Evidence map›Paper›PMID 26582357›Full record

ArticlePharmaceutical research2016

Controlled Release from Zein Matrices: Interplay of Drug Hydrophobicity and pH.

Jacob Bouman, Peter Belton, Paul Venema, Erik van der Linden, Renko de Vries, Sheng Qi

Open access · hybridAbstract read
In one paragraph

Article in Pharmaceutical research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
6.3field-weighted citation impact, top 4% 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

21 citing papers in PubMed, 82 citations in OpenAlex.

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  19. Protein-Based Fiber Materials in Medicine: A Review.Nanomaterials (Basel, Switzerland) · 2018
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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

6 authors at 3 institutions in 2 countries.

Jacob BoumanLaboratory of Physical Chemistry and Soft Matter, Wageningen University, Wageningen, The Netherlands. jacob.bouman@wur.nl.ORCID http://orcid.org/0000-0002-1713-6006
Peter BeltonSchool of Chemistry, University of East Anglia, Norwich, UK.
Paul VenemaLaboratory of Physics and Physical Chemistry of Foods, Wageningen University, Wageningen, The Netherlands.
Erik van der LindenLaboratory of Physics and Physical Chemistry of Foods, Wageningen University, Wageningen, The Netherlands.
Renko de VriesLaboratory of Physical Chemistry and Soft Matter, Wageningen University, Wageningen, The Netherlands.
Sheng QiSchool of Pharmacy, University of East Anglia, Norwich, UK.
University of East Anglia · GBWageningen University & Research · NLUniversity Medical Center Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeIn earlier studies, the corn protein zein is found to be suitable as a sustained release agent, yet the range of drugs for which zein has been studied remains small. Here, zein is used as a sole excipient for drugs differing in hydrophobicity and isoelectric point: indomethacin, paracetamol and ranitidine.

methodsCaplets were prepared by hot-melt extrusion (HME) and injection moulding (IM). Each of the three model drugs were tested on two drug loadings in various dissolution media. The physical state of the drug, microstructure and hydration behaviour were investigated to build up understanding for the release behaviour from a zein based matrix for drug delivery.

resultsDrug crystallinity of the caplets increases with drug hydrophobicity. For ranitidine and indomethacin, swelling rates, swelling capacity and release rates were pH dependent as a consequence of the presence of charged groups on the drug molecules. Both hydration rates and release rates could be approached by existing models.

conclusionThe drug state and pH dependant electrostatic interactions are hypothesised to influence release kinetics. Both factors can potentially be used to influence release kinetics release, thereby broadening the horizon for zein as a tuneable release agent.

Indexed as

AcetaminophenDelayed-Action PreparationsDrug CarriersDrug CompoundingDrug Delivery SystemsExcipientsHydrogen-Ion ConcentrationHydrophobic and Hydrophilic InteractionsIndomethacinKineticsRanitidineStatic ElectricityTabletsZeinAcetaminophenDelayed-Action PreparationsDrug CarriersExcipientsIndomethacinRanitidineTabletsZeincontrolled releasediffusion mechanismdissolution kinetics modellingextrusion-injection mouldingZein

Identifiers

PMID26582357
PMCPMC4744255
OpenAlexW2172734873

What OpenQuestion holds

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LicenceCC BY
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.