ArticleJournal of materials science. Materials in medicine2010
Self-assembled particles of N-phthaloylchitosan-g-polycaprolactone molecular bottle brushes as carriers for controlled release of indometacin.
Article in Journal of materials science. Materials in medicine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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
0 citing papers in PubMed, 16 citations in OpenAlex.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
A series of amphiphilic N-phthaloylchitosan-g-polycaprolactone molecular bottle brushes were prepared by "graft onto" method. The narrow distribution of polycaprolactone macromonomers ensures that the molecular bottle brushes can self-assemble into highly monodisperse particles, which have the ability to get a high loading efficiency of the hydrophobic drug, indometacin (INN). Searching for the effective drug loading ratio, three parameters such as polycaprolactone chain length, the grafting content and concentration of the molecular bottle brushes were tested to entrap INN. These encapsulated drug particles show sustained release of the encapsulated INN, of which 91.7% was released in 22 h at 37 degrees C in phosphate buffered saline. The self-assembled particles of the molecular bottle brushes as carriers for INN can effectively prevent the drug from releasing quickly and prolong the release time, which is a promising candidate for potential clinical applications.
Indexed as
Identifiers
What OpenQuestion holds
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.