Niclosamide nanoemulsion for colorectal cancer: development, physicochemical characterization, and in vitro anticancer activity

IF 2.1 4区 材料科学 Q3 CHEMISTRY, MULTIDISCIPLINARY
Eduardo José Barbosa, Claudio Fukumori, Sarah de Araújo Sprengel, Thayná Lopes Barreto, Kelly Ishida, Gabriel Lima Barros de Araujo, Nádia Araci Bou-Chacra, Luciana Biagini Lopes
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引用次数: 0

Abstract

The BCS class II (Biopharmaceutical Classification System) niclosamide has shown promising anticancer activity for colorectal cancer. However, its low water solubility compromises its oral absorption and systemic action. Incorporating niclosamide in nanoemulsion allows to optimize its cell uptake and tumor penetration. This study aimed at the development, physicochemical characterization, and in vitro anticancer activity of a niclosamide nanoemulsion, with HCT-116 as the cell model. Medium- and long-chain lipids were tested to prepare the nanoemulsions, obtained by high-pressure homogenization. Design of experiments was used to optimize the formulations, which were subjected to a stability study at 30 °C/75% relative humidity (RH) and 4 °C. Nanoemulsion efficacy was evaluated in an HCT-116 viability assay and 3D cell culture model. Medium-chain lipids provided better solubility results than long-chain. Miglyol® 812 and poloxamer 188 proved to be suitable components for the system. Niclosamide nanoemulsion (~ 200 nm) was stable for 56 days, presenting monomodal particle size distribution. The cell viability assay with HCT-116 cell line demonstrated that niclosamide cytoxicity was both time and concentration dependent. In the 3D cell culture model, size and zeta potential may have influenced drug penetration in the spheroid. Incorporating the drug substance in a nanostructured system was pivotal to potentiate niclosamide activity. Our results encourage further research to understand and optimize niclosamide performance as an anticancer drug substance aiming at its repositioning.

Graphical Abstract

用于治疗结直肠癌的烟酰胺纳米乳液:开发、理化表征和体外抗癌活性
BCS II 级(生物制药分类系统)烟酰胺对结直肠癌具有良好的抗癌活性。然而,尼可刹米的水溶性较低,影响了其口服吸收和全身作用。在纳米乳液中加入尼可刹米可优化其细胞吸收和肿瘤穿透。本研究旨在以 HCT-116 为细胞模型,研究尼可刹米纳米乳液的开发、理化特性和体外抗癌活性。研究人员测试了中链和长链脂质来制备纳米乳液,并通过高压均质化获得了纳米乳液。实验设计用于优化配方,并在 30 °C/75% 相对湿度 (RH) 和 4 °C 下进行稳定性研究。在HCT-116活力测定和三维细胞培养模型中评估了纳米乳剂的功效。中链脂质的溶解度优于长链脂质。事实证明,Miglyol® 812 和 poloxamer 188 是该系统的合适成分。尼可刹米纳米乳液(约 200 nm)可稳定使用 56 天,呈现单模粒度分布。用 HCT-116 细胞系进行的细胞活力测定表明,尼可刹米的细胞毒性与时间和浓度有关。在三维细胞培养模型中,粒度和zeta电位可能会影响药物在球体内的渗透。在纳米结构体系中加入药物物质是增强尼可刹米活性的关键。我们的研究结果鼓励人们进一步研究如何了解和优化尼可刹米作为抗癌药物的性能,以实现其重新定位。
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来源期刊
Journal of Nanoparticle Research
Journal of Nanoparticle Research 工程技术-材料科学:综合
CiteScore
4.40
自引率
4.00%
发文量
198
审稿时长
3.9 months
期刊介绍: The objective of the Journal of Nanoparticle Research is to disseminate knowledge of the physical, chemical and biological phenomena and processes in structures that have at least one lengthscale ranging from molecular to approximately 100 nm (or submicron in some situations), and exhibit improved and novel properties that are a direct result of their small size. Nanoparticle research is a key component of nanoscience, nanoengineering and nanotechnology. The focus of the Journal is on the specific concepts, properties, phenomena, and processes related to particles, tubes, layers, macromolecules, clusters and other finite structures of the nanoscale size range. Synthesis, assembly, transport, reactivity, and stability of such structures are considered. Development of in-situ and ex-situ instrumentation for characterization of nanoparticles and their interfaces should be based on new principles for probing properties and phenomena not well understood at the nanometer scale. Modeling and simulation may include atom-based quantum mechanics; molecular dynamics; single-particle, multi-body and continuum based models; fractals; other methods suitable for modeling particle synthesis, assembling and interaction processes. Realization and application of systems, structures and devices with novel functions obtained via precursor nanoparticles is emphasized. Approaches may include gas-, liquid-, solid-, and vacuum-based processes, size reduction, chemical- and bio-self assembly. Contributions include utilization of nanoparticle systems for enhancing a phenomenon or process and particle assembling into hierarchical structures, as well as formulation and the administration of drugs. Synergistic approaches originating from different disciplines and technologies, and interaction between the research providers and users in this field, are encouraged.
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