Evidence map›Paper›PMID 34959655›Full record

ArticlePharmaceuticals (Basel, Switzerland)2021

Improved Bioavailability of Poorly Water-Soluble Drug by Targeting Increased Absorption through Solubility Enhancement and Precipitation Inhibition.

Ju-Hyun Lee, Chulhun Park, Kwon-Yeon Weon, Chin-Yang Kang, Beom-Jin Lee, Jun-Bom Park

Abstract read
In one paragraph

Article in Pharmaceuticals (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
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

6 authors.

Ju-Hyun LeeCollege of Pharmacy, Sahmyook University, Seoul 01795, Korea.
Chulhun ParkFaculty of Pharmacy & Pharmaceutical Sciences, University of Alberta, Edmonton, AB T6G 2E1, Canada.ORCID 0000-0003-4951-3213
Kwon-Yeon WeonCollege of Pharmacy, Catholic University of Daegu, Gyeongsan-si 38430, Korea.
Chin-Yang KangCollege of Pharmacy, Sahmyook University, Seoul 01795, Korea.
Beom-Jin LeeCollege of Pharmacy, Ajou University, Suwon 16499, Korea.ORCID 0000-0003-0922-3289
Jun-Bom ParkCollege of Pharmacy, Sahmyook University, Seoul 01795, Korea.ORCID 0000-0001-6193-0023

Funding

National Research Foundation of Korea NRF-2019R1F1A1056572
6 · The paper itself

Abstract

Itraconazole (ITZ) is a class II drug according to the biopharmaceutical classification system. Its solubility is pH 3-dependent, and it is poorly water-soluble. Its pKa is 3.7, which makes it a weak base drug. The aim of this study was to prepare solid dispersion (SD) pellets to enhance the release of ITZ into the gastrointestinal environment using hot-melt extrusion (HME) technology and a pelletizer. The pellets were then filled into capsules and evaluated in vitro and in vivo. The ITZ changed from a crystalline state to an amorphous state during the HME process, as determined using DSC and PXRD. In addition, its release into the gastrointestinal tract was enhanced, as was the level of ITZ recrystallization, which was lower than the marketed drug (Sporanox

Indexed as

absorption areahot-melt extrusionitraconazolemodified drug releasesolid dispersion

Identifiers

PMID34959655
PMCPMC8707685

What OpenQuestion holds

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Registered trials

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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.