TY - JOUR
T1 - Nanoparticle impregnated self-supporting protein gel for enhanced reduction in oxidative stress
T2 - A molecular dynamics insight for lactoferrin-polyphenol interaction
AU - Raychaudhuri, Ruchira
AU - Pandey, Abhijeet
AU - Das, Subham
AU - Nannuri, Shivanand H.
AU - Joseph, Alex
AU - George, Sajan D.
AU - Vincent, Anita P.
AU - Mutalik, Srinivas
N1 - Funding Information:
The authors are thankful to Nanomission, Department of Science and Technology, Government of India , New Delhi for providing financial support for the research project ( DST/NM/NT/2018/133 ). The authors express their gratitude to Council for Scientific and Industrial Research (CSIR), Government of India, New Delhi (for providing Senior Research Fellowship to Ruchira Raychaudhuri) and Manipal Academy of Higher Education, Manipal (for providing Postdoctoral Research Fellowship to Dr. Abhijeet Pandey and Dr. TMA Pai Doctoral Fellowship to Subham Das and Shivanand H. Nannuri). The authors are grateful to Manipal College of Pharmaceutical Sciences, Department of Atomic and Molecular Physics, and Manipal Academy of Higher Education, Manipal for providing necessary facilities and support.
Funding Information:
The authors are thankful to Nanomission, Department of Science and Technology, Government of India, New Delhi for providing financial support for the research project (DST/NM/NT/2018/133). The authors express their gratitude to Council for Scientific and Industrial Research (CSIR), Government of India, New Delhi (for providing Senior Research Fellowship to Ruchira Raychaudhuri) and Manipal Academy of Higher Education, Manipal (for providing Postdoctoral Research Fellowship to Dr. Abhijeet Pandey and Dr. TMA Pai Doctoral Fellowship to Subham Das and Shivanand H. Nannuri). The authors are grateful to Manipal College of Pharmaceutical Sciences, Department of Atomic and Molecular Physics, and Manipal Academy of Higher Education, Manipal for providing necessary facilities and support.
Publisher Copyright:
© 2021 Elsevier B.V.
PY - 2021/10/31
Y1 - 2021/10/31
N2 - In the present work, lactoferrin (Lf) based nanoparticle incorporated self-supporting gel encapsulating a flavonoid, quercetin (Q), was developed. The complex formation between Lf and Q was assessed using molecular docking and dynamics simulation that lactoferrin and quercetin showed strong interaction and binding supporting hydrophobic interaction. The microscopic, spectroscopic, and x-ray techniques were used to characterize the gel extensively. In vitro drug release was studied to understand the release pattern of quercetin from the protein gel. The viscosity of the gel and its rheological characteristics were determined using a Brookfield viscometer. Ex vivo skin permeation studies using vertical diffusion cells were carried out to understand its skin permeation properties. The gel showed strong anti-oxidant activity using the DPPH scavenging assay. The enhanced effect of the Lf-Q complex on antioxidant enzyme activity (superoxide dismutase, catalase, and malondialdehyde), was supported by molecular dynamics, surface hydrophobicity, and in vitro studies. To investigate the effect of the gel on angiogenesis, the chorioallantoic membrane assay was performed and its compatibility with erythrocytes was also assessed. Suitability for topical administration was assessed using skin irritation studies performed on Sprague Dawley rats. The overall results suggest that the developed NiPG is suitable for cutaneous localization of quercetin with enhanced antioxidant activity.
AB - In the present work, lactoferrin (Lf) based nanoparticle incorporated self-supporting gel encapsulating a flavonoid, quercetin (Q), was developed. The complex formation between Lf and Q was assessed using molecular docking and dynamics simulation that lactoferrin and quercetin showed strong interaction and binding supporting hydrophobic interaction. The microscopic, spectroscopic, and x-ray techniques were used to characterize the gel extensively. In vitro drug release was studied to understand the release pattern of quercetin from the protein gel. The viscosity of the gel and its rheological characteristics were determined using a Brookfield viscometer. Ex vivo skin permeation studies using vertical diffusion cells were carried out to understand its skin permeation properties. The gel showed strong anti-oxidant activity using the DPPH scavenging assay. The enhanced effect of the Lf-Q complex on antioxidant enzyme activity (superoxide dismutase, catalase, and malondialdehyde), was supported by molecular dynamics, surface hydrophobicity, and in vitro studies. To investigate the effect of the gel on angiogenesis, the chorioallantoic membrane assay was performed and its compatibility with erythrocytes was also assessed. Suitability for topical administration was assessed using skin irritation studies performed on Sprague Dawley rats. The overall results suggest that the developed NiPG is suitable for cutaneous localization of quercetin with enhanced antioxidant activity.
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U2 - 10.1016/j.ijbiomac.2021.08.089
DO - 10.1016/j.ijbiomac.2021.08.089
M3 - Article
AN - SCOPUS:85113610491
SN - 0141-8130
VL - 189
SP - 100
EP - 113
JO - International Journal of Biological Macromolecules
JF - International Journal of Biological Macromolecules
ER -