Evidence map›Paper›PMID 32605162›Full record

ArticleBiomolecules2020

Development and Characterization of a Fucoidan-Based Drug Delivery System by Using Hydrophilic Anticancer Polysaccharides to Simultaneously Deliver Hydrophobic Anticancer Drugs.

Yen-Ho Lai, Chih-Sheng Chiang, Chin-Hao Hsu, Hung-Wei Cheng, San-Yuan Chen

Open access · goldAbstract read
In one paragraph

Article in Biomolecules, 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
5.7field-weighted citation impact, top 4% 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, 65 citations in OpenAlex.

  1. Review
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  10. Nanoparticle-Mediated Immunotherapy in Triple-Negative Breast Cancer.ACS biomaterials science & engineering · 2024
    Review
  11. Review
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  13. Article
  14. Evaluation of MScientific reports · 2022
    Article
  15. Article
  16. Bioactive Carbohydrate Polymers-Between Myth and Reality.Molecules (Basel, Switzerland) · 2021
    Review
  17. Review
  18. 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

5 authors at 3 institutions in 1 country.

Yen-Ho LaiDepartment of Materials Science and Engineering, National Chiao Tung University, Hsinchu 30010, Taiwan.
Chih-Sheng ChiangCell Therapy Center, China Medical University Hospital, Taichung 40454, Taiwan.
Chin-Hao HsuDepartment of Materials Science and Engineering, National Chiao Tung University, Hsinchu 30010, Taiwan.
Hung-Wei ChengDepartment of Materials Science and Engineering, National Chiao Tung University, Hsinchu 30010, Taiwan.
San-Yuan ChenDepartment of Materials Science and Engineering, National Chiao Tung University, Hsinchu 30010, Taiwan.
National Yang Ming Chiao Tung University · TWChina Medical University · TWNational Tsing Hua University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fucoidan, a natural sulfated polysaccharide, which can activate the immune response and lessen adverse effects, is expected to be an adjuvant agent in combination with chemotherapy. Using natural hydrophilic anticancer polysaccharides to simultaneously encapsulate hydrophobic anticancer drugs is feasible, and a reduced side effect can be achieved to amplify the therapeutic efficacy. In this study, a novel type of fucoidan-PLGA nanocarrier (FPN-DTX) was developed for the encapsulation of the hydrophobic anticancer drug, docetaxel (DTX), as a drug delivery system. From the comparison between FPN-DTX and the PLGA particles without fucoidan (PLGA-DTX), FPNs-DTX with fucoidan were highly stable with smaller sizes and dispersed well without aggregations in an aqueous environment. The drug loading and release can be further modified by modulating relative ratios of Fucoidan (Fu) to PLGA. The (FPN 3-DTX) nanoparticles with a 10:3 ratio of Fu:PLGA displayed uniform particle size with higher encapsulation efficiency than PLGA NPs and sustained drug release ability. The biocompatible fucoidan-PLGA nanoparticles displayed low cytotoxicity without drug loading after incubation with MDA-MB-231 triple-negative breast cancer cells. Despite lower cellular uptake than that of PLGA-DTX due to a higher degree of negative zeta potential and hydrophilicity, FPN 3-DTX effectively exerted better anticancer ability, so FPN 3-DTX can serve as a competent drug delivery system.

Indexed as

Antineoplastic AgentsCell Line, TumorCell ProliferationCell SurvivalDelayed-Action PreparationsDocetaxelDrug Delivery SystemsDrug StabilityFemaleHumansNanoparticlesParticle SizePolylactic Acid-Polyglycolic Acid CopolymerPolysaccharidesTriple Negative Breast NeoplasmsAntineoplastic AgentsDelayed-Action PreparationsDocetaxelfucoidanPolylactic Acid-Polyglycolic Acid CopolymerPolysaccharidesanticancer therapy/cancer treatmentdocetaxeldrug delivery systemfucoidanPLGA

Identifiers

PMID32605162
PMCPMC7408464
OpenAlexW3037413757

What OpenQuestion holds

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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.