Publications by authors named "Al-Bogami A"

The emergence of poses a significant global health threat due to its high mortality rates and multidrug resistance. The development of new antifungal drugs is essential to effectively combat this pathogen. Antimicrobial peptides, such as Dermaseptin, have demonstrated potent anti- activity.

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Changes in the neurotransmitters are indications for several diseases. Several sensors were reported for monitoring dopamine (DA), but the simple and accurate DA detection in biological samples still faces many challenges. The research proposal aims to develop an optical sensor for detecting neurotransmitters based on luminescence emission spectra in different biological samples.

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In impoverished nations, the COVID-19 pandemic has led to a widespread occurrence of deadly fungal diseases like mucormycosis. The limited availability of effective antifungal treatments and the emergence of drug-resistant fungal strains further exacerbate the situation. Factors such as systemic steroid use, intravenous drug misuse, and overutilization of broad-spectrum antimicrobials contribute to the prevalence of hospital-acquired infections caused by drug-resistant fungi.

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Article Synopsis
  • The Raman technique, particularly using surface-enhanced Raman scattering (SERS) with noble metal nanostructures, offers high sensitivity and ease of use for detecting pyocyanin without requiring sample preparation.
  • The study focuses on the use of anodic aluminum oxide (AAO) as a substrate with controlled roughness to enhance Raman signals, achieving a sensitive detection limit of 96 nM for pyocyanin concentrations.
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, a recent addition to the species, poses a significant threat with its association to numerous hospital outbreaks globally, particularly affecting immunocompromised individuals. Given its resistance to existing antifungal therapies, there is a pressing need for innovative treatments. In this study, novel triazole bridged quinoline derivatives were synthesized and evaluated for their antifungal activity against .

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Heteroleptic metal complexes containing Cu, Co, and Zn, incorporating curcumin and a Schiff base ligand (L), were synthesized and characterized, and their antifungal activity was evaluated. Their antifungal activities were investigated individually and in combination with fluconazole. Utilizing various analytical techniques such as UV-Vis, FT-IR, NMR, ESI-MS, TGA-DTG, elemental analyses, conductance, and magnetic susceptibility measurements, complex C1 ([Cu(Cur)LCl(HO)]) was assigned a distorted octahedral geometry, while complexes C2 ([Co(Cur)LCl(HO)]) and C3 ([Zn(Cur)LCl(HO)]) were assigned octahedral geometries.

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Palladium and platinum complexes, especially those that include cisplatin, can be useful chemotherapeutic drugs. Alternatives that have less adverse effects and require lower dosages of treatment could be provided by complexes containing pyridine bases. The complexes [Pd(SCN)(4-Acpy)] (1), [Pd(N)(4-Acpy)] (2) [Pd(paOH)].

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Cancer poses a formidable challenge, necessitating improved treatment strategies. Metal-based drugs and nanotechnology offer new hope in this battle. Versatile gold complexes and functionalized gold nanoparticles exhibit unique properties like biologically inert behaviour, outstanding light absorption, and heat-conversion abilities.

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Article Synopsis
  • Candida auris is a fungi causing serious infections in humans, known for its resistance to common antifungal treatments, leading to outbreaks in healthcare settings.
  • Researchers synthesized and tested various eugenol tosylate congeners (ETCs) to find an effective antifungal, identifying C5 as the most potent compound against C. auris with a minimal inhibitory concentration (MIC) of 0.98 g/mL.
  • C5 not only showed strong antifungal activity but also induced cell death in Candida auris through apoptotic mechanisms, while exhibiting low toxicity, suggesting it could be a safe option for future treatments—but further animal studies are necessary to support these findings.
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Although Candida auris was only identified in the year 2009, it has rapidly spread in more than a dozen countries and is proving more deadly and notorious. In our previous studies, we reported on the tremendous antifungal potential of a series of cinnamaldehyde based azole derivatives against fluconazole susceptible and resistant clinical isolates of Candida albicans and identified a promising lead molecule (6f). In this study, the effect of this compound on the viability and physiology of cell death in C.

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Coordination compounds from simple transition metals are robust substitutes for platinum-based complexes due to their remarkable anticancer properties. In a quest to find new metal complexes that could substitute or augment the platinum based chemotherapy we synthesized three transition metal complexes C1-C3 with Cu(ii), Ni(ii), and Co(ii) as the central metal ions, respectively, and evaluated them for their anticancer activity against the human keratinocyte (HaCaT) cell line and human cervical cancer (HeLa) cell lines. These complexes showed different activity profiles with the square planar copper complex C1 being the most active with IC values lower than those of the widely used anticancer drug cisplatin.

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Population of drug-resistant bacteria have increased at an alarming rate in the past few decades. The major reason for increasing drug resistance is the lack of new antibiotics and limited drug targets. It has therefore been a vital task to develop new antibiotics with different drug targets.

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For combating life-threatening infections caused by Candida albicans there is an urgent requirement of new antifungal agents with a targeted activity and low host cytotoxicity. Manipulating the mechanistic basis of cell death decision in yeast may provide an alternative approach for future antifungal therapeutics. Herein, the effect of an active citral derivative (Cd1) over the physiology of cell death in C.

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Article Synopsis
  • There is a growing urgency for effective COVID-19 biosensors as infections rise, pushing the need for methods that are fast, simple, and accurate.
  • A gold microcuboid pattern was utilized in an electrochemical biosensor to detect the COVID-19 S protein, achieving detection limits down to 276 fmol/L.
  • The biosensor successfully identified COVID-19 from a nasal swab sample, with results corroborated by the PCR technique, demonstrating high sensitivity and efficiency.
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Here, we reported the synthesis of reduced porous graphene oxide (rPGO) decorated with gold nanoparticles (Au NPs) to modify the ITO electrode. Then we used this highly uniform Au NPs@rPGO modified ITO electrode as a surface-enhanced Raman spectroscopy-active surface and a working electrode. The uses of the Au nanoparticles and porous graphene enhance the Raman signals and the electrochemical conductivity.

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The fungal pathogen , is a serious threat to public health and is associated with bloodstream infections causing high mortality particularly in patients with serious medical problems. As this pathogen is generally resistant to all the available classes of antifungals, there is a constant demand for novel antifungal drugs with new mechanisms of antifungal action. Therefore, in this study we synthesised six novel piperidine based 1,2,3-triazolylacetamide derivatives (pta1-pta6) and tested their antifungal activity and mechanism of action against clinical isolates.

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With an upsurge in multidrug resistant bacteria backed by biofilm defence armours, there is a desperate need of new antibiotics with a non-traditional mechanism of action. Targeting bacteria by misguiding them or halting their communication is a new approach that could offer a new way to combat the multidrug resistance problem. Quorum sensing is considered to be the achilles heel of bacteria that has a lot to offer.

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Opportunistic fungal pathogens including are responsible for the alarming rise in hospital acquired infections and millions of deaths worldwide. The current treatment modalities are not enough to handle this situation, and therefore, new treatment modalities and strategies are desperately needed. In this direction, we synthesized a series of azole based acetohydrazide derivatives of cinnamaldehyde and subjected it to antifungal activity evaluation.

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Though abundant studies have targeted the sorption of Cr(VI) and As(V) anions by organic polymers or magnetic metal oxides, there is no research literature on the sorption characteristics of Cr(VI) and As(V) by thiourea-formaldehyde resin (TF) and its magnetic derivative (MTF). TF resin is a strong chelating agent, which has several practical applications. This paper reports on the removal of Cr(VI) and As(V) oxoanions by TF and MTF sorbents.

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Development of new chemotherapeutic agents to treat microbial infections and recurrent cancers is of pivotal importance. Metal based drugs particularly ruthenium complexes have the uniqueness and desired properties that make them suitable candidates for the search of potential chemotherapeutic agents. In this study, two mixed ligand Ru(III) complexes [Ru(Cl)(SB)(Phen] (RC-1) and [Ru(Cl)(SB)(Bipy)] (RC-2) were synthesised and characterized by elemental analysis, IR, UV-Vis, H, C NMR spectroscopic techniques and their molecular structure was confirmed by X-ray crystallography.

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The occurrence of invasive fungal diseases, particularly in immunocompromised patients, is life-threatening and increases the economic burden. The rising problem of multi-drug resistance is becoming a major concern for clinicians. In addition, a repertoire of antifungal agents is far less in number than antibacterial drugs.

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Background: The prevalence of obesity and vitamin D deficiency in Saudi Arabia has increased recently. Decreased physical activity might play a role in obesity. Previous studies showed an association between low vitamin D level and its receptor polymorphism with obesity development.

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The immobilization of Mo(VI) on magnetic poly p-phenylenediamine-thiourea-formaldehyde composite polymer (MpPDTF) (through an intermediary adsorption step) increased sorption of As(V) ions: retention capacity increased from 35.15mg As g for MpPDTF to 99.04mg As g for MpPDTF immobilized Mo(VI) at 298±1K.

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The atom-efficient and green protocol for formation of pyrano[3,4-e][1,3]oxazines utilizing dimethyl carbonate under ultrasound irradiation in a presence of KF/basic alumina was reported. We provide a novel series of pyrano[3,4-e][1,3]oxazine derivatives interesting for biological screening tests. In general, it was found that ultrasound irradiations enable the reactions to occur which could not be carried out under silent conditions.

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Research on sodium batteries has made a comeback because of concern regarding the limited resources and cost of lithium for Li-ion batteries. From the standpoint of electrochemistry and economics, Mn- or Fe-based layered transition metal oxides should be the most suitable cathode candidates for affordable sodium batteries. Herein, this paper reports a novel cathode material, layered Na1+x(Fey/2Niy/2Mn1-y)1-xO2 (x = 0.

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