Publications by authors named "O Abdullah"

Purpose of the study was to enhance the solubility of chlorthalidone, poorly soluble diuretic that has been the used for lowering high blood pressure for the past half-century. Solubility is a challenge for approximately 90% of drug candidates. Chlorthalidone is BCS Class IV drug whose poor solubility needs to be improved in order to optimize its efficacy.

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Article Synopsis
  • Enterovirus D68 (EV-D68) is linked to severe respiratory illness and acute flaccid myelitis (AFM), with 2022 showing increased infections but no rise in AFM cases unlike in 2018, which had a significant surge in AFM.
  • A study of 351 EV-D68 cases mainly involved children under 5, revealing that infections in 2018 led to more hospitalizations compared to 2022, and identified specific viral genomic changes associated with severe outcomes.
  • The findings emphasize the need for ongoing viral genomic surveillance to better understand the connections between genomic changes, immune responses, and the severity of diseases like AFM.
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Disulfiram (DSF), an irreversible aldehyde dehydrogenase 2 (ALDH2) inhibitor, is an U.S. Food and Drug Administration (FDA)-approved drug for the treatment of chronic alcoholism.

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Effervescent formulation helps in faster and better absorption of drugs, especially those that are rapidly soluble in water. However, these tablets require special packaging in order to prevent them from absorbing moisture, hence increasing cost. We compared an effervescent tablet prepared using an in-house developed method (multi-layer tablet with acid and base part separated by an inert layer) to a European effervescent tablet (Efferalgan®) in a single-center, randomized cross-over study among twelve healthy volunteers.

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Geldanamycin, an -macrolide composed of a rigid benzoquinone ring and an aliphatic -bridge, was isolated from . Geldanamycin is a potent heat shock protein inhibitor with remarkable antiproliferative activity. However, it shows pronounced hepatotoxicity in animal models and unfavorable pharmacokinetic properties.

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