Khadivi-Derakhshan Saeedeh, Pirouzmand Mahtab, Soleymani Jafar, Esrafili Mehdi D
Department of Inorganic Chemistry, Faculty of Chemistry, University of Tabriz Tabriz 5166616471 Iran
Pharmaceutical Analysis Research Center and Faculty of Pharmacy, Tabriz University of Medical Sciences Tabriz Iran.
RSC Adv. 2025 Jul 4;15(27):22006-22017. doi: 10.1039/d5ra02118a. eCollection 2025 Jun 23.
The scientific community is very interested in investigating antioxidant activity using various assays to treat oxidative stress and reduce the harmful effects of free radicals. Cysteine, a sulfur-containing compound can treat oxidative stress. The primary objective of this study was to create a novel ligand through the combination of l-cysteine with malic acid and its metal complexes with copper and manganese. The following discussion focuses on how the complexes mimic natural antioxidant enzymes and explains how they could be used to remove reactive oxygen species. Various methods were used to verify the synthesis, including FT-IR, UV-vis, TGA, CHNS, EDX, SEM, mass, and fluorescence. These techniques indicated structural changes upon complexation and integration with β-CD. Spectrophotometric tests were used to evaluate the compounds' peroxidase-, catalase-, and superoxide dismutase-like activities under different conditions. Cytotoxicity was evaluated using HFF-2 cells and the MTT test. The amounts of carbon, hydrogen, nitrogen, and sulfur were 39.48, 4.7, 6.58, and 15.23, and the ligand formula is CHNSO. Changes in infrared spectral signals upon metal interaction, particularly in the carboxylate region, indicate significant metal-ligand bonding. The results showed that the β-CD-modified complexes, especially Cu-complex/β-CD and Mn-complex/β-CD, had better antioxidant activity (91% and 78%, respectively). They were better at scavenging O˙ radicals and breaking down HO into safe byproducts. Additionally, Mn-complex/β-CD was less cytotoxic. In conclusion, the produced complexes are promising antioxidants and potential treatments for diseases linked to oxidative stress, especially the β-CD derivatives.
科学界对使用各种测定方法研究抗氧化活性以治疗氧化应激和减少自由基的有害影响非常感兴趣。半胱氨酸,一种含硫化合物,可以治疗氧化应激。本研究的主要目的是通过将L-半胱氨酸与苹果酸及其与铜和锰的金属配合物相结合来制备一种新型配体。以下讨论重点关注这些配合物如何模拟天然抗氧化酶,并解释它们如何用于去除活性氧。使用了各种方法来验证合成,包括傅里叶变换红外光谱(FT-IR)、紫外可见光谱(UV-vis)、热重分析(TGA)、元素分析(CHNS)、能量色散X射线光谱(EDX)、扫描电子显微镜(SEM)、质谱和荧光分析。这些技术表明了络合以及与β-环糊精(β-CD)整合后的结构变化。使用分光光度法测试来评估化合物在不同条件下的过氧化物酶、过氧化氢酶和超氧化物歧化酶样活性。使用人包皮成纤维细胞(HFF-2)和MTT试验评估细胞毒性。碳、氢、氮和硫的含量分别为39.48、4.7、6.58和15.23,配体化学式为CHNSO。金属相互作用时红外光谱信号的变化,特别是在羧酸盐区域,表明存在显著的金属-配体键合。结果表明,β-CD修饰的配合物,特别是铜配合物/β-CD和锰配合物/β-CD,具有更好的抗氧化活性(分别为91%和78%)。它们在清除氧自由基和将过氧化氢分解为安全副产物方面表现更好。此外,锰配合物/β-CD的细胞毒性较小。总之,所制备的配合物是有前景的抗氧化剂,也是与氧化应激相关疾病的潜在治疗药物,尤其是β-CD衍生物。