Evidence map›Paper›PMID 41857404›Full record

ReviewAAPS PharmSciTech2026

Innovative Nanocarriers of Sorafenib in the Optimisation of Therapeutic Outcome: Challenges and Applications in Breast Cancer.

Nishtha Chaurawal, Amalia Ruiz Estrada, Klaus Pors, Kaisar Raza, Muhammad Wahajuddin

Abstract readReview
PubMed Publisher
In one paragraph

Review in AAPS PharmSciTech, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Nishtha ChaurawalDepartment of Pharmacy, School of Chemical Sciences and Pharmacy, Central University of Rajasthan, Bandarsindri, Ajmer, Rajasthan, 305817, India.ORCID http://orcid.org/0009-0004-6764-8597
Amalia Ruiz EstradaInstitute of Cancer Therapeutics, Faculty of Life Sciences, University of Bradford, BD7 1DP, Bradford, UK. g.ruizestrada@bradford.ac.uk.ORCID http://orcid.org/0000-0001-8358-5304
Klaus PorsInstitute of Cancer Therapeutics, Faculty of Life Sciences, University of Bradford, BD7 1DP, Bradford, UK. K.Pors1@bradford.ac.uk.ORCID http://orcid.org/0000-0002-0837-5208
Kaisar RazaDepartment of Pharmacy, School of Chemical Sciences and Pharmacy, Central University of Rajasthan, Bandarsindri, Ajmer, Rajasthan, 305817, India. drkaisar@curaj.ac.in.ORCID http://orcid.org/0000-0001-8159-8005
Muhammad WahajuddinInstitute of Cancer Therapeutics, Faculty of Life Sciences, University of Bradford, BD7 1DP, Bradford, UK. m.wahajuddin@bradford.ac.uk.ORCID http://orcid.org/0000-0003-3362-7558

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sorafenib is an oral tyrosine kinase inhibitor which inhibits the growth of cancer cells by inhibiting several tyrosine kinase receptors taking part in the perpetuation and pathogenesis of breast tumours. Sorafenib was approved in 2005 for the treatment of liver and prostate cancers. In recent years, focused studies have explored the drugs clinical potential in breast cancer. There are several clinical trials (ongoing and completed) of sorafenib to treat metastatic breast cancer patients. Interestingly, these have shown encouraging results in particular in combination with other clinically-used drugs. However, effective clinical use has been somewhat hampered due to the drug's hydrophobicity, rapid first pass metabolism, short half-life, low oral bioavailability and side effects including hand and foot reaction as well as hypersensitivity. In attempts to overcome some of these drawbacks, nanotechnology-based delivery systems have been explored including nanocarriers like liposomes, niosomes, lipid-polymer hybrid nanoparticles, solid lipid nanocarriers, microemulsions, nanovectors and gel matrices. We will describe current state-of-the-art nanocarrier-based strategies, and discuss how such approaches can be harnessed to enhance the clinical efficacy of sorafenib for breast cancer treatment.

Indexed as

Antineoplastic AgentsBreast NeoplasmsDrug CarriersNanoparticlesNiacinamidePhenylurea CompoundsAnimalsBiological AvailabilityDrug Delivery SystemsFemaleHumansLiposomesProtein Kinase InhibitorsSorafenibAntineoplastic AgentsDrug CarriersLiposomesNiacinamidePhenylurea CompoundsProtein Kinase InhibitorsSorafenibanticancerbioavailabilityclinical trialsefficacynanotechnologysorafenib

Identifiers

PMID41857404

What OpenQuestion holds

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Registered trials

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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.