Evidence map›Paper›PMID 30348025›Full record

ArticleDrug delivery2018

Stacking of doxorubicin on folic acid-targeted multiwalled carbon nanotubes for in vivo chemotherapy of tumors.

Yan Yan, Ruizhi Wang, Yong Hu, Rongyue Sun, Tian Song, Xiangyang Shi, Shimeng Yin

Open access · goldAbstract read
In one paragraph

Article in Drug delivery, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

26 citing papers in PubMed, 71 citations in OpenAlex.

  1. Bridging solubility, stability, and translation: advances in carbon nanotube-based drug delivery systems.Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences · 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

7 authors at 4 institutions in 1 country.

Yan Yana Department of Obstetrics , Shanghai First Maternity and Infant Hospital, Tongji University School of Medicine , Shanghai , P. R. China.
Ruizhi Wangb Department of Radiology , Huadong Hospital, Fudan University , Shanghai , P. R. China.
Yong Huc College of Chemistry, Chemical Engineering and Biotechnology , Donghua University , Shanghai , P. R. China.
Rongyue Sunb Department of Radiology , Huadong Hospital, Fudan University , Shanghai , P. R. China.
Tian Songb Department of Radiology , Huadong Hospital, Fudan University , Shanghai , P. R. China.
Xiangyang Shic College of Chemistry, Chemical Engineering and Biotechnology , Donghua University , Shanghai , P. R. China.
Shimeng Yinb Department of Radiology , Huadong Hospital, Fudan University , Shanghai , P. R. China.
Donghua University · CNFudan University · CNHuadong Hospital · CNShanghai First Maternity and Infant Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this work, we developed a novel active targeting and pH-responsive system for delivering the drug doxorubicin (DOX) to tumor sites using folic acid (FA)-modified multiwalled carbon nanotubes (MWCNTs). Acid-treated MWCNTs with carboxyl groups were first covalently conjugated with polyethyleneimine (PEI). Subsequent sequential modification with FA (via a polyethylene glycol spacer), fluorescein isothiocyanate (FI), and acetic anhydride/triethylamine resulted in multifunctional FA-bound MWCNT (MWCNT-PEI.Ac-FI-PEG-FA) nanomaterials that possessed exceptional colloidal stability and good biocompatibility in a given concentration range. The FA-bound MWCNTs were characterized using various techniques and exhibited a high drug loading and an encapsulation efficiency as high as 70.4%. DOX/MWCNT-PEI.Ac-FI-PEG-FA nanocomplexes (DOX/MWCNT NCs) exhibited pH-responsive release in acidic environments. Importantly, the DOX/MWCNT NCs targeted tumor cells overexpressing FA receptors (FARs) and effectively inhibited their growth. In vivo anticancer experiments demonstrated that DOX/MWCNT NCs not only enhanced the suppression of tumor growth but also decreased the side effects of free DOX. The developed FA-modified MWCNTs with an unconventionally high DOX loading boosted in vivo anti-tumor efficacy, and the lower systemic toxicity may be utilized for tumor therapy upon clinical translation.

Indexed as

AnimalsAntibiotics, AntineoplasticCell Line, TumorCell SurvivalDoxorubicinDrug CarriersDrug CompoundingDrug Delivery SystemsFolic AcidHumansHydrogen-Ion ConcentrationMiceNanotubes, CarbonNeoplasmsSolubilityTissue DistributionAntibiotics, AntineoplasticDoxorubicinDrug CarriersFolic AcidNanotubes, Carbondoxorubicinfolic acidMultiwalled carbon nanotubespolyethyleneiminetumor targeting

Identifiers

PMID30348025
PMCPMC6201812
OpenAlexW2895977609

What OpenQuestion holds

Textmetadata
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.