Evidence map›Paper›PMID 36994202›Full record

ReviewFrontiers in oncology2023

The use of nanoparticles for targeted drug delivery in non-small cell lung cancer.

Jessica E Holder, Christopher Ferguson, Elisabete Oliveira, Carlos Lodeiro, Carol M Trim, Lee J Byrne, Emilia Bertolo, Cornelia M Wilson

Open access · goldFull text readReview
In one paragraph

Review in Frontiers in oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

16 citing papers in PubMed, 36 citations in OpenAlex.

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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

8 authors at 2 institutions in 2 countries.

Jessica E HolderCanterbury Christ Church University, School of Psychology and Life Sciences, Life Sciences Industry Liaison Lab, Sandwich, United Kingdom.
Christopher FergusonCanterbury Christ Church University, School of Psychology and Life Sciences, Life Sciences Industry Liaison Lab, Sandwich, United Kingdom.
Elisabete OliveiraBIOSCOPE Research Group, Laboratório Associado para a Química Verde- Rede de Química e Tecnologia (LAQV- REQUIMTE), Chemistry Department, NOVA School of Science and Technology, Universidade NOVA de Lisboa, Caparica, Portugal.
Carlos LodeiroBIOSCOPE Research Group, Laboratório Associado para a Química Verde- Rede de Química e Tecnologia (LAQV- REQUIMTE), Chemistry Department, NOVA School of Science and Technology, Universidade NOVA de Lisboa, Caparica, Portugal.
Carol M TrimCanterbury Christ Church University, School of Psychology and Life Sciences, Life Sciences Industry Liaison Lab, Sandwich, United Kingdom.
Lee J ByrneCanterbury Christ Church University, School of Psychology and Life Sciences, Life Sciences Industry Liaison Lab, Sandwich, United Kingdom.
Emilia BertoloCanterbury Christ Church University, School of Psychology and Life Sciences, Life Sciences Industry Liaison Lab, Sandwich, United Kingdom.
Cornelia M WilsonCanterbury Christ Church University, School of Psychology and Life Sciences, Life Sciences Industry Liaison Lab, Sandwich, United Kingdom.
Canterbury Christ Church University · GBAssociação Científica Proteomass

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer is a global health problem affecting millions of people each year. Non-small cell lung cancer (NSCLC) is the most common form of lung cancer with various conventional treatment available in the clinic. Application of these treatments alone often results in high rates of cancer reoccurrence and metastasis. In addition, they can cause damage to healthy tissues, resulting in many adverse effects. Nanotechnology has emerged as a modality for the treatment of cancer. When used in combination with nanoparticles, it is possible to improve the pharmacokinetic and pharmacodynamic profiles of pre-existing drugs used in cancer treatment. Nanoparticles have physiochemical properties such as small size which allowing passage through challenging areas of the body, and large surface area allows for higher doses of drugs to be brought to the tumor site. Nanoparticles can be functionalized which involves modifying the surface chemistry of the particles and allows for the conjugation of ligands (small molecules, antibodies, and peptides). Ligands can be chosen for their ability to target components that are specific to or are upregulated in cancer cells, such as targeting receptors on the tumor surface that are highly expressed in the cancer. This ability to precisely target the tumor can improve the efficacy of drugs and decrease toxic side effects. This review will discuss approaches used for targeting drugs to tumors using nanoparticles, provide examples of how this has been applied in the clinic and highlight future prospects for this technology.

Indexed as

cancerdrug deliverylung cancernanoparticlestherapeutics

Identifiers

PMID36994202
PMCPMC10042133
OpenAlexW4323668225

What Socratic holds

Textfull text, public
LicenceCC BY
measurements read16
identifiers read3
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.