阴蒂花提取物辅助合成Pluronic F127和l -组氨酸包被SrO2作为具有抗癌、抗氧化和抗菌活性的多模态纳米复合材料。

IF 3.6 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Bioprocess and Biosystems Engineering Pub Date : 2025-11-01 Epub Date: 2025-07-31 DOI:10.1007/s00449-025-03213-6
Aakash Sharma, Suhas Ballal, Deeplata Sharma, Jaivik Pathak, AbdulAziz A AlGhamdi, Srinivas Tadepalli, Indumathi Thangavelu
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引用次数: 0

摘要

肝细胞癌(HepG2)是一种高度侵袭性的肝癌,预后差,治疗选择有限,死亡率高,使其成为严重的全球健康问题,迫切需要开发更有效和更安全的治疗方法。本研究以阴蒂花提取物为原料,利用Pluronic F127 (PF127)和l -组氨酸(LH)对其表面进行修饰,制备SrO2-PF127-LH纳米复合材料,研究其对HepG2细胞系的潜在抗癌作用。利用各种分析技术对纳米复合材料进行表征,并对其对HePG2肝癌细胞的抗癌活性、抗氧化性能和对上述细菌的抗菌活性进行了评价。XRD分析表明,SrO2具有四方相的结晶性质。FTIR光谱证实SrO2-PF127-LH纳米复合材料在573 cm-1处存在Sr-O拉伸带。紫外可见分析表明,SrO2和SrO2- pf127 - lh纳米复合材料的能带能分别为4.13 eV和4.07 eV。利用PL分析研究了SrO2-PF127-LH纳米复合材料的表面缺陷,包括氧空位。与单独的SrO2纳米颗粒相比,SrO2- pf127 - lh纳米复合材料具有优异的抗菌和抗氧化活性。此外,SrO2-PF127-LH纳米复合材料对肝癌(HePG2)细胞株具有增强的抗癌活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clitoria ternatea flower extract assisted synthesis of Pluronic F127 and L-histidine coated SrO2 as a multimodality nanocomposite for anti-cancer, anti-oxidant, and antimicrobial activities.

Hepatocellular carcinoma (HepG2) is a highly aggressive liver cancer with poor prognosis, limited treatment options, and high mortality rates, making it a serious global health concern that demands urgent development of more effective and safer therapeutic approaches. In this context, the present study focuses on the green synthesis of SrO2 nanoparticles using Clitoria ternatea flower extract, followed by surface modification with Pluronic F127 (PF127) and L-histidine (LH), to fabricate SrO2-PF127-LH nanocomposites aimed at evaluating their potential anticancer efficacy against the HepG2 cell line. Various analytical techniques were used to characterize the nanocomposite, and then their anticancer activity against HePG2 liver cancer cells, antioxidant properties, and antimicrobial activity against the bacteria mentioned above were evaluated. XRD revealed the crystalline nature of SrO2 with a tetragonal phase. FTIR spectrum confirmed the Sr-O stretching band at 573 cm-1 for SrO2-PF127-LH nanocomposite. UV-visible analysis revealed the band gap energies of 4.13 eV for SrO2 and 4.07 eV for SrO2-PF127-LH nanocomposite. The surface defects including oxygen vacancies of SrO2-PF127-LH nanocomposite were investigated using PL analysis. The SrO2-PF127-LH nanocomposite exhibited excellent antibacterial and antioxidant activities when compared to SrO2 nanoparticles alone. In addition, the SrO2-PF127-LH nanocomposite had enhanced anticancer activity against liver cancer (HePG2) cell lines.

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来源期刊
Bioprocess and Biosystems Engineering
Bioprocess and Biosystems Engineering 工程技术-工程:化工
CiteScore
7.90
自引率
2.60%
发文量
147
审稿时长
2.6 months
期刊介绍: Bioprocess and Biosystems Engineering provides an international peer-reviewed forum to facilitate the discussion between engineering and biological science to find efficient solutions in the development and improvement of bioprocesses. The aim of the journal is to focus more attention on the multidisciplinary approaches for integrative bioprocess design. Of special interest are the rational manipulation of biosystems through metabolic engineering techniques to provide new biocatalysts as well as the model based design of bioprocesses (up-stream processing, bioreactor operation and downstream processing) that will lead to new and sustainable production processes. Contributions are targeted at new approaches for rational and evolutive design of cellular systems by taking into account the environment and constraints of technical production processes, integration of recombinant technology and process design, as well as new hybrid intersections such as bioinformatics and process systems engineering. Manuscripts concerning the design, simulation, experimental validation, control, and economic as well as ecological evaluation of novel processes using biosystems or parts thereof (e.g., enzymes, microorganisms, mammalian cells, plant cells, or tissue), their related products, or technical devices are also encouraged. The Editors will consider papers for publication based on novelty, their impact on biotechnological production and their contribution to the advancement of bioprocess and biosystems engineering science. Submission of papers dealing with routine aspects of bioprocess engineering (e.g., routine application of established methodologies, and description of established equipment) are discouraged.
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