Literature DB >> 1448420

Regional jejunal perfusion, a new in vivo approach to study oral drug absorption in man.

H Lennernäs1, O Ahrenstedt, R Hällgren, L Knutson, M Ryde, L K Paalzow.   

Abstract

Recently a new in vivo approach in man, using a regional intestinal perfusion technique, has been developed. The perfusion tube consists of a multichannel tube with two inflatable balloons, which are placed 10 cm apart. The tube is introduced orally and the time required for insertion and positioning of the tube is approximately 1 hr. In the present study eight healthy subjects were perfused in the proximal jejunum on three separate occasions. The first two perfusion experiments used the same flow rate, 3 ml/min, and the third experiment used 6 ml/min. Phenazone (antipyrine) was chosen as the model drug. The recovery of PEG 4000 in the outlet intestinal perfusate was complete in experiments 1 and 2, but slightly lower (90%) when the higher flow rate was used. The mean (+/- SD) fraction of phenazone absorbed calculated from perfusion data was 51 +/- 12% (3 ml/min), 64 +/- 19% (3 ml/min), and 42 +/- 27% (6 ml/min) for the three experiments, respectively. The mean fraction absorbed estimated by deconvolution of the plasma data was 47 +/- 16%, 51 +/- 19%, and 38 +/- 26%, respectively. The effective permeability of phenazone was 5.3 +/- 2.5, 11 +/- 6.8, and 11 +/- 12 (x 10(4) cm/sec, respectively. We have shown that it was possible to establish a tight intestinal segment which behaved as a well-mixed compartment. The low perfusion rate of 3 ml/min was preferred, since it resulted in the lowest variability in absorption.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1992        PMID: 1448420     DOI: 10.1023/a:1015888813741

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


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Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1974       Impact factor: 3.000

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  45 in total

1.  Dissolution of hydrocortisone in human and simulated intestinal fluids.

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Journal:  Pharm Res       Date:  2000-02       Impact factor: 4.200

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Journal:  Pharm Res       Date:  1999-02       Impact factor: 4.200

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Journal:  AAPS PharmSciTech       Date:  2003       Impact factor: 3.246

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Journal:  Pharm Res       Date:  1997-09       Impact factor: 4.200

Review 5.  Why is it challenging to predict intestinal drug absorption and oral bioavailability in human using rat model.

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Journal:  Pharm Res       Date:  2006-08       Impact factor: 4.200

6.  The use of BDDCS in classifying the permeability of marketed drugs.

Authors:  Leslie Z Benet; Gordon L Amidon; Dirk M Barends; Hans Lennernäs; James E Polli; Vinod P Shah; Salomon A Stavchansky; Lawrence X Yu
Journal:  Pharm Res       Date:  2008-01-31       Impact factor: 4.200

Review 7.  Mechanistic approaches to predicting oral drug absorption.

Authors:  Weili Huang; Sau Lawrence Lee; Lawrence X Yu
Journal:  AAPS J       Date:  2009-04-21       Impact factor: 4.009

8.  The influence of net water absorption on the permeability of antipyrine and levodopa in the human jejunum.

Authors:  D Nilsson; U Fagerholm; H Lennernäs
Journal:  Pharm Res       Date:  1994-11       Impact factor: 4.200

9.  Regional rectal perfusion: a new in vivo approach to study rectal drug absorption in man.

Authors:  H Lennernäs; U Fagerholm; Y Raab; B Gerdin; R Hällgren
Journal:  Pharm Res       Date:  1995-03       Impact factor: 4.200

10.  A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability.

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Journal:  Pharm Res       Date:  1995-03       Impact factor: 4.200

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