Biogenic synthesis of AgNPs via polyherbal formulation: Mechanistic neutralization and toxicological impact on acetylcholinesterase from Bungarus sindanus venom

乙酰胆碱酯酶 化学 银纳米粒子 毒液 阿切 核化学 傅里叶变换红外光谱 酶动力学 纳米颗粒 生物化学 活动站点 纳米技术 化学工程 材料科学 工程类
作者
Noshaba Afshin,Nadia Mushtaq,Mushtaq Ahmed,Naila Sher,Sadeq K. Alhag,Fatma Mohamed Ameen Khalil,Laila A. Al‐Shuraym,Hajra Hameed,Farhad Badshah,Riaz Hussain
出处
期刊:Microscopy Research and Technique [Wiley]
标识
DOI:10.1002/jemt.24701
摘要

Abstract This study aims to examine the biogenic production, characterization, and anti‐acetylcholinesterase (AAChE) properties of polyherbal formulation PHF‐extract‐synthesized silver nanoparticles (PHF‐AgNPs). The Elapidae snake Bungarus sindanus has extremely dangerous venom for humans and contains a high amount of AChE (acetylcholinesterase). Inhibiting AChE leads to acetylcholine buildup, affecting neurotransmission. The study tested silver nanoparticles as AChE inhibitors using kinetics. Their production was confirmed through ultraviolet (UV) spectrometry at 425 nm (SPR peak of 1.94), and stabilizing functional groups were identified via Fourier transform infrared spectroscopy (FT‐IR). The average length of 20 nm was confirmed by analyzing the scanning electron microscopy (SEM) data. Energy‐dispersive X‐ray spectroscopy (EDX) identified silver as the primary component of PHF‐AgNPs (26%). Statistical analysis showed that the activity of AChE in krait venom decreased by up to 45% and 37% at a given dose of ACh (0.5 mM) by PHF and AgNPs, respectively. Utilizing the Lineweaver‐Burk plot for kinetic analysis, a competitive type of inhibition is found. Research Highlights Successfully synthesized PHF‐extract‐induced silver nanoparticles (PHF‐AgNPs) demonstrated through UV spectrometry and characterized as crystalline with an average size of 45 nm by X‐ray diffraction. PHF‐AgNPs effectively inhibited acetylcholinesterase (AChE), an enzyme critical in neurotransmission, reducing its activity in krait venom by up to 45% at certain concentrations. Kinetic analysis revealed that the inhibition mechanism of AChE by PHF‐AgNPs is competitive, offering potential for therapeutic applications in neurologically related conditions.
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