Nanomedicine-Based Drug-Targeting in Breast Cancer: Pharmacokinetics, Clinical Progress, and Challenges
- PMID: 38162753
- PMCID: PMC10753706
- DOI: 10.1021/acsomega.3c07345
Nanomedicine-Based Drug-Targeting in Breast Cancer: Pharmacokinetics, Clinical Progress, and Challenges
Abstract
Breast cancer (BC) is a malignant neoplasm that begins in the breast tissue. After skin cancer, BC is the second most common type of cancer in women. At the end of 2040, the number of newly diagnosed BC cases is projected to increase by over 40%, reaching approximately 3 million worldwide annually. The hormonal and chemotherapeutic approaches based on conventional formulations have inappropriate therapeutic effects and suboptimal pharmacokinetic responses with nonspecific targeting actions. To overcome such issues, the use of nanomedicines, including liposomes, nanoparticles, micelles, hybrid nanoparticles, etc., has gained wider attention in the treatment of BC. Smaller dimensional nanomedicine (especially 50-200 nm) exhibited improved in vivo effectiveness, such as better tissue penetration and more effective tumor suppression through enhanced retention and permeation, as well as active targeting of the drug. Additionally, nanotechnology, which further extended and developed theranostic nanomedicine by incorporating diagnostic and imaging agents in one platform, has been applied to BC. Furthermore, hybrid and theranostic nanomedicine has also been explored for gene delivery as anticancer therapeutics in BC. Moreover, the nanocarriers' size, shape, surface charge, chemical compositions, and surface area play an important role in the nanocarriers' stability, cellular absorption, cytotoxicity, cellular uptake, and toxicity. Additionally, nanomedicine clinical translation for managing BC remains a slow process. However, a few cases are being used clinically, and their progress with the current challenges is addressed in this Review. Therefore, this Review extensively discusses recent advancements in nanomedicine and its clinical challenges in BC.
© 2023 The Authors. Published by American Chemical Society.
Conflict of interest statement
The authors declare no competing financial interest.
Figures




Similar articles
-
Functionalization of curcumin nanomedicines: a recent promising adaptation to maximize pharmacokinetic profile, specific cell internalization and anticancer efficacy against breast cancer.J Nanobiotechnology. 2023 Mar 25;21(1):106. doi: 10.1186/s12951-023-01854-x. J Nanobiotechnology. 2023. PMID: 36964547 Free PMC article. Review.
-
The Clinical Translation of Organic Nanomaterials for Cancer Therapy: A Focus on Polymeric Nanoparticles, Micelles, Liposomes and Exosomes.Curr Med Chem. 2018;25(34):4224-4268. doi: 10.2174/0929867324666170830113755. Curr Med Chem. 2018. PMID: 28875844 Review.
-
Receptor-Targeted Surface-Engineered Nanomaterials for Breast Cancer Imaging and Theranostic Applications.Crit Rev Ther Drug Carrier Syst. 2022;39(6):1-44. doi: 10.1615/CritRevTherDrugCarrierSyst.2022040686. Crit Rev Ther Drug Carrier Syst. 2022. PMID: 35997100
-
Multi-functionalization, a Promising Adaptation to Overcome Challenges to Clinical Translation of Nanomedicines as Nano-diagnostics and Nano-therapeutics for Breast Cancer.Curr Pharm Des. 2021;27(43):4356-4375. doi: 10.2174/1381612827666210830092539. Curr Pharm Des. 2021. PMID: 34459374 Review.
-
Nano-Based Theranostic Platforms for Breast Cancer: A Review of Latest Advancements.Bioengineering (Basel). 2022 Jul 15;9(7):320. doi: 10.3390/bioengineering9070320. Bioengineering (Basel). 2022. PMID: 35877371 Free PMC article. Review.
Cited by
-
Nanoscale strides: exploring innovative therapies for breast cancer treatment.RSC Adv. 2024 Apr 29;14(20):14017-14040. doi: 10.1039/d4ra02639j. eCollection 2024 Apr 25. RSC Adv. 2024. PMID: 38686289 Free PMC article. Review.
-
A comprehensive review on doxorubicin: mechanisms, toxicity, clinical trials, combination therapies and nanoformulations in breast cancer.Drug Deliv Transl Res. 2025 Jan;15(1):102-133. doi: 10.1007/s13346-024-01648-0. Epub 2024 Jun 17. Drug Deliv Transl Res. 2025. PMID: 38884850 Review.
-
LINC00870 promotes imatinib resistance in gastrointestinal stromal tumor via inhibiting PIGR glycosylation modifications.Heliyon. 2025 Jan 13;11(3):e41934. doi: 10.1016/j.heliyon.2025.e41934. eCollection 2025 Feb 15. Heliyon. 2025. PMID: 39968132 Free PMC article.
-
Interleukin-6 Modulation in Ovarian Cancer Necessitates a Targeted Strategy: From the Approved to Emerging Therapies.Cancers (Basel). 2024 Dec 16;16(24):4187. doi: 10.3390/cancers16244187. Cancers (Basel). 2024. PMID: 39766086 Free PMC article. Review.
-
Radiolabelling and bioequivalence of modified Tamoxifen solid lipid nanoparticles as a targeted chemotherapeutic drug.Drug Deliv Transl Res. 2025 May 7. doi: 10.1007/s13346-025-01865-1. Online ahead of print. Drug Deliv Transl Res. 2025. PMID: 40335856
References
-
- Data Explorer. ECIS - European Cancer Information System. https://ecis.jrc.ec.europa.eu/explorer.php?$0-0 (accessed 2023-09-04).
Publication types
LinkOut - more resources
Full Text Sources