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Synergistic Effects of Platinum-Based Drugs and Curcumin on Liposomal Delivery in Hsc-3 Oral Cancer Cells Publisher



Amiri F1 ; Ghanbarikondori P2 ; Amoozegar H3 ; Kazemi K4 ; Sadrian S5 ; Afsharibehbahanizadeh S6, 7 ; Akbarzadehkhayavi A8
Authors
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Authors Affiliations
  1. 1. DDS, Tehran University of Medical Sciences, Dental School, Tehran, Iran
  2. 2. Department of Pharmaceutics, Pharmaceutical Sciences Branch, Islamic Azad University (IAU), Tehran, Iran
  3. 3. School of Pharmacy, Zanjan University of Medical Sciences, Zanjan, Iran
  4. 4. Faculty of Nursing, Golestan University of Medical Sciences, Golestan, Iran
  5. 5. Department of Biological Sciences and Technologies, Shahid Beheshti University, Tehran, Iran
  6. 6. Department of Experimental Medicine (DIMES), University of Genoa, Via Leon Battista Alberti, 2, Genoa, 16132, Italy
  7. 7. Department of Internal Medicine (DiMI), University of Genoa, Viale Benedetto XV, 6, Genoa, 16132, Italy
  8. 8. Institute Pasteur of Iran in Department Nanobiechnology, Tehran, Iran

Source: Indian Journal of Clinical Biochemistry Published:2025


Abstract

This study delves into the potentiation of cytotoxic effects through the strategic incorporation of curcumin within two distinct nanoliposomal formulations: cisplatin-loaded and carboplatin-loaded nanoliposomes, specifically targeting HSC-3 oral carcinoma cells. The formulations were rigorously characterized to ascertain their physicochemical properties, with particle sizes measured in the range of 220–240 nm, zeta potentials surpassing − 28 mV, and polydispersity indices (PDI) below 0.30, collectively signifying robust colloidal stability and a uniform size distribution—both essential attributes for efficient drug delivery. The cytotoxic potential of these nanoliposomal systems was systematically evaluated using MTT assays across three temporal checkpoints (24, 48, and 72 h), wherein the inclusion of 4 mM curcumin markedly augmented the induction of cell death compared to the control cohorts. This enhancement underscores the synergistic interplay between curcumin and the platinum-based chemotherapeutics in amplifying therapeutic efficacy. Furthermore, drug release kinetics were meticulously examined, revealing a sustained release pattern where approximately 21% and 27% of the encapsulated cisplatin and carboplatin, respectively, were released over 35 h. Such controlled release dynamics not only prolong the therapeutic window of these agents within the tumor microenvironment but also mitigate systemic toxicity risks associated with burst release phenomena. Collectively, this finding highlight the advantage of heightened cytotoxic efficacy by curcumin integration, positioning nanoliposomal formulations as a transformative approach in the realm of oral cancer therapeutics. Future endeavors will pivot towards in vivo validations to substantiate these in vitro observations and unravel the molecular underpinnings of the observed synergistic effects. © The Author(s), under exclusive licence to Association of Clinical Biochemists of India 2025.