Biomedical subjects

Masato Sano

Publications and source records attributed to Masato Sano.

3 recordsLinked to original sources

PubMed2006

Estimation of membrane permeability and intracellular diffusion coefficients.

We propose a method for estimating membrane permeability and the intracellular diffusion coefficient using pulsed-gradient spin-echo measurement in combination with numerical simulation. The diffusion signal attenuation of leukocytes was measured with 4pi(2)q(2)(Delta-delta/3) values up to 6000 s/mm(2). For numerical simulations, the cell was modeled as a 15 x 15 microm(2) square with various membrane permeabilities and intracellular diffusion coefficients. Minimization of the difference in signal attenuations between the measurement and the simulation enabled estimations of these unknown parameters for the leukocytes. A cell sample of 2.17 x 10(8) cells/mL had a membrane permeability and an intracellular diffusion coefficient of 23 mum/s and 8.9 x 10(-4) mm(2)/s, respectively.

Cell Membrane Permeability↗

PubMed2003

Testicular metastasis from squamous cell carcinoma of the lung.

We present a case of squamous cell carcinoma of the testis that metastasized from lung cancer. The patient, who had received left pneumonectomy 2 years earlier for squamous cell carcinoma (SCC) of the lung, developed pulmonary metastasis, which was treated with chemotherapy. Although the recurrence regressed after treatment, the testicular tumor progressed gradually. Left radical orchiectomy was performed. Pathological examination revealed metastatic SCC. Testicular metastasis from lung cancer is a very rare disease.

Carcinoma, Squamous Cell↗

PubMed1999

Inhibitory action of clarithromycin on glycocalyx produced by MRSA.

We determined whether clarithromycin (CAM) had the ability to eliminate glycocalyx and biofilm produced by methicillin-resistant Staphylococcus aureus (MRSA) using an in-vitro experimental system (consisting of a bladder model and a kidney model) simulating complicated urinary tract infection (UTI). We also examined whether a combination of CAM and vancomycin (VCM) was effective for eliminating the MRSA biofilm. VCM (urinary concentration simulating drip infusion of 500 mg twice a day for 5 days; minimum inhibitory concentration (MIC) 0.5 &mgr;g/ml) eliminated MRSA from the bladder model medium at 48 h, but reproliferation occurred immediately after withdrawal of the agent. No disappearance of MRSA biofilm was noted, and this appeared to be the cause of the bacterial regrowth. CAM (urinary concentration simulating oral administration of 200 mg twice a day for 5 days; MIC, 128 &mgr;g/ml) allowed microbial recovery to the initial level within 48 h, but led to the disappearance of the glycocalyx-forming biofilm. A combination of VCM and CAM caused microbial elimination from the bladder model medium at 46 h with no regrowth after withdrawal of the antimicrobial agents. Scanning electron microscopy confirmed that the MRSA biofilm disappeared completely and no microbial adhesion was noted. These results suggest that CAM has an inhibitory action on glycocalyx and biofilm of MRSA, and that the combined use of VCM and CAM may be efficacious for the treatment of MRSA UTI

Journal Article↗