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31.
Ischemic or infarcted bowel: CT findings 总被引:4,自引:0,他引:4
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Rajaretinam Rajesh Kannan Appadurai Muthamil Iniyan Vincent Samuel Gnana Prakash 《Asian Pacific Journal of Tropical Biomedicine》2011,1(5):341-347
Objective
The aim of the present study was to isolate the anti-MRSA (Methicillin Resistant Staphylococcus aureus) molecule from the Mangrove symbiont Streptomyces and its biomedical studies in Zebrafish embryos.Methods
MRSA was isolated from the pus samples of Colachal hospitals and confirmed by amplification of mecA gene. Anti-MRSA molecule producing strain was identified by 16s rRNA gene sequencing. Anti-MRSA compound production was optimized by Solid State Fermentation (SSF) and the purification of the active molecule was carried out by TLC and RP-HPLC. The inhibitory concentration and LC50 were calculated using Statistical software SPSS. The Biomedical studies including the cardiac assay and organ toxicity assessment were carried out in Zebrafish.Results
The bioactive anti-MRSA small molecule A2 was purified by TLC with Rf value of 0.37 with 1.389 retention time at RP-HPLC. The Inhibitory Concentration of the purified molecule A2 was 30 µg/mL but, the inhibitory concentration of the MRSA in the infected embryo was 32-34 µg/mL for TLC purified molecule A2 with LC50 mean value was 61.504 µg/mL. Zebrafish toxicity was assessed in 48-60 µg/mL by observing the physiological deformities and the heart beat rates (HBR) of embryos for anti MRSA molecule showed the mean of 41.33-41.67 HBR/15 seconds for 40 µg/mL and control was 42.33-42.67 for 15 seconds which significantly showed that the anti-MRSA molecule A2 did not affected the HBR.Conclusions
Anti-MRSA molecule from Streptomyces sp PVRK-1 was isolated and biomedical studies in Zebrafish model assessed that the molecule was non toxic at the minimal inhibitory concentration of MRSA. 相似文献37.
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W Dörr S Schlichting MA Bray IR Flockhart JW Hopewell 《International journal of radiation biology》2013,89(3):243-250
Purpose: To define the effect of dexpanthenol with or without Aloe vera extract on radiation-induced oral mucositis.Materials and methods: Mouse tongue mucosal ulceration was analysed as the clinically relevant endpoint. Graded single or fractionated dose irradiation (10 x 3?Gy/2 weeks, graded test doses on day 14) were combined with topical administration of dexpanthenol or a base, with or without Aloe vera extract. The formulations were applied for 14 days (single dose) or 24 days after the first fraction.Results: Single dose irradiation resulted in an ED50 (dose at which a positive mucosal response was expected in 50% of the animals irradiated) of 11.9?±?1.2?Gy. None of the formulations yielded a significant change in incidence or time course of ulceration. Test irradiation after 10 x 3?Gy gave an ED50 of 9.0?±?0.1?Gy. Base treatment increased the ED50-values to 10.5?±?0.8?Gy (p?=?0.0095) and 9.9?±?0.7?Gy (p?=?0.0445) without or with Aloe vera. Dexpanthenol resulted in ED50 values of 9.5?±?0.1?Gy without Aloe vera (p?>?0.05), and of 10.9?±?0.9?Gy (p?=?0.0035) with Aloe vera. The latent time to ulceration was prolonged, compared to the control (6.3 days) without Aloe vera (8.0?–?8.2 days, p?<?0.001) and with dexpanthenol and Aloe vera (7.3 days, p?=?0.0239).Conclusions: With single dose irradiation, neither dexpanthenol nor Aloe vera extract significantly changed the oral mucosal radiation response. With fractionated irradiation, drug administration significantly increased the isoeffective radiation doses, independent of dexpanthenol or Aloe vera content. Neither dexpanthenol nor Aloe vera display a prophylactic potential. 相似文献
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