Arzneimittelforschung 2009; 59(8): 392-396
DOI: 10.1055/s-0031-1296413
Antihypertensives
Editio Cantor Verlag Aulendorf (Germany)

Bioequivalence Study of Two Tablet Formulations of Ramipril in Healthy Volunteers

Alessandro Allegrini
1   Clinical Research Centre, Centre of Excellence on Aging, “G. D’Annunzio”, University Foundation, Chieti, (Italy)
,
Loredana Nuzzo
1   Clinical Research Centre, Centre of Excellence on Aging, “G. D’Annunzio”, University Foundation, Chieti, (Italy)
,
Mirco Zucchelli
1   Clinical Research Centre, Centre of Excellence on Aging, “G. D’Annunzio”, University Foundation, Chieti, (Italy)
,
Andrea Tavella-Scaringi
1   Clinical Research Centre, Centre of Excellence on Aging, “G. D’Annunzio”, University Foundation, Chieti, (Italy)
,
Marco Bucci
1   Clinical Research Centre, Centre of Excellence on Aging, “G. D’Annunzio”, University Foundation, Chieti, (Italy)
,
Daniele Pavone
1   Clinical Research Centre, Centre of Excellence on Aging, “G. D’Annunzio”, University Foundation, Chieti, (Italy)
,
Elena Toniato
1   Clinical Research Centre, Centre of Excellence on Aging, “G. D’Annunzio”, University Foundation, Chieti, (Italy)
,
Andrea Mezzetti
1   Clinical Research Centre, Centre of Excellence on Aging, “G. D’Annunzio”, University Foundation, Chieti, (Italy)
,
Stefano Martinotti
1   Clinical Research Centre, Centre of Excellence on Aging, “G. D’Annunzio”, University Foundation, Chieti, (Italy)
,
Stefano Bonani
1   Segix Italia S. r. l., Rome, (Italy)
› Author Affiliations
Further Information

Publication History

Publication Date:
13 December 2011 (online)

This study was conducted in order to assess the bioequivalence of a test and reference tablet formulation containing 10 mg of ramipril ((lS,5S,7S)-8-[(2S)-2-[[(lS)-l-ethoxycarbonyl-3-phenyl-pro-pyl]amino]propanoyl]-8-azabicyclo[3.3.0] octane-7-carboxylic acid, CAS 87333-19-5). Forty healthy male and female volunteers were treated in a single-centre randomised, single-dose, open-label, 2-way crossover study, with a washout period of 35 days between treatments. Plasma samples were collected up to 168 h post-dosing for the determination of ramipril and its active metabolite, ramiprilat, by LC-MS/MS. The evaluation of bioequivalence was based on the following pharmacokinetic parameters that were calculated by standard non-com-partmental methods: the area under the plasma concentration-time curve from zero to the time of the last quantifiable concentration (AUC,) and that extrapolated to infinity (AUC) and the maximum observed concentration (Cmax). The 90% confidence interval of the ratios (test/reference) (obtained by analysis of variance, ANOVA) were 0.83–1.20 for Cmax of ramipril, 0.90–1.10 for Cmax of ramiprilat, 0.95–1.23 for AUC0–48 of ramipril, 0.97–1.11 for AUC0–168 of ramiprilat, 0.96–1.23 for AUC of ramipril and 0.98–1.15 for AUC of ramiprilat, i. e. within the predefined acceptable range for the conclusion of bioequivalence. Tmax of the test formulation was 0.67 ± 0.33 h for ramipril and 2.28 ± 0.74 h for ramiprilat; Tmax of the reference formulation was 0.71 ± 0.32 h for ramipril and 2.40 ± 0.88 for ramiprilat. The ramipril and ramiprilat Tmax values estimated for the test and the reference formulations were not significantly different (p-value > 0.05). The study indicated that the test and reference formulations containing 10 mg of ramipril were equivalent in terms of both the rate and extent of bioavailability.

 
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