Safety data on 19 vehicles for use in 1 month oral rodent pre-clinical studies: administration of hydroxypropyl-ß-cyclodextrin causes renal toxicity-Reference-Cited by-同舟云学术

Safety data on 19 vehicles for use in 1 month oral rodent pre-clinical studies: administration of hydroxypropyl-ß-cyclodextrin causes renal toxicity

Published:2015-05-10 Issue:1 Volume:36 Page:140-150
ISSN:0260-437X
Container-title:Journal of Applied Toxicology
language:en
Short-container-title:J. Appl. Toxicol.

Author:

Healing Guy¹,Sulemann Tabassum²,Cotton Peter¹,Harris Jayne³,Hargreaves Adam¹,Finney Rowena¹,Kirk Sarah⁴,Schramm Carolin¹,Garner Clare¹,Pivette Perrine²,Burdett Lisa¹

Affiliation:

1. AstraZeneca; Drug Safety and Metabolism; Mereside, Alderley Park Macclesfield Cheshire SK10 4TG UK

2. AstraZeneca; Pharmaceutical Development; Mereside, Alderley Park Macclesfield Cheshire SK10 4TG UK

3. AstraZeneca; Drug Safety and Metabolism; 310 Darwin Building, Science Park Cambridge CB40 0WG UK

4. AstraZeneca; Discovery Sciences; Mereside, Alderley Park Macclesfield Cheshire SK10 4TG UK

Publisher

Wiley

Subject

Toxicology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/jat.3155/fullpdf

Reference38 articles.

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2. Cyclodextrins as pharmaceutical solubilizers;Brewster;Adv. Drug Deliver. Rev.,2007

3. Assessment of Labrasol®/Labrafil®/Transcutol® (4/4/2, v/v/v) as non-clinical vehicle for poorly water-soluble compounds after 4-weeks oral toxicity study in Wistar rats;Delongeas;Regul. Toxicol. Pharm.,2010

4. One-month intravenous toxicity studies of poloxamer 188 in male Sprague-Dawley rats and in beagle dogs;Duvinage;Toxicol. Lett.,1996

5. European Medicines Agency (EMA) 2013 Guideline on the Use of Phthalates as Excipients in Human Medicinal Products - Draft

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