Ecofriendly one pot fabrication of methyl gallate@ZIF-L nanoscale hybrid as pH responsive drug delivery system for lung cancer therapy
[Display omitted] •Green synthesis of metal organic framework using Gracilaria debilis extract.•In vitro and In vivo toxicity studies illustrated that MG@ZIF-L nanocomposite is nontoxic in nature.•MG@ZIF-L exhibited potent anticancer potential against lung cancer cell line A549.•MG@ZIF-L possesses h...
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Veröffentlicht in: | Process biochemistry (1991) 2019-09, Vol.84, p.39-52 |
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Format: | Artikel |
Sprache: | eng |
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•Green synthesis of metal organic framework using Gracilaria debilis extract.•In vitro and In vivo toxicity studies illustrated that MG@ZIF-L nanocomposite is nontoxic in nature.•MG@ZIF-L exhibited potent anticancer potential against lung cancer cell line A549.•MG@ZIF-L possesses high loading efficiency, pH stimuli based drug delivery.
Zeolitic imidazole frame work, a special class of porous crystalline material with tunable pore size has emerged as a promising candidate for biomedical applications. The present work enlightens the fabrication of methyl gallate encapsulated ZIF-L (MG@ZIF-L) by utilizing red seaweed Gracilaria debilis and evaluating its anticancer potential against lung cancer cell lines A549. The material structure and physicochemical behaviors were systemically investigated using several spectroscopic techniques. Results showed that MG@ZIF-L possessed high loading efficiency, biocompatibility and fast drug release in tumor microenvironment, revealing that ZIF-L would act as a promising drug delivery system for cancer therapy. In vitro anticancer experiments illustrated that MG@ZIF-L exhibited high cytotoxic effects against A549 cells. Fluorescent microscopic analysis confirmed that MG@ZIF-L enhanced intracellular reactive oxygen species, causing mitochondrial dysfunction, releasing cytochrome C, the key factor for apoptosis. Moreover, in vitro and in vivo toxicity studies using PBMC and zebra fish embryo as model systems confirmed the nontoxic nature of MG@ZIF-L. Overall, the present work highlights the possibility of developing MG@ZIF-L nanocomposite as a suitable candidate for lung cancer therapy. |
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ISSN: | 1359-5113 1873-3298 |
DOI: | 10.1016/j.procbio.2019.06.015 |