Proguanil

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(Redirected from Chloroguanide)

Proguanil structure
Proguanil SF

Proguanil, commonly recognized under the names chlorguanide and chloroguanide, is primarily utilized as a prophylactic agent against malaria. Commercially distributed under the brand name Paludrine by AstraZeneca, Proguanil has been pivotal in malaria prevention, particularly among vulnerable groups, such as children with sickle cell disease residing in regions where malaria is endemic.

Pharmacodynamics[edit | edit source]

Upon ingestion, Proguanil undergoes biotransformation to generate its active derivative, cycloguanil. This metabolite is specifically potent against the malarial parasite sporozoites, disrupting their life cycle and inhibiting infection progression.

Medical Uses[edit | edit source]

Historically, Proguanil is administered in tandem with other antimalarial agents to enhance its efficacy. Some commonly used combinations include:

  • Proguanil and Atovaquone: This combination, branded as Malarone by GlaxoSmithKline, is preferred for treating infections by chloroquine-resistant and multidrug-resistant strains of Plasmodium falciparum and Plasmodium vivax. Malarone is generally well-tolerated, exhibiting fewer side effects than alternatives like mefloquine. However, its daily dosing schedule might render it a pricier choice.
  • Proguanil and Chloroquine: Another frequently used combination in malarial prophylaxis.

Precautions[edit | edit source]

While Proguanil is typically safe for consumption, extended use spanning several months might occasionally lead to subtle psychological effects, including heightened feelings of melancholy and anxiety. It's crucial for users to remain vigilant to any changes in mood or behavior, even if they manifest slowly or ambiguously.

Mechanism of Action[edit | edit source]

Proguanil exerts its antimalarial activity by targeting the malarial parasites Plasmodium falciparum and Plasmodium vivax residing within the red blood cells.

It achieves this by inhibiting the enzyme dihydrofolate reductase. This enzyme plays a crucial role in the synthesis of tetrahydrofolate, an essential compound that facilitates the synthesis of purine bases and dTMP in the body.

Recognition[edit | edit source]

Signifying its importance in global health, Proguanil has secured a place on the World Health Organization's List of Essential Medicines, which enumerates the quintessential medications indispensable for a foundational health infrastructure.

See Also[edit | edit source]

Proguanil Resources
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