(Q42207382)

18 October 2017

Influence of drug release properties of conventional solid dosage forms on the systemic exposure of highly soluble drugs (English)

1 reference

18 October 2017

L X Yu

1

1 reference

18 October 2017

C D Ellison

2

1 reference

18 October 2017

D P Conner

3

1 reference

18 October 2017

L J Lesko

4

1 reference

18 October 2017

A S Hussain

5

1 reference

18 October 2017

1 January 2001

1 reference

18 October 2017

1 reference

18 October 2017

3

1 reference

18 October 2017

3

1 reference

18 October 2017

E24

1 reference

Tablet dissolution affected by a moisture mediated solid-state interaction between drug and disintegrant

18 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2751019

The biopharmaceutics classification system (BCS): class III drugs - better candidates for BA/BE waiver?

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2751019

Saturable small intestinal drug absorption in humans: modeling and interpretation of cefatrizine data

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2751019

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

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2751019

Transit of pharmaceutical dosage forms through the small intestine

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2751019

A compartmental absorption and transit model for estimating oral drug absorption.

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2751019

The effect of in vivo dissolution, gastric emptying rate, and intestinal transit time on the peak concentration and area-under-the-curve of drugs with different gastrointestinal permeabilities.

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2751019

A comparison between direct determination of in vivo dissolution and the deconvolution technique in humans.

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2751019

A heterogeneous tube model of intestinal drug absorption based on probabilistic concepts

17 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11741275

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Development of predictive pharmacokinetic simulation models for drug discovery

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11741275

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Dependence of in vitro-in vivo correlation analysis acceptability on model selections

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11741275

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1208/PS030324

1 reference

18 October 2017

1 reference

18 October 2017

PubMed publication ID

11741275

1 reference