Evidence map›Paper›PMID 27706041›Full record

ArticleMarine drugs2016

Controlling Properties and Cytotoxicity of Chitosan Nanocapsules by Chemical Grafting.

Laura De Matteis, Maria Alleva, Inés Serrano-Sevilla, Sonia García-Embid, Grazyna Stepien, María Moros, Jesús M de la Fuente

Open access · goldAbstract read
In one paragraph

Article in Marine drugs, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

8 citing papers in PubMed, 34 citations in OpenAlex.

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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

7 authors at 3 institutions in 2 countries.

Laura De MatteisInstituto de Nanociencia de Aragón (INA), Universidad de Zaragoza, Edificio I+D, calle Mariano Esquillor s/n, 50018 Zaragoza, Spain. lauradem@unizar.es.
Maria AllevaInstituto de Nanociencia de Aragón (INA), Universidad de Zaragoza, Edificio I+D, calle Mariano Esquillor s/n, 50018 Zaragoza, Spain. mariaalleva1234@gmail.com.
Inés Serrano-SevillaInstituto de Nanociencia de Aragón (INA), Universidad de Zaragoza, Edificio I+D, calle Mariano Esquillor s/n, 50018 Zaragoza, Spain. inessersev@gmail.com.
Sonia García-EmbidInstituto de Nanociencia de Aragón (INA), Universidad de Zaragoza, Edificio I+D, calle Mariano Esquillor s/n, 50018 Zaragoza, Spain. sonia.garcia.embid@gmail.com.
Grazyna StepienInstituto de Nanociencia de Aragón (INA), Universidad de Zaragoza, Edificio I+D, calle Mariano Esquillor s/n, 50018 Zaragoza, Spain. gstepien@unizar.es.
María MorosIstituto di Scienze Applicate e Sistemi Intelligenti "E. Caianiello", Consiglio Nazionale delle Ricerche, Pozzuoli 80078, Italy. m.moros@isasi.cnr.it.
Jesús M de la FuenteInstituto de Ciencia de Materiales de Aragón (ICMA), CSIC-Universidad de Zaragoza, Edificio I+D, calle Mariano Esquillor s/n, 50018 Zaragoza, Spain. jmfuente@unizar.es.
Universidad de Zaragoza · ESInstitute of Applied Science and Intelligent Systems · ITInstituto de Nanociencia y Materiales de Aragón · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The tunability of the properties of chitosan-based carriers opens new ways for the application of drugs with low water-stability or high adverse effects. In this work, the combination of a nanoemulsion with a chitosan hydrogel coating and the following poly (ethylene glycol) (PEG) grafting is proven to be a promising strategy to obtain a flexible and versatile nanocarrier with an improved stability. Thanks to chitosan amino groups, a new easy and reproducible method to obtain nanocapsule grafting with PEG has been developed in this work, allowing a very good control and tunability of the properties of nanocapsule surface. Two different PEG densities of coverage are studied and the nanocapsule systems obtained are characterized at all steps of the optimization in terms of diameter, Z potential and surface charge (amino group analysis). Results obtained are compatible with a conformation of PEG molecules laying adsorbed on nanoparticle surface after covalent linking through their amino terminal moiety. An improvement in nanocapsule stability in physiological medium is observed with the highest PEG coverage density obtained. Cytotoxicity tests also demonstrate that grafting with PEG is an effective strategy to modulate the cytotoxicity of developed nanocapsules. Such results indicate the suitability of chitosan as protective coating for future studies oriented toward drug delivery.

Indexed as

AnimalsCell SurvivalChitosanChlorocebus aethiopsDrug CarriersDrug Delivery SystemsDrug StabilityElectrochemical TechniquesEmulsionsHydrogen-Ion ConcentrationNanocapsulesParticle SizePolyethylene GlycolsSurface PropertiesThermogravimetryVero CellsChitosanDrug CarriersEmulsionsNanocapsulesPolyethylene Glycolschitosanhydrogelnanocapsulesstabilitysurface grafting

Identifiers

PMID27706041
PMCPMC5082323
OpenAlexW2526311572

What OpenQuestion holds

Textmetadata
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.