Literature DB >> 8008697

Controlled drug release of highly water-soluble pentoxifylline from time-limit disintegration-type wax matrix tablets.

M Otsuka1, Y Matsuda.   

Abstract

A pulsatile drug release system with a dry-coated tablet containing pentoxifylline was investigated for controlling drug release in the gastrointestinal tract. The system consisted of a core tablet with disintegrator and outer layer, which obtained compression from the ground mixtures of pentoxifylline and behenic acid. Drug release from a dry-coated tablet was investigated at 37 degrees C in JPXII 2nd fluid at pH 6.8. The drug release from the outer layer was fitted to the Cobby model. The drug release from the wax matrix increased significantly after tablet distintegration; therefore, the drug release profiles showed typical sigmoidal curves. The disintegration time depended on the weight fraction of the core tablet, and the drug release rate after disintegration increased with increasing drug concentration in the core tablet. The relationship between the time required for 50% drug release and the disintegration time was linear, indicating that the drug release rate was controlled by regulating the disintegration time.

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Year:  1994        PMID: 8008697     DOI: 10.1023/a:1018944516678

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


  9 in total

1.  MECHANISM OF SUSTAINED-ACTION MEDICATION. THEORETICAL ANALYSIS OF RATE OF RELEASE OF SOLID DRUGS DISPERSED IN SOLID MATRICES.

Authors:  T HIGUCHI
Journal:  J Pharm Sci       Date:  1963-12       Impact factor: 3.534

2.  THE USE OF SILICONE RUBBER AS A CARRIER FOR PROLONGED DRUG THERAPY.

Authors:  J FOLKMAN; D M LONG
Journal:  J Surg Res       Date:  1964-03       Impact factor: 2.192

3.  Design and preparation of pulsatile release tablet as a new oral drug delivery system.

Authors:  R Ishino; H Yoshino; Y Hirakawa; K Noda
Journal:  Chem Pharm Bull (Tokyo)       Date:  1992-11       Impact factor: 1.645

4.  Release of highly water-soluble medicinal compounds from inert, heterogeneous matrixes. I: Physical mixture.

Authors:  T P Foster; E L Parrott
Journal:  J Pharm Sci       Date:  1990-09       Impact factor: 3.534

5.  Release of highly water-soluble medicinal compounds from inert, heterogeneous matrixes. II: Melt.

Authors:  T P Foster; E L Parrott
Journal:  J Pharm Sci       Date:  1990-10       Impact factor: 3.534

6.  Influence of shape factors on kinetics of drug release from matrix tablets. I. Theoretical.

Authors:  J Cobby; M Mayersohn; G C Walker
Journal:  J Pharm Sci       Date:  1974-05       Impact factor: 3.534

7.  A pharmacokinetic analysis program (multi) for microcomputer.

Authors:  K Yamaoka; Y Tanigawara; T Nakagawa; T Uno
Journal:  J Pharmacobiodyn       Date:  1981-11

8.  Investigation of factors influencing release of solid drug dispersed in inert matrices. 3. Quantitative studies involving the polyethylene plastic matrix.

Authors:  S J Desai; P Singh; A P Simonelli; W I Higuchi
Journal:  J Pharm Sci       Date:  1966-11       Impact factor: 3.534

9.  Absorption of diltiazem in beagle dog from pulsatile release tablet.

Authors:  R Ishino; H Yoshino; Y Hirakawa; K Noda
Journal:  Chem Pharm Bull (Tokyo)       Date:  1992-11       Impact factor: 1.645

  9 in total
  1 in total

Review 1.  Applications of Nanobiomaterials in the Therapy and Imaging of Acute Liver Failure.

Authors:  Yuanyuan Jin; Haixia Wang; Ke Yi; Shixian Lv; Hanze Hu; Mingqiang Li; Yu Tao
Journal:  Nanomicro Lett       Date:  2020-11-19
  1 in total

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