Lascufloxacin Hydrochloride is a novel fluoroquinolone antibiotic that has garnered significant attention in recent years for its effectiveness in treating a range of
bacterial infections. Marketed under the trade name "Lasvic", Lascufloxacin Hydrochloride targets bacterial DNA gyrase and
topoisomerase IV, both of which are essential enzymes for bacterial DNA replication and transcription. This drug has been the subject of extensive research by institutions worldwide, including Japan's
Kyorin Pharmaceutical Co., Ltd., which is at the forefront of its development. Lascufloxacin Hydrochloride is primarily indicated for the treatment of
respiratory tract infections, including
acute bacterial exacerbation of chronic bronchitis,
community-acquired pneumonia, and other bacterial infections. As of the latest updates, this drug has passed through various stages of clinical trials, showing promising results in terms of efficacy and safety.
The mechanism of action of Lascufloxacin Hydrochloride is similar to other fluoroquinolones but with some unique properties that make it a potent antimicrobial agent. It inhibits bacterial DNA gyrase and topoisomerase IV, enzymes that are vital for DNA replication, transcription, and repair. By binding to these enzymes, Lascufloxacin Hydrochloride induces the formation of double-stranded breaks in bacterial DNA, thereby inhibiting bacterial cell division and leading to cell death. This dual targeting mechanism enhances its antibacterial activity and reduces the likelihood of resistance development. Notably, this drug exhibits broad-spectrum activity against Gram-positive and Gram-negative bacteria, making it a versatile option for treating various infections.
Administering Lascufloxacin Hydrochloride is straightforward, with options for both oral and intravenous administration, depending on the severity of the
infection and patient needs. For oral administration, the typical dosage is 75 mg once daily, although the exact dosage may vary based on the infection being treated and the patient's medical condition. The drug is rapidly absorbed, with peak plasma concentrations achieved within one to two hours after oral administration. For intravenous use, the dosage is generally the same, but it allows for quicker delivery to the bloodstream, which can be crucial for
severe infections.
The onset of action for Lascufloxacin Hydrochloride is relatively fast, given its high bioavailability and rapid absorption. Most patients start to experience symptom relief within 24 to 48 hours of beginning treatment. However, the full course of the medication, usually lasting 7 to 14 days, must be completed to ensure the eradication of the infection and to prevent the development of antibiotic resistance.
Like all medications, Lascufloxacin Hydrochloride comes with potential side effects, although it is generally well-tolerated. Common side effects include gastrointestinal disturbances such as
nausea,
vomiting, and
diarrhea. Some patients may also experience
headaches,
dizziness, and
insomnia. Serious but rare side effects can include
tendonitis and
tendon rupture,
peripheral neuropathy, and central nervous system effects like
seizures and psychiatric symptoms. Due to these potential severe side effects, it is contraindicated in patients with a history of tendon disorders related to fluoroquinolone use, those with
myasthenia gravis, and individuals with known hypersensitivity to the drug.
Pregnant and breastfeeding women are advised against using Lascufloxacin Hydrochloride due to insufficient data on its safety in these populations. Additionally, caution is advised in elderly patients and those with
renal impairment, as dosage adjustments may be necessary to avoid toxicity.
Interaction with other drugs is a critical consideration when prescribing Lascufloxacin Hydrochloride. Concomitant use with antacids containing magnesium or aluminum, as well as supplements containing iron or zinc, can significantly reduce the absorption of Lascufloxacin Hydrochloride, thereby decreasing its efficacy. To avoid this, it is recommended that such products be taken at least two hours before or four hours after the antibiotic.
Nonsteroidal anti-inflammatory drugs (NSAIDs) may increase the risk of central nervous system stimulation and seizures when taken with Lascufloxacin Hydrochloride. This is a crucial interaction to monitor, especially in patients with a history of
seizure disorders. Additionally, the drug can prolong the QT interval, and its use with other medications that have the same effect (such as certain antiarrhythmics, antipsychotics, and antidepressants) should be carefully managed to avoid the risk of serious cardiac events.
In summary, Lascufloxacin Hydrochloride represents a significant advancement in the treatment of bacterial infections, offering a broad spectrum of activity and a rapid onset of action. While it is generally well-tolerated, healthcare providers must be mindful of its potential side effects and interactions with other medications. With ongoing research and clinical use, Lascufloxacin Hydrochloride is poised to become a valuable tool in the fight against bacterial infections, providing new hope for patients and clinicians alike.
How to obtain the latest development progress of all drugs?
In the Synapse database, you can stay updated on the latest research and development advances of all drugs. This service is accessible anytime and anywhere, with updates available daily or weekly. Use the "Set Alert" function to stay informed. Click on the image below to embark on a brand new journey of drug discovery!


