The DOI matches its Crossref record; 336 of the 343 references it cites were found in a registry or an index.
Nanotechnology-based drug delivery for breast cancer treatment: Current applications and future directions
Open accessAbstract
Breast cancer (BC) is one of the most prevalent cancers in women worldwide. Limited specificity, systemic toxicity, risk of recurrence, and drug resistance are some of the drawbacks of traditional BC treatment approaches. Therefore, it is crucial to develop more effective, safe, and customized management plans for BC. The application of nanoparticle-based systems, such as liposomes, nanostructured lipid carriers, polymeric micelles, polymeric nanoparticles, dendrimers, and hybrid nanoparticles, has drawn significant interest in BC treatment. Nanomedicine can enhance the efficacy of drugs through active targeting, better tissue penetration, and more efficient tumor suppression via improved retention and permeability. Additionally, gene delivery using hybrid and theranostic nanomedicine has also been explored in BC treatment. Numerous nanomedicines have been used clinically for the treatment of breast cancer, some of which have already received U.S. Food and Drug Administration (USFDA) approval. Here, we focus on nanotechnology-based therapeutic approaches for BC treatment and highlighted their enhanced efficacy and reduced side effects. In addition, we have also explored on the possible utilization of Artificial Intelligence (AI) nanomedicine and bioinspired nanocarriers for BC treatment, which could pave the way for more precise, effective, and personalized therapies by improving nanoparticle design, optimizing drug delivery systems, and leveraging big data analytics.
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“The route of administration also remains a practical limitation, as intratumoral delivery may not be feasible for all anatomical sites, whereas systemic administration raises concerns regarding off-target accumulation and toxicity [25,97].”
From Nanoparticle-Mediated Radiosensitization in Breast Cancer: A Systematic Review of Preclinical Evidence and Translational Challenges (2026) · cites this paper as [97]
In the citing paper
“Many preclinical studies rely on passive targeting through the enhanced permeability and retention (EPR) effect, which is highly variable and generally less pronounced in human tumors than in experimental models [5,97].”
From Nanoparticle-Mediated Radiosensitization in Breast Cancer: A Systematic Review of Preclinical Evidence and Translational Challenges (2026) · cites this paper as [97]
In the citing paper
“These systems established the proof-of-concept that nanomaterials could enhance radiation-induced damage, but they also highlighted important limitations related to tumor hypoxia, antioxidant defenses, heterogeneous intratumoral distribution, and variable nanoparticle accumulation [11,12,25,95,97].”
From Nanoparticle-Mediated Radiosensitization in Breast Cancer: A Systematic Review of Preclinical Evidence and Translational Challenges (2026) · cites this paper as [97]
In the citing paper
“Although these combinatorial systems often demonstrate enhanced efficacy experimentally, their clinical development is challenged by issues related to reproducibility, manufacturing consistency, regulatory approval, scalability, and long-term safety [25,96,97].”
From Nanoparticle-Mediated Radiosensitization in Breast Cancer: A Systematic Review of Preclinical Evidence and Translational Challenges (2026) · cites this paper as [97]
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Flagged first, then by citations
7 of the 343 references couldn’t be matched to a known paper.
Research works printed but not linked: 10
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Cited by
Sorted by citations
Breast Cancer: Molecular Pathogenesis and Targeted Therapy
Samad, M. A., Ahmad, I., Khan, M. R., Suhail, M., Zughaibi, T. A., Al-Abbasi, F. A., Alhosaini, K. A., Khan, M. S., Kumer, A., & Tabrez, S. S. M. (2025) · MedComm · doi:10.1002/mco2.70404 · Cited by 28
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Natural-Based Magnetite/Hydroxyapatite/Chitosan Nanocomposite as Effective Drug Delivery Systems
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Radiopaque Silk Sericin Nanoparticles for Computed Tomography Imaging of Solid Tumors
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Aneja, P., Guleria, R., & Dahiya, D. P. (2025) · Assay and Drug Development Technologies · doi:10.1089/adt.2025.026 · Cited by 6
Metadata
- Authors
- Samad, M. A., Ahmad, I., Zughaibi, T. A., Suhail, M., Zaidi, S. K., Al-Abbasi, F. A., & Tabrez, S.
- Affiliations
- King Abdulaziz University (SA)
- Corresponding author
- Tabrez, Shams
- ORCID
- Venue
- European Journal of Medicinal Chemistry Reports
- Publisher
- Elsevier BV
- Published
- 2025-08
- Volume
- 14
- Pages
- 100268
- ISSN
- 2772-4174 (ISSN-L)
- OpenAlex
- W4409392096
- Cited by
- 35
- References
- 343
- Citations by year
- 2026: 21 · 2025: 14
- FWCI
- 7.40
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- European Journal of Medicinal Chemistry Reports (publishedVersion, cc-by-nc-nd)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- King Fahad Medical City
- King Abdulaziz University
- Topics
- Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Drug Discovery › Pharmacology and Nanomedicine Research
- Physical Sciences › Materials Science › Polymers and Plastics › Dendrimers and Hyperbranched Polymers
- Keywords
- breast cancer, nanomedicine, drug delivery systems, liposomes, nanostructured lipid carriers, polymeric micelles, polymeric nanoparticles, dendrimers, hybrid nanostructures, nanotheranostics, gene delivery, targeted drug delivery, drug resistance
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