Evidence map›Paper›PMID 22300622›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2012

Polyelectrolyte multilayer nanoshells with hydrophobic nanodomains for delivery of Paclitaxel.

Thomas Boudou, Prathamesh Kharkar, Jing Jing, Raphael Guillot, Isabelle Paintrand, Rachel Auzely-Velty, Catherine Picart

Abstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2012. 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. Layer-by-Layer Assemblies for Cancer Treatment and Diagnosis.Advanced materials (Deerfield Beach, Fla.) · 2016
    Review
  4. Thiol-ene click hydrogels for therapeutic delivery.ACS biomaterials science & engineering · 2016
    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

7 authors.

Thomas Boudou *Grenoble Institute of Technology and CNRS, UMR 5628, LMGP, 3 parvis Louis Néel, 38 016 Grenoble, France.
Prathamesh Kharkar *Grenoble Institute of Technology and CNRS, UMR 5628, LMGP, 3 parvis Louis Néel, 38 016 Grenoble, France.
Jing JingCentre de Recherches sur les Macromolécules Végétales (CERMAV-CNRS), affiliated with Université Joseph Fourier, and member of the Institut de Chimie Moléculaire de Grenoble, 601 rue de la piscine, Grenoble, France.
Raphael GuillotGrenoble Institute of Technology and CNRS, UMR 5628, LMGP, 3 parvis Louis Néel, 38 016 Grenoble, France.
Isabelle PaintrandCentre de Recherches sur les Macromolécules Végétales (CERMAV-CNRS), affiliated with Université Joseph Fourier, and member of the Institut de Chimie Moléculaire de Grenoble, 601 rue de la piscine, Grenoble, France.
Rachel Auzely-VeltyCentre de Recherches sur les Macromolécules Végétales (CERMAV-CNRS), affiliated with Université Joseph Fourier, and member of the Institut de Chimie Moléculaire de Grenoble, 601 rue de la piscine, Grenoble, France.
Catherine PicartGrenoble Institute of Technology and CNRS, UMR 5628, LMGP, 3 parvis Louis Néel, 38 016 Grenoble, France.

Funding

European Research Council 259370
6 · The paper itself

Abstract

Efficient and effective delivery of poorly water-soluble drug molecules, which constitute a large part of commercially available drugs, is a major challenge in the field of drug delivery. Several drugs including paclitaxel (PTX) which are used for cancer treatment are hydrophobic, exhibit poor aqueous solubility and need to be delivered using an appropriate carrier. In the present work, we engineered PTX-loaded polyelectrolyte films and microcapsules by pre-complexing PTX with chemically modified derivative of hyaluronic acid (alkylamino hydrazide) containing hydrophobic nanocavities, and subsequent assembly with either poly(l-lysine) (PLL) or quaternized chitosan (QCHI) as polycations. The PTX loading capacity of the films was found to be dependent on number of layers in the films as well as on the initial concentration of PTX pre-complexed to hydrophobic HA, with a loading capacity up to 5000-fold the initial PTX concentration. The films were stable in physiological medium and were degraded in the presence of hyaluronidase. The PTX-loaded microcapsules were found to decrease the viability and proliferation of MDA MB 231 breast cancer cells, while unloaded microcapsules did not impact cell viability. All together, our results highlight the potential of hyaluronan-based assemblies containing hydrophobic nanodomains for hydrophobic drug delivery.

Indexed as

Antineoplastic Agents, PhytogenicCell Line, TumorCell ProliferationCell SurvivalChitosanDrug CarriersDrug CompoundingDrug StabilityHumansHyaluronic AcidHydrophobic and Hydrophilic InteractionsMolecular StructureNanoshellsPaclitaxelPolyaminesPolyelectrolytesAntineoplastic Agents, PhytogenicChitosanDrug CarriersHyaluronic AcidPaclitaxelPolyaminesPolyelectrolytesPolylysine

Identifiers

PMID22300622
PMCPMC4111540

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.