Nanoformulations for Hydrazones; Synthesis, Characterization, Parasitology, and Histopathology Investigations

In the creation of medicine delivery systems, nanotechnology has become an innovator, especially for organic compounds. The manipulation of materials at the nanoscale (1-100 nm) allows for unique physicochemical properties that can enhance the efficacy and bioavailability of therapeutic agents. The objective of the current research is to synthesize the hydrazones nanoparticles <b>3-(a*-c*)</b> which utilizes the ionic gelation method via chitosan as a matrix, and their size was measured via both scanning (SEM) and transmission (TEM) electronic microscopes. Interestingly, the formulated nanoparticles are found to be relatively stable, with a positive net charge and high entrapment efficiency up to 82.6%. The studied compounds were further subjected to molecular docking in the active site of protein TgCDPK1, Lipinski's rule, and Swiss ADMET filter, which showed greater activity for all hydrazones <b>3-(a-c)</b>. Furthermore, these compounds were tested for their parasitological activity. The results revealed that the nanoformulation of synthesized hydrazones <b>3-(a*-c*)</b> had great activity against Toxoplasma infection compared to the synthesized hydrazone <b>3-(a-c)</b>. Moreover, in brain homogenates from mice infected with Toxoplasma, the nanoformulation <b>3c*</b> demonstrated a noteworthy (64%) decrease in the percentage of cyst burden, which is more effective compared to hydrazone <b>3c</b> (49%).

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Publication Details

Journal
ACS Omega
Published
2025-05-15
DOI
https://doi.org/10.1021/acsomega.4c10965
Citations
2
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
3.01

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article

Nanoformulations for Hydrazones; Synthesis, Characterization, Parasitology, and Histopathology Investigations

Esraa Abdelhamid Moneer, Ahmed S. Zakaria, Assem Barakat, Sherif Ramadan et al.
2 citations
ACS Omega
Computational Drug Discovery Methods
3.01
article

Nanoformulations for Hydrazones; Synthesis, Characterization, Parasitology, and Histopathology Investigations

Esraa Abdelhamid Moneer, Ahmed S. Zakaria, Assem Barakat, Sherif Ramadan, Saied M. Soliman, Mohamed Hagar, Hamida Abdel‐Hamid, Hanaa A. Rasheed, Eman M. Hassan, Ahmed R. Rabee
article en
2 citations

Abstract

In the creation of medicine delivery systems, nanotechnology has become an innovator, especially for organic compounds. The manipulation of materials at the nanoscale (1-100 nm) allows for unique physicochemical properties that can enhance the efficacy and bioavailability of therapeutic agents. The objective of the current research is to synthesize the hydrazones nanoparticles <b>3-(a*-c*)</b> which utilizes the ionic gelation method via chitosan as a matrix, and their size was measured via both scanning (SEM) and transmission (TEM) electronic microscopes. Interestingly, the formulated nanoparticles are found to be relatively stable, with a positive net charge and high entrapment efficiency up to 82.6%. The studied compounds were further subjected to molecular docking in the active site of protein TgCDPK1, Lipinski's rule, and Swiss ADMET filter, which showed greater activity for all hydrazones <b>3-(a-c)</b>. Furthermore, these compounds were tested for their parasitological activity. The results revealed that the nanoformulation of synthesized hydrazones <b>3-(a*-c*)</b> had great activity against Toxoplasma infection compared to the synthesized hydrazone <b>3-(a-c)</b>. Moreover, in brain homogenates from mice infected with Toxoplasma, the nanoformulation <b>3c*</b> demonstrated a noteworthy (64%) decrease in the percentage of cyst burden, which is more effective compared to hydrazone <b>3c</b> (49%).

ACS OmegaVol. 10(20)
Pharos University in Alexandria (EG), Benha University (EG), King Saud University (SA), Division of Chemistry (US), Alexandria University (EG), Michigan State University (US)
King Saud University, Science and Technology Development Fund
Openalex Percentile: Top 9%
Computational Drug Discovery Methods
3.01
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