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Anti-amyloidogenic property of gold nanoparticle decorated quercetin polymer nanorods in pH and temperature induced aggregation of lysozyme

Quercetin is an abundant plant polyphenol effective against several diseases due to its antioxidant and anti-inflammatory activity. Herein, we report novel polymeric quercetin nanorods and the former decorated with gold nanoparticles for the first time. The prepared conjugates quercetin-polyvinylpyr...

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Autores principales: Rananaware, Pranita, Pandit, Parimal, Naik, Seekha, Mishra, Monalisa, Keri, Rangappa S., Brahmkhatri, Varsha P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9389553/
https://www.ncbi.nlm.nih.gov/pubmed/36090438
http://dx.doi.org/10.1039/d2ra03121c
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author Rananaware, Pranita
Pandit, Parimal
Naik, Seekha
Mishra, Monalisa
Keri, Rangappa S.
Brahmkhatri, Varsha P.
author_facet Rananaware, Pranita
Pandit, Parimal
Naik, Seekha
Mishra, Monalisa
Keri, Rangappa S.
Brahmkhatri, Varsha P.
author_sort Rananaware, Pranita
collection PubMed
description Quercetin is an abundant plant polyphenol effective against several diseases due to its antioxidant and anti-inflammatory activity. Herein, we report novel polymeric quercetin nanorods and the former decorated with gold nanoparticles for the first time. The prepared conjugates quercetin-polyvinylpyrrolidone (Q-PVP) and quercetin-polyvinylpyrrolidone-gold nanoparticles (Q-PVP-Au) were characterized by UV-visible spectroscopy, Fourier transform infrared, dynamic light scattering, and zeta potential measurements. The surface morphology of conjugates was analyzed by field emission scanning electron microscopy. These conjugates exhibit harmonized rod-like morphology with a narrow size distribution. Furthermore, the quercetin conjugates with nanorod morphology exhibited enhanced and prolonged drug release over a long period. The synthesized conjugates were investigated for lysozyme aggregation kinetics. ThT binding assay, fibril size measurement, and electron microscopy results revealed that conjugates could suppress fibrillogenesis in lysozyme. The highest amyloid aggregation inhibition activity (IC(50)) was obtained against Q-PVP and Q-PVP-Au at 32 μg mL(−1) and 30 μg mL(−1) respectively. The amyloid aggregate disintegration activity (DC(50)) obtained against Q-PVP and Q-PVP-Au was 27 μg mL(−1) and 29 μg mL(−1) respectively. The present quercetin conjugates exhibit enhanced bioavailability and stability. They were potent inhibitors of lysozyme aggregation that may find applications as a therapeutic agent in neurological diseases like Alzheimer's and Parkinson's.
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spelling pubmed-93895532022-09-08 Anti-amyloidogenic property of gold nanoparticle decorated quercetin polymer nanorods in pH and temperature induced aggregation of lysozyme Rananaware, Pranita Pandit, Parimal Naik, Seekha Mishra, Monalisa Keri, Rangappa S. Brahmkhatri, Varsha P. RSC Adv Chemistry Quercetin is an abundant plant polyphenol effective against several diseases due to its antioxidant and anti-inflammatory activity. Herein, we report novel polymeric quercetin nanorods and the former decorated with gold nanoparticles for the first time. The prepared conjugates quercetin-polyvinylpyrrolidone (Q-PVP) and quercetin-polyvinylpyrrolidone-gold nanoparticles (Q-PVP-Au) were characterized by UV-visible spectroscopy, Fourier transform infrared, dynamic light scattering, and zeta potential measurements. The surface morphology of conjugates was analyzed by field emission scanning electron microscopy. These conjugates exhibit harmonized rod-like morphology with a narrow size distribution. Furthermore, the quercetin conjugates with nanorod morphology exhibited enhanced and prolonged drug release over a long period. The synthesized conjugates were investigated for lysozyme aggregation kinetics. ThT binding assay, fibril size measurement, and electron microscopy results revealed that conjugates could suppress fibrillogenesis in lysozyme. The highest amyloid aggregation inhibition activity (IC(50)) was obtained against Q-PVP and Q-PVP-Au at 32 μg mL(−1) and 30 μg mL(−1) respectively. The amyloid aggregate disintegration activity (DC(50)) obtained against Q-PVP and Q-PVP-Au was 27 μg mL(−1) and 29 μg mL(−1) respectively. The present quercetin conjugates exhibit enhanced bioavailability and stability. They were potent inhibitors of lysozyme aggregation that may find applications as a therapeutic agent in neurological diseases like Alzheimer's and Parkinson's. The Royal Society of Chemistry 2022-08-19 /pmc/articles/PMC9389553/ /pubmed/36090438 http://dx.doi.org/10.1039/d2ra03121c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Rananaware, Pranita
Pandit, Parimal
Naik, Seekha
Mishra, Monalisa
Keri, Rangappa S.
Brahmkhatri, Varsha P.
Anti-amyloidogenic property of gold nanoparticle decorated quercetin polymer nanorods in pH and temperature induced aggregation of lysozyme
title Anti-amyloidogenic property of gold nanoparticle decorated quercetin polymer nanorods in pH and temperature induced aggregation of lysozyme
title_full Anti-amyloidogenic property of gold nanoparticle decorated quercetin polymer nanorods in pH and temperature induced aggregation of lysozyme
title_fullStr Anti-amyloidogenic property of gold nanoparticle decorated quercetin polymer nanorods in pH and temperature induced aggregation of lysozyme
title_full_unstemmed Anti-amyloidogenic property of gold nanoparticle decorated quercetin polymer nanorods in pH and temperature induced aggregation of lysozyme
title_short Anti-amyloidogenic property of gold nanoparticle decorated quercetin polymer nanorods in pH and temperature induced aggregation of lysozyme
title_sort anti-amyloidogenic property of gold nanoparticle decorated quercetin polymer nanorods in ph and temperature induced aggregation of lysozyme
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9389553/
https://www.ncbi.nlm.nih.gov/pubmed/36090438
http://dx.doi.org/10.1039/d2ra03121c
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