Classification of Dyes by Chemical Structure
In pharmacology, the group of dyes is generally divided into three main categories based on their chemical structure:
- Triphenylmethane derivatives. This group includes the well-known brilliant green.
- Phenothiazine derivatives. The main representative is methylthioninium chloride, better known in medical practice as methylene blue.
- Acridine derivatives. Includes ethacridine lactate (rivanol).
Brilliant Green (*Viride nitens*)
This is a highly active antiseptic that exerts a pronounced bactericidal effect on Gram-positive bacteria. In addition, the drug possesses fungicidal activity against pathogenic fungi.
Main indications for use:
- Traumatic skin lesions: treatment of fresh cuts, abrasions, as well as post-traumatic and postoperative scars.
- Pyoderma (purulent-inflammatory diseases): treatment of furunculosis and carbunculosis.
- Neonatology: standard umbilical cord care in newborns.
- Ophthalmology: treatment of blepharitis and hordeolum (sty).
The drug is available in aqueous and alcoholic solutions, as well as convenient medical pencils. Brilliant green is actively used for impregnating antibacterial adhesive bandages and is an active component of corn liquids and Novikov's liquid.
Methylthioninium Chloride (Methylene Blue)
As an antiseptic, this drug is somewhat inferior to brilliant green. Its mechanism of action is based on direct interaction with microbial proteins and mucopolysaccharides. Alcoholic solutions are used topically for burns and pyodermas, while aqueous solutions are used locally and internally for flushing bladder and urethral infections.
Toxicological Properties and Antidote Role A unique feature of methylene blue is its ability to act as a hydrogen ion donor or acceptor in redox reactions. The effect strictly depends on the administered dose (given intravenously in a glucose solution):
- Low concentrations: the drug reduces methemoglobin back to normal hemoglobin. This property is used in treating methemoglobinemia caused by aniline or nitrite poisoning.
- High concentrations: the drug conversely oxidizes hemoglobin, converting it into methemoglobin. This is life-saving in cyanide (hydrocyanic acid) poisoning. The resulting methemoglobin tightly binds cyanides, forming a non-toxic complex—cyanmethemoglobin. High doses are also used for hydrogen sulfide and carbon monoxide (CO) intoxication.
Ethacridine Lactate (Rivanol)
The drug is active primarily against coccal flora, primarily streptococci. Its mechanism of action is also dose-dependent:
- At low concentrations it exhibits a certain selectivity, specifically inhibiting microbial cell enzyme activity.
- At high concentrations it causes total coagulation of microbial proteins.
Application in Surgery and Traumatology: Ethacridine lactate is widely used topically. As lotions and tampons, it is prescribed for treating purulent-inflammatory lesions of soft tissues and skin (furuncles, carbuncles, abscesses, phlegmons, infected wounds, and ulcers). Additionally, rivanol solutions are used for prophylactic and therapeutic flushing of cavities during purulent processes: peritoneal, pleural, joint, as well as the urinary bladder.