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Antineoplastic Effect of PAC Capped Silver Nanoparticles Promote Apoptosis in HT-29 Human Colon Cancer Cells
Proanthocyanidin (PAC) is an anti-cancer drug that effectively treat various cancers, including colon cancer. Whereas, the chemotherapeutic potential has restricted to low bioavailability and more defects. To overcome these complications, PAC produces a selective intend of AgNPs as a medicine for ca...
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Published in: | Journal of cluster science 2019-03, Vol.30 (2), p.483-493 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Proanthocyanidin (PAC) is an anti-cancer drug that effectively treat various cancers, including colon cancer. Whereas, the chemotherapeutic potential has restricted to low bioavailability and more defects. To overcome these complications, PAC produces a selective intend of AgNPs as a medicine for cancer cells and growing modern antineoplastic promoter, an innovative nano-capped drug was enhanced bioavailability of tumor cells. The synthesized PAC-AgNPs was described by spectroscopy analysis. Phenolic compound has hydroxyl groups which are able to bind to metals and reduce the metal salt and provide stability against agglomeration was confirmed by FTIR and spherical or polygonal shape with an average size of 72.35 nm found through FE-SEM analysis, applicable for targeted delivery to specific tissues. The potential of this nano-incorporate drug had been caused apoptosis in colon cancer cells was measured. Significantly, it was found in decreasing cell growth by MTT assay, morphological changes such as membrane blebbing and chromatin condensation exhibited in AO/EB staining. At the end, the mitochondrial pathway of apoptotic cell death confirmed by cell cycle progression as well as annexin V/PI. These results strongly suggest that PAC-AgNPs could be used as a major nano-composite therapeutic drug for effectively treated with colon cancer. |
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ISSN: | 1040-7278 1572-8862 |
DOI: | 10.1007/s10876-019-01510-1 |