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PJB-2025-468

GREEN SYNTHESIS IN BIOLOGICAL APPLICATION OF NANO DOTS FROM THE SEED EXTRACT OF ERIOBOTRYA JAPONICA

Akhtar Alai Khan

Abstract

Nanotechnology has revolutionized material science and biomedicine by enabling the eco-friendly synthesis of carbon nanodots using plant-based biomolecules like Eriobotrya japonica seeds, offering a sustainable alternative to conventional toxic methods. In this study, nitrogen–sulfur co-doped carbon nanodots (N–S CDs) were successfully synthesized from Eriobotrya japonica seed extract through a green hydrothermal route at 180 °C without using any hazardous chemicals. The resulting N–S CDs displayed a uniform quasi-spherical morphology with an average size of 4.2 ± 1.1 nm and excellent aqueous stability (zeta potential = –21.4 mV). Optical characterization revealed bright blue fluorescence at 450 nm under 360 nm excitation, with a high quantum yield of 32.4%, nearly twice that of undoped CDs. The nanodots retained over 91.7% fluorescence intensity after 120 minutes of UV exposure, demonstrating exceptional photostability. Structural analyses (TEM, XRD, Raman, and XPS) confirmed a partially graphitic carbon framework with successful nitrogen and sulfur incorporation, enhancing electronic conjugation and surface passivation. The synthesized N–S CDs exhibited remarkable sensitivity and selectivity toward Fe³⁺ ions with a detection limit of 0.04 µM and recovery of 96.8–103.4% in tap water, indicating strong analytical potential. Cytotoxicity studies confirmed >92% cell viability at 500 µg mL⁻¹, showing excellent biocompatibility, while antioxidant assays demonstrated up to 90% DPPH radical scavenging, comparable to ascorbic acid. Overall, Eriobotrya japonica-based N–S CDs represent a low-cost, sustainable, and multifunctional nanomaterial with promising applications in biosensing, bioimaging, and environmental monitoring, highlighting the potential of green nanotechnology for future biomedical innovations. Keywords:co-doping; Eriobotrya japonica seed extract; Hydrothermal synthesis; Photoluminescence; Fe³⁺ ion sensing

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