureus (S. aureus), Streptococcus pneumoniae (S. pneumoniae), and Escherichia coli (E. coli) were injected intramuscularly into the left caudal thighs of three groups of rats to create soft tissue infection. In addition, normal saline was injected into the left caudal thighs of ten rats which were used as controls. Before and 48 hr after inoculation of the bacilli, a blood sample (0.5 ml) was taken from each rat and analyzed to determine the white blood cell count and differentiated cell count. In addition, 48 hr after the inoculation, 0.2 mCi of gallium-67 was injected via the tail vein. Gallium scan was performed at 24 hr and 48 hr after administration of the radiotracer. The dorsal view of both hind legs was imaged and analyzed by computers to calculate the lesion-to-normal (L/N) ratio. After imaging, all rats were sacrificed and specimens from portions of the infected thigh muscle were sent for histopathologic investigation to confirm the infection. The increase in both the WBC counts and the segmented polymorphonuclear leukocytes (PMNs) were most significant in the S. aureus group, followed by the S. pneumoniae group, E. coli group and normal control groups. The rats with S. aureus infection had significant gallium uptake at the site of infection and the highest L/N ratio of 2.14 on the 24-hr image and 2.0 on the 48-hr image. The rats with S. pneumoniae had the second highest L/N ratio (1.41 at 24 hr, and 1.48 at 48 hr). The L/N ratio for the E. coli group was 1.27 at 24 hr and 1.35 at 48 hr. No obviously abnormal gallium uptake was demonstrated in the normal controls. We conclude that all three bacilli induced a soft tissue infection in SD rats. S. aureus resulted in the most significant infectious signs.

Animals↗