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一锅法合成、AuNPs 及 Au-阿莫西林缀合物的生物功效,该缀合物功能化于 的粗黄酮提取物

One Pot Synthesis, Biological Efficacy of AuNPs and Au-Amoxicillin Conjugates Functionalized with Crude Flavonoids Extract of .

机构信息

Chemistry Department, Islamia College University, Peshawar 25000, Pakistan.

Department of Chemistry, Government Degree College Hayatabad, Peshawar 25000, Pakistan.

出版信息

Molecules. 2023 Apr 9;28(8):3320. doi: 10.3390/molecules28083320.

Abstract

Amoxicillin is the most widely used antibiotic in human medicine for treating bacterial infections. However, in the present research, extract mediated gold nanoparticles (AuNPs) were conjugated with amoxicillin (Au-amoxi) to study their efficacy against the inflammation and pain caused by bacterial infections. The formation of AuNPs and Au-amoxi conjugates were confirmed by UV-visible surface plasmon peaks at 535 nm and 545 nm, respectively. The scanning electron microscopy (SEM), zeta potential (ZP), and X-ray diffraction (XRD) studies reveal that the size of AuNPs and Au-amoxi are found to be 42 nm and 45 nm, respectively. Fourier-transform infrared spectroscopy (FT-IR) absorption bands at 3200 cm, 1000 cm, 1500 cm, and 1650 cm reveal the possible involvement of different moieties for the formation of AuNPs and Au-amoxi. The pH studies show that AuNPs and Au-amoxi conjugates are stable at lower pH. The carrageenan-induced paw edema test, writhing test, and hot plate test were used to conduct in vivo anti-inflammatory and antinociceptive studies, respectively. According to in vivo anti-inflammatory activity, Au-amoxi compounds have higher efficiency (70%) after 3 h at a dose of 10 mg/kg body weight as compared to standard diclofenac (60%) at 20 mg/kg, amoxicillin (30%) at 100 mg/kg, and extract (35%) at 100 mg/kg. Similarly, for antinociceptive activities, writhing test results show that Au-amoxi conjugates produced the same number of writhes (15) but at a lower dose (10 mg/kg) compared to standard diclofenac (20 mg/kg). The hot plate test results demonstrate that the Au-amoxi has a better latency time of 25 s at 10 mg/kg dose when compared to standard Tramadol of 22 s at 30 mg/ kg, amoxicillin of 14 s at 100 mg/kg, and extract of 14 s at 100 mg/kg after placing the mice on the hot plate for 30, 60, and 90 min with a significance of ( ≤ 0.001). These findings show that the conjugation of AuNPs with amoxicillin to form Au-amoxi can boost its anti-inflammatory and antinociceptive potential caused by bacterial infections.

摘要

阿莫西林是人类医学中治疗细菌感染最广泛使用的抗生素。然而,在本研究中, 提取物介导的金纳米粒子(AuNPs)与阿莫西林(Au-amoxi)缀合,以研究它们对细菌感染引起的炎症和疼痛的疗效。通过在 535nm 和 545nm 处分别出现紫外可见表面等离子体峰,证实了 AuNPs 和 Au-amoxi 缀合物的形成。扫描电子显微镜(SEM)、Zeta 电位(ZP)和 X 射线衍射(XRD)研究表明,AuNPs 和 Au-amoxi 的尺寸分别为 42nm 和 45nm。傅里叶变换红外光谱(FT-IR)在 3200cm、1000cm、1500cm 和 1650cm 处的吸收带表明,AuNPs 和 Au-amoxi 的形成可能涉及不同的基团。pH 研究表明,AuNPs 和 Au-amoxi 缀合物在较低 pH 值下稳定。角叉菜胶诱导的足肿胀试验、扭体试验和热板试验分别用于进行体内抗炎和镇痛研究。根据体内抗炎活性,在 10mg/kg 体重的剂量下,Au-amoxi 化合物在 3 小时后效率更高(70%),而标准双氯芬酸(60%)在 20mg/kg,阿莫西林(30%)在 100mg/kg, 提取物(35%)在 100mg/kg。同样,在镇痛活性方面,扭体试验结果表明,与标准双氯芬酸钠(20mg/kg)相比,Au-amoxi 缀合物在较低剂量(10mg/kg)下产生相同数量的扭体(15 次)。热板试验结果表明,与标准曲马多(30mg/kg)的 22s、阿莫西林(100mg/kg)的 14s 和 提取物(100mg/kg)的 14s 相比,Au-amoxi 在 10mg/kg 剂量下具有更好的潜伏期 25s,在将小鼠放置在热板上 30、60 和 90 分钟后,差异有统计学意义( ≤ 0.001)。这些发现表明,将 AuNPs 与阿莫西林缀合形成 Au-amoxi 可以增强其对细菌感染引起的抗炎和镇痛潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2ab/10140876/d9719a115a4f/molecules-28-03320-g001a.jpg

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