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Synthesis, characterization & evaluation of venom neutralization potential of silver nanoparticles mediated Alstonia scholaris Linn bark extract

OBJECTIVE: The venom neutralization potential of silver nanoparticle(AgNP-AS) mediated bark extract of Alstonia scholaris Linn R.Br was investigated in the study. METHODS & MATERIALS: AgNP-AS was synthesized with respect to optimal temperature, pH of extract. UV–vis, FT-IR, XRD, TEM, SEM studies...

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Autores principales: Ghosh, Rituparna, Sarkhel, Sumana, Saha, Kanchan, Parua, Poulami, Chatterjee, Upasana, Mana, Koushik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8091482/
https://www.ncbi.nlm.nih.gov/pubmed/33996502
http://dx.doi.org/10.1016/j.toxrep.2021.04.006
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author Ghosh, Rituparna
Sarkhel, Sumana
Saha, Kanchan
Parua, Poulami
Chatterjee, Upasana
Mana, Koushik
author_facet Ghosh, Rituparna
Sarkhel, Sumana
Saha, Kanchan
Parua, Poulami
Chatterjee, Upasana
Mana, Koushik
author_sort Ghosh, Rituparna
collection PubMed
description OBJECTIVE: The venom neutralization potential of silver nanoparticle(AgNP-AS) mediated bark extract of Alstonia scholaris Linn R.Br was investigated in the study. METHODS & MATERIALS: AgNP-AS was synthesized with respect to optimal temperature, pH of extract. UV–vis, FT-IR, XRD, TEM, SEM studies were used to characterize silver nanoparticles of Alstonia scholaris Linn(AgNP-AS). The potential of AgNP-AS in neutralization of venom lethality, rise in myotoxicity markers(LDH) and proinflammatory cytokines(IL6, TNFα) were evaluated in animal models. RESULTS: AgNP-AS was synthesized optimally with AgNO(3) (2 mM); extract concentration, 0.2 gm/l (1% w/v); extract (pH 9) and optimal temperature (40 °C). The colour change and synthesis of AgNP-AS was validated by UV–vis analysis at 432 nm. Transmission electron microscopy of AgNP-AS showed that the particle size for AgNP-AS was 14 nm-20 nm. FT-IR revealed peaks at 3445 cm(−1), 1646 cm(−1), 1346 cm(−1) and 1108 cm(−1). From the dynamic light scattering studies the hydrodynamic diameter (115.87 nm) and zeta potential(-29.8 mV) were estimated. The EDAX exhibited a peak for silver validating that the synthesized silver was pure. The biosynthesized (AgNP-AS) could significantly neutralize Viper russelli venom(VRV) induced rise in serum lactate dehydrogenase(LDH) and proinflammatory cytokines(IL6, TNFα) in animal models. CONCLUSION: The culmination of nanotechnology with herbal medicine might endow with a really constructive tool in coming up with future drugs with fewer toxicity.
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spelling pubmed-80914822021-05-13 Synthesis, characterization & evaluation of venom neutralization potential of silver nanoparticles mediated Alstonia scholaris Linn bark extract Ghosh, Rituparna Sarkhel, Sumana Saha, Kanchan Parua, Poulami Chatterjee, Upasana Mana, Koushik Toxicol Rep Regular Article OBJECTIVE: The venom neutralization potential of silver nanoparticle(AgNP-AS) mediated bark extract of Alstonia scholaris Linn R.Br was investigated in the study. METHODS & MATERIALS: AgNP-AS was synthesized with respect to optimal temperature, pH of extract. UV–vis, FT-IR, XRD, TEM, SEM studies were used to characterize silver nanoparticles of Alstonia scholaris Linn(AgNP-AS). The potential of AgNP-AS in neutralization of venom lethality, rise in myotoxicity markers(LDH) and proinflammatory cytokines(IL6, TNFα) were evaluated in animal models. RESULTS: AgNP-AS was synthesized optimally with AgNO(3) (2 mM); extract concentration, 0.2 gm/l (1% w/v); extract (pH 9) and optimal temperature (40 °C). The colour change and synthesis of AgNP-AS was validated by UV–vis analysis at 432 nm. Transmission electron microscopy of AgNP-AS showed that the particle size for AgNP-AS was 14 nm-20 nm. FT-IR revealed peaks at 3445 cm(−1), 1646 cm(−1), 1346 cm(−1) and 1108 cm(−1). From the dynamic light scattering studies the hydrodynamic diameter (115.87 nm) and zeta potential(-29.8 mV) were estimated. The EDAX exhibited a peak for silver validating that the synthesized silver was pure. The biosynthesized (AgNP-AS) could significantly neutralize Viper russelli venom(VRV) induced rise in serum lactate dehydrogenase(LDH) and proinflammatory cytokines(IL6, TNFα) in animal models. CONCLUSION: The culmination of nanotechnology with herbal medicine might endow with a really constructive tool in coming up with future drugs with fewer toxicity. Elsevier 2021-04-19 /pmc/articles/PMC8091482/ /pubmed/33996502 http://dx.doi.org/10.1016/j.toxrep.2021.04.006 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Ghosh, Rituparna
Sarkhel, Sumana
Saha, Kanchan
Parua, Poulami
Chatterjee, Upasana
Mana, Koushik
Synthesis, characterization & evaluation of venom neutralization potential of silver nanoparticles mediated Alstonia scholaris Linn bark extract
title Synthesis, characterization & evaluation of venom neutralization potential of silver nanoparticles mediated Alstonia scholaris Linn bark extract
title_full Synthesis, characterization & evaluation of venom neutralization potential of silver nanoparticles mediated Alstonia scholaris Linn bark extract
title_fullStr Synthesis, characterization & evaluation of venom neutralization potential of silver nanoparticles mediated Alstonia scholaris Linn bark extract
title_full_unstemmed Synthesis, characterization & evaluation of venom neutralization potential of silver nanoparticles mediated Alstonia scholaris Linn bark extract
title_short Synthesis, characterization & evaluation of venom neutralization potential of silver nanoparticles mediated Alstonia scholaris Linn bark extract
title_sort synthesis, characterization & evaluation of venom neutralization potential of silver nanoparticles mediated alstonia scholaris linn bark extract
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8091482/
https://www.ncbi.nlm.nih.gov/pubmed/33996502
http://dx.doi.org/10.1016/j.toxrep.2021.04.006
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