Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/596056
Title: Synthesis and Characterization of Methotrexate Loaded Zinc Oxide Nano Particles for Efficient Delivery to Breast Cancer Cells
Researcher: Joshi Mitesh Manojkumar
Guide(s): Bhatt Purvi
Keywords: Biology
Biology and Biochemistry
Life Sciences
Triple-negative breast cancer
University: Narsee Monjee Institute of Management Studies
Completed Date: 2024
Abstract: Breast cancer is the most common cancer among women and is the second leading cause of cancer-related deaths in women, following lung cancer. Early detection and treatment play a crucial role in improving survival rates. However, metastasis and cancer resistance to therapies continue to contribute to cancer mortality. Triple-negative breast cancer (TNBC) is a type of breast cancer that does not have any hormonal receptors or HER2, which makes it more difficult to treat. Combination therapy, which involves the use of multiple agents that target different genes, disease pathways, or cell-cycle checkpoints, has shown promise in enhancing the efficacy of standard single-agent treatments. newlineFolic acid receptor (FAR) is a molecular marker that is highly expressed in certain cancers, including breast cancer. Targeting FAR allows for the specific delivery of antitumor agents to FAR-overexpressing cancer cells while minimizing non-specific tissue absorption. Methotrexate (MTX) is a commonly used chemotherapy drug that has shown potential in targeting FAR-overexpressing cells. Nanotechnology offers passive and active targeting strategies to enhance drug concentration within cancer cells and reduce toxicity to normal cells. Zinc oxide nanoparticles (ZnONPs) have proved its efficacy as a potential anticancer agent for various different cancer types in vitro. ZnONPs are cytotoxic as they release soluble Zn+2 ions in the surrounding environment which is the major factor involved into ZnONPs related toxicity. newlineIn this study, we aimed to develop a novel system combining ZnONPs and MTX to enhance therapeutic effectiveness and minimize side effects. The synthesized MTX-ZnONPs were characterized using various techniques, revealing hexagonal crystal morphology with an average size of 30 nm and positive Zeta potential. A drug release study demonstrated biphasic drug release, with approximately 90% of the drug released within 24 hours. newline
Pagination: i-x;194p
URI: http://hdl.handle.net/10603/596056
Appears in Departments:Department of Biological Sciences

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01_title.pdfAttached File178.99 kBAdobe PDFView/Open
02_prelim pages.pdf858.95 kBAdobe PDFView/Open
03_contents.pdf138.45 kBAdobe PDFView/Open
04_abstract.pdf139.76 kBAdobe PDFView/Open
05_chapter 1.pdf395.07 kBAdobe PDFView/Open
06_chapter 2.pdf1.33 MBAdobe PDFView/Open
07_chapter 3.pdf181.57 kBAdobe PDFView/Open
08_chapter 4.pdf2.1 MBAdobe PDFView/Open
09_chapter 5.pdf5.59 MBAdobe PDFView/Open
10_chapter 6.pdf624.08 kBAdobe PDFView/Open
11_chapter 7.pdf300.96 kBAdobe PDFView/Open
12_annexures.pdf16.37 MBAdobe PDFView/Open
80_recommendation.pdf111.06 kBAdobe PDFView/Open
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