Evidence map›Paper›PMID 25724161›Full record

ArticlePharmaceutical research2015

Curdlan-Conjugated PLGA Nanoparticles Possess Macrophage Stimulant Activity and Drug Delivery Capabilities.

Matshawandile Tukulula, Rose Hayeshi, Pascaline Fonteh, Debra Meyer, Abongile Ndamase, Michael T Madziva, Vincent Khumalo, Philip Labuschagne, Philip Lubuschagne, Brendon Naicker and 2 more

Erratum issuedAbstract read
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In one paragraph

Article in Pharmaceutical research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
  2. Synthesis of immunomodulatory biomimetic lipid polymer hybrid nanoparticles and application of zebrafish larvae in immunomodulation screening.European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 1 country.

Matshawandile TukululaEncapsulation and Delivery Group, Council for Scientific and Industrial Research, 1 Meiring Naude Road, Brummeria, Pretoria, 0001, South Africa.
Rose Hayeshi
Pascaline Fonteh
Debra Meyer
Abongile Ndamase
Michael T Madziva
Vincent Khumalo
Philip Labuschagne
Philip Lubuschagne
Brendon Naicker
Hulda Swai
Admire Dube
Council for Scientific and Industrial Research · ZAUniversity of Pretoria · ZAUniversity of the Western Cape · ZAUniversity of the Witwatersrand · ZA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThere is significant interest in the application of nanoparticles to deliver immunostimulatory signals to cells. We hypothesized that curdlan (immune stimulating polymer) could be conjugated to PLGA and nanoparticles from this copolymer would possess immunostimulatory activity, be non-cytotoxic and function as an effective sustained drug release system.

methodsCarbodiimide chemistry was employed to conjugate curdlan to PLGA. The conjugate (C-PLGA) was characterized using (1)H and (13)C NMR, FTIR, DSC and TGA. Nanoparticles were synthesized using an emulsion-solvent evaporation technique. Immunostimulatory activity was characterized in THP-1 derived macrophages. MTT assay and real-time impedance measurements were used to characterize polymer and nanoparticle toxicity and uptake in macrophages. Drug delivery capability was assessed across Caco-2 cells using rifampicin as a model drug.

resultsSpectral characterization confirmed successful synthesis of C-PLGA. C-PLGA nanoparticles enhanced phosphorylated ERK production in macrophages indicating cell stimulation. Nanoparticles provided slow release of rifampicin across Caco-2 cells. Polymers but not nanoparticles altered the adhesion profiles of the macrophages. Impedance measurements suggested Ca(2+) dependent uptake of nanoparticles by the macrophages.

conclusionsPLGA nanoparticles with macrophage stimulating and sustained drug delivery capabilities have been prepared. These nanoparticles can be used to stimulate macrophages and concurrently deliver drug in infectious disease therapy.

Indexed as

Antitubercular Agentsbeta-GlucansBiological Transport, ActiveCaco-2 CellsCarbohydrate SequenceCell Membrane PermeabilityCell SurvivalChemistry, PharmaceuticalDrug Delivery SystemsExcipientsHumansIntestinal AbsorptionLactic AcidMacrophagesMolecular Sequence DataNanoparticlesAntitubercular Agentsbeta-GlucanscurdlanExcipientsLactic AcidPolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerRifampin

Identifiers

PMID25724161
OpenAlexW2079358581

What OpenQuestion holds

Textmetadata
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.