Publications by authors named "Carlos Alonso-Moreno"

Article Synopsis
  • - The Tetrahedron approach is an innovative tool designed to evaluate the sustainability of human activities through a four-step process involving key parameter identification, evaluation, diagram construction, and global sustainability estimation.
  • - It considers multiple sustainability dimensions—economic, social, and environmental—and has been applied in five case studies related to carbon capture and various production processes.
  • - The Tetrahedron is shown to be effective and reliable for quantifying sustainability, offering a holistic, simple, and adaptable alternative to existing environmental assessment methods.
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Article Synopsis
  • The study focuses on the synthesis of five small molecules featuring a guanidine core through guanylation reactions, a key method in medicinal chemistry.
  • These compounds were tested against various strains of bacteria, including extended-spectrum beta-lactamase (ESBL) producers and methicillin-resistant Staphylococcus aureus (MRSA), using minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) tests.
  • Results indicate that these guanidine-core molecules show potential as new treatments for bacterial infections, especially against drug-resistant strains, suggesting further research is necessary to optimize their effectiveness.
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  • Colorectal cancer (CRC) is the third most prevalent cancer globally, and recent research highlights CDK12 as a promising target for therapy.
  • A new CDK12 inhibitor (CDK12-IN-E9, CDK12i) and its lipid-based formulation (LP-CDK12i) were tested on various CRC cell lines to evaluate their effectiveness in reducing cell growth and inducing cell death.
  • Results showed that the lipid formulation LP-CDK12i had a significantly greater effect on reducing cell proliferation and enhancing apoptosis compared to the free CDK12i, confirming the potential of targeting CDK12 in CRC treatment.
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The effective measurement of temperature in living systems at the nano and microscopic scales continues to be a challenge to this day. Here, we study the use of 2-(anthracen-2-yl)-1,3-diisopropylguanidine, 1, as a nanothermometer based on fluorescence lifetime measurements and its bioimaging applications. In aqueous solution, 1 is shown in aggregated form and the equilibrium between the two main aggregate types (T-shaped and π-π) is highly sensitive to the temperature.

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The modular synthesis of the heteroscorpionate core is explored as a tool for the rapid development of ruthenium-based therapeutic agents. Starting with a series of structurally diverse alcohol-NN ligands, a family of heteroscorpionate-based ruthenium derivatives was synthesized, characterized, and evaluated as an alternative to platinum therapy for breast cancer therapy. In vitro, the antitumoral activity of the novel derivatives was assessed in a series of breast cancer cell lines using UNICAM-1 and cisplatin as metallodrug control.

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Article Synopsis
  • The research developed a modular method to create guanidine compounds, which are being explored as potential anti-cancer drugs, using a catalyst called ZnEt.
  • A group of different phenyl-guanidines was synthesized efficiently, with one specific compound identified as the top candidate based on its promising antitumoral activity.
  • Various biological tests revealed that this lead compound induces cancer cell death, halts the cell cycle, and reduces cell adhesion and colony formation, highlighting its potential for cancer treatment.
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AIEgens have emerged as a promising alternative to molecular rotors in bioimaging applications. However, transferring the concept of aggregation-induced emission (AIE) from solution to living systems remains a challenge. Given the highly heterogeneous nature and the compartmentalization of the cell, different approaches are needed to control the self-assembly within the crowded intricate cellular environment.

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Background: Artificial insemination (AI) is a routine breeding technology in animal reproduction. Nevertheless, the temperature-sensitive nature and short fertile lifespan of ram sperm samples hamper its use in AI. In this sense, nanotechnology is an interesting tool to improve sperm protection due to the development of nanomaterials for AI, which could be used as delivery vehicles.

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Piperine (PIP), a compound found in , has shown promise as a potential chemotherapeutic agent for breast cancer. However, its inherent toxicity has limited its application. To overcome this challenge, researchers have developed PIP@MIL-100(Fe), an organic metal-organic framework (MOF) that encapsulates PIP for breast cancer treatment.

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is one of the species with the greatest clinical importance and greatest impact on public health. In fact, methicillin-resistant (MRSA) is considered a pandemic pathogen, being essential to develop effective medicines and combat its rapid spread. This study aimed to foster the translation of clinical research outcomes based on metallodrugs into clinical practice for the treatment of MRSA.

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Article Synopsis
  • The increasing global population and resource depletion necessitate the development of sustainable materials, particularly from biodegradable and renewable sources.
  • Researchers are exploring a "metal-free" copolymerization method to transform biomass-derived carvone into unique luminescent biopolymers.
  • The study found that the luminescence characteristics of these copolymers are affected by their structural folding and environment, making them highly sensitive to temperature changes, which could lead to applications in smart photothermal imaging technologies.
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The advent of nanotechnology in the field of animal reproduction has led to the development of safer and more efficient therapies. The use of nanotechnology allows us to avoid the detrimental effects of certain traditional antioxidants, such as Vitamin E. Its hydrophobic nature makes mandatory the use of organic solvents, which are toxic to sperm cells.

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BRCA1/2 protein-deficient or mutated cancers comprise a group of aggressive malignancies. Although PARPis have shown considerably efficacy in their treatment, the widespread use of these agents in clinical practice is restricted by various factors, including the development of acquired resistance due to the presence of compensatory pathways. BETis can completely disrupt the HR pathway by repressing the expression of BRCA1 and could be aimed at generation combination regimes to overcome PARPi resistance and enhance PARPi efficacy.

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The incessant developments in the pharmaceutical and biomedical fields, particularly, customised solutions for specific diseases with targeted therapeutic treatments, require the design of multicomponent materials with multifunctional capabilities. Biodegradable polymers offer a variety of tailored physicochemical properties minimising health adverse side effects at a low price and weight, which are ideal to design matrices for hybrid materials. PLAs emerge as an ideal candidate to develop novel materials as are endowed withcombined ambivalent performance parameters.

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A series of bionanocomposites composed of shark gelatin hydrogels and PLA nanoparticles featuring different nanostructures were designed to generate multifunctional drug delivery systems with tailored release rates required for personalized treatment approaches. The global conception of the systems was considered from the desired customization of the drug release while featuring the viscoelastic properties needed for their ease of storage and posterior local administration as well as their biocompatibility and cell growth capability for the successful administration at the biomolecular level. The hydrogel matrix offers the support to develop a direct thermal method to convert the typical kinetic trapped nanostructures afforded by the formulation method whilst avoiding the detrimental nanoparticle agglomeration that diminishes their therapeutic effect.

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Degradation of targeted proteins using proteolysis targeting chimeras (PROTACs) has gained momentum. A PROTAC is a bifunctional molecule that consists of three parts: a ligand that interacts with the protein to be degraded, another ligand that binds to an E3 ubiquitin ligase and a linker that connects both. Identification of the right proteins as targets to be degraded and a ligase that is highly expressed in tumors compare with normal tissue is mandatory, as can augment efficacy reducing toxicity.

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Article Synopsis
  • Classical cancer targeting typically focuses on creating chemical compounds that bind to proteins critical for tumor growth, particularly those with enzymatic activity like kinases.
  • Researchers are now exploring innovative strategies like PROTACs, which facilitate the degradation of both enzymatic and non-enzymatic oncogenic proteins, including transcription factors.
  • The article discusses the potential of PROTACs in solid tumor treatments while addressing challenges such as enhancing drug delivery, bioavailability, and ensuring safety in clinical applications.
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Objective: The purpose of this study was to evaluate the in vitro antibacterial effects of a Cymene-based bis(pyrazolyl)methane derivative (SC-19) to advance in developing alternative therapeutic compounds to fight against bacterial isolates from patients with otitis externa (OE).

Methods: Eighteen swab specimens were collected from patients aged over 18 years diagnosed with OE within at least 7 days of symptom onset, contaminated by only one bacterium type: ( = 5); ( = 8); ( = 2); ( = 1); ( = 2). To appraise antibacterial activity, minimal inhibitory concentration (MIC), minimal bactericidal concentration (MBC), minimum biofilm inhibitory concentration (MBIC), and minimum biofilm eradication concentration (MBEC) assays were run at different SC-19 concentrations.

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Stereo-diblock copolymers of high molecular weight polylactide (PLA) were synthetized by the one pot-sequential addition method assisted by a heteroscorpionate catalyst without the need of a co-initiator. The alkyl zinc organometallic heteroscorpionate derivative (Zn(Et)(κ-bpzteH)] (bpzteH = 2,2-bis(3,5-dimethylpyrazol-1-yl)-1-para-tolylethoxide) proved to assist in the mechanism of reaction following a coordination-insertion process. Kinetic studies along with the linear correlation between monomer and number average molecular weight (M) conversion, and the narrow polydispersities supported the truly living polymerization character of the initiator, whereas matrix-assisted laser desorption/Ionization-time of flight (MALDI-TOF) studies showed a very low order of transesterification.

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Oxidative stress has become a major concern in the field of spermatology, and one of the possible solutions to this acute problem would be the use of antioxidant protection; however, more studies are required in this field, as highly contradictory results regarding the addition of antioxidants have been obtained. Vitamin E is a powerful biological antioxidant, but its low stability and high hydrophobicity limit its application in spermatology, making the use of organic solvents necessary, which renders spermatozoa practically motionless. Keeping this in mind, we propose the use of hydrogels (HVEs) and nanoemulsions (NVEs), alone or in combination, as carriers for the controlled release of vitamin E, thus, improving its solubility and stability and preventing oxidative stress in sperm cells.

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Article Synopsis
  • Platinum compounds are important treatments for solid tumors but have limitations like long-term side effects and resistance issues.
  • Researchers propose organometallic ruthenium(II) compounds as safer and more effective alternatives due to their better toxicity profile and potential for optimized drug design.
  • The study details the modification of ruthenium compounds for breast cancer treatment, focusing on their synthesis, stability, cytotoxicity, and mechanism of action, which could lead to new therapies.
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Background: Sarcomas comprise a group of aggressive malignancies with very little treatment options beyond standard chemotherapy. Reposition of approved drugs represents an attractive approach to identify effective therapeutic compounds. One example is mithramycin (MTM), a natural antibiotic which has demonstrated a strong antitumour activity in several tumour types, including sarcomas.

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Quantitative analysis of sulfate anions in water still remains an important challenge for the society. Among all the methodologies, the most successful one is based on optical supramolecular receptors because the presence of small concentrations of sulfate anion modifies the photophysical properties of the receptor. In this case, fluorescence anion sensors have been designed by the incorporation of guanidine motifs into fluorenyl cores.

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This study was designed to propose alternative therapeutic compounds to fight against bacterial pathogens. Thus, a library of nitrogen-based compounds bis(triazolyl)methane (1T-7T) and bis(pyrazolyl)methane (1P-11P) was synthesised following previously reported methodologies and their antibacterial activity was tested using the collection strains of Staphylococcus aureus, Enterococcus faecalis, Escherichia coli, and Pseudomonas aeruginosa. Moreover, the novel compound 2P was fully characterized by IR, UV-Vis and NMR spectroscopy.

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Article Synopsis
  • Many therapeutic agents fail in clinical development due to toxic effects on healthy tissues, prompting the use of nanotechnology to improve drug delivery.
  • Biodegradable and biocompatible polymers are highlighted as effective materials for creating polymeric nanoparticles, which enhance drug targeting and circulation time.
  • The text discusses various applications of polymeric nanoparticles in cancer treatment, covering their materials, formulation methods, mechanisms, and ongoing clinical research.
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