Evidence map›Paper›PMID 29588586›Full record

ArticleInternational journal of nanomedicine2018

Paclitaxel-loaded redox-sensitive nanoparticles based on hyaluronic acid-vitamin E succinate conjugates for improved lung cancer treatment.

Yu Song, Han Cai, Tingjie Yin, Meirong Huo, Ping Ma, Jianping Zhou, Wenfang Lai

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

21 citing papers in PubMed, 96 citations in OpenAlex.

  1. Review
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  6. Rutin and Hesperidin Revoke the Hepatotoxicity Induced by Paclitaxel in Male Wistar RatsEvidence-based complementary and alternative medicine : eCAM · 2023
    Article
  7. Review
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  9. The emergence of nanoporous materials in lung cancer therapy.Science and technology of advanced materials · 2022
    Review
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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.

Yu SongDepartment of Pharmaceutics, China Pharmaceutical University, Nanjing, People's Republic of China.
Han CaiDepartment of Pharmaceutics, China Pharmaceutical University, Nanjing, People's Republic of China.
Tingjie YinDepartment of Pharmaceutics, China Pharmaceutical University, Nanjing, People's Republic of China.
Meirong HuoDepartment of Pharmaceutics, China Pharmaceutical University, Nanjing, People's Republic of China.
Ping MaFormulation Development, Tolmar Inc, Fort Collins, CO, USA.
Jianping ZhouDepartment of Pharmaceutics, China Pharmaceutical University, Nanjing, People's Republic of China.
Wenfang LaiCollege of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou, People's Republic of China.
China Pharmaceutical University · CNFujian University of Traditional Chinese Medicine · CNTolmar (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLung cancer is the primary cause of cancer-related death worldwide. A redox-sensitive nanocarrier system was developed for tumor-targeted drug delivery and sufficient drug release of the chemotherapeutic agent paclitaxel (PTX) for improved lung cancer treatment.

methodsThe redox-sensitive nanocarrier system constructed from a hyaluronic acid-disulfide-vitamin E succinate (HA-SS-VES, HSV) conjugate was synthesized and PTX was loaded in the delivery system. The physicochemical properties of the HSV nanoparticles were characterized. The redox-sensitivity, tumor-targeting and intracellular drug release capability of the HSV nanoparticles were evaluated. Furthermore, in vitro and in vivo antitumor activity of the PTX-loaded HSV nanoparticles was investigated in a CD44 over-expressed A549 tumor model.

resultsThis HSV conjugate was successfully synthesized and self-assembled to form nanoparticles in aqueous condition with a low critical micelle concentration of 36.3 μg mL

conclusionThe results of our study indicated the redox-sensitive HSV nanoparticle was a promising nanocarrier for lung cancer therapy.

Indexed as

alpha-TocopherolAnimalsAntineoplastic AgentsApoptosisCell SurvivalDrug Delivery SystemsDrug LiberationHumansHyaluronan ReceptorsHyaluronic AcidLung NeoplasmsMice, Inbred BALB CMicellesNanoparticlesOxidation-ReductionPaclitaxelalpha-TocopherolAntineoplastic AgentsCD44 protein, humanHyaluronan ReceptorsHyaluronic AcidMicellesPaclitaxelnanoparticlesredox-sensitivetumor targeting

Identifiers

PMID29588586
PMCPMC5858821
OpenAlexW2791437922

What OpenQuestion holds

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LicenceCC BY-NC
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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.