Preparation of Lipid Microbubble/Paclitaxel Nanoparticle Complex and Its In Vitro Antigastric Tumor Effect Mediating the STAT3-NF-κB Pathway

IF 0.9 4区 材料科学
Wenhao Sun, Tianyuan Chen, Yuehua Yan, Heng Chen, Yang Yang, Yulan Wang
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Abstract

In this research, lipid microbubbles (MBs) were prepared first, and then Tat peptide, carboxylated heparin, amino biotin, and amino folic acid were successively synthesized. After a certain amount of paclitaxel was added, paclitaxel nanoparticles (NPs) with a double-ligand were obtained through reaction. The lipid MBs prepared above were added to streptavidin. After washing and purification, the lipid MBs and double-ligand paclitaxel NPs were added. After incubation on ice, the lipid MB-double-ligand paclitaxel NP complex was obtained. In addition to the physical characterization of the materials, human breast cancer cells MDA-MB-231 and lung cancer cells A549 were first utilized to test the biological properties of the NP complex In Vitro and then utilized to study the effects of gastric cancer (GC) cells. The results revealed that the lipid MBs were uniformly distributed and did not aggregate. The concentration of the NP complex reached 7.75±0.93×10 8 NPs/mL, and the particle size was 2.23±0.68 μ m. At various radiation intensities, blue fluorescently stained MDA-MB-231 cells and A549 cells showed greener fluorescently labeled double-ligand paclitaxel NPs around and inside the nucleus of Hoechst 33342. According to the prepared products and byproducts, they were grouped to compare different prepared products. The fluorescence uptake of the two cells at 4 h was the highest under the condition of the NP complex combined with ultrasonic radiation, and the destruction of cancer cells (MDA-MB-231 and A549) was the strongest under the condition of the NP complex combined with ultrasonic radiation. In GC cells, NP complexes inhibited cell migration and invasion relative to the other groups ( P <0.05), the level of Bax protein increased ( P <0.05), while that of Bcl-2, pSTAT3/STAT3, and phosphorylation of NF-kappa B (PNF- κ B)/NF- κ B protein were markedly decreased ( P <0.05).
脂质微泡/紫杉醇纳米颗粒复合物的制备及其介导STAT3-NF-κB通路的体外抗胃肿瘤作用
本研究首先制备脂质微泡(mb),然后依次合成Tat肽、羧化肝素、氨基生物素和氨基叶酸。加入一定量的紫杉醇后,通过反应得到具有双配体的紫杉醇纳米颗粒。将上述制备的脂质mb加入链霉亲和素中。洗涤纯化后,加入脂质MBs和双配体紫杉醇NPs。冰孵育后,得到脂质mb -双配体紫杉醇NP复合物。在对材料进行物理表征的基础上,首先利用人乳腺癌细胞MDA-MB-231和肺癌细胞A549在体外测试NP复合物的生物学特性,然后利用其对胃癌(GC)细胞的作用进行研究。结果表明,脂质mb分布均匀,不聚集。NP复合物的浓度达到7.75±0.93×10 8 NPs/mL,粒径为2.23±0.68 μ m。在不同的辐射强度下,蓝色荧光染色的MDA-MB-231细胞和A549细胞在Hoechst 33342细胞核周围和内部显示绿色荧光标记的双配体紫杉醇NPs。根据制备产物和副产物进行分组,比较不同的制备产物。两种细胞在4 h时的荧光摄取在NP复合物联合超声辐射条件下最高,对癌细胞(MDA-MB-231和A549)的破坏作用在NP复合物联合超声辐射条件下最强。在GC细胞中,NP复合物相对于其他组抑制细胞迁移和侵袭(P <0.05), Bax蛋白水平升高(P <0.05), Bcl-2、pSTAT3/STAT3和NF- κ B (PNF- κ B)/NF- κ B蛋白磷酸化水平明显降低(P <0.05)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Science of Advanced Materials
Science of Advanced Materials NANOSCIENCE & NANOTECHNOLOGY-MATERIALS SCIENCE, MULTIDISCIPLINARY
自引率
11.10%
发文量
98
审稿时长
4.4 months
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