An Experimental Design Approach for Producing Curcumin-Loaded Solid Lipid Nanoparticles

<b>Background/Objectives</b>: Curcumin has well-established efficacy in a variety of disorders due to its prominent antioxidant, antiaging, anti-inflammatory, chemosensitizing, and anticancer activities. Despite its numerous benefits, curcumin exhibits low bioavailability mainly due to its poor solubility, poor absorption, rapid metabolism, and quick excretion, consequently limiting its clinical applications. In this study, we investigated the most convenient ingredients in SLNs to enhance curcumin's solubility by examining the effects of multiple independent variables simultaneously using an experimental design. <b>Methods</b>: After curcumin's saturation solubility was investigated, SLN formulations were produced. The optimum formulation was determined with the help of experimental design. The SLNs were characterized in terms of the particle size and distribution, zeta potential, shape, entrapment efficiency, drug loading capacity, and drug release. The cell viability and cell internalization were also evaluated. <b>Results</b>: An impressive synergistic effect was achieved with the combination of Brij and Gelucire 48/16, which increased curcumin's solubility in water by 452.5 times. Curcumin-loaded SLNs were successfully produced with a spherical shape and particle size of 389.3 ± 9.95 nm. The encapsulation efficiency was directly proportionate to the amount of curcumin and the stirring speed. Curcumin in the SLNs entered the cancer cells more easily than curcumin alone. <b>Conclusions</b>: Our results demonstrate that the quantity of surfactant is a significant factor influencing the efficiency of drug loading. Finally, the 3:1 (Brij-Gelucire48/16) ratio markedly enhanced the loading efficiency. The cellular internalization and, consequently, the anticancer efficacy against adenocarcinomic human alveolar basal epithelial cells were improved with SLNs. This could be a promising approach for lipid-based colloidal drug delivery systems.

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Publication Details

Journal
Pharmaceuticals
Published
2025-03-27
DOI
https://doi.org/10.3390/ph18040470
Citations
7
Primary Topic
Curcumin's Biomedical Applications
Type
article
Field-Weighted Citation Impact
4.14
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article

An Experimental Design Approach for Producing Curcumin-Loaded Solid Lipid Nanoparticles

Emirhan Nemutlu, Ongun Mehmet Saka, Cemre İrem Aygüler, Bilge Sürücü et al.
7 citations
Pharmaceuticals
Curcumin's Biomedical Applications
4.14
article

An Experimental Design Approach for Producing Curcumin-Loaded Solid Lipid Nanoparticles

Emirhan Nemutlu, Ongun Mehmet Saka, Cemre İrem Aygüler, Bilge Sürücü, Neval Sevinç Özdemir, Egemen Çakırlı, Gülen Melike Demirbolat
article en
7 citations

Abstract

<b>Background/Objectives</b>: Curcumin has well-established efficacy in a variety of disorders due to its prominent antioxidant, antiaging, anti-inflammatory, chemosensitizing, and anticancer activities. Despite its numerous benefits, curcumin exhibits low bioavailability mainly due to its poor solubility, poor absorption, rapid metabolism, and quick excretion, consequently limiting its clinical applications. In this study, we investigated the most convenient ingredients in SLNs to enhance curcumin's solubility by examining the effects of multiple independent variables simultaneously using an experimental design. <b>Methods</b>: After curcumin's saturation solubility was investigated, SLN formulations were produced. The optimum formulation was determined with the help of experimental design. The SLNs were characterized in terms of the particle size and distribution, zeta potential, shape, entrapment efficiency, drug loading capacity, and drug release. The cell viability and cell internalization were also evaluated. <b>Results</b>: An impressive synergistic effect was achieved with the combination of Brij and Gelucire 48/16, which increased curcumin's solubility in water by 452.5 times. Curcumin-loaded SLNs were successfully produced with a spherical shape and particle size of 389.3 ± 9.95 nm. The encapsulation efficiency was directly proportionate to the amount of curcumin and the stirring speed. Curcumin in the SLNs entered the cancer cells more easily than curcumin alone. <b>Conclusions</b>: Our results demonstrate that the quantity of surfactant is a significant factor influencing the efficiency of drug loading. Finally, the 3:1 (Brij-Gelucire48/16) ratio markedly enhanced the loading efficiency. The cellular internalization and, consequently, the anticancer efficacy against adenocarcinomic human alveolar basal epithelial cells were improved with SLNs. This could be a promising approach for lipid-based colloidal drug delivery systems.

PharmaceuticalsVol. 18(4)
Yeditepe University (TR), Ankara University (TR), Kent Hastanesi (TR), Pharmaceutical Biotechnology (Czechia) (CZ), Acıbadem Adana Hospital (TR), Hacettepe University (TR), Istanbul University (TR)
Good health and well-being
Openalex Percentile: Top 6%
Curcumin's Biomedical Applications
4.14
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