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A simple green method for the production of silver/gold bimetallic nanoparticles (Ag/Au BNPs) using a Heliotropium eichwaldi L. (HE) extract was designed in this study. The reduction of Ag/Au metals to stable Ag/Au BNPs within 24 h at pH 5 using 1 mL of HE at 40 °C signifies a greater rate of reaction compared with chemically elaborated synthesis. The confirmation of the synthesis and the examination of the size, shape, and elemental composition of these BNPs were performed using visible absorption spectroscopy, Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy dispersive X-ray spectroscopy (EDX). Stable, irregular-rod-shaped, and crystalline Ag/Au BNPs with a well-defined 6-nm diameter and a blue shift λmax of 532 nm were synthesized using the HE extract. Moreover, the anti-cholinesterase (anti-AChE) potential of the Ag/Au BNPs was tested as a treatment for Alzheimer’s disease (AD). An excellent anti-AChE activity (IC50, 71.2 ± 0.22 μg/mL) was observed for these biogenic-synthesized NPs. A statistical analysis revealed that Ag/Au BNPs inhibited AChE competitively, according to a Lineweaver–Burk plot, with Km increasing from 0.019 to 0.063 (288%–1185.7%) and Vmax remaining constant. The Ag/Au BNPs also caused an increase in KIapp, from 128 to 1184 (236%–828%), whereas they did not affect Vmaxiapp. The Km, KI, and Ki values were also calculated to be 0.0053 mmol/L, 595.25 µg, and 80 µg, respectively. Therefore, it is concluded that small-size, stable, and potent Ag/Au BNPs were synthesized successfully from HE extracts that exhibited anti-AChE activity, which renders them a significant remedy for AD.


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Acetylcholinesterase Activity in the Brain of Rats: Presence of an Inhibitor of Enzymatic Activity in Heliotropium eichwaldi L. Induced Silver/Gold Allied Bimetallic Nanoparticles

Show Author's information Naila Sher1Mushtaq Ahmed1( )Nadia Mushtaq2Rahmat Ali khan1
Department of Biotechnology, University of Science and Technology Bannu-KPK, Pakistan
Department of Botany, University of Science and Technology Bannu-KPK, Pakistan

Abstract

A simple green method for the production of silver/gold bimetallic nanoparticles (Ag/Au BNPs) using a Heliotropium eichwaldi L. (HE) extract was designed in this study. The reduction of Ag/Au metals to stable Ag/Au BNPs within 24 h at pH 5 using 1 mL of HE at 40 °C signifies a greater rate of reaction compared with chemically elaborated synthesis. The confirmation of the synthesis and the examination of the size, shape, and elemental composition of these BNPs were performed using visible absorption spectroscopy, Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy dispersive X-ray spectroscopy (EDX). Stable, irregular-rod-shaped, and crystalline Ag/Au BNPs with a well-defined 6-nm diameter and a blue shift λmax of 532 nm were synthesized using the HE extract. Moreover, the anti-cholinesterase (anti-AChE) potential of the Ag/Au BNPs was tested as a treatment for Alzheimer’s disease (AD). An excellent anti-AChE activity (IC50, 71.2 ± 0.22 μg/mL) was observed for these biogenic-synthesized NPs. A statistical analysis revealed that Ag/Au BNPs inhibited AChE competitively, according to a Lineweaver–Burk plot, with Km increasing from 0.019 to 0.063 (288%–1185.7%) and Vmax remaining constant. The Ag/Au BNPs also caused an increase in KIapp, from 128 to 1184 (236%–828%), whereas they did not affect Vmaxiapp. The Km, KI, and Ki values were also calculated to be 0.0053 mmol/L, 595.25 µg, and 80 µg, respectively. Therefore, it is concluded that small-size, stable, and potent Ag/Au BNPs were synthesized successfully from HE extracts that exhibited anti-AChE activity, which renders them a significant remedy for AD.

Keywords: Alzheimer’s disease (AD), Heliotropium eichwaldi L., silver/gold bimetallic nanoparticles (Ag/Au BNPs)

References(54)

[1]

M. Rafique, I. Sadaf, M.S. Rafique, et al. A review on green synthesis of silver nanoparticles and their applications. Artificial Cells,Nanomedicine,and Biotechnology, 2017, 45(7): 1272−1291. https://doi.org/10.1080/21691401.2016.1241792

[2]
M. Rai, M. Patel, R. Patel. Nanotechnology in Medicine: Toxicity and Safety. John Wiley & Sons, 2021.
DOI
[3]

A. Zaleska-Medynska, M. Marchelek, M. Diak, et al. Noble metal-based bimetallic nanoparticles: The effect of the structure on the optical, catalytic and photocatalytic properties. Advances in Colloid and Interface Science, 2016, 229: 80−107. https://doi.org/10.1016/j.cis.2015.12.008

[4]
G. Sharma, A. Kumar, M.Naushad,et al. Polyacrylamide@Zr(IV) vanadophosphate nanocomposite: Ion exchange properties, antibacterial activity, and photocatalytic behavior. Journal of Industrial and Engineering Chemistry, 2016, 33: 201–208.
DOI
[5]

N. Sher, M. Ahmed, N. Mushtaq. Synthesis, optimization, and characterization of silver/gold allied bimetallic from Hippeastrum hybridum (L.) and their ex vivo anti-acetylcholinesterase activity in rat brain. Applied Organometallic Chemistry, 2023, 37(5): e7082. https://doi.org/10.1002/aoc.7082

[6]

N. Sher, D.H.M. Alkhalifah, M. Ahmed, et al. Comparative study of antimicrobial activity of silver, gold, and silver/gold bimetallic nanoparticles synthesized by green approach. Molecules, 2022, 27(22): 7895. https://doi.org/10.3390/molecules27227895

[7]

C. Wang, Z.G. Xie, , K.E. de Krafft, et al. Doping metal–organic frameworks for water oxidation, carbon dioxide reduction, and organic photocatalysis. Journal of the American Chemical Society, 2011, 133(34): 13445−13454. https://doi.org/10.1021/ja203564w

[8]

D. Philip, C. Unni, S.A. Aromal, et al. Murraya koenigii leaf-assisted rapid green synthesis of silver and gold nanoparticles, Spectrochim. Spectrochimica Acta Part A:Molecular and Biomolecular Spectroscopy, 2011, 78(2): 899−904. https://doi.org/10.1016/j.saa.2010.12.060

[9]

J. Jacob, T. Mukherjee, S. Kapoor. A simple approach for facile synthesis of Ag, anisotropic Au and bimetallic (Ag/Au) nanoparticles using cruciferous vegetable extracts. Materials Science and Engineering:C, 2012, 32(7): 1827−1834. https://doi.org/10.1016/j.msec.2012.04.072

[10]

M. Meena Kumari, J. Jacob, D. Philip. Green synthesis and applications of Au–Ag bimetallic nanoparticles. Spectrochimica Acta Part A:Molecular and Biomolecular Spectroscopy, 2015, 137: 185−192. https://doi.org/10.1016/j.saa.2014.08.079

[11]

K. Gopinath, S. Kumaraguru, K. Bhakyaraj, et al. Green synthesis of silver, gold and silver/gold bimetallic nanoparticles using the Gloriosa superba leaf extract and their antibacterial and antibiofilm activities. Microbial Pathogenesis, 2016, 101: 1−11. https://doi.org/10.1016/j.micpath.2016.10.011

[12]

S. Amor, F. Puentes, D. Baker, et al. Inflammation in neurodegenerative diseases. Immunology, 2010, 129(2): 154−169. https://doi.org/10.1111/j.1365-2567.2009.03225.x

[13]

H. Chen, J.C. Kwong, R. Copes, et al. Living near major roads and the incidence of dementia, Parkinson’s disease, and multiple sclerosis: A population-based cohort study. The Lancet, 2017, 389(10070): 718−726. https://doi.org/10.1016/S0140-6736(16)32399-6

[14]

A. Arsalan, O. Khurram, S. Maimoona, et al. Dementia in pakistan: national guidelines for clinicians. Pakistan Journal of Neurological Sciences, 2013, 8(3): 7.

[15]

C.C. Tan, J.T. Yu, M.S. Tan, et al. Autophagy in aging and neurodegenerative diseases: Implications for pathogenesis and therapy. Neurobiology of Aging, 2014, 35(5): 941−957. https://doi.org/10.1016/j.neurobiolaging.2013.11.019

[16]

M. Takalo, A. Salminen, H. Soininen, et al. Protein aggregation and degradation mechanisms in neurodegenerative diseases. American Journal of Neurodegenerative Disease, 2013, 2(1): 1−14.

[17]

R. Schliebs, T. Arendt. The cholinergic system in aging and neuronal degeneration. Behavioural Brain Research, 2011, 221(2): 555−563. https://doi.org/10.1016/j.bbr.2010.11.058

[18]

W.W. Chen, X. Zhang, W.J. Huang. Role of neuroinflammation in neurodegenerative diseases (review). Molecular Medicine Reports, 2016, 13(4): 3391−3396. https://doi.org/10.3892/mmr.2016.4948

[19]

D.A. Butterfield, A.M. Swomley, R. Sultana. Amyloidβ-peptide (1–42)-induced oxidative stress in alzheimer disease: Importance in disease pathogenesis and progression. Antioxidants &Redox Signaling, 2013, 19(8): 823−835. https://doi.org/10.1089/ars.2012.5027

[20]

M. Ahmed, S.Z. Khan, N. Sher, et al. Kinetic and toxicological effects of synthesized palladium(II) complex on snake venom (Bungarus sindanus) acetylcholinesterase. Journal of Venomous Animals and Toxins Including Tropical Diseases, 2021, 27: e20200047. https://doi.org/10.1590/1678-9199-JVATITD-2020-0047

[21]

I. Solanki, P. Parihar, M.L. Mansuri, et al. Flavonoid-based therapies in the early management of neurodegenerative diseases. Advances in Nutrition, 2015, 6(1): 64−72. https://doi.org/10.3945/an.114.007500

[22]

M. Ahmed, N. Mushtaq, N. Sher, et al. New synthesized tri-peptide as inhibitor of krait (Bungarus sindanus) venom acetylcholinesterase. International Journal of Peptide Research and Therapeutics, 2022, 28: 154. https://doi.org/10.1007/s10989-022-10462-6

[23]

P.K. Mukherjee, V. Kumar, M. Mal, et al. Acetylcholinesterase inhibitors from plants. Phytomedicine, 2007, 14(4): 289−300. https://doi.org/10.1016/j.phymed.2007.02.002

[24]

M. Öztürk. Anticholinesterase and antioxidant activities of Savoury (Satureja thymbra L.) with identified major terpenes of the essential oil. Food Chemistry, 2012, 134(1): 48−54. https://doi.org/10.1016/j.foodchem.2012.02.054

[25]

S. Ijaz, A. Perveen, N. Ghaffar. Preliminary phytochemical screening of seeds of Phytolacca latbenia (moq.) walte. A wild medicinal plant of tropical and sub-tropical region of Pakistan. Organic &Medicinal Chemistry International Journal, 2019, 9(1): 555754. https://doi.org/10.19080/omcij.2019.09.555754

[26]
M. Alamzeb, M.R. Khan, S. Ali, et al. Antimicrobial properties of extracts and compounds isolated from Berberis jaeschkeana. Bangladesh Journal of Pharmacology, 2013, 8(2): 107–109.
DOI
[27]

K.S. Prasad, N. Savithramma. Biosynthesis and validation of SNPs from Nymphaea caerulea savigny. American Journal of Advanced Drug Delivery, 2015, 3: 3149−159.

[28]

A. Johri, M.F. Beal. Mitochondrial dysfunction in neurodegenerative diseases. Journal of Pharmacology and Experimental Therapeutics, 2012, 342(3): 619−630. https://doi.org/10.1124/jpet.112.192138

[29]

O.H. Lowry, N.J. Rosebrough, A.L. Farr, et al. Protein measurement with the folin phenol reagent. Journal of Biological Chemistry, 1951, 193(1): 265−275. https://doi.org/10.1016/s0021-9258(19)52451-6

[30]

M. Ahmed, A. Ahmad, N. Mushtaq, et al. Protective role of antibiotics (anisomycin and puromycin) against snake venom acetylcholinesterase (AChE). International Journal of Peptide Research and Therapeutics, 2022, 29: 13. https://doi.org/10.1007/s10989-022-10482-2

[31]

H. Lineweaver, D. Burk. The determination of enzyme dissociation constants. Journal of the American Chemical Society, 1934, 56(3): 658−666. https://doi.org/10.1021/ja01318a036

[32]
M. Dixon, E.C. Webb. Enzymes. Longmans, 1964.
[33]

A. Cornish-Bowden, M.L. Cárdenas. Hexokinase and 'glucokinase' in liver metabolism. Trends in Biochemical Science, 1991, 16(8): 281−282. https://doi.org/10.1016/0968-0004(91)90115-C

[34]

A. Ahmed, A. Rauf, H.A. Hemeg, et al. Green synthesis of gold and silver nanoparticles using opuntia dillenii aqueous extracts: Characterization and their antimicrobial assessment. Journal of Nanomaterials, 2022, 2022: 4804116. https://doi.org/10.1155/2022/4804116

[35]

M. Kamali, S. Khosroyar, M.R. Jalilvand. Evaluation of phenolic, flavonoids, anthocyanin contents and antioxidant capacities of different extracts of aerial parts of Dracocephalum kotschyi. Journal of North Khorasan University of Medical Sciences, 2014, 6(3): 627−634. https://doi.org/10.29252/jnkums.6.3.627

[36]

B. Ajitha, Y. Ashok Kumar Reddy, P. Sreedhara Reddy. Enhanced antimicrobial activity of silver nanoparticles with controlled particle size by pH variation. Powder Technology, 2015, 269: 110−117. https://doi.org/10.1016/j.powtec.2014.08.049

[37]

N. Islam, K. Miyazaki. Nanotechnology innovation system: Understanding hidden dynamics of nanoscience fusion trajectories. Technological Forecasting and Social Change, 2009, 76(1): 128−140. https://doi.org/10.1016/j.techfore.2008.03.021

[38]

M. Azizi, S. Sedaghat, K. Tahvildari, et al. Synthesis of silver nanoparticles using Peganum harmala extract as a green route. Green Chemistry Letters and Reviews, 2017, 10(4): 420−427. https://doi.org/10.1080/17518253.2017.1395081

[39]

N. Sher, M. Ahmed, N. Mushtaq, et al. Calligonum polygonoides reduced nanosilver: A new generation of nanoproduct for medical applications. European Journal of Integrative Medicine, 2020, 33: 101042. https://doi.org/10.1016/j.eujim.2019.101042

[40]

R.K. Das, N. Gogoi, U. Bora. Green synthesis of gold nanoparticles using Nyctanthes arbortristis flower extract. Bioprocess and Biosystems Engineering, 2011, 34: 615−619. https://doi.org/10.1007/s00449-010-0510-y

[41]
S. Ghosh, S. Patil, N.B. Chopade, et al. Gnidia glauca leaf and stem extract mediated synthesis of gold nanocatalysts with free radical scavenging potential. Journal of Nanomedicine & Nanotechnology, 2016, 7: 358.
DOI
[42]

S.I. Thakore, P.S. Nagar, R.N. Jadeja, et al. Sapota fruit latex mediated synthesis of Ag, Cu mono and bimetallic nanoparticles and their in vitro toxicity studies. Arabian Journal of Chemistry, 2019, 12(5): 694−700. https://doi.org/10.1016/j.arabjc.2014.12.042

[43]

N. Sher, M. Ahmed, N. Mushtaq, et al. Enhancing antioxidant, antidiabetic, and antialzheimer performance of Hippeastrum hybridum (L.) using silver nanoparticles. Applied Organometallic Chemistry, 2022, 36(7): e6724. https://doi.org/10.1002/aoc.6724

[44]

B.H. Xia, F. He, L.D. Li. Preparation of bimetallic nanoparticles using a facile green synthesis method and their application. Langmuir, 2013, 29(15): 4901−4907. https://doi.org/10.1021/la400355u

[45]

W.T. Yang, W.S. Guo, W.J. Le, et al. Albumin-bioinspired Gd: CuS nanotheranostic agent for in vivo photoacoustic/magnetic resonance imaging-guided tumor-targeted photothermal therapy. ACS Nano, 2016, 10(11): 10245−10257. https://doi.org/10.1021/acsnano.6b05760

[46]

S.Y. Fu, H.L. Chen, W.T. Yang, et al. ROS-targeted depression therapy via BSA-incubated ceria nanoclusters. Nano Letters, 2022, 22(11): 4519−4527. https://doi.org/10.1021/acs.nanolett.2c01334

[47]

V. Ganesh Kumar, S. Dinesh Gokavarapu, A. Rajeswari, et al. Facile green synthesis of gold nanoparticles using leaf extract of antidiabetic potent Cassia auriculata. Colloids and Surfaces B:Biointerfaces, 2011, 87(1): 159−163. https://doi.org/10.1016/j.colsurfb.2011.05.016

[48]

E.E. Elemike, D.C. Onwudiwe, N. Nundkumar, et al. Green synthesis of Ag, Au and Ag-Au bimetallic nanoparticles using Stigmaphyllon ovatum leaf extract and their in vitro anticancer potential. Materials Letters, 2019, 243: 148−152. https://doi.org/10.1016/j.matlet.2019.02.049

[49]
M.E. Pereira, A.I.H. Adams, N.S. Silva. 2, 5-Hexanedione inhibits rat brain acetylcholinesterase activity in vitro. Toxicology Letters, 2004, 146(3): 269–274.
DOI
[50]

C.Y. Shin, H.S. Kim, K.H. Cha, et al. The effects of donepezil, an acetylcholinesterase inhibitor, on impaired learning and memory in rodents. Biomolecules &Therapeutics, 2018, 26(3): 274−281. https://doi.org/10.4062/biomolther.2017.189

[51]

N. Dorosti, F. Jamshidi. Plant-mediated gold nanoparticles by Dracocephalum kotschyi as anticholinesterase agent: Synthesis, characterization, and evaluation of anticancer and antibacterial activity. Journal of Applied Biomedicine, 2016, 14(3): 235−245. https://doi.org/10.1016/j.jab.2016.03.001

[52]

Z.Y. Wang, J. Zhao, F.M. Li, et al. Adsorption and inhibition of acetylcholinesterase by different nanoparticles. Chemosphere, 2009, 77(1): 67−73. https://doi.org/10.1016/j.chemosphere.2009.05.015

[53]

G. Rajakumar, T. Gomathi, M. Thiruvengadam, et al. Evaluation of anti-cholinesterase, antibacterial and cytotoxic activities of green synthesized silver nanoparticles using from Millettia pinnata flower extract. Microbial Pathogenesis, 2017, 103: 123−128. https://doi.org/10.1016/j.micpath.2016.12.019

[54]

N. Sher, M. Ahmed, N. Mushtaq. Biogenic synthesis of gold nanoparticles using Heliotropium eichwaldi L and neuroprotective potential via anticholinesterase inhibition in rat brain. Applied Organometallic Chemistry, 2023, 37(4): e7000. https://doi.org/10.1002/aoc.7000

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Publication history

Received: 28 May 2023
Revised: 15 July 2023
Accepted: 29 July 2023
Published: 12 October 2023
Issue date: September 2023

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