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Original Research Article | OPEN ACCESS

Nanostructured lipid carriers loaded with capecitabine modulate apoptosis via IL-6 signaling: A novel approach to targeted cancer therapy

Mohammad Intakhab Alam1, Syam Mohan2,3, Mohammad Ashafaq4, Ahmad Salawi1, Dalin A Hassan4, Wedad Mawkili4, Rahimullah Siddiqui4, Sohail Hussain4

1Department of Pharmaceutics, College of Pharmacy, Jazan University, Jazan, Saudi Arabia; 2School of Health Sciences, University of Petroleum and Energy Studies, Dehradun, Uttarakhand; 3Center for Global Health Research, Saveetha Medical College and Hospitals, Saveetha Institute of Medical and Technical Sciences, Saveetha University, India; 4Department of Pharmacology and Toxicology, College of Pharmacy, Jazan University, Jazan, Saudi Arabia.

For correspondence:-  Sohail Hussain   Email: shussainamu@gmail.com   Tel:+966-5314389

Received: 21 January 2024        Accepted: 13 April 2025        Published: 07 May 2025

Citation: Alam MI, Mohan S, Ashafaq M, Salawi A, Hassan DA, Mawkili W, et al. Nanostructured lipid carriers loaded with capecitabine modulate apoptosis via IL-6 signaling: A novel approach to targeted cancer therapy. Trop J Pharm Res 2025; 24(4):459-468 doi: https://dx.doi.org/10.4314/tjpr.v24i4.2

© 2025 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To examine the impact of capecitabine-loaded nanostructured lipid carriers (NLC) on cancer cell death mechanisms and apoptosis through interleukin-6 (IL-6) signaling system. Method: In a triplicate MTT assay, cell viability was assessed using 100 μg/mL capecitabine-loaded nanostructured lipid carrier (NLC) formulation. Apoptotic DNA degradation was determined by DNA fragmentation analysis. The molecular processes behind cellular responses were clarified by gene expression profiling of IL-6 pathway components. The formulations were characterized using zeta potential, particle size, and polydispersity index (PDI). Furthermore, morphological analysis, MTT testing, DNA fragmentation assay, and qRT-PCR were used to examine gene expression of interleukin cytokines IL-6, IL-6R, gp130, Bcl-2, Bax, NF-kB, and JAK-STAT. Results: Microscopic examination of cell lines revealed morphological alterations suggestive of cell death and apoptosis. Results from MTT assay showed that nano-formulation had a much lower IC50 (8 μg/mL) compared to pure drug (48 μg/mL). There were statistically significant (p < 0.05) differences between nano formulation and pure drug in each treatment concentration. expression of inflammatory and apoptotic genes was significantly lower in pure and Nano-Cap treated cell lines compared to control (p < 0.05). However, treatment with Nano-Cap significantly reduced expression of inflammatory and apoptotic markers compared to pure drug (p < 0.05). Furthermore, level of Bax was significantly increased (p < 0.001) in Nano-Cap-treated cell lines compared to pure drug and control Conclusion: Capecitabine-loaded nanostructured lipid carriers (NLC) are more effective than pure drug in treating colon cancer. The results may contribute to developing more effective, targeted cancer therapies and personalized treatment strategies by elucidating the interplay between nanoparticle drug delivery, chemotherapy agents, and intracellular signaling pathways.

Keywords: Capecitabine, NLC, Apoptosis, MTT, Interleukin, IL-6 signaling

Impact Factor
Thompson Reuters (ISI): 0.6 (2023)
H-5 index (Google Scholar): 49 (2023)

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