Effect of crystal size on the in vitro dissolution and oral absorption of nitrendipine in rats. (Q43002669)

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6 February 2020

title

Effect of crystal size on the in vitro dissolution and oral absorption of nitrendipine in rats (English)

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1

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author name string

Fude Cui

2

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Hongze Piao

3

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Dongmei Cun

4

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Hongyu Piao

5

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Yanbo Jiang

6

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Mei Ouyang

7

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Peng Quan

8

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publication date

29 June 2010

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published in

Pharmaceutical Research

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volume

27

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issue

9

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page(s)

1965-1976

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

6 February 2020

cites work

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Dissolution of slightly soluble drugs. IV. Effect of particle size of sulfonamides on in vitro dissolution rate and in vivo absorption rate, and their relation to solubility

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Stereoselective pharmacokinetics of oral and intravenous nitrendipine in healthy male subjects

21 January 2018

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Dissolution of slightly soluble drugs. V. Effect of particle size on gastrointestinal drug absorption and its relation to solubility

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Effect of nanonization on absorption of 301029: ex vivo and in vivo pharmacokinetic correlations determined by liquid chromatography/mass spectrometry

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Influence of hydrodynamics and particle size on the absorption of felodipine in labradors

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The effect of particle size on the absorption of digoxin

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In vitro permeability of PBCA nanoparticles through porcine small intestine

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Handling of computational in vitro/in vivo correlation problems by Microsoft Excel: III. Convolution and deconvolution

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Understanding the effect of API properties on bioavailability through absorption modeling

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Dissolution testing as a prognostic tool for oral drug absorption: dissolution behavior of glibenclamide

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Lectin-conjugated PLGA nanoparticles loaded with thymopentin: ex vivo bioadhesion and in vivo biodistribution

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Preparation of stable nitrendipine nanosuspensions using the precipitation-ultrasonication method for enhancement of dissolution and oral bioavailability

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12 December 2020

Estimating the fraction dose absorbed from suspensions of poorly soluble compounds in humans: a mathematical model.

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10.1007/S11095-010-0200-0

Identifiers

DOI

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6 February 2020

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