Investigating the self-assembling of nicotinic hydrazide-based amphiphile into nano-range vesicles and its amphotericin B loading applications

Most of the drugs are hydrophobic and have low water solubility, therefore posing issues in their absorption and bioavailability. Nonionic surfactants improve the solubility of hydrophobic drugs by entrapping them in their lipid bilayers. Two nonionic surfactants NODNH-16 and NODNH-18 are synthesized and characterized using different techniques i.e. EI-MS, H-1 NMR, and FTIR. These newly synthesized surfactants were screened for blood hemolysis assay and cell toxicity studies using the NIH/3T3 cell line to assess their biocompatibility. Then amphotericin B was loaded into niosomal vesicles, and the drug entrapment efficiency of these surfactants was measured using UV-visible spectroscopy. The morphology of drug-loaded niosomes of synthesized surfactants was investigated using AFM, and their size, polydispersity, and zeta potential were measured with the Zetasizer instrument. Finally, a simulation study was performed to determine the pattern of self-assembly of the synthesized amphiphiles. Both synthesized nonionic surfactants showed good entrapment efficiency of 60.65 +/- 2.12% and 68.45 +/- 2.12%, respectively. It was also confirmed that both these synthesized nonionic surfactants were safe and biocompatible and showed less blood hemolysis (i.e. 21.13 +/- 2.11% and 23.32 +/- 2.45%) and higher 3T3 cells' viability at 150 mu g/mL concentration as compared to Tween (R)-80. The antifungal potential of amphotericin B-loaded niosomes has been evaluated against unicellular multi-fungal species, which showed a promising potential for fungicidal activity. These results are substantiated by constructing a safe vehicle system for drug delivery.

Automated summary

Due to the low solubility of hydrophobic drugs, nonionic surfactants are used to improve their solubility by entrapping them in lipid bilayers. Two newly synthesized nonionic surfactants, NODNH-16 and NODNH-18, were characterized and demonstrated good drug entrapment efficiency. They also showed biocompatibility and low blood hemolysis, making them safe for use. The antifungal potential of niosomes loaded with amphotericin B has been evaluated, showing promising fungicidal activity and providing a safe vehicle system for drug delivery.