ArticleJournal of materials science. Materials in medicine2004
In vitro release dynamics of insulin from a loaded hydrophilic polymeric network.
Article in Journal of materials science. Materials in medicine, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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.
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.
Who cites it
2 citing papers in PubMed, 24 citations in OpenAlex.
- A novel amphiphilic nano hydrogel using ketene based polyester with polyacrylamide for controlled drug delivery system.Journal of materials science. Materials in medicine · 2008Article
- Preparation, characterization and microhardness study of semi interpenetrating polymer networks of polyvinyl alcohol and crosslinked polyacrylamide.Journal of materials science. Materials in medicine · 2006Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors at 2 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
A hydrophilic semi-interpenetrating polymer network of polyvinyl alcohol (PVA), poly(ethylene glycol) (PEG) and crosslinked polyacrylamide (PAM) chains has been synthesized and its potential for controlled release of macromolecular drugs has been assessed by taking insulin as a representative drug. The semi-IPN was characterized by IR studies and network parameters such as the average molecular weight between crosslinks (Mc), crosslink density (q), and number of elastically effective chains (Ve) were evaluated. The effect of chemical architecture of the IPN was investigated on the percent loading of insulin and its subsequent release from the loaded device. Other parameters such as the thickness of the gel, molecular weight of PEG and pH and temperature of the release medium were also studied for their possible impact on the release of insulin. The whole release data was analyzed by Ficks power law and the influence of various factors on the plausible mechanism of insulin release was investigated.
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Registered trials
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.