Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/502937
Title: Investigation on Surface Functionalized Mesoporous Silicon Dioxide Sio2 Nanoparticles Fabricated with Reduced Graphene Oxide Rgo Nanosheet for Targeted Drug Delivery on Breast Cancer Cells
Researcher: Vignesh, K
Guide(s): Kalaivani, T
Keywords: Physical Sciences
Physics
Physics Nuclear
University: SRM Institute of Science and Technology
Completed Date: 2023
Abstract: Mesoporous nanoparticles (MNPs) have gained considerable attention in the biomedical field as trustworthy drug delivery systems for the treatment of cancer. Due to their high surface area, tunable pore size, huge pore volume, simplicity in adjusting the interior and exterior surfaces, and high drug loading potential, they have a number of benefits over conventional drug carriers. Synthesis of mesoporous silicon dioxide nanoparticles (MNPs) with different pore volumes and their toxicity effects on zebrafish. The structural and morphological analyses of MNPs were carried out through XRD and HRTEM, functional groups have been identified by FTIR and N2 adsorption/desorption isotherm and the pore size distribution was determined by BET analysis. The maximum pore volume of 1.5 cm3/g and a pore size of 8.0 nm, were reported. Survival percentage of zebrafish was reported to be above 85% newline
Pagination: 
URI: http://hdl.handle.net/10603/502937
Appears in Departments:Department of Physics

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01_title.pdfAttached File211.71 kBAdobe PDFView/Open
02_preliminary page.pdf.pdf314.26 kBAdobe PDFView/Open
03_content.pdf267.83 kBAdobe PDFView/Open
04_abstract.pdf240.81 kBAdobe PDFView/Open
05_chapter 1.pdf578.33 kBAdobe PDFView/Open
06_chapter 2.pdf504.95 kBAdobe PDFView/Open
07_chapter 3.pdf833.6 kBAdobe PDFView/Open
08_chapter 4.pdf1.05 MBAdobe PDFView/Open
09_chapter 5.pdf905.77 kBAdobe PDFView/Open
10_chapter 6.pdf959.42 kBAdobe PDFView/Open
11_chapter 7.pdf310.86 kBAdobe PDFView/Open
12_annexures.pdf412.27 kBAdobe PDFView/Open
80_recommendation.pdf367.08 kBAdobe PDFView/Open
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