Evidence map›Paper›PMID 30874284›Full record

ArticleNanoscale2019

Triple conjugated carbon dots as a nano-drug delivery model for glioblastoma brain tumors.

Sajini D Hettiarachchi, Regina M Graham, Keenan J Mintz, Yiqun Zhou, Steven Vanni, Zhilli Peng, Roger M Leblanc

Open access · greenAbstract read
In one paragraph

Article in Nanoscale, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 98 papers.

0numbers the graph read from it
0cells of the map it votes in
98citing papers in PubMed
13.6field-weighted citation impact, top 1% 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

98 citing papers in PubMed, 280 citations in OpenAlex.

  1. Article
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  11. Nanoparticle-Functionalized Cellulose Through Biosynthesis-Only Approach.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  12. Review
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  14. Immunotherapy in central nervous system tumors.International journal of surgery (London, England) · 2025
    Review
  15. Article
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  19. Article
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38 more citing papers are in PubMed but not listed here.

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 1 institution in 1 country.

Sajini D HettiarachchiDepartment of Chemistry, University of Miami, 1301 Memorial Drive, Coral Gables, Florida 33146, USA. rml@miami.edu.
Regina M Graham
Keenan J Mintz
Yiqun Zhou
Steven Vanni
Zhilli Peng
Roger M Leblanc
University of Miami · US

Funding

Testing the therapeutic potential of carbon nanodots in bone mineralization diseasesR21AR072226 · NIAMS · UNIVERSITY OF RICHMOND · PI SKROMNE, ISAAC · 2017 to 2018
$316k
NIAMS NIH HHS R21 AR072226
6 · The paper itself

Abstract

Most of the dual nano drug delivery systems fail to enter malignant brain tumors due to a lack of proper targeting systems and the size increase of the nanoparticles after drug conjugation. Therefore, a triple conjugated system was developed with carbon dots (C-dots), which have an average particle size of 1.5-1.7 nm. C-dots were conjugated with transferrin (the targeted ligand) and two anti-cancer drugs, epirubicin and temozolomide, to build the triple conjugated system in which the average particle size was increased only up to 3.5 nm. In vitro studies were performed with glioblastoma brain tumor cell lines SJGBM2, CHLA266, CHLA200 (pediatric) and U87 (adult). The efficacy of the triple conjugated system (dual drug conjugation along with transferrin) was compared to those of dual conjugated systems (single drug conjugation along with transferrin), non-transferrin C-dots-drugs, and free drug combinations. Transferrin conjugated samples displayed the lowest cell viability even at a lower concentration. Among the transferrin conjugated samples, the triple conjugated system (C-dots-trans-temo-epi (C-DT)) was more strongly cytotoxic to brain tumor cell lines than dual conjugated systems (C-dots-trans-temo (C-TT) and C-dots-trans-epi (C-ET)). C-DT increased the cytotoxicity to 86% in SJGBM2 at 0.01 μM while C-ET and C-TT reduced it only to 33 and 8%, respectively. Not only did triple conjugated C-DT increase the cytotoxicity, but also the two-drug combination in C-DT displayed a synergistic effect.

Indexed as

Brain NeoplasmsCarbonCell Line, TumorCell ProliferationCell SurvivalDrug CarriersDrug SynergismEpirubicinGlioblastomaHumansModels, BiologicalQuantum DotsSpectrometry, FluorescenceTemozolomideTransferrinCarbonDrug CarriersEpirubicinTemozolomideTransferrin

Identifiers

PMID30874284
PMCPMC6459689
OpenAlexW2918597707

What OpenQuestion holds

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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.