Literature DB >> 9358548

Evaluation of direct curve comparison metrics applied to pharmacokinetic profiles and relative bioavailability and bioequivalence.

S A Marston1, J E Polli.   

Abstract

PURPOSE: The intent was to investigate three direct curve comparison metrics, the Rescigno Index, f1, and the Chinchilli Metric as tools to assess relative bioavailability (BA) and bioequivalence (BE). The specific objectives were to 1) estimate relative bioavailability and bioequivalence and 2) compare detection of profile shape differences with typical (i.e. AUC and Cmax) criteria.
METHODS: Product bioequivalence was estimated and the degree of concordance with typical criteria in detecting profile differences was determined from the eighteen bioequivalence studies (390 subjects). Descriptive statistical analysis was carried out on the concordant and discordant profile subsets.
RESULTS: 1) Three of the eighteen studies failed typical criteria (AUC and Cmax). Of the curve metrics, 12 studies failed the Chinchilli metric criteria and 13 failed f1 criteria. Using three different exponents in the Rescigno Index calculation, 17 (exponent = 3), 13 (exponent = 1), and 11 (exponent = 1/3) failed the criteria for bioequivalence. The frequency of profiles found to be different was comparable across the metrics, but the specific profiles found to be different or not different varied across the metrics. The Chinchilli Metric and f1 agreed 71% and 72% with typical criteria in judging profiles to be different or not different. Descriptive evaluation suggested that the direct curve metrics more effectively detect differences in absorption time lags but less effectively detect differences in Cmax. The Rescigno Index showed dependence on the direction of the difference between test and reference concentrations.
CONCLUSIONS: With the limits used here, the direct curve metrics represent a more conservative approach to evaluate product bioequivalence. With further investigation and development, the direct curve approach may be used effectively to evaluate relative BA and BE.

Mesh:

Year:  1997        PMID: 9358548     DOI: 10.1023/a:1012160419520

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  8 in total

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Authors:  A Rescigno
Journal:  Pharm Res       Date:  1992-07       Impact factor: 4.200

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Authors:  M L Chen
Journal:  Pharm Res       Date:  1992-11       Impact factor: 4.200

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Journal:  Pharm Res       Date:  1995-12       Impact factor: 4.200

5.  The multivariate assessment of bioequivalence.

Authors:  V M Chinchilli; R K Elswick
Journal:  J Biopharm Stat       Date:  1997-03       Impact factor: 1.051

6.  Methods to compare dissolution profiles and a rationale for wide dissolution specifications for metoprolol tartrate tablets.

Authors:  J E Polli; G S Rekhi; L L Augsburger; V P Shah
Journal:  J Pharm Sci       Date:  1997-06       Impact factor: 3.534

7.  Sensitivity of indirect metrics for assessing "rate" in bioequivalence studies--moving the "goalposts" or changing the "game".

Authors:  A Rostami-Hodjegan; P R Jackson; G T Tucker
Journal:  J Pharm Sci       Date:  1994-11       Impact factor: 3.534

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Authors:  F Y Bois; T N Tozer; W W Hauck; M L Chen; R Patnaik; R L Williams
Journal:  Pharm Res       Date:  1994-07       Impact factor: 4.200

  8 in total
  6 in total

1.  Novel direct curve comparison metrics for bioequivalence.

Authors:  J E Polli; A M McLean
Journal:  Pharm Res       Date:  2001-06       Impact factor: 4.200

2.  Biometrical evaluation of bioequivalence trials using a bootstrap individual direct curve comparison method.

Authors:  E Zintzaras; P Bouka; A Kowald
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2002 Jan-Mar       Impact factor: 2.441

3.  When is a metric not a metric? Remarks on direct curve comparison in bioequivalence studies.

Authors:  Wojciech Jawień
Journal:  J Pharmacokinet Pharmacodyn       Date:  2009-06-21       Impact factor: 2.745

4.  Use of partial AUC (PAUC) to evaluate bioequivalence--a case study with complex absorption: methylphenidate.

Authors:  Jeanne Fourie Zirkelbach; Andre J Jackson; Yaning Wang; Donald J Schuirmann
Journal:  Pharm Res       Date:  2012-09-25       Impact factor: 4.200

5.  Trapezoid bioequivalence: A rational bioavailability evaluation approach on account of the pharmaceutical-driven balance of population average and variability.

Authors:  Sara Soufsaf; Fahima Nekka; Jun Li
Journal:  CPT Pharmacometrics Syst Pharmacol       Date:  2022-03-18

6.  IVIVC for Extended Release Hydrophilic Matrix Tablets in Consideration of Biorelevant Mechanical Stress.

Authors:  Valentyn Mohylyuk; Seyedreza Goldoozian; Gavin P Andrews; Andriy Dashevskiy
Journal:  Pharm Res       Date:  2020-10-22       Impact factor: 4.200

  6 in total

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