In vitro cytotoxicity assessment of biosynthesized Apis mellifera bee venom nanoparticles (BVNPs) against MCF-7 breast cancer cell lines

Abstract In this work, we reported the synthesis of honey bee (Apis mellifera) venom-derived nanoparticles via a hydrothermal method. This method not only ensures the preservation of the bee venom’s bioactive components but also enhances their potential stability, thus broadening the scope for their...

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Main Authors: Vikram Jadhav, Arun Bhagare, Ashwini Palake, Kisan Kodam, Akshay Dhaygude, Anant Kardel, Dnyaneshwar Lokhande, Jayraj Aher
Format: Article
Language:English
Published: Springer 2024-10-01
Series:Discover Nano
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Online Access:https://doi.org/10.1186/s11671-024-04123-4
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author Vikram Jadhav
Arun Bhagare
Ashwini Palake
Kisan Kodam
Akshay Dhaygude
Anant Kardel
Dnyaneshwar Lokhande
Jayraj Aher
author_facet Vikram Jadhav
Arun Bhagare
Ashwini Palake
Kisan Kodam
Akshay Dhaygude
Anant Kardel
Dnyaneshwar Lokhande
Jayraj Aher
author_sort Vikram Jadhav
collection DOAJ
description Abstract In this work, we reported the synthesis of honey bee (Apis mellifera) venom-derived nanoparticles via a hydrothermal method. This method not only ensures the preservation of the bee venom’s bioactive components but also enhances their potential stability, thus broadening the scope for their applications in the biomedicinal field. The synthesis method started with the homogenization suspension of bee venom, followed by its hydrothermal process to synthesize bee venom nanoparticles (BVNPs). The successful synthesis of BVNPs was characterized using various characteristic techniques such as Ultraviolet–visible (UV–Vis) spectroscopy, Fourier Transforms Infrared (FTIR) Spectroscopy, Zeta Potential (ZP), Liquid Chromatography-Mass Spectrometry (LCMS), and Transmission Electron Microscopy (TEM). The synthesis of BVNPs through biosynthesis is shown by the visible violet-brown color development at 347 nm by UV–Vis spectroscopy. FTIR analysis revealed the presence of several functional groups in the BVNPs, including alcohols (–OH), phenols (C6H5–), carboxylic acids (–COOH), amines (–NH2, –NH–), aldehydes (–CHO), ketones (–CO–), nitriles (–CN), amides (–CO–N–), imines (–CNH–), esters (–COO–), and polysaccharides. These functional groups, as confirmed by their specific stretching and bending vibrational modes, contribute to the diverse biological activities of BVNPs, including cytotoxicity against MCF-7 breast cancer cells. The ZP of the BVNPs indicated good colloidal stability at − 45 mV. LCMS analysis confirmed the presence of major bioactive molecules, including melittin & apamin and TEM analysis shows the BVNPs exhibited a quasi-spherical shape with good dispersion, the average size was approximately 25 nm, with some being smaller (quantum dots) and interplanar spacing of 0.236 nm indicated a highly ordered crystalline structure. Moreover, the anticancer efficacy of the BVNPs was ascertained through in vitro assays against MCF-7 breast cancer cells, showing a dose-dependent cytotoxic effect. The findings of this study underscore the viability of hydrothermal synthesis in producing biologically active and structurally stable BVNPs, with a significant potential for anticancer activities. Graphical Abstract
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spelling doaj-art-1c14b70c5cd54cdd8a3b855bca483cb02025-08-20T02:17:48ZengSpringerDiscover Nano2731-92292024-10-0119111510.1186/s11671-024-04123-4In vitro cytotoxicity assessment of biosynthesized Apis mellifera bee venom nanoparticles (BVNPs) against MCF-7 breast cancer cell linesVikram Jadhav0Arun Bhagare1Ashwini Palake2Kisan Kodam3Akshay Dhaygude4Anant Kardel5Dnyaneshwar Lokhande6Jayraj Aher7Department of Chemistry, M. V. P. Samaj’s K. K. Wagh Arts, Science, and Commerce CollegeDepartment of Chemistry, M. V. P. Samaj’s K. K. Wagh Arts, Science, and Commerce CollegeBiochemistry Division, Department of Chemistry, Savitribai Phule Pune UniversityBiochemistry Division, Department of Chemistry, Savitribai Phule Pune UniversityDepartment of Chemistry, M. V. P. Samaj’s K. K. Wagh Arts, Science, and Commerce CollegeDepartment of Chemistry, M. V. P. Samaj’s K. K. Wagh Arts, Science, and Commerce CollegePost Graduate Department of Chemistry, K. R. T. Arts, B. H. Commerce, and A. M. Science CollegePost Graduate Department of Chemistry, K. R. T. Arts, B. H. Commerce, and A. M. Science CollegeAbstract In this work, we reported the synthesis of honey bee (Apis mellifera) venom-derived nanoparticles via a hydrothermal method. This method not only ensures the preservation of the bee venom’s bioactive components but also enhances their potential stability, thus broadening the scope for their applications in the biomedicinal field. The synthesis method started with the homogenization suspension of bee venom, followed by its hydrothermal process to synthesize bee venom nanoparticles (BVNPs). The successful synthesis of BVNPs was characterized using various characteristic techniques such as Ultraviolet–visible (UV–Vis) spectroscopy, Fourier Transforms Infrared (FTIR) Spectroscopy, Zeta Potential (ZP), Liquid Chromatography-Mass Spectrometry (LCMS), and Transmission Electron Microscopy (TEM). The synthesis of BVNPs through biosynthesis is shown by the visible violet-brown color development at 347 nm by UV–Vis spectroscopy. FTIR analysis revealed the presence of several functional groups in the BVNPs, including alcohols (–OH), phenols (C6H5–), carboxylic acids (–COOH), amines (–NH2, –NH–), aldehydes (–CHO), ketones (–CO–), nitriles (–CN), amides (–CO–N–), imines (–CNH–), esters (–COO–), and polysaccharides. These functional groups, as confirmed by their specific stretching and bending vibrational modes, contribute to the diverse biological activities of BVNPs, including cytotoxicity against MCF-7 breast cancer cells. The ZP of the BVNPs indicated good colloidal stability at − 45 mV. LCMS analysis confirmed the presence of major bioactive molecules, including melittin & apamin and TEM analysis shows the BVNPs exhibited a quasi-spherical shape with good dispersion, the average size was approximately 25 nm, with some being smaller (quantum dots) and interplanar spacing of 0.236 nm indicated a highly ordered crystalline structure. Moreover, the anticancer efficacy of the BVNPs was ascertained through in vitro assays against MCF-7 breast cancer cells, showing a dose-dependent cytotoxic effect. The findings of this study underscore the viability of hydrothermal synthesis in producing biologically active and structurally stable BVNPs, with a significant potential for anticancer activities. Graphical Abstracthttps://doi.org/10.1186/s11671-024-04123-4Apis melliferaBee venom nanoparticlesCytotoxicityHydrothermal synthesisAnticancer activityMCF-7 cells
spellingShingle Vikram Jadhav
Arun Bhagare
Ashwini Palake
Kisan Kodam
Akshay Dhaygude
Anant Kardel
Dnyaneshwar Lokhande
Jayraj Aher
In vitro cytotoxicity assessment of biosynthesized Apis mellifera bee venom nanoparticles (BVNPs) against MCF-7 breast cancer cell lines
Discover Nano
Apis mellifera
Bee venom nanoparticles
Cytotoxicity
Hydrothermal synthesis
Anticancer activity
MCF-7 cells
title In vitro cytotoxicity assessment of biosynthesized Apis mellifera bee venom nanoparticles (BVNPs) against MCF-7 breast cancer cell lines
title_full In vitro cytotoxicity assessment of biosynthesized Apis mellifera bee venom nanoparticles (BVNPs) against MCF-7 breast cancer cell lines
title_fullStr In vitro cytotoxicity assessment of biosynthesized Apis mellifera bee venom nanoparticles (BVNPs) against MCF-7 breast cancer cell lines
title_full_unstemmed In vitro cytotoxicity assessment of biosynthesized Apis mellifera bee venom nanoparticles (BVNPs) against MCF-7 breast cancer cell lines
title_short In vitro cytotoxicity assessment of biosynthesized Apis mellifera bee venom nanoparticles (BVNPs) against MCF-7 breast cancer cell lines
title_sort in vitro cytotoxicity assessment of biosynthesized apis mellifera bee venom nanoparticles bvnps against mcf 7 breast cancer cell lines
topic Apis mellifera
Bee venom nanoparticles
Cytotoxicity
Hydrothermal synthesis
Anticancer activity
MCF-7 cells
url https://doi.org/10.1186/s11671-024-04123-4
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