Evidence map›Paper›PMID 39071505›Full record

ReviewInternational journal of nanomedicine2024

Research Progress of Disulfide Bond Based Tumor Microenvironment Targeted Drug Delivery System.

Weiran Ma, Xiaoying Wang, Dongqi Zhang, Xupeng Mu

Abstract readReview
In one paragraph

Review in International journal of nanomedicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
–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

35 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  7. On-Demand Chemically Degradable Hydrogels for Biological Applications.Chembiochem : a European journal of chemical biology · 2026
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  8. [Exploration and application of nanotechnology in precision transarterial chemoembolization for hepatocellular carcinoma].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2026
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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

4 authors.

Weiran MaScientific Research Center, China-Japan Union Hospital of Jilin University, Changchun, 130033, People's Republic of China.ORCID 0009-0006-0421-6759
Xiaoying WangJilin University School of Pharmaceutical Sciences, Changchun, 130021, People's Republic of China.ORCID 0009-0005-8287-1145
Dongqi ZhangDepartment of Urology, The First Hospital of Jilin University, Changchun, 130021, People's Republic of China.
Xupeng MuScientific Research Center, China-Japan Union Hospital of Jilin University, Changchun, 130033, People's Republic of China.ORCID 0000-0002-4330-4456

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer poses a significant threat to human life and health. Chemotherapy is currently one of the effective cancer treatments, but many chemotherapy drugs have cell toxicity, low solubility, poor stability, a narrow therapeutic window, and unfavorable pharmacokinetic properties. To solve the above problems, target drug delivery to tumor cells, and reduce the side effects of drugs, an anti-tumor drug delivery system based on tumor microenvironment has become a focus of research in recent years. The construction of a reduction-sensitive nanomedicine delivery system based on disulfide bonds has attracted much attention. Disulfide bonds have good reductive responsiveness and can effectively target the high glutathione (GSH) levels in the tumor environment, enabling precise drug delivery. To further enhance targeting and accelerate drug release, disulfide bonds are often combined with pH-responsive nanocarriers and highly expressed ligands in tumor cells to construct drug delivery systems. Disulfide bonds can connect drug molecules and polymer molecules in the drug delivery system, as well as between different drug molecules and carrier molecules. This article summarized the drug delivery systems (DDS) that researchers have constructed in recent years based on disulfide bond drug delivery systems targeting the tumor microenvironment, disulfide bond cleavage-triggering conditions, various drug loading strategies, and carrier design. In this review, we also discuss the controlled release mechanisms and effects of these DDS and further discuss the clinical applicability of delivery systems based on disulfide bonds and the challenges faced in clinical translation.

Indexed as

Antineoplastic AgentsDisulfidesDrug Delivery SystemsNeoplasmsTumor MicroenvironmentAnimalsDelayed-Action PreparationsDrug CarriersDrug LiberationGlutathioneHumansHydrogen-Ion ConcentrationNanomedicineNanoparticlesAntineoplastic AgentsDelayed-Action PreparationsDisulfidesDrug CarriersGlutathionedisulfide bonddrug delivery systemsGSH/ROStumor microenvironment

Identifiers

PMID39071505
PMCPMC11283832

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.