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肉桂酸丁酯壳聚糖纳米粒的理化性质及其抗乳腺癌活性。

Cinnamon cassia oil chitosan nanoparticles: Physicochemical properties and anti-breast cancer activity.

机构信息

Key Laboratory of Modern Preparation of Traditional Chinese Medicine, Ministry of Education, Jiangxi University of Chinese Medicine, Nanchang 330004, China.

Key Laboratory of Modern Preparation of Traditional Chinese Medicine, Ministry of Education, Jiangxi University of Chinese Medicine, Nanchang 330004, China.

出版信息

Int J Biol Macromol. 2023 Jan 1;224:1065-1078. doi: 10.1016/j.ijbiomac.2022.10.191. Epub 2022 Nov 7.

DOI:10.1016/j.ijbiomac.2022.10.191
PMID:36367479
Abstract

The aim of this study was to prepare Cinnamomum cassia essential oil (CEO) impregnated chitosan nanoparticles (CS-CEO) and assess its pharmacological activity against breast cancer. Cinnamon oil-loaded chitosan nanoparticles were investigated for their physicochemical properties, stability, and anti-cancer activities both in vitro and in vivo. The prepared CS-CEO nanoparticles have a particle size, zeta-potential, entrapment efficiency and drug loading of (215.40 ± 3.90) nm, (51.70 ± 1.90) mV, (83.37 ± 0.4)% and (26.42 ± 0.65)%, respectively. CS-CEO showed a regular, uniform, and spherical or quasi-spherical structure under a transmission electron microscope. CS-CEO remained stable upon storage at 4 °C. CS-CEO exhibited enhanced in vitro antitumor activity (52 μg/mL) compared to CEO. The mechanism might be related to the up-regulation of Caspase-3 and AIF protein expression. In in vivo experiments, CS-CEO suppressed the growth of 4T1 breast cancer cells transplanted into mice, inhibited tumor cell proliferation, and induced apoptosis by reducing the expression of the Ki-67 protein. These results indicated that CEO encapsulated in chitosan had a higher physical stability and was also more effective against 4T1 breast tumor model, which can be used as a reference for the application of volatile oil components in traditional Chinese medicine.

摘要

本研究旨在制备肉桂精油(CEO)浸渍壳聚糖纳米粒(CS-CEO),并评估其对乳腺癌的药理活性。研究了肉桂油负载壳聚糖纳米粒的物理化学性质、稳定性以及在体外和体内的抗癌活性。所制备的 CS-CEO 纳米粒的粒径、Zeta 电位、包封效率和载药量分别为(215.40±3.90)nm、(51.70±1.90)mV、(83.37±0.4)%和(26.42±0.65)%。CS-CEO 在透射电子显微镜下呈现出规则、均匀、球形或准球形的结构。CS-CEO 在 4°C 下储存时保持稳定。CS-CEO 在体外表现出增强的抗肿瘤活性(52μg/mL),优于 CEO。其机制可能与 Caspase-3 和 AIF 蛋白表达上调有关。在体内实验中,CS-CEO 抑制了移植到小鼠体内的 4T1 乳腺癌细胞的生长,通过降低 Ki-67 蛋白的表达抑制肿瘤细胞增殖并诱导细胞凋亡。这些结果表明,包封在壳聚糖中的 CEO 具有更高的物理稳定性,对 4T1 乳腺癌模型也更有效,可为挥发油成分在中药中的应用提供参考。

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