PTSA-induced synthesis, in silico and nano study of novel ethylquinolin-thiazolo-triazole in cervical cancer.
Priyanka SonkerRupen TamangAbhishesh K MehataManisha NidharVishal P SharmaVipin KumarMadaswamy S MuthuBiplob KochAshish K TewariPublished in: Future medicinal chemistry (2024)
Aim: p-Toluenesulfonic acid-(PTSA) and grinding-induced novel synthesis of ethylquinolin-thiazolo-triazole derivatives was performed using green chemistry. Materials & methods: Development of a nanoconjugate drug-delivery system of ethylquinolin-thiazolo-triazole was carried out with D-α-tocopheryl polyethylene glycol succinate (TPGS) and the formulation was further characterized by transmission electron microscopy, atomic force microscopy, dynamic light scattering and in vitro drug release assay. The effect of 3a nanoparticles was assessed against a cervical cancer cell line (HeLa) through the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, and the effect on apoptosis was determined. Results & discussion: The 3a nanoparticles triggered the apoptotic mode of cell death after increasing the intracellular reactive oxygen level by enhancing cellular uptake of micelles. Furthermore, in silico studies revealed higher absorption, distribution, metabolism, elimination and toxicity properties and bioavailability of the enzyme tyrosine protein kinase. Conclusion: The 3a nanoparticles enhanced the therapeutic potential and have higher potential for targeted drug delivery against cervical cancer.
Keyphrases
- drug delivery
- drug release
- cell death
- cell cycle arrest
- cancer therapy
- atomic force microscopy
- diabetic rats
- high glucose
- oxidative stress
- electron microscopy
- high throughput
- molecular docking
- protein kinase
- high speed
- drug induced
- endoplasmic reticulum stress
- endothelial cells
- walled carbon nanotubes
- cell proliferation
- anti inflammatory