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Therapeutic Drug Monitoring: Drug Analysis Methods01:26

Therapeutic Drug Monitoring: Drug Analysis Methods

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Therapeutic Drug Monitoring (TDM) is a clinical practice that measures specific drug levels in a patient's blood or body tissues to tailor drug therapy effectively. This monitoring is critical for managing drugs with narrow therapeutic indices like digoxin and phenytoin, ensuring they are both safe and effective. For instance, monitoring theophylline levels in asthma patients involves precision and sensitivity to adjust doses according to individual responses to therapy, ensuring efficacy and...
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Therapeutic Drug Monitoring: Affecting Factors01:29

Therapeutic Drug Monitoring: Affecting Factors

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Therapeutic Drug Monitoring (TDM) is the clinical practice of measuring specific drug levels in a patient's blood or body tissues to manage and optimize therapy. TDM is crucial for drugs with narrow therapeutic windows, like warfarin and phenytoin, where incorrect doses can lead to treatment failure or severe side effects. This monitoring ensures the dosage administered is within a safe and effective range. The factors affecting therapeutic drug monitoring include:Patient-Specific Factors:a.
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Therapeutic Drug Monitoring: Overview and Classification01:16

Therapeutic Drug Monitoring: Overview and Classification

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Therapeutic Drug Monitoring (TDM) is a clinical practice that measures specific drug levels in a patient's blood at designated intervals to ensure the drug concentration stays within a therapeutic range. This monitoring is crucial for optimizing individual dosage regimens, enhancing therapeutic efficacy, and minimizing drug-related toxicity. TDM is vital for drugs with narrow therapeutic windows, significant variability in pharmacokinetics, and a clear correlation between plasma levels and...
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ABC Transporters: Exporter01:31

ABC Transporters: Exporter

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ATP-binding cassette or ABC transporter is the largest superfamily of integral membrane proteins. The transporters have transmembrane-binding domains (TMDs) and nucleotide-binding domains (NBDs). The TMDs are specific to their substrates, whereas the NBDs are similar to engines that complete ATP hydrolysis to complete the substrate transport. They can be full transporters consisting of two TMDs and NBDs, half transporters with one TMD and NBD, while some encoded with a single TMD or NBD are...
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Antidepressant Drugs: MAOIs and Other Agents01:23

Antidepressant Drugs: MAOIs and Other Agents

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Atypical antidepressants, including bupropion (Wellbutrin), mirtazapine (Remeron), nefazodone (Serzone), trazodone (Desyrel), and vilazodone (Viibryd), offer unique mechanisms of action. Bupropion weakly inhibits dopamine and norepinephrine reuptake, aiding depression treatment and smoking cessation, with a low risk of sexual dysfunction. Mirtazapine enhances serotonin and norepinephrine neurotransmission, leading to sedation, increased appetite, and weight gain. As a result, it helps treat...
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SnapShot: Las drogas antipalúdicas

Madeline R Luth1, Elizabeth A Winzeler2

  • 1Department of Pediatrics, University of California, San Diego, La Jolla, CA 92093, USA.

Cell
|October 16, 2020
PubMed
Resumen
Este resumen es generado por máquina.

La malaria, una enfermedad causada por el parásito Plasmodium, se enfrenta a los desafíos de la resistencia a los medicamentos. Esta revisión detalla cómo los medicamentos antimaláricos actuales y nuevos se dirigen al parásito

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Área de la Ciencia:

  • Parasitología
  • Enfermedades infecciosas
  • Descubrimiento de drogas

Sus antecedentes:

  • La malaria es una enfermedad transmitida por vectores causada por parásitos Plasmodium.
  • La resistencia a los medicamentos en Plasmodium falciparum complica las intervenciones terapéuticas y los esfuerzos de erradicación.

Objetivo del estudio:

  • Para resumir las etapas relevantes para el hombre del ciclo de vida de P. falciparum.
  • Describir cómo los compuestos antipalúdicos se dirigen a diferentes etapas del ciclo de vida.

Principales métodos:

  • Revisión de los antipalúdicos autorizados.
  • Análisis de los candidatos clínicos.
  • Examen de los nuevos compuestos antimaláricos.

Principales resultados:

  • Los medicamentos autorizados, los candidatos clínicos y los compuestos novedosos se dirigen a varias etapas del ciclo de vida de P. falciparum.
  • Comprender los objetivos de los medicamentos a lo largo del ciclo de vida es crucial para el control de la malaria.

Conclusiones:

  • Apuntar a etapas específicas del ciclo de vida de P. falciparum con diversos compuestos antimaláricos es esencial para prevenir, tratar y bloquear la transmisión de la malaria.
  • La lucha contra la resistencia a los medicamentos requiere el desarrollo continuo de nuevas estrategias antimaláricas.