In vivo safety and tolerability study of QR-441(a) using three dose formulations and three routes of administration in chickens
Autor: | Michael P Petteruti, Richard A Rosenbloom, Carolyn LeFante, Timothy S. Cummings, Mario Guralnik, Kelly Digian |
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Rok vydání: | 2007 |
Předmět: |
Drinking
Pharmacology Irritability Antiviral Agents Eating Random Allocation In vivo Toxicity Tests medicine Animals Pharmacology (medical) Palatability Organic Chemicals Adverse effect Administration Intranasal Plants Medicinal Dose-Response Relationship Drug business.industry Plant Extracts Body Weight Water General Medicine Animal Feed Tolerability Tolerability Study Taste Toxicity Nasal administration medicine.symptom business Chickens |
Zdroj: | American journal of therapeutics. 14(5) |
ISSN: | 1075-2765 |
Popis: | The current study assessed the safety, tolerability, and palatability of the experimental drug QR-441(a) using three dose formulations and three routes of administration. A 4-day study was carried out using a total of 132 chickens. A total of 11 groups were formed (12 chickens per group) subjected to varying concentrations and routes of administration of QR-441(a). Chickens were given a high, medium, or low dose of QR-441(a) in either feed, water, or both for a period of 4 days. In addition, one group was dosed intranasally, one drop per nostril four times a day. Although no lesions were found to suggest toxicity or irritability, the medium- and high-dose water groups reduced their water intake. This reduction in water intake suggests that chickens may find the medium and high water doses unpalatable. There was no reduction in water intake in the low-dose water groups or in any of the formulated feed groups. There was also no evidence of toxicity or irritability in the nasal-dose group. These data support the use of the low, medium, and high doses in feed and the use of the low-dose concentration in water for the administration of QR-441(a). The data also suggest that QR-441(a) can be administered intranasally without the presence of any adverse events. |
Databáze: | OpenAIRE |
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