Toxicity evaluation of methoxy poly(ethylene oxide)- block -poly(ε-caprolactone) polymeric micelles following multiple oral and intraperitoneal administration to rats
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Le résumé fourni par la source
Methoxy poly(ethylene oxide)-block-poly(ɛ-caprolactone) (PEO-b-PCL) copolymers are amphiphilic and biodegradable copolymers designed to deliver a variety of drugs and diagnostic agents. The aim of this study was to synthesize PEO-b-PCL block copolymers and assess the toxic effects of drug-free PEO-b-PCL micelles after multiple-dose administrations via oral or intraperitoneal (ip) administration in rats. Assembly of block copolymers was achieved by co-solvent evaporation method. To investigate the toxicity profile of PEO-b-PCL micelles, sixty animals were divided into two major groups: The first group received PEO-b-PCL micelles (100 mg/kg) by oral gavage daily for seven days, while the other group received the same dose of micelles by ip injections daily for seven days. Twenty-four hours following the last dose, half of the animals from each group were sacrificed and blood and organs (lung, liver, kidneys, heart and spleen) were collected. Remaining animals were observed for further 14 days and was sacrificed at the end of the third week, and blood and organs were collected. None of the polymeric micelles administered caused any significant effects on relative organ weight, animal body weight, leucocytes count, % lymphocytes, liver and kidney toxicity markers and organs histology. Although the dose of copolymers used in this study is much higher than those used for drug delivery, it did not cause any significant toxic effects in rats. Histological examination of all the organs confirmed the nontoxic nature of the micelles.
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Le contrôle bibliographique ouvert
DOI retrouvé dans Crossref DOI retrouvé ; titre concordant.
- Titre Crossref
- Toxicity evaluation of methoxy poly(ethylene oxide)- block -poly(ε-caprolactone) polymeric micelles following multiple oral and intraperitoneal administration to rats
- Date Crossref
- 01/09/2017
- Éditeur
- Springer Science and Business Media LLC
- Type
- journal-article
Ce recoupement confirme des métadonnées liées au DOI. Il ne confirme ni la méthode ni les conclusions de l’étude, et il ne compte pas comme une seconde source scientifique indépendante.
Où se fait cette recherche
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King Saud University King Salman Bin Abdulaziz Chair for Kidney Disease pays non établi dans la noticeUniversité ou école supérieure
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College of Pharmacy Department of Pharmaceutics pays non établi dans la noticeUniversité ou école supérieure
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College of Medicine Department of Pathology pays non établi dans la noticeUniversité ou école supérieure
King Salman Bin Abdulaziz Chair for Kidney Disease — King Saud University, Department of Pharmaceutics — College of Pharmacy et Department of Pathology — College of Medicine.
Une affiliation ne permet pas de déduire la nationalité d’un auteur.