Abstract

A facile, eco-friendly fluorescence approach based on the biogenic formation of zinc oxide nanoparticles using the biomass of Plicosepalus curviflorus shoots was developed. The suggested approach was employed to analyze three phenolic compounds (catechin, curviflorside, and curviflorin) isolated from the shoots of P. curviflorus. The surface morphology of the prepared ZnONPs was characterized by carrying out different microscopic and spectroscopic investigations. A significant UV-Vis absorption peak of ZnONPs was recognized at 345 nm and the FT-IR spectra of the isolated catechin, curviflorside, and curviflorin in the presence of sodium dodecyl sulfate (SDS) and ZnONPs were recorded at λem 470, 490, and 484 nm after excitation at λex 380, 420, and 410 nm. The suggested fluorescence method displayed linear concentration ranges of 10–120, 5–100, and 10–150 μg mL−1 for the three isolated compounds, respectively. The shoot extract, isolated compounds, and ZnONPs were screened for antibacterial and anticancer effects against four different types of bacterial strains and HeLa cells, respectively. The ZnONPs exhibited the highest zone of inhibition against Escherichia coli and Staphylococcus aureus strains when compared with pure, isolated compounds and shoot extract. The anticancer potential of ZnONPs (64%) was stronger as compared to the 160 µg mL−1 of shoot extract (49%), catechin (52%), curviflorside (54%), and curviflorin (58%) at 160 µg mL−1. Moreover, all the samples were investigated for hemolysis activity and showed a potent anti-hemolytic effect. The developed analytical method showed excellent sensitivity and reliability for the concurrent analysis of the isolated bioactive markers.

Highlights

  • Nowadays, enormous focus on the progress of powerful, inexpensive, and sensitive identification techniques for analyzing natural isolated chemical makers, preferably bioactive ones in herbal extracts for their acceptance in global markets [1,2]

  • Several advanced analytical techniques, including chromatographic (HPLC, UPLC, HPTLC) separations [3], electrochemical analysis [4], surface plasmon resonance [5], quartz crystal microbalance [6], and optical methods such as chemiluminescence and fluorescence are used for the bioactive markers detection and quantification based on the principle of different corresponding signal appearance [7,8]

  • Methanol (96.0%), n-hexane (95.0%), chloroform (96.0%), ethyl acetate (99.0%), n-Butanol (95.5%), acetone (99.0%), acetone-d6 (99.5%), methanol-d4 (99.8%), dimethyl sulfoxide (DMSO, 99.9%), p-anisaldehyde (98.0%), sulfuric acid (95.0%), zinc acetate dihydrate (Zn(CH3COO)2.2H2O) (99.9%), sodium dodecyl sulfate (SDS), 3-(4,5-dimethylthiazol-2yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT), 2% osmium tetroxide, 2% triton x-100, 3% glutaraldehyde, Dulbecco’s Modified Eagle Medium (DMEM), and 10% of fetal bovine serum (FBS) were purchased from Sigma-Aldrich (Hamburg, Germany)

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Summary

Introduction

Enormous focus on the progress of powerful, inexpensive, and sensitive identification techniques for analyzing natural isolated chemical makers, preferably bioactive ones in herbal extracts for their acceptance in global markets [1,2]. The advancement in the making and designing of nanostructures has resulted in the rapid development of several nanoparticles with unique chemical and physical features such as a large surface area and distinctive optical, magnetic, and electronic properties [15]. These nanoparticles have a unique biocompatible nature that makes them highly suitable for bio-detection applications. Zinc oxide nanoparticles with unique inherent properties such as easy synthesis, facile functionalization, outstanding fluorescence intensity, rapid dissolution, the quick formation of ZnO ions, biocompatibility, and stability have grabbed enormous interest in the areas of energy storage, photocatalysis, optical devices, and signal detection [22,23]. Studies in the literature have claimed that ZnONPs prepared from plant extracts have elevated the fluorescence detection as well as the biological properties of the ZnONPs due to the presence of fluorescent active phytocompounds in the plant extracts [26,27,28]

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