Saad S. M. Hassan

Saad S. M. Hassan


Research Focus & Metrics

Academic Career Length

30Years (1997-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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12 November 2015 in Advances in Natural Sciences: Nanoscience and Nanotechnology
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Journal Article
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SHSaad S. M. Hassan
Saad S. M. Hassan
WAWaleed I M El Azab
Waleed I M El Azab
HAHager R Ali
Hager R Ali
MMMona S M Mansour
Mona S M Mansour
Enhancement removal of tartrazine dye using HCl-doped polyaniline

21 September 2020 in RSC Advances
Verified
Journal Article
Open access
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AIA. M. Ismael
A. M. Ismael
AEAyat El-Shazly
Ayat El-Shazly
SGS. E. Gaber
S. E. Gaber
Mohamed M. RashadMohamed M. Rashad
Mohamed M. Rashad
Ayman H. KamelAyman H. Kamel
Ayman H. Kamel
SHSaad S. M. Hassan
Saad S. M. Hassan
A TiO2/GO/CuFe2O4 heterostructure photocatalyst is fabricated by a simple and low cost ball milling pathway for enhancing the photocatalytic degradation of chlorinated pesticides under UV light irradiation.

1 June 2006 in Analytica Chimica Acta
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Journal Article
Closed access
SHSaad S. M. Hassan
Saad S. M. Hassan
MHMohamed S.A. Hamza
Mohamed S.A. Hamza
Ayman H. KamelAyman H. Kamel
Ayman H. Kamel

1 June 2008 in Journal of Hazardous Materials
Verified
Journal Article
Closed access
SHSaad S. M. Hassan
Saad S. M. Hassan
NANasser S. Awwad
Nasser S. Awwad
AAAwaad H.A. Aboterika
Awaad H.A. Aboterika

27 October 2022 in Scientific Reports
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Journal Article
Open access
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HHHeba M. Hashem
Heba M. Hashem
AMAmira Motawea
Amira Motawea
AKAyman H. Kamel
Ayman H. Kamel
EBE. M. Abdel Bary
E. M. Abdel Bary
SHSaad S. M. Hassan
Saad S. M. Hassan
Recently, drug-controlled release nanotechnology has gained special attention in biomedicine. This work focuses on developing novel electrospun polymeric nanofibers (NFs) for buccal delivery of VEN to avoid the hepatic metabolism and enzymatic degradation in the GIT and develop an effective control of drug release. The optimized NFs were obtained by blending polylactic acid (PLA), and poly (ɛ-caprolactone) (PCL) fixed at a ratio of 1:1. It was characterized for morphology, drug-loading, FTIR, XRD, DSC, and in vitro drug release. Ex vivo permeability of the blend NFs was assessed using chicken pouch mucosa compared to VEN suspension, followed by histopathological examination. Further, the cytotoxic effect in three different cell lines using WST-1 assay. SEM morphologies refer to defect-free uniform NFs of PLA, PCL, and PLA/PCL mats. These fibers had a diameter ranging from 200 to 500 nm. The physico-thermal characterization of NFs depicted that the drug was successfully loaded and in an amorphous state in the PLA/PCL NFs. In vitro release of NFs substantiated a bi-phasic profile with an initial burst release of about 30% in the initial 0.5 h and a prolonged cumulative release pattern that reached 80% over 96 h following a non-Fickian diffusion mechanism. Ex vivo permeation emphasizes the major enhancement of the sustained drug release and the noticeable decrease in the permeability of the drug from NFs. Cytotoxicity data found that IC50 of VEN alone was 217.55 μg/mL, then VEN-NFs recorded an IC50 value of 250.62 μg/mL, and plain NFs showed the lowest toxicity and IC50 440.48 μg/mL in oral epithelial cells (OEC). Histopathology and cell toxicity studies demonstrated the preserved mucosal architecture and the preclinical safety. The developed PLA/PCL NFs can be promising drug carriers to introduce a step-change in improved psychiatric treatment healthcare.

1 March 2009 in Journal of Hazardous Materials
Verified
Journal Article
Closed access
SHSaad S. M. Hassan
Saad S. M. Hassan
NANasser S. Awwad
Nasser S. Awwad
AAAwaad H.A. Aboterika
Awaad H.A. Aboterika