Chitosan based sorafenib tosylate loaded magnetic nanoparticles: Formulation and in-vitro characterization

纳米颗粒 分散性 超顺磁性 Zeta电位 壳聚糖 磁性纳米粒子 材料科学 核化学 顺磁性 分析化学(期刊) 化学 粒径 纳米技术 磁化 色谱法 物理化学 有机化学 高分子化学 磁场 物理 量子力学
作者
Mandeep Dahiya,Rajendra Awasthi,Jaya Parkash Yadav,Shammi Sharma,Kamal Dua,Harish Dureja
出处
期刊:International Journal of Biological Macromolecules [Elsevier BV]
卷期号:242: 124919-124919
标识
DOI:10.1016/j.ijbiomac.2023.124919
摘要

Biocompatible magnetic nanoparticles are used for various biomedical applications. This study reported the development of nanoparticles with magnetic properties by embedding magnetite particles in the drug-loaded, crosslinked matrix of chitosan. Sorafenib tosylate-loaded magnetic nanoparticles were prepared by a modified ionic-gelation method. Particle size, zeta potential, polydispersity index, and entrapment efficiency of nanoparticles were in the range of 95.6 ± 3.4 nm to 440.9 ± 7.3 nm, 12.8 ± 0.8 mV to 27.3 ± 1.1 mV, 0.289 ± 0.011 to 0.571 ± 0.011, and 54.36 ± 1.26 % to 79.67 ± 1.40 %, respectively. The XRD spectrum of formulation CMP-5 confirmed the amorphous nature of the loaded drug in nanoparticles. TEM image confirmed the spherical shape of nanoparticles. Atomic force microscopic image of formulation CMP-5 indicated a mean surface roughness of 10.3597 nm. The magnetization saturation of formulation CMP-5 was 24.74 emu/g. Electron paramagnetic resonance spectroscopy revealed that formulation CMP-5's g-Lande's factor was 4.27, which was extremely near to the 4.30 (usual for Fe3+ ions). Residual paramagnetic Fe3+ ions may be responsible for paramagnetic origin. The data suggests superparamagnetic nature of particles. Formulations released 28.66 ± 1.22 % to 53.24 ± 1.95 % and 70.13 ± 1.72 % to 92.48 ± 1.32 % of the loaded drug after 24 h in pH 6.8 and pH 1.2, respectively. The IC50 value of formulation CMP-5 was 54.75 μg/mL in HepG2 (human hepatocellular carcinoma cell lines).

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