Evidence map›Paper›PMID 29288412›Full record

ArticlePharmaceutical research2017

Closed-Loop Doluisio (Colon, Small Intestine) and Single-Pass Intestinal Perfusion (Colon, Jejunum) in Rat-Biophysical Model and Predictions Based on Caco-2.

Isabel Lozoya-Agullo, Isabel Gonzalez-Alvarez, Moran Zur, Noa Fine-Shamir, Yael Cohen, Milica Markovic, Teresa M Garrigues, Arik Dahan, Marta Gonzalez-Alvarez, Matilde Merino-Sanjuán and 2 more

Abstract read
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In one paragraph

Article in Pharmaceutical research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.6field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 29 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 2 countries.

Isabel Lozoya-AgulloPharmacokinetics and Pharmaceutical Technology, Miguel Hernandez University, Alicante, Spain.
Isabel Gonzalez-AlvarezPharmacokinetics and Pharmaceutical Technology, Miguel Hernandez University, Alicante, Spain.
Moran ZurDepartment of Clinical Pharmacology, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Noa Fine-ShamirDepartment of Clinical Pharmacology, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Yael CohenDepartment of Clinical Pharmacology, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Milica MarkovicDepartment of Clinical Pharmacology, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Teresa M GarriguesPharmacokinetics and Pharmaceutical Technology, University of Valencia, Valencia, Spain.
Arik DahanDepartment of Clinical Pharmacology, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Marta Gonzalez-AlvarezPharmacokinetics and Pharmaceutical Technology, Miguel Hernandez University, Alicante, Spain.
Matilde Merino-SanjuánPharmacokinetics and Pharmaceutical Technology, University of Valencia, Valencia, Spain.
Marival BermejoPharmacokinetics and Pharmaceutical Technology, Miguel Hernandez University, Alicante, Spain. mbermejo@goumh.umh.es.ORCID http://orcid.org/0000-0001-5022-0544
Alex Avdeefin-ADME Research, 1732 First Avenue, No.102, New York, New York, 10128, USA.
Ben-Gurion University of the Negev · ILUniversitat de Miguel Hernández d'Elx · ESUniversitat de València · ES

Funding

European Commission DCI-ALA/19.09.01/10/21526/245-297/ALFA 111(2010)29Ministerio de Economía y Competitividad SAF2016-78756-PMinisterio de Educación, Cultura y Deporte FPU 2012-00280
6 · The paper itself

Abstract

purposeThe effective rat intestinal permeability (P

methodsFour types of rat intestinal perfusion data were considered: single-pass intestinal perfusion (SPIP) in the jejunum (n = 40), and colon (n = 15), closed-loop (Doluisio type) in the small intestine (n = 78), and colon (n = 74). Moreover, in vitro Caco-2 permeability values were used to predict rat in vivo values in the rat data studied.

resultsComparable number of molecules permeate via paracellular water channels as by the lipoidal transcellular route in the SPIP method, although in the closed-loop method, the paracellular route appears dominant in the colon. The aqueous boundary layer thickness in the small intestine is comparable to that found in unstirred in vitro monolayer assays; it is thinner in the colon. The mucosal surface area in anaesthetized rats is 0.96-1.4 times the smooth cylinder calculated value in the colon, and it is 3.1-3.6 times in the small intestine. The paracellular permeability of the intestine appeared to be greater in rat than human, with the colon showing more leakiness (higher P

conclusionBased on log intrinsic permeability values, the correlations between the in vitro and in vivo models ranged from r

Indexed as

Models, BiologicalAnimalsCaco-2 CellsColonDatabases, PharmaceuticalHumansIntestinal AbsorptionIntestinal MucosaIntestine, SmallJejunumMaleOrganic ChemicalsPerfusionPermeabilityPharmaceutical PreparationsPharmacokineticsOrganic ChemicalsPharmaceutical Preparationsaqueous boundary layer permeabilityCaco-2dynamic range window (DRW)paracellular permeabilityrat colon and small intestinal perfusion methods

Identifiers

PMID29288412
OpenAlexW2778414657

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.