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首页> 外文期刊>Advances in Therapy >Besifloxacin Ophthalmic Suspension, 0.6%: a Novel Topical Fluoroquinolone for Bacterial Conjunctivitis
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Besifloxacin Ophthalmic Suspension, 0.6%: a Novel Topical Fluoroquinolone for Bacterial Conjunctivitis

机译:贝西沙星滴眼液,0.6%:一种用于细菌性结膜炎的新型局部用氟喹诺酮

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摘要

Acute bacterial conjunctivitis, the most common cause of conjunctivitis, is responsible for approximately 1% of all primary-care consultations. Of the topical ophthalmic antibiotics used to treat acute bacterial conjunctivitis, fluoroquinolones are especially useful because they possess a broad antibacterial spectrum, are bactericidal in action, are generally well tolerated, and have been less prone to development of bacterial resistance. Besifloxacin, the latest advanced fluoroquinolone approved for treating bacterial conjunctivitis, is the first fluoroquinolone developed specifically for topical ophthalmic use. It has a C-8 chlorine substituent and is known as a chloro-fluoroquinolone. Besifloxacin possesses relatively balanced dual-targeting activity against bacterial topoisomerase IV and DNA gyrase (topoisomerse II), two essential enzymes involved in bacterial DNA replication, leading to increased potency and decreased likelihood of bacterial resistance developing to besifloxacin. Microbiological data suggest a relatively high potency and rapid bactericidal activity for besifloxacin against common ocular pathogens, including bacteria resistant to other fluoroquinolones, especially resistant staphylococcal species. Randomized, double-masked, controlled clinical studies demonstrated the clinical efficacy of besifloxacin ophthalmic suspension 0.6% administered three-times daily for 5 days to be superior to the vehicle alone and similar to moxifloxacin ophthalmic solution 0.5% for bacterial conjunctivitis. In addition, besifloxacin ophthalmic suspension 0.6% administered two-times daily for 3 days was clinically more effective than the vehicle alone for bacterial conjunctivitis. Besifloxacin has also been shown in preclinical animal studies to be potentially effective for the “off-label” treatment of infections following ocular surgery, prophylaxis of endophthalmitis, and the treatment of bacterial keratitis. Taken together, clinical and preclinical animal studies indicate that besifloxacin is an important new option for the treatment of ocular infections.
机译:急性细菌性结膜炎是结膜炎的最常见原因,约占所有初级保健会诊的1%。在用于治疗急性细菌性结膜炎的局部眼用抗生素中,氟喹诺酮类药物特别有用,因为它们具有广谱的抗菌谱,具有杀菌作用,通常具有良好的耐受性,并且不易产生细菌耐药性。贝西沙星是批准用于治疗细菌性结膜炎的最新先进氟喹诺酮,是首款专门用于局部眼科用途的氟喹诺酮。它具有一个C-8氯取代基,被称为氯氟喹诺酮。贝西沙星对细菌拓扑异构酶IV和DNA促旋酶(拓扑异构酶II)(参与细菌DNA复制的两种必需酶)具有相对平衡的双重靶向活性,从而提高了药效,并降低了细菌对贝西沙星产生耐药性的可能性。微生物学数据表明,贝西沙星对常见的眼部病原体,包括对其他氟喹诺酮类耐药的细菌,特别是对葡萄球菌具有抗性的细菌,具有相对较高的效力和快速的杀菌活性。随机,双掩蔽,对照的临床研究表明,每天3次每天0.6%的贝西沙星眼用混悬液连续5天给药的临床疗效优于单独的赋形剂,类似于0.5%的莫西沙星眼用溶液对细菌性结膜炎的疗效。此外,对于细菌性结膜炎,每天两次连续3天服用0.6%的贝西沙星眼用混悬液,在临床上比单独的载体更有效。临床前动物研究还显示,贝西沙星对眼外科手术后感染的“非常规”治疗,预防眼内炎和细菌性角膜炎的治疗可能有效。综合起来,临床和临床前动物研究表明,贝西沙星是治疗眼部感染的重要新选择。

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