Tunç Tutku, Hepokur Ceylan, Kari Per Afşin
Department of Pharmaceutical Microbiology, Faculty of Pharmacy, Sivas Cumhuriyet University, Sivas, Türkiye.
Department of Biochemistry, Faculty of Pharmacy, Sivas Cumhuriyet University, Sivas, Türkiye.
Bioinorg Chem Appl. 2024 Feb 13;2024:9916187. doi: 10.1155/2024/9916187. eCollection 2024.
Carrier system therapies based on combining cancer drugs with nanoparticles have been reported to control tumor growth and significantly reduce the side effects of cancer drugs. We thought that paclitaxel-loaded silver nanoparticles (AgNPs-PTX) were the right carrier to target cancer cells. We also carried out antimicrobial activity experiments as systems formed with nanoparticles have been shown to have antimicrobial activity. In our study, we used easy-to-synthesize and low-cost silver nanoparticles (AgNPs) with biocatalytic and photocatalytic advantages as drug carriers. We investigated the antiproliferative activities of silver nanoparticles synthesized by adding paclitaxel on MCF-7 (breast adenocarcinoma cell line), A549 (lung carcinoma cell line), C6 (brain glioma cell line) cells, and healthy WI-38 (fibroblast normal cell line) cell lines and their antimicrobial activities on 10 different microorganisms. The synthesized AgNPs and AgNPs-PTX were characterized by dynamic light scattering (DLS), scanning transmission electron microscopy, UV-visible spectroscopy, Fourier transform infrared spectroscopy, and X-ray spectroscopy. The nanoparticles were spherical in shape, with AgNPs ranging in size from 2.32 to 5.6 nm and AgNPs-PTXs from 24.36 to 58.77 nm. AgNPs demonstrated well stability of -47.3 mV, and AgNPs-PTX showed good stability of -25.4 mV. The antiproliferative effects of the synthesized nanoparticles were determined by XTT (tetrazolium dye; 2,3-bis-(2-methoxy-4-nitro-5-sulfenyl)-(2H)-tetrazolium-5-carboxanilide), and the proapoptotic effects were determined by annexin V/propidium iodide (PI) staining. The effect of AgNPs-PTX was more effective, and anticancer activity was higher than PTX in all cell lines. When selectivity indices were calculated, AgNPs-PTX was more selective in the A549 cell line (SI value 6.53 g/mL). AgNPs-PTX was determined to increase apoptosis cells by inducing DNA fragmentation. To determine the antimicrobial activity, the MIC (minimum inhibitory concentration) test was performed using 8 different bacteria and 2 different fungi. Seven of the 10 microorganisms tested exhibited high antimicrobial activity according to the MIC ≤100 g/mL standard, reaching MIC values below 100 g/mL and 100 g/mL for both AgNPs and AgNPs-PTX compared to reference sources. Compared to standard antibiotics, AgNPs-PTX was highly effective against 4 microorganisms.
据报道,基于将抗癌药物与纳米颗粒相结合的载体系统疗法能够控制肿瘤生长,并显著降低抗癌药物的副作用。我们认为负载紫杉醇的银纳米颗粒(AgNPs-PTX)是靶向癌细胞的合适载体。由于已证明由纳米颗粒形成的系统具有抗菌活性,我们还开展了抗菌活性实验。在我们的研究中,我们使用了具有生物催化和光催化优势、易于合成且成本低廉的银纳米颗粒(AgNPs)作为药物载体。我们研究了添加紫杉醇合成的银纳米颗粒对MCF-7(乳腺腺癌细胞系)、A549(肺癌细胞系)、C6(脑胶质瘤细胞系)细胞以及健康的WI-38(成纤维细胞正常细胞系)细胞系的抗增殖活性,以及它们对10种不同微生物的抗菌活性。通过动态光散射(DLS)、扫描透射电子显微镜、紫外可见光谱、傅里叶变换红外光谱和X射线光谱对合成的AgNPs和AgNPs-PTX进行了表征。纳米颗粒呈球形,AgNPs的尺寸范围为2.32至5.6纳米,AgNPs-PTX的尺寸范围为24.36至58.77纳米。AgNPs表现出良好的稳定性,ζ电位为-47.3毫伏,AgNPs-PTX表现出良好的稳定性,ζ电位为-25.4毫伏。通过XTT(四唑盐染料;2,3-双-(2-甲氧基-4-硝基-5-磺基)-(2H)-四唑-5-甲酰苯胺)测定合成纳米颗粒的抗增殖作用,通过膜联蛋白V/碘化丙啶(PI)染色测定促凋亡作用。在所有细胞系中,AgNPs-PTX的效果更显著,抗癌活性高于紫杉醇。计算选择性指数时,AgNPs-PTX在A549细胞系中更具选择性(SI值为6.53微克/毫升)。经测定,AgNPs-PTX通过诱导DNA片段化增加凋亡细胞。为测定抗菌活性,使用8种不同细菌和2种不同真菌进行了最低抑菌浓度(MIC)试验。根据MIC≤100微克/毫升的标准,所测试的10种微生物中有7种表现出高抗菌活性,与参考来源相比,AgNPs和AgNPs-PTX的MIC值均低于100微克/毫升和100微克/毫升。与标准抗生素相比,AgNPs-PTX对4种微生物具有高效性。