L-Cysteine capped zinc oxide nanoparticles induced cellular response on adenocarcinomic human alveolar basal epithelial cells using a conventional and organ-on-a-chip approach.

Zinc oxide nanoparticles (ZnO NPs) are among the well-characterized nanomaterials with multifaceted biomedical applications, including biomedical imaging, drug delivery, and pharmaceutical preparations. The high surface charge of ZnO NPs leads to the agglomeration of the particles. Therefore, surface coating with a suitable ligand can increase colloidal stability. In this present study, in-vitro responses of ZnO NPs capped with a sulfur-containing amino acid, L-cysteine (Cys-ZnO NPs), on A549 cells was investigated. Fourier Transform Infrared Spectroscopy (FTIR) studies were carried out to confirm the capping of ZnO NPs with L-cysteine. Cytotoxic studies using A549 cells demonstrated reduced cytotoxicity in comparison with already reported pristine Zinc Oxide nanoparticles. The cellular uptake is confirmed by fluorescent cytometry. However, a higher concentration (160 µg/mL) of Cys-ZnO NPs led to apoptotic cell death marked by nuclear condensation, mitochondrial membrane depolarization, actin filament condensation, lysosomal damage LDH leakage, intracellular ROS production, blebbing, upregulation of Bax and downregulation of Bcl-2 gene expression. Cys-ZnO NPs treatment was also carried out in cells cultured in a microfluidic lung-on-a-chip device under a physiologically relevant flow rate. The study concluded that the microfluidic-based lung-on-a-chip culture resulted in reduced cell death compared to the conventional condition.

Effect of cyanide ions (CN-) extracted from cassava (Manihotesculenta Crantz) on Alveolar Epithelial Cells (A549 cells).

Cassava (Manihotesculenta Crantz) is one of the most important root crops in tropical countries. It is a major source of cyanogenic glycosides viz. linamarin and lotaustralin, and these on breakdown liberate HCN and ketone. Cassava cyanide extract (CCE) from cassava leaves and tuber rinds were formulated as a biopesticide against certain borer insect pests of horticultural crops. Adenocarcinomic human alveolar basal epithelial cells (A549) were treated with three different concentrations (100, 200, 400 ppm) of CCE. The MTT and NRU assays showed dose-dependent cytotoxicity. The DCFH-DA assay does not show any free radical scavenging activity, whereas the NRR assay showed a reduction in the nitrile radicals with an increase in the concentration of the bioactive compound. A negative correlation was found between the concentration of the bioactive principles and mitochondrial and lysosomal functions. Various cellular assays demonstrated the cellular response of the CCE, and it was found that at higher concentration (400 ppm), the CCE exert a significant necrotic cell death rather than apoptosis. The results of the study indicated that the CCE have a remarkable tendency of anti-proliferative ability.