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Journal ArticleDOI

Modeling and comparison of dissolution profiles.

TLDR
Drug dissolution from solid dosage forms has been described by kinetic models in which the dissolved amount of drug (Q) is a function of the test time, t or Q=f(t).
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This article is published in European Journal of Pharmaceutical Sciences.The article was published on 2001-05-01. It has received 4794 citations till now. The article focuses on the topics: Dissolution testing & Dosage form.

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Citations
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Journal ArticleDOI

The morphology of salt crystals affects the perception of saltiness

TL;DR: Crystal morphology may be a variable to consider to achieve sodium reduction while maintaining salt intensity in order to correlate the findings with the perception of saltiness over time.
Journal ArticleDOI

Masking the Bitter Taste of Injectable Lidocaine HCl Formulation for Dental Procedures

TL;DR: The taste evaluation study indicated that HP-β-CD (1:1 and 1:2 M ratios) significantly improved the bitter taste of LID injectable formulation, and inclusion complex in the 1:1 M ratio with 0.09% sodium saccharin was considered to be optimum in masking the bitter tasted LID.
Journal ArticleDOI

Evaluation of acetylated moth bean starch as a carrier for controlled drug delivery.

TL;DR: A new hydrophobic polymer is synthesized using acetylation of native moth bean starch for controlled release excipient for pharmaceutical formulation development and the results revealed that the acetylated mothbean starch can be used as controlled release polymer.
Journal ArticleDOI

Sintering of wax for controlling release from pellets

TL;DR: In vitro drug release profiles indicated an increase in drug release retardation with increasing carnauba wax concentration, and sintered pellets had a higher hydrophobicity than did the unsintered pellets.
References
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Book

The mathematics of diffusion

John Crank
TL;DR: Though it incorporates much new material, this new edition preserves the general character of the book in providing a collection of solutions of the equations of diffusion and describing how these solutions may be obtained.
Book

Introduction to percolation theory

TL;DR: In this paper, a scaling solution for the Bethe lattice is proposed for cluster numbers and a scaling assumption for cluster number scaling assumptions for cluster radius and fractal dimension is proposed.
Book

Introduction to percolation theory

TL;DR: In this article, a scaling solution for the Bethe lattice is proposed for cluster numbers and a scaling assumption for cluster number scaling assumptions for cluster radius and fractal dimension is proposed.
Journal ArticleDOI

Mechanisms of solute release from porous hydrophilic polymers

TL;DR: In this article, the role of dynamic swelling and the dissolution of the polymer matrix on the release mechanism was discussed, as well as the effect of the tracer/excipient ratio on the poly(vinyl alcohol) release profile.
Journal ArticleDOI

Mechanism of sustained‐action medication. Theoretical analysis of rate of release of solid drugs dispersed in solid matrices

TL;DR: The analyses suggest that for the latter system the time required to release 50% of the drug would normally be expected to be approximately 10 per cent of that required to dissolve the last trace of the solid drug phase in the center of the pellet.
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