Preparation of poly(N-isopropylacrylamide) copolymers and preliminary assessment of their acute and subacute toxicity in mice
Autor: | Anne Otto, Frédéric Eeckman, David Fontaine, Hugues Malonne, André Jules Moes, Louis De Vos, Jeanine Fontaine, Karim Amighi |
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Rok vydání: | 2005 |
Předmět: |
medicine.medical_specialty
Polymers Subacute toxicity Pharmaceutical Science Pharmacology Dosage form Mice chemistry.chemical_compound Internal medicine medicine Animals Organ weight Acrylamides No-Observed-Adverse-Effect Level Hematology Cumulative toxicity business.industry Health condition General Medicine Acute toxicity Surgery Acrylates chemistry Poly(N-isopropylacrylamide) business Biotechnology |
Zdroj: | European Journal of Pharmaceutics and Biopharmaceutics. 61:188-194 |
ISSN: | 0939-6411 |
DOI: | 10.1016/j.ejpb.2005.05.007 |
Popis: | A subacute toxicity study was conducted to evaluate the oral toxicity profile of poly(N-isopropylacrylamide) (PNIPAAm) derivatives. These thermoresponsive polymers may have several potential pharmaceutical applications such as ingredient for oral solid dosage form. A preliminary acute oral toxicity study was performed with one of the polymer (PNIPAAm-co-NVA) at a unique dose of 4000 mg/kg body weight administered to six male and six female mice, to determine the dosage for further evaluation. No treatment-related effect was observed on behavior and health condition of the experimental animals during the 14 days observational period. The autopsy of the treated animals did not revealed any macroscopic changes in major organ aspects. Based on these preliminary results we selected a 2000 mg/kg body weight/day dose for the 28 days long subacute study. Three polymers were tested, namely PNIPAAm, PNIPAAm-co-NVA and PNIPAAm-co-AAc and compared to a saline control. No significant changes in clinical signs, body weight and food consumption, hematology, clinical chemistry or absolute organ weight were observed. Histological examination of excised major organs showed no marked differences between treated and control mice. In conclusion, PNIPAAm-co-NVA is well tolerated up to 4000 mg/kg body weight when administered orally. In addition, the subacute study indicated the absence of cumulative toxicity and a no-observed-adverse-effect level (NOAEL) of 2000 mg/kg was identified for PNIPAAm and its two copolymers. Further studies are mandatory. |
Databáze: | OpenAIRE |
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