Publications by authors named "Nabil A Shoman"

This research investigates the formulation of a nanogel complex using pectin and poly(acrylic acid) (PAAc) to encapsulate rutin. The nanogel's pH-responsive behavior and its potential as a targeted drug delivery platform are investigated. The gamma irradiation-induced crosslinking mechanism is elucidated, highlighting its role in creating a stable three-dimensional network structure within the polymer matrix.

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Article Synopsis
  • As of July 2024, there were over 775 million confirmed COVID-19 cases and more than 7 million deaths globally, despite over 13.5 billion vaccine doses administered.
  • The relationship between vitamin D levels and COVID-19 severity is significant, with vitamin D deficiency linked to worse outcomes and immune dysfunction in severely ill patients.
  • Research highlights the potential therapeutic role of vitamin D in enhancing the efficacy of antiviral treatments, but conclusive evidence is still lacking, necessitating large-scale randomized trials for clearer insights.
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This paper presents an extensive analysis of COVID-19 with a specific focus on VEGFR-2 inhibitors as potential treatments. The investigation includes an overview of computational methodologies employed in drug repurposing and highlights research aimed at developing treatments for SARS-CoV-2. The study explores the possible effects of twenty-eight established VEGFR-2 inhibitors, which include amide and urea linkers, against SARS-CoV-2.

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In this study, a new gastro-floating sustained-release tablet (GFT) with a combination of Etoricoxib (ET) and Famotidine (FM) was successfully developed. GFTs were prepared by using a combination of hydrophilic swellable natural/semi-synthetic polymers as a controlled-release layer. Through a 2 full factorial statistical experimental design, the effects of formulation factors on the release of GFTs were conducted.

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Article Synopsis
  • - This study developed a floating raft system to deliver etoricoxib (ETO) and famotidine (FAM) using polysaccharides like glucomannan, focusing on factors like gelation and release time.
  • - The optimal formulation included specific percentages of ingredients, resulting in fast gelation and floating times while allowing controlled drug release over 8 hours.
  • - X-ray studies confirmed the raft's buoyancy for about 8 hours and showed that this new system had better bioavailability compared to existing products, indicating effective dual drug delivery.
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A PEGylated Tween 80-functionalized chitosan-lipidic (PEG-T-Chito-Lip) nano-vesicular hybrid was developed for intranasal administration as an alternative delivery route to help improve the poor oral bioavailability of BCS class-III model/antiemetic (metoclopramide hydrochloride; MTC). The influence of varying levels of chitosan, cholesterol, PEG 600, and Tween 80 on the stability/release parameters of the formulated nanovesicles was optimized using Draper-Lin Design. Two optimized formulations (Opti-Max and Opti-Min) with both maximized and minimized MTC-release goals, were predicted, characterized, and proved their vesicular outline light/electron microscopy, along with the mutual prompt/extended release patterns.

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To design and evaluate hyaluronan-based cubosomes loaded with bromfenac sodium (BS) for ocular application to enhance the corneal permeation and retention in pterygium and cataract treatment. BS-loaded cubosomes were prepared by the emulsification method, employing 2 full factorial design using Design-Expert® software. Glycerol monoolein (GMO) and poloxamer 407 (P407) as lipid phase and polyvinyl alcohol (PVA) as stabilizer were the used ingredients.

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The aim of this study was to formulate, evaluate, and compare satiety-enhancing floating raft system (FRS) of bupropion as gastroretentive drug delivery systems (GRDDS) using in-situ gelling pectin and alginate. Bupropion was considered as a good candidate for such systems due to high water solubility that requires frequent dosing. Pectin and alginate could prolong satiety sensation augmenting weight loss of bupropion.

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Purpose: Bupropion is an antidepressant drug that facilitates weight loss. It is a highly water-soluble drug that needs multiple dosing, so it is considered a potential candidate for oral controlled-release dosage form. The aim of this research was to formulate and evaluate satiety-inducing swellable floating bupropion tablets by direct compression targeting depression associated with eating disorders.

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