Literature DB >> 3322836

The hydrodynamically balanced system: a novel principle of controlled drug release.

W Erni1, K Held.   

Abstract

Madopar HBS (125 mg) is a controlled-release dosage form with 100 mg L-dopa and 25 mg benserazide. The 'hydrodynamically balanced system' (HBS) used for this novel dosage form of Madopar is a dosage form which, when in contact with gastric fluid and after dissolution of the gelatine shell of the capsule, forms a mucous body and a bulk density of less than 1 and releases the drug(s) at a desired rate whereas the dosage form remains in the stomach for a prolonged period of time. Drugs--in the present case L-dopa and benserazide--are released through the hydrated layer by diffusion principle. This system is valuable for drugs which are soluble at lower pH. By varying the composition of the excipients, desired release rates can be achieved. The in vitro dissolution rate of Madopar HBS formulation is as follows: L-dopa t75% = about 6 h and benserazide t75% = about 4 h. The floating behavior was tested in an in vitro test. These in vitro floating properties could be confirmed in man and were investigated in 10 healthy volunteers by means of gamma camera measurements using a poly-marker technique carried out in connection with a Valium CR study. It is expected that this novel drug delivery system proffers a valuable dosage form which delivers the drug at a specific rate allowing a better control of fluctuations in parkinsonian patients.

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Year:  1987        PMID: 3322836     DOI: 10.1159/000116171

Source DB:  PubMed          Journal:  Eur Neurol        ISSN: 0014-3022            Impact factor:   1.710


  15 in total

1.  Novel gastroretentive dosage forms: evaluation of gastroretentivity and its effect on levodopa absorption in humans.

Authors:  Eytan A Klausner; Eran Lavy; Miklos Barta; Eva Cserepes; Michael Friedman; Amnon Hoffman
Journal:  Pharm Res       Date:  2003-09       Impact factor: 4.200

Review 2.  Soluble and controlled-release preparations of levodopa: do we really need them?

Authors:  Giovanni Fabbrini; Flavio Di Stasio; Maria Bloise; Alfredo Berardelli
Journal:  J Neurol       Date:  2010-11       Impact factor: 4.849

Review 3.  Floating drug delivery systems: a review.

Authors:  Shweta Arora; Javed Ali; Alka Ahuja; Roop K Khar; Sanjula Baboota
Journal:  AAPS PharmSciTech       Date:  2005-10-19       Impact factor: 3.246

Review 4.  Current drug therapy for Parkinson's disease. A review.

Authors:  R J Coleman
Journal:  Drugs Aging       Date:  1992 Mar-Apr       Impact factor: 3.923

Review 5.  New directions in the drug treatment of Parkinson's disease.

Authors:  J L Montastruc; O Rascol; J M Senard
Journal:  Drugs Aging       Date:  1996-09       Impact factor: 3.923

Review 6.  Old Drugs, New Delivery Systems in Parkinson's Disease.

Authors:  Harsh V Gupta; Kelly E Lyons; Rajesh Pahwa
Journal:  Drugs Aging       Date:  2019-09       Impact factor: 3.923

7.  The bilayer floating capsule: a stomach-directed drug delivery system for misoprostol.

Authors:  M Oth; M Franz; J Timmermans; A Möes
Journal:  Pharm Res       Date:  1992-03       Impact factor: 4.200

8.  Controlled-release levodopa/benserazide (Madopar HBS): clinical observations and levodopa and dopamine plasma concentrations in fluctuating parkinsonian patients.

Authors:  A O Ceballos-Baumann; R von Kummer; W Eckert; H Weicker
Journal:  J Neurol       Date:  1990-02       Impact factor: 4.849

9.  Defining small differences in efficacy between anti-parkinsonian agents using gait analysis: a comparison of two controlled release formulations of levodopa/decarboxylase inhibitor.

Authors:  C Weller; C J O'Neill; A Charlett; S G Bowes; A Purkiss; P W Nicholson; R J Dobbs; S M Dobbs
Journal:  Br J Clin Pharmacol       Date:  1993-04       Impact factor: 4.335

Review 10.  Pharmacokinetic optimisation in the treatment of Parkinson's disease.

Authors:  M Contin; R Riva; F Albani; A Baruzzi
Journal:  Clin Pharmacokinet       Date:  1996-06       Impact factor: 6.447

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