Evidence map›Paper›PMID 35517745›Full record

ArticleRSC advances2020

Amino acid-modified PAMAM dendritic nanocarriers as effective chemotherapeutic drug vehicles in cancer treatment: a study using zebrafish as a cancer model.

Szu-Yuan Wu, Hsiao-Ying Chou, Hsieh-Chih Tsai, Rajeshkumar Anbazhagan, Chiou-Hwa Yuh, Jen Ming Yang, Yen-Hsiang Chang

Open access · goldAbstract read
In one paragraph

Article in RSC advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 26% 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

8 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
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  7. Article
  8. Zebrafish as a Model for Anticancer Nanomedicine Studies.Pharmaceuticals (Basel, Switzerland) · 2021
    Review
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 5 institutions in 5 countries.

Szu-Yuan WuDepartment of Food Nutrition and Health Biotechnology, College of Medical and Health Science, Asia University Taichung Taiwan.
Hsiao-Ying ChouGraduate Institute of Applied Science and Technology, National Taiwan University of Science and Technology Taipei Taiwan h.c.tsai@mail.ntust.edu.tw arrajeshkumar6@gmail.com +886-2-27303625 +886-984252998.
Hsieh-Chih TsaiGraduate Institute of Applied Science and Technology, National Taiwan University of Science and Technology Taipei Taiwan h.c.tsai@mail.ntust.edu.tw arrajeshkumar6@gmail.com +886-2-27303625 +886-984252998.ORCID https://orcid.org/0000-0002-7034-6205
Rajeshkumar AnbazhaganGraduate Institute of Applied Science and Technology, National Taiwan University of Science and Technology Taipei Taiwan h.c.tsai@mail.ntust.edu.tw arrajeshkumar6@gmail.com +886-2-27303625 +886-984252998.
Chiou-Hwa YuhInstitute of Molecular and Genomic Medicine, National Health Research Institutes Zhunan Miaoli Taiwan.
Jen Ming YangDepartment of Chemical and Materials Engineering, Chang Gung University Tao-Yuan Taiwan jmyang@mail.cgu.edu.tw +886-3-2118800-529.
Yen-Hsiang ChangDepartment of General Dentistry, Chang Gung Memorial Hospital Tao-Yuan, 333 Taiwan.
National Taiwan University of Science and Technology · TWAsia University · TWChang Gung University · TWMemorial Hospital of South Bend · USNational Yang Ming Chiao Tung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The use of nanomaterials for drug delivery offers many advantages including the targeted delivery of drugs and their controlled release. Nonetheless, entry into the target cells remains a challenge for many nanomaterials used for drug delivery. Moreover, cellular uptake limits the therapeutic efficiency of many anticancer drugs. An important goal is to increase the specific accumulation of these nanoparticles (NPs) at the desired cancerous tissues. Notably, cancer cells show a high demand for some amino acids and we have used this knowledge to develop novel carrier systems. In this study, drug carriers were produced by the conjugation of multiple amino acids such as l-histidine (H) and l-cysteine (C) or single amino acids such as only H with the G4.5 dendrimers (G) to produce GHC aggregates and GH NP carriers, respectively. Doxorubicin was loaded into the G4.5, GH, and GHC dendrimers (G/DOX, GH/DOX and GHC/DOX, respectively) and the release mechanism was demonstrated at pH 7.4 and pH 5.0. GH/DOX and GHC/DOX showed better stability under physiological conditions than the dendrimer alone (G/DOX). GH/DOX and GHC/DOX exhibited higher inhibition of HeLa cell proliferation in

Identifiers

PMID35517745
PMCPMC9054295
OpenAlexW3031177352

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.