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In vitro anticancer effects of frankincense and its nanoemulsions for enhanced cancer cell targeting

Affiliation
Department of Basic and Applied Sciences ,College of Applied and Health Sciences ,A’Sharqiyah University ,Ibra ,Oman
Al-Balushi, Rayya A.;
Affiliation
Department of Pharmaceutical Engineering and Technology ,Indian Institute of Technology (BHU) ,Varanasi ,India
Chaudhuri, Aiswarya;
Affiliation
Brown Cancer Center ,University of Louisville ,Louisville ,KY ,United States
Kandimalla, Raghuram;
Affiliation
Department of Chemistry ,College of Science ,University of Hail ,Hail ,Saudi Arabia
Haque, Ashanul;
Affiliation
Department of Chemistry ,College of Science ,University of Hail ,Hail ,Saudi Arabia
Alenezi, Khalaf M.;
Affiliation
Department of Biology ,College of Science ,University of Hail ,Hail ,Saudi Arabia
Saeed, Mohd.;
Affiliation
College of Health Sciences ,University of Buraimi ,Al Buraimi ,Oman
Changez, Mohammad;
Affiliation
Department of Basic and Applied Sciences ,College of Applied and Health Sciences ,A’Sharqiyah University ,Ibra ,Oman
Al Harthy, Thuraya;
Affiliation
Department of Basic and Applied Sciences ,College of Applied and Health Sciences ,A’Sharqiyah University ,Ibra ,Oman
Al Hinaai, Mohammed;
Affiliation
Department Health Services Management ,College of Public Health and Health Informatics ,University of Hail ,Hail ,Saudi Arabia
Siddiqui, Samra;
Affiliation
Department of Pharmaceutical Engineering and Technology ,Indian Institute of Technology (BHU) ,Varanasi ,India
Agrawal, Ashish Kumar;
Affiliation
Brown Cancer Center ,University of Louisville ,Louisville ,KY ,United States
Aqil, Farrukh

Introduction Frankincense has demonstrated promising in vitro anticancer activity. However, its conventional delivery methods face significant challenges due to limited oral bioavailability. To address these limitations, this study focuses on developing optimized nanoemulsions (NEs) of Frankincense oil (FO) to enhance its therapeutic efficacy. Methods Frankincense resins were extracted and characterized using gas chromatography-mass spectrometry (GC-MS) and liquid chromatography-mass spectrometry (LC-MS), identifying key metabolites including isopinocarveol, α-thujene, p-cymene, carvone, germacrene A, and various methyl esters. FO-based nanoemulsions (FO-NEs) were prepared and optimized using a 3-factor, 3-level Box-Behnken Design (BBD), with 10% FO (v/v), 40% surfactant (cremophor EL), and co-surfactant (Transcutol P). The optimized FO-NEs were evaluated for particle size, polydispersity index (PDI), zeta potential, and morphology using scanning electron microscopy (SEM) and atomic force microscopy (AFM). Cytotoxicity, wound healing, mitochondrial membrane potential (MMP), and reactive oxygen species (ROS) assays were performed against breast cancer (MDA-MB-231, MDA-MB-231-TR) and lung cancer (A549, A549-TR, H1299) cell lines. Results The optimized FO-NEs exhibited an average particle size of 65.1 ± 4.21 nm, a PDI of 0.258 ± 0.04, and a zeta potential of −22.3 ± 1.2 mV. SEM and AFM confirmed the spherical morphology of the FO-NEs. In vitro cytotoxicity studies revealed enhanced anticancer activity of FO-NEs (IC50 = 13.2 μg/mL) compared to free FO (IC50 = 22.5 μg/mL) against resistant breast cancer MDA-MB-231-TR cells. FO-NEs significantly improved cancer cell internalization, disrupted mitochondrial membrane potential, and increased ROS generation, leading to enhanced cytotoxic effects. Discussion The results demonstrate that nanoemulsion-based delivery significantly enhances the bioactivity and cellular uptake of frankincense oil compared to its free form. FO-NEs exhibit potent anticancer activity, particularly against drug-resistant cancer cell lines, suggesting their potential as a viable strategy for improving the therapeutic efficacy of frankincense in cancer treatment.

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License Holder: Copyright © 2025 Al-Balushi, Chaudhuri, Kandimalla, Haque, Alenezi, Saeed, Changez, Al Harthy, Al Hinaai, Siddiqui, Agrawal and Aqil.

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