Saxena Juhi, Upadhyay Tarun Kumar, Jyoti Anupam, Joshi Unnati, Joshi Anand, Rathore Mahendra Singh, Thakor Sanketsinh, Pathak Jaivik, Das Lala Sumit, Deb Payel
Department of Biotechnology, Parul Institute of Technology, Parul University, Vadodara, 391760, Gujarat, India.
Department of Life Sciences, Parul Institute of Applied Sciences and Research and Development Cell, Parul University, Vadodara, 391760, Gujarat, India.
Naunyn Schmiedebergs Arch Pharmacol. 2025 May 27. doi: 10.1007/s00210-025-04302-9.
Infectious diseases and cancers are the leading causes of mortality worldwide. Despite the discovery of antimicrobials and anticancer drugs, the mortality rate has not declined significantly. Hence, new novel agents with antibacterial and anticancer properties without toxicity are urgently needed. In the present study, carbonaceous hybrid nanocomposites multi-walled carbon nanotubes (MWCNT)/hydroxyapatite (HAp)/polyetheretherketone (PEEK)-MWCNT/HAp/PEEK were synthesized using Alphie 3D Tumbler Mixer (Synthesis Method-1), solid-state mixing (Synthesis Method-2), and chemical mixing and solvent casting (Synthesis Method-3). Synthesis Method-2 and Method-3 exhibited antibacterial activities at 250 and 500 µg/mL concentrations, and no antibacterial activity in the nanocomposite fabricated by Synthesis Method-1. However, nanocomposites prepared by Synthesis Method-1 demonstrated enhanced anticancer activity compared to Synthesis Method-2 and Synthesis Method-3. Moreover, these nanocomposites did not show any haemolytic activity at 250 and 500 µg/mL concentrations. These nanocomposites were characterized by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and transmission electron microscopy (TEM). SEM data demonstrated that nanocomposites fabricated by Synthesis Method-3 were a homogeneous, defect-free PEEK matrix with well-dispersed MWCNTs and HAp compared to Methods-1 and 2. EDS analysis showed that Synthesis Methods-2 and -3 exhibited enhanced PEEK and MWCNT dispersion. TGA analysis exhibited that Synthesis Method-3 led to the highest thermal stability. FTIR data demonstrated the presence of various functional groups in hybrid nanocomposites. XRD analysis confirmed that these nanocomposites were crystalline in nature. The TEM analysis confirms that amine-functionalized MWCNTs and HAp nanoparticles are well dispersed within the PEEK matrix. In conclusion, the synthesis strategy adopted has influenced and resulted in safe and bi-functional nanocomposites having antibacterial and anticancer activity in line with SDG-3.
传染病和癌症是全球主要的死亡原因。尽管发现了抗菌药物和抗癌药物,但死亡率并未显著下降。因此,迫切需要具有抗菌和抗癌特性且无毒的新型药物。在本研究中,使用Alphie 3D Tumbler Mixer(合成方法-1)、固态混合(合成方法-2)以及化学混合和溶剂浇铸(合成方法-3)合成了碳质杂化纳米复合材料多壁碳纳米管(MWCNT)/羟基磷灰石(HAp)/聚醚醚酮(PEEK)-MWCNT/HAp/PEEK。合成方法-2和方法-3在浓度为250和500μg/mL时表现出抗菌活性,而通过合成方法-1制备的纳米复合材料没有抗菌活性。然而,与合成方法-2和合成方法-3相比,通过合成方法-1制备的纳米复合材料表现出增强的抗癌活性。此外,这些纳米复合材料在浓度为250和500μg/mL时未表现出任何溶血活性。这些纳米复合材料通过扫描电子显微镜(SEM)、能量色散X射线光谱(EDS)、热重分析(TGA)、傅里叶变换红外光谱(FTIR)、X射线衍射(XRD)和透射电子显微镜(TEM)进行表征。SEM数据表明,与方法-1和方法-2相比,通过合成方法-3制备的纳米复合材料是一种均匀、无缺陷的PEEK基质,MWCNT和HAp分散良好。EDS分析表明,合成方法-2和-3表现出增强的PEEK和MWCNT分散性。TGA分析表明,合成方法-3具有最高的热稳定性。FTIR数据表明杂化纳米复合材料中存在各种官能团。XRD分析证实这些纳米复合材料本质上是晶体。TEM分析证实胺功能化的MWCNT和HAp纳米颗粒在PEEK基质中分散良好。总之,所采用的合成策略影响并产生了符合可持续发展目标-3的具有抗菌和抗癌活性的安全双功能纳米复合材料。