Evidence map›Paper›PMID 37583664›Full record

ArticleRSC advances2023

Dual targeting multiwalled carbon nanotubes for improved neratinib delivery in breast cancer.

Amr Selim Abu Lila, Rohini Bhattacharya, Afrasim Moin, Turki Al Hagbani, Marwa Helmy Abdallah, Syed Mohd Danish Rizvi, El-Sayed Khafagy, Talib Hussain, Hosahalli Veerabhadrappa Gangadharappa

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in RSC advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

4 citing papers in PubMed, 13 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
    Review
  2. Article
  3. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 3 countries.

Amr Selim Abu LilaDepartment of Pharmaceutics, College of Pharmacy, University of Ha'il Ha'il 81442 Saudi Arabia.
Rohini BhattacharyaDepartment of Pharmaceutics, JSS College of Pharmacy, JSS Academy of Higher Education and Research Mysuru 570015 India hvgangadharappa@jssuni.edu.in.
Afrasim MoinDepartment of Pharmaceutics, College of Pharmacy, University of Ha'il Ha'il 81442 Saudi Arabia.
Turki Al HagbaniDepartment of Pharmaceutics, College of Pharmacy, University of Ha'il Ha'il 81442 Saudi Arabia.
Marwa Helmy AbdallahDepartment of Pharmaceutics, College of Pharmacy, University of Ha'il Ha'il 81442 Saudi Arabia.
Syed Mohd Danish RizviDepartment of Pharmaceutics, College of Pharmacy, University of Ha'il Ha'il 81442 Saudi Arabia.
El-Sayed KhafagyDepartment of Pharmaceutics, College of Pharmacy, Prince Sattam Bin Abdulaziz University Al-kharj 11942 Saudi Arabia.
Talib HussainDepartment of Pharmacology and Toxicology, College of Pharmacy, University of Ha'il Ha'il 81442 Saudi Arabia.
Hosahalli Veerabhadrappa GangadharappaDepartment of Pharmaceutics, JSS College of Pharmacy, JSS Academy of Higher Education and Research Mysuru 570015 India hvgangadharappa@jssuni.edu.in.ORCID https://orcid.org/0000-0002-2961-4108
University of Ha'il · SAJSS Academy of Higher Education and Research · INZagazig University · EGSuez Canal University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to develop biotinylated chitosan (Bio-Chi) decorated multi-walled carbon nanotubes (MWCNTs) for breast cancer therapy with the tyrosine kinase inhibitor, neratinib (NT). For achieving such a purpose, carboxylic acid functionalized multiwalled carbon nanotubes (c-MWCNTs) were initially decorated non-covalently with biotin-chitosan (Bio-Chi) coating for achieving a dual targeting mode; pH-dependent release with chitosan and biotin-receptor mediated active targeting with biotin. Afterwards, Bio-Chi decorated c-MWCNTs were loaded with the tyrosine kinase inhibitor, neratinib (NT). The formulation was then characterized by dynamic light scattering, FTIR and EDX. The drug loading efficiency was estimated to be 95.6 ± 1.2%.

Identifiers

PMID37583664
PMCPMC10424192
OpenAlexW4385817384

What Socratic 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 Socratic graph.