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一种用于合成具有理想物理化学特性的壳聚糖纳米颗粒的快速方案。

A rapid protocol for synthesis of chitosan nanoparticles with ideal physicochemical features.

作者信息

Dadashi Hamed, Vandghanooni Somayeh, Karamnejad-Faragheh Shahrbanoo, Karimian-Shaddel Alireza, Eskandani Morteza, Jahanban-Esfahlan Rana

机构信息

Research Center for Pharmaceutical Nanotechnology, Biomedicine Institute, Tabriz University of Medical Sciences, Tabriz, Iran.

Department of Medical Biotechnology, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran.

出版信息

Heliyon. 2024 Jun 3;10(11):e32228. doi: 10.1016/j.heliyon.2024.e32228. eCollection 2024 Jun 15.

Abstract

In this research, an innovative protocol is introduced to address crucial deficiencies in the formulation of chitosan nanoparticles (Cs NPs). While NPs show potential in drug delivery systems (DDSs), their application in the clinic is hindered by various drawbacks, such as toxicity, high material costs, and time-consuming and challenging preparation procedures. Within polymer-based NPs, Cs is a plentiful natural substance derived from the deacetylation of chitin, which can be sourced from the shells of shrimp or crab. Cs NPs can be formulated using the ionic gelation technique, which involves the use of a negatively charged agent, such as tripolyphosphate (TPP), as a crosslinking agent. Even though Cs is a cost-effective and biocompatible material, the formulation of Cs NPs with the correct size and surface electrical charge (zeta potential) presents a persistent challenge. In this study, various techniques were employed to analyze the prepared Cs NPs. The size and surface charge of the NPs were evaluated using dynamic light scattering (DLS). Morphological analysis was conducted using field emission-scanning electron microscopy (FE-SEM). The chemical composition and formation of Cs NPs were investigated using Fourier transform infrared (FTIR). The stability analysis was confirmed through X-ray diffraction (XRD) analysis. Lastly, the biocompatibility of the NPs was assessed through cell cytotoxicity evaluation using the MTT assay. Moreover, here, 11 formulations with different parameters such as reaction pH, Cs:TPP ratio, type of Cs/TPP, and ultrasonication procedure were prepared. Formulation 11 was chosen as the optimized formulation based on its high stability of more than three months, biocompatibility, nanosize of 75.6 ± 18.24 nm, and zeta potential of +26.7 mV. To conclude, the method described here is easy and reproducible and can be used for facile preparation of Cs NPs with desirable physicochemical characteristics and engineering ideal platforms for drug delivery purposes.

摘要

在本研究中,引入了一种创新方案来解决壳聚糖纳米颗粒(Cs NPs)制剂中的关键缺陷。虽然纳米颗粒在药物递送系统(DDSs)中显示出潜力,但其在临床上的应用受到各种缺点的阻碍,如毒性、高材料成本以及耗时且具有挑战性的制备程序。在基于聚合物的纳米颗粒中,Cs是一种从几丁质脱乙酰化得到的丰富天然物质,几丁质可来源于虾或蟹的壳。Cs NPs可以使用离子凝胶化技术来制备,该技术涉及使用带负电荷的试剂,如三聚磷酸钠(TPP),作为交联剂。尽管Cs是一种具有成本效益且生物相容性良好的材料,但制备具有正确尺寸和表面电荷(zeta电位)的Cs NPs仍然是一个持续的挑战。在本研究中,采用了各种技术来分析制备的Cs NPs。使用动态光散射(DLS)评估纳米颗粒的尺寸和表面电荷。使用场发射扫描电子显微镜(FE-SEM)进行形态分析。使用傅里叶变换红外光谱(FTIR)研究Cs NPs的化学成分和形成。通过X射线衍射(XRD)分析确认稳定性分析。最后,通过使用MTT法的细胞毒性评估来评估纳米颗粒的生物相容性。此外,在此制备了11种具有不同参数的制剂,如反应pH、Cs:TPP比例、Cs/TPP类型和超声处理程序。基于其超过三个月的高稳定性、生物相容性、75.6±18.24nm的纳米尺寸和+26.7mV的zeta电位,制剂11被选为优化制剂。总之,这里描述的方法简单且可重复,可用于轻松制备具有理想物理化学特性的Cs NPs,并为药物递送目的构建理想的平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35e1/11219308/72bdaceb8c1d/ga1.jpg

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