In vitro / in vivo correlation of biperiden tablets

碩士 === 高雄醫學大學 === 藥學研究所 === 88 === Biperiden is helpful in managing significant tremor of Parkinson’s disease and antipsychotic-induced extrapyramidal symptoms (EPS). The major purposes of the study are fixed to compare the difference of the brand product (A) and the four generic products...

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Main Authors: Hsing-Jung Chou, 周幸蓉
Other Authors: Yi-Hung Tsai
Format: Others
Language:zh-TW
Published: 2000
Online Access:http://ndltd.ncl.edu.tw/handle/16306191114787247526
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spelling ndltd-TW-088KMC005510202015-10-13T10:56:27Z http://ndltd.ncl.edu.tw/handle/16306191114787247526 In vitro / in vivo correlation of biperiden tablets Biperiden錠體內與體外相關性之研究 Hsing-Jung Chou 周幸蓉 碩士 高雄醫學大學 藥學研究所 88 Biperiden is helpful in managing significant tremor of Parkinson’s disease and antipsychotic-induced extrapyramidal symptoms (EPS). The major purposes of the study are fixed to compare the difference of the brand product (A) and the four generic products (B, C, D, and E) in vitro, then to find the most different generic product from the brand product and administrate to rabbits to figure out the appropriate in vitro/in vivo correlation of biperiden tablets. In this study, simulated intestinal fluid, water, and 0.1N hydrochloric acid were used as the dissolution media to confirm the relationship between pH value and dissolution profile. The difference factor (f1) and similarity factor (f2) published by FDA were employed to compare the similarity of multipoint dissolution profiles of brand and the generic products in the media. The pharmacokinetic parameters were determined by PCNONLIN software. Thereafter, the appropriate in vitro/in vivo correlation of biperiden tablets could be approached. Biperiden tablets were fast dissolved in first 20 minutes. The pH value and biperiden concentration in media was found to be an inverse relationship. All f1 values of generic products are more than 15 and f2 values of generic products are less than 50. This means no significant similarity was observed in dissolution profiles between the brand and the generic products. Peak concentration (Cmax) of brand and the generic biperiden tablets were 25 to 28 ng ml-1 reached after 1.1 to 1.5 h (Tmax). Absorption rate constant (Kabs) of brand and the generic biperiden tablets were 1.084 h-1. No significant difference was observed in pharmacokinetic parameters between the brand and the generic products. Therefore, there is no close in vitro/in vivo correlation in the biperiden tablets studied. Yi-Hung Tsai 蔡義弘 2000 學位論文 ; thesis 86 zh-TW
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language zh-TW
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description 碩士 === 高雄醫學大學 === 藥學研究所 === 88 === Biperiden is helpful in managing significant tremor of Parkinson’s disease and antipsychotic-induced extrapyramidal symptoms (EPS). The major purposes of the study are fixed to compare the difference of the brand product (A) and the four generic products (B, C, D, and E) in vitro, then to find the most different generic product from the brand product and administrate to rabbits to figure out the appropriate in vitro/in vivo correlation of biperiden tablets. In this study, simulated intestinal fluid, water, and 0.1N hydrochloric acid were used as the dissolution media to confirm the relationship between pH value and dissolution profile. The difference factor (f1) and similarity factor (f2) published by FDA were employed to compare the similarity of multipoint dissolution profiles of brand and the generic products in the media. The pharmacokinetic parameters were determined by PCNONLIN software. Thereafter, the appropriate in vitro/in vivo correlation of biperiden tablets could be approached. Biperiden tablets were fast dissolved in first 20 minutes. The pH value and biperiden concentration in media was found to be an inverse relationship. All f1 values of generic products are more than 15 and f2 values of generic products are less than 50. This means no significant similarity was observed in dissolution profiles between the brand and the generic products. Peak concentration (Cmax) of brand and the generic biperiden tablets were 25 to 28 ng ml-1 reached after 1.1 to 1.5 h (Tmax). Absorption rate constant (Kabs) of brand and the generic biperiden tablets were 1.084 h-1. No significant difference was observed in pharmacokinetic parameters between the brand and the generic products. Therefore, there is no close in vitro/in vivo correlation in the biperiden tablets studied.
author2 Yi-Hung Tsai
author_facet Yi-Hung Tsai
Hsing-Jung Chou
周幸蓉
author Hsing-Jung Chou
周幸蓉
spellingShingle Hsing-Jung Chou
周幸蓉
In vitro / in vivo correlation of biperiden tablets
author_sort Hsing-Jung Chou
title In vitro / in vivo correlation of biperiden tablets
title_short In vitro / in vivo correlation of biperiden tablets
title_full In vitro / in vivo correlation of biperiden tablets
title_fullStr In vitro / in vivo correlation of biperiden tablets
title_full_unstemmed In vitro / in vivo correlation of biperiden tablets
title_sort in vitro / in vivo correlation of biperiden tablets
publishDate 2000
url http://ndltd.ncl.edu.tw/handle/16306191114787247526
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AT zhōuxìngróng biperidendìngtǐnèiyǔtǐwàixiāngguānxìngzhīyánjiū
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