Evidence map›Paper›PMID 32260469›Full record

ArticlePolymers2020

Investigating Novel Syntheses of a Series of Unique Hybrid PLGA-Chitosan Polymers for Potential Therapeutic Delivery Applications.

Jason Thomas Duskey, Cecilia Baraldi, Maria Cristina Gamberini, Ilaria Ottonelli, Federica Da Ros, Giovanni Tosi, Flavio Forni, Maria Angela Vandelli, Barbara Ruozi

Abstract read
In one paragraph

Article in Polymers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Heterocycles in Medicinal Chemistry III.Molecules (Basel, Switzerland) · 2026
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  13. TweenNanomaterials (Basel, Switzerland) · 2021
    Article
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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

9 authors.

Jason Thomas DuskeyTe.Far.T.I.-Nanotech Lab, Department of Life Sciences, University of Modena and Reggio Emilia, 41121 Modena, Italy.
Cecilia BaraldiDepartment of Life Sciences, University of Modena and Reggio Emilia, 41121 Modena, Italy.
Maria Cristina GamberiniDepartment of Life Sciences, University of Modena and Reggio Emilia, 41121 Modena, Italy.
Ilaria OttonelliTe.Far.T.I.-Nanotech Lab, Department of Life Sciences, University of Modena and Reggio Emilia, 41121 Modena, Italy.
Federica Da RosTe.Far.T.I.-Nanotech Lab, Department of Life Sciences, University of Modena and Reggio Emilia, 41121 Modena, Italy.
Giovanni TosiTe.Far.T.I.-Nanotech Lab, Department of Life Sciences, University of Modena and Reggio Emilia, 41121 Modena, Italy.
Flavio ForniTe.Far.T.I.-Nanotech Lab, Department of Life Sciences, University of Modena and Reggio Emilia, 41121 Modena, Italy.
Maria Angela VandelliTe.Far.T.I.-Nanotech Lab, Department of Life Sciences, University of Modena and Reggio Emilia, 41121 Modena, Italy.
Barbara RuoziTe.Far.T.I.-Nanotech Lab, Department of Life Sciences, University of Modena and Reggio Emilia, 41121 Modena, Italy.

Funding

Fondazione Umberto Veronesi Individual researcher grantMinistero degli Affari Esteri e della Cooperazione Internazionale US19GR23POR FESR: Mat2Rep DGR 986/2018UNIMORE GRANT FAR UNIMORE GRANT FAR
6 · The paper itself

Abstract

Discovering new materials to aid in the therapeutic delivery of drugs is in high demand. PLGA, a FDA approved polymer, is well known in the literature to form films or nanoparticles that can load, protect, and deliver drug molecules; however, its incompatibility with certain drugs (due to hydrophilicity or charge repulsion interactions) limits its use. Combining PLGA or other polymers such as polycaprolactone with other safe and positively-charged molecules, such as chitosan, has been sought after to make hybrid systems that are more flexible in terms of loading ability, but often the reactions for polymer coupling use harsh conditions, films, unpurified products, or create a single unoptimized product. In this work, we aimed to investigate possible innovative improvements regarding two synthetic procedures. Two methods were attempted and analytically compared using nuclear magnetic resonance (NMR), fourier-transform infrared spectroscopy (FT-IR), and dynamic scanning calorimetry (DSC) to furnish pure, homogenous, and tunable PLGA-chitosan hybrid polymers. These were fully characterized by analytical methods. A series of hybrids was produced that could be used to increase the suitability of PLGA with previously non-compatible drug molecules.

Indexed as

chitosanchitosan-PLGA polymerDSCFT-IRhybrid polymersNMRPLGA

Identifiers

PMID32260469
PMCPMC7249265

What OpenQuestion holds

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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.