What is Lomefloxacin used for?

15 June 2024
Lomefloxacin is a synthetic broad-spectrum antibiotic belonging to the fluoroquinolone class. It is marketed under several trade names, including Maxaquin, Okacyn, and Dekloflox. The drug primarily targets bacterial DNA gyrase and topoisomerase IV, enzymes crucial for DNA replication and transcription. Lomefloxacin was first developed in the late 1980s and has since been extensively researched by various pharmaceutical companies and academic institutions. It is indicated for the treatment of infections such as urinary tract infections (UTIs), bronchitis, and certain types of skin infections. Research has shown it to be effective against a broad range of Gram-negative and some Gram-positive bacteria. However, its usage has decreased over the years due to the development of newer fluoroquinolones with improved safety profiles and broader antimicrobial activity.

Lomefloxacin Mechanism of Action

Lomefloxacin functions by inhibiting bacterial DNA gyrase and topoisomerase IV, enzymes that play a pivotal role in DNA replication, recombination, and repair. DNA gyrase introduces negative supercoils into DNA using energy from ATP hydrolysis, which is essential for DNA condensation and efficient replication. By binding to the DNA-enzyme complex, lomefloxacin stabilizes the complex and prevents the ligation step of the DNA replication process, thus inducing breaks in the double-stranded DNA. This results in the inhibition of bacterial cell division and ultimately leads to cell death. Unlike human cells, bacterial cells rely heavily on these enzymes for their replication machinery, making them an excellent target for antibiotics like lomefloxacin.

How to Use Lomefloxacin

Lomefloxacin is usually administered orally in the form of tablets. The typical dosage for adults ranges from 400 mg once daily, depending on the type and severity of the infection being treated. For instance, uncomplicated urinary tract infections may require a shorter treatment duration compared to chronic bronchitis. It is advised to take the medication at the same time each day to maintain an even level in the bloodstream. The onset of action is relatively fast, with peak plasma concentrations achieved within 1 to 2 hours post-ingestion.

It is crucial to complete the entire prescribed course, even if symptoms improve before the medication is finished, to prevent the development of antibiotic-resistant bacteria. The tablets should be swallowed whole with a full glass of water and can be taken with or without food. However, it is advisable to avoid dairy products or calcium-fortified juices within two hours before or after taking the medication, as these can interfere with its absorption.

What is Lomefloxacin Side Effects

Like all medications, lomefloxacin comes with a spectrum of potential side effects. Common side effects include gastrointestinal issues such as nausea, diarrhea, and abdominal pain. Central nervous system side effects can also occur, including dizziness, headache, and insomnia. Skin reactions such as rash and photosensitivity are relatively rare but can be severe, requiring immediate medical attention.

Serious but less common side effects include tendonitis and tendon rupture, particularly in the elderly or those who are on concomitant corticosteroid therapy. Peripheral neuropathy, which manifests as tingling or numbness in the limbs, is another serious side effect that warrants discontinuation of the drug.

Lomefloxacin is contraindicated in individuals with a known hypersensitivity to fluoroquinolones. It should also be used with caution in patients with a history of seizure disorders, as it can lower the seizure threshold. Pregnant and breastfeeding women should avoid using this drug due to the potential for adverse effects on the developing fetus and newborn.

What Other Drugs Will Affect Lomefloxacin

Lomefloxacin can interact with a variety of other medications, affecting its efficacy and safety. Co-administration with antacids containing aluminum or magnesium, as well as supplements containing iron or zinc, can significantly reduce the absorption of lomefloxacin. Therefore, it is recommended to take these substances at least two hours before or after lomefloxacin.

Non-steroidal anti-inflammatory drugs (NSAIDs) can increase the risk of CNS stimulation and seizures when taken in conjunction with lomefloxacin. Drugs such as theophylline and caffeine can also have elevated serum concentrations due to the inhibited metabolism by lomefloxacin, leading to potential toxicity.

Patients on anticoagulant therapy with warfarin may experience an increased risk of bleeding, necessitating close monitoring of their coagulation parameters. Additionally, drugs that prolong the QT interval, such as certain antiarrhythmics and antipsychotics, should be used with caution as they can exacerbate this effect when taken with lomefloxacin.

In conclusion, while lomefloxacin is a potent antibiotic effective against a variety of bacterial infections, its use must be carefully managed to minimize risks and interactions. Always consult healthcare providers for personalized advice and conduct thorough monitoring when lomefloxacin is part of the therapeutic regimen.

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