N-acetyl-d-glucosamine decorated solid lipid nanoparticles for targeted tamoxifen delivery to breast cancer cells

IF 2.1 4区 材料科学 Q3 CHEMISTRY, MULTIDISCIPLINARY Journal of Nanoparticle Research Pub Date : 2024-10-25 DOI:10.1007/s11051-024-06166-1
Mahavir Narwade, Saili Jagdale, Kavita R. Gajbhiye
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Abstract

One of the primary challenges associated with current chemotherapy lies in its inherent toxicity to healthy cells, leading to severe side effects. Recognizing the need for a more targeted approach, we have focused on tumor-specific drug delivery. Cancer cells, being highly metabolic, exhibit a significant increase in glucose consumption approximately 200 times more than normal cells for their rapid growth. To address this, we have engineered GLcNAc-modified solid lipid nanoparticles (SLNPs) designed to be actively internalized by cancer cells, thereby facilitating precise drug delivery to tumors. The developed GLcNAc-TMX-SLNPs are characterized by a size range of 200 to 250 nm and a surface charge of -25 to -35 mV. Their structural properties were thoroughly examined using techniques such as DSC, FTIR, and TEM. In the evaluation of drug release within the tumor microenvironment pH, a biphasic release pattern was observed, with 73.54 ± 0.73% release of TMX within 48 h. Importantly, the hemolysis caused by these developed SLNPs was found to be less than 5%, indicating their suitability for intravenous administration. Cellular uptake studies conducted on MDA-MB-231 cells underscored the targeted characteristics of the developed formulations. With a stable lipid composition, these SLNPs present a promising and stable platform for anticancer treatment. By minimizing off-target effects and enhancing drug delivery precision, our approach holds potential to improve the therapeutic efficacy of chemotherapy while mitigating its impact on healthy cells.

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N-acetyl-d-glucosamine decorated solid lipid nanoparticles for targeted tamoxifen delivery to breast cancer cells
当前化疗面临的主要挑战之一在于其对健康细胞的固有毒性,从而导致严重的副作用。我们认识到需要一种更具针对性的方法,因此将重点放在肿瘤特异性给药方面。癌细胞新陈代谢旺盛,其快速生长所需的葡萄糖消耗量是正常细胞的 200 倍。为此,我们设计了 GLcNAc 修饰的固体脂质纳米颗粒(SLNPs),可被癌细胞主动内化,从而促进向肿瘤精确给药。所开发的 GLcNAc-TMX-SLNPs 尺寸范围为 200 到 250 nm,表面电荷为 -25 到 -35 mV。使用 DSC、FTIR 和 TEM 等技术对其结构特性进行了全面检测。在肿瘤微环境 pH 值内的药物释放评估中,观察到了双相释放模式,48 小时内 TMX 的释放量为 73.54 ± 0.73%。在 MDA-MB-231 细胞上进行的细胞吸收研究强调了所开发制剂的靶向特性。这些 SLNPs 具有稳定的脂质成分,为抗癌治疗提供了一个前景广阔的稳定平台。通过最大限度地减少脱靶效应和提高给药精确度,我们的方法有望提高化疗的疗效,同时减轻化疗对健康细胞的影响。 图文摘要
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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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