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Exact(3)
In order to explore the time-dependent effects of the probiotics, AAD mice models were administered with probiotics for short term (5 days) and long term (15 days).
AAD mice models were administered with ceftriaxone (8 g/kg body weight, Rocephin, Shanghai Roche Pharmaceuticals Ltd., Shanghai, China) intragastrically through a ball-tipped stainless steel gavage needle once daily for 5 days except the normal group [ 5, 6].
AAD models were administered with single probiotic strain and probiotic mixture for short term and long term to evaluate the changes of the composition and diversity of intestinal microbiota, histopathology of the colon, and the systemic inflammation.
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A questionnaire based on attitude-social norms-self efficacy model was administered to a convenience sample of critical care HCWs (n = 77 physicians, n = 100 nurses; response rate 81%).
Model mice were administered G-Re intragastrically (4 mg/kg/day as a high dose and 1 mg/kg/day as a low dose) for 30 days.
In the experiment (18 55 days), mice of the blank group and the model group were administered with normal saline gavage, while the drug groups were given 80, 40, and 20 mg/kg of TSRDN.
To sustain the growth of the ER-positive ZR-75-1 cell model, animals were administered a 1.7 mg, 60-day slow-release estrogen pellet from Innovative Research of America (Sarasota, FL) subcutaneously in the dorsal space of the neck.
In the A673 rhabdomyosarcoma xenograft model, antibodies were administered intraperitoneally at 5 mg/kg/dose, 3 times per week for a total of 9 doses.
Rats in sham and model groups were administered with the same volume of distilled water.
Behavioural variables derived from Gebbie and Merrill's model 14 were administered to participants if (1) they can identify and locate the agency's emergency response plan, (2) they can describe the agency's role in responding to emergencies that might arise and (3) they can describe one's own functions and roles in responding to emergencies that might arise.
Although there is clinical relevance for testing reversal agents in a trauma model, all agents were administered ex vivo.
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