Nanosomal-Mediated Lipid Suspension Delivery of Docetaxel as a Promising Landscape to Enhance the Therapeutic Potential in Triple-Negative Breast Cancer
The challenging subtype of breast cancer known as Triple-Negative Breast Cancer (TNBC) is characterized by the absence of HER2 expression, progesterone receptors, and estrogen receptors. TNBC is linked to a harsh treatment trajectory, elevated rates of recurrence, and restricted therapeutic alternatives. The mainstay of treatment for TNBC has historically been conventional chemotherapy, especially taxanes like Docetaxel. However, the effectiveness of these drugs is frequently compromised by systemic toxicity and resistance mechanisms. The development of Nanosomal Docetaxel Lipid Suspension (NDLS) offers a promising alternative, designed to enhance Docetaxel's therapeutic index by improving solubility, reducing side effects, and optimizing tumor-targeted drug delivery. NDLS has potential as a delivery system for additional chemotherapy drugs or combination treatments. This study addresses the cellular and molecular causes of TNBC, emphasizes the drawbacks of traditional treatments, and offers a thorough examination of NDLS in preclinical and clinical settings. This review provides a thorough analysis of NDLS in TNBC, laying the groundwork for further studies and therapeutic applications.
Authors
- Faraat Ali (ORCID: https://orcid.org/0000-0002-1438-4223)
- Varisha Anjum (ORCID: https://orcid.org/0000-0001-6916-5653)
- Irina Potoroko (ORCID: https://orcid.org/0000-0003-1941-6754)
- Ammar Kadi (ORCID: https://orcid.org/0000-0003-2755-1497)
- Rabia Choudhary
- Pritya Jha
Institutions
- Banasthali University (IN)
- South Ural State University (RU)
- Charles University (CZ)
- Sunderland College (GB)
- University of Hradec Králové (CZ)
Publication Details
- Journal
- Anti-Cancer Agents in Medicinal Chemistry
- Published
- 2025-05-30
- DOI
- https://doi.org/10.2174/0118715206366378250519105734
- Primary Topic
- Nanoparticle-Based Drug Delivery
- Type
- article
- Field-Weighted Citation Impact
- 0.00