Comparative effects of two different aluminum nanoparticle formulations on the histological and physiological aspects of Drosophila melanogaster (Diptera: Drosophilidae) as a model
Data files
Jul 16, 2025 version files 63.80 MB
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Transmission_electron_microscope_for_nanoparticles_(1).zip
3.51 MB
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Raw_data_of_Biological_experiments.csv
2.40 KB
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Histological_examination__Ball_milling_(1).zip
25.28 MB
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FTIR_for_NPs_sythetized_by_Ball_milling.txt
69.96 KB
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FTIR_for_NPs_sythetized_by_conventional_grinding.txt
69.94 KB
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Histological_examination_Control.zip
6.05 MB
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Histological_examination_Conventional_grinding.zip
9.55 MB
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README.md
4.94 KB
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Scanning_electron_microscope_for_nanoparticles.zip
2.76 MB
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TEM_of_Drosophila_midgut_exposed_to_control_food_media.zip
5.08 MB
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TEM_of_Drosophila_midgut_treated_with_NPs_synthetized_by_Ball_milling_method.zip
7.93 MB
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TEM_of_Drosophila_midgut_treated_with_NPs_synthetized_by_Conventional_grinding_method.zip
3.44 MB
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XDR_for_NPs_sythetized_by_Ball_milling.txt
25.83 KB
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XDR_for_NPs_sythetized_by_conventional_grinding.txt
37.45 KB
Abstract
Recycling aluminum, which is widely utilized in industries such as packaging, poses a significant challenge in selecting the most efficient method that retains its properties while minimizing environmental impact. This study investigates the potential adverse effects of aluminum oxide nanoparticles (Al2O3 NPs) synthesized from disposable aluminum foil waste using two different recycling methods: conventional grinding (CG) and ball milling (BM). This study employs Drosophila melanogaster as a well-established in vivo model organism to determine which recycling technique yields nanoparticles (NPs) that are less harm to non-targets. To assess this, relevant concentration of Al2O3 NPs formulations was added into the food media. Seven days post feeding, alterations of adult’s midgut were analyzed at physiological and ultrastructure levels. The results showed that Al2O3 NPs had significant effects on digestive enzymes, regardless of how they are synthesized. In contrast to chitinase and protease, the activities of digestive enzymes such as lipase, phospholipase A2, and carboxypeptidase were significantly higher in flies exposed to Al2O3 NPs synthesized by BM than those in fed on control food media or those supplemented with Al2O3 NPs synthesized by CG. Histological and ultrastructural analyses revealed that both formulations of Al2O3 NPs negatively impacted the midgut cells. However, the harmful effects were more pronounced in NPs synthesized by the BM method compared to those produced using the CG method. Where indistinct peritrophic membrane and disrupted microvilli, columnar and goblet cells with numerous vacuoles were recorded. Collectively, while the findings confirm the toxicity of Al2O3 NPs to Drosophila, the synthesis method used to process aluminum and convert it into nanoparticle form plays a significant role in determining its potential hazards and should be carefully considered.
Authors: Hanaa Elbrense, Marwa N. El-Nahass, Samar El-Kholy
Corresponding author: Samar El Kholy (samar_elkholy@science.tanta.edu.eg) ORCID number: 0000-0003-2816-7243
Dataset DOI:10.5061/dryad.wwpzgmsxf
Description of the data and file structure
The present study investigates the potential adverse effects of aluminum oxide nanoparticles (Al2O3 NPs) synthesized from disposable aluminum foil waste using two different recycling methods: conventional grinding (CG) and ball milling (BM). This study employs Drosophila melanogaster as in vivo model organism to determine which recycling technique yields nanoparticles (NPs) that are less harm to non-targets. To assess this, relevant concentration of Al2O3 NPs formulations was added into the food media. Seven days post feeding, alterations of adultís midgut were analyzed at physiological and ultrastructure levels.
Files and variables
Raw_data_of_Biological_experiments.csv
Description: This data file includes the quantification of the amount of food consumed (in µl), defecation rate (No. of fecal pellets per fly), digestive enzymes (amylase, lipase, protease, alpha glycosidase, phospholipase A2, chitinase and carboxy peptidase) activity (U/ml) in Drosophila adults supplemented with control or aluminum oxide NPs synthesized by CG and BM methods. The file also contains an evaluation of aluminum oxide NPs (synthesized by CG or BM) adverse effects at cellular level based on Transmission Electron Microscope imaging. This data includes vacuoles number and area (µm-2), nuclear (µm-2) and nucleolar area (µm-2).
Histological_examination_Control.zip
Description: This file contains images of sections stained with eosin and hematoxylin to illustrate Drosophila adult midgut tissue after feeding of control food media.
Histological_examination__Ball_milling_(1).zip
Description: This file contains images of sections stained with eosin and hematoxylin to illustrate abnormalities of Drosophila adult midgut tissue after feeding of food media supplemented with aluminum oxide NPs synthesized by BM.
Histological_examination_Conventional_grinding.zip
Description: This file contains images of sections stained with eosin and hematoxylin to illustrate abnormalities of Drosophila adult midgut tissue after feeding of food media supplemented with aluminum oxide NPs synthesized by CG.
TEM_of_Drosophila_midgut_exposed_to_control_food_media.zip
Description: This data files includes transmission electron microscopic imaging of midgut tissues of adult Drosophila supplemented with control food media.
TEM_of_Drosophila_midgut_treated_with_NPs_synthetized_by_Conventional_grinding_method.zip
Description: This data file includes transmission electron microscopic imaging of midgut tissues of adult Drosophila fed on food media supplemented with aluminum oxide NPS synthesized by CG.
TEM_of_Drosophila_midgut_treated_with_NPs_synthetized_by_Ball_milling_method.zip
Description: This data files includes transmission electron microscopic imaging of midgut tissues of adult Drosophila fed on food media supplemented with aluminum oxide NPS synthesized by BM.
FTIR_for_NPs_sythetized_by_Ball_milling.txt
Description: This data file includes characterization of surface chemistry of aluminum oxide NPs synthesized by BM using Fourier-transform infrared spectroscopy.
Y-axis, T%, x-axis (Wavenumber (cm-1))
FTIR_for_NPs_sythetized_by_conventional_grinding.txt
Description: This data file includes characterization of surface chemistry of aluminum oxide NPs synthesized by CG using Fourier-transform infrared spectroscopy.
Y-axis, T%, x-axis (Wavenumber (cm-1))
XDR_for_NPs_sythetized_by_Ball_milling.txt
Description: This data file includes characterization of Crystalline Structure of aluminum oxide NPs synthesized by BM using Small-angle X-ray diffraction.
I (Intensity in arbitrary unit), 2 Theta (angle between the incident X-ray and the atomic planes in the sample)
XDR_for_NPs_sythetized_by_conventional_grinding.txt
Description: This data file includes characterization of Crystalline Structure of aluminum oxide NPs synthesized by CG using Small-angle X-ray diffraction.
I (Intensity in arbitrary unit), 2 Theta (angle between the incident X-ray and the atomic planes in the sample)
Scanning_electron_microscope_for_nanoparticles.zip
Description: This data file includes scanning electron microscopic imaging of aluminum oxide NPS synthesized by CG and BM.
Transmission_electron_microscope_for_nanoparticles_(1).zip
Description: This data file includes transmission electron microscopic imaging of aluminum oxide NPS synthesized by CG and BM.
This dataset originates from a study investigating the biological effects of aluminum oxide nanoparticles (Al₂O₃ NPs) synthesized from recycled aluminum foil waste. The synthesis involved dissolving cleaned and shredded aluminum foil in hydrochloric acid, followed by precipitation using sodium carbonate to form aluminum oxide. The resulting material was washed, dried, calcined at 800°C, and then ground using two methods—conventional grinding (CG) and ball milling (BM)—to obtain nanoscale particles. These formulations were characterized using FTIR, XRD, SEM, and TEM.
Biological assays were conducted on Drosophila melanogaster (wild-type Canton S) to assess the physiological effects of CG and BM Al₂O₃ NPs. Flies were exposed to nanoparticle-supplemented food media, and multiple endpoints were evaluated: food intake using the capillary feeding (CAFE) assay, defecation rate via fecal pellet count, digestive enzyme activities in dissected midguts (seven enzymes assessed using colorimetric kits), and tissue-level effects using histological and ultrastructural analyses (light microscopy and TEM). All experimental conditions were replicated appropriately and analyzed using standard statistical tools (ANOVA).
This dataset includes quantitative and image-based measurements capturing ingestion behavior, gut enzyme activity, and cellular morphology under nanoparticle exposure.