Pharmacokinetic Equivalence of Taxotere and SID530, a Novel Docetaxel Formulation Containing Hydroxypropyl-beta-cyclodextrin in Monkeys
- Authors
- Kim, Tae-kon; Yoo, H. H.; Kim, Eun-jeong; Lee, Bongyong; Park , Jeonghill
- Issue Date
- Jun-2012
- Publisher
- Editio Cantor Verlag
- Keywords
- docetaxel; bioequivalence; HP-beta-CD; polysorbate 80; LC-MS/MS
- Citation
- Arzneimittel-Forschung/Drug Research, v.62, no.6, pp 280 - 284
- Pages
- 5
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- Arzneimittel-Forschung/Drug Research
- Volume
- 62
- Number
- 6
- Start Page
- 280
- End Page
- 284
- URI
- https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/32671
- DOI
- 10.1055/s-0032-1306305
- ISSN
- 0004-4172
1616-7066
- Abstract
- SID530 is a new parenteral formulation of docetaxel containing hydroxypropyl-beta-cyclodextrin (HP-beta-CD). In this study, a comparative pharmacokinetic study of 2 docetaxel parenteral solutions, SID530 and Taxotere, was carried out. In a crossover experimental design, 6 male cynomolgus monkeys received each formulation by intravenous infusion of a single dose. The concentration of docetaxel in whole blood and plasma was determined using liquid chromatography-tandem mass spectrometry (LC-MS/MS). The 2 formulations showed similar pharmacokinetic parameters in both whole blood and plasma, and displayed comparable values for maximum serum concentration (C-max), time to peak concentration (T-max), and area under the concentration-time curve (AUC). The 90% confidence intervals for the ratios of C-max and AUC values for SID530 to Taxotere were within the acceptable range of 0.80-1.20 in both plasma and whole blood. These findings indicate that SID530 and Taxotere are comparable in terms of their distribution in the blood and their plasma profile; consequently, these drugs are bioequivalent in the monkey.
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