Matsumoto Tetsuya
Department of Microbiology, Tokyo Medical University, Tokyo, Japan.
Clin Pharmacol. 2014 Sep 26;6:139-48. doi: 10.2147/CPAA.S44377. eCollection 2014.
Arbekacin sulfate (ABK), an aminoglycoside antibiotic, was discovered in 1972 and was derived from dibekacin to stabilize many common aminoglycoside modifying enzymes. ABK shows broad antimicrobial activities against not only Gram-positive bacteria including methicillin-resistant Staphylococcus aureus (MRSA) but also Gram-negative bacteria such as Escherichia coli, Pseudomonas aeruginosa, and Klebsiella pneumoniae. ABK has been approved as an injectable formulation in Japan since 1990, under the trade name Habekacin, for the treatment of patients with pneumonia and sepsis caused by MRSA. The drug has been used in more than 250,000 patients, and its clinical benefit and safety have been proven over two decades. ABK currently shows promise for the application for the treatment of multidrug-resistant Gram-negative bacterial infections such as multidrug-resistant strains of P. aeruginosa and Acinetobacter baumannii because of its synergistic effect in combination with beta-lactams.
硫酸阿贝卡星(ABK)是一种氨基糖苷类抗生素,于1972年被发现,由双去氧卡那霉素B衍生而来,可抑制多种常见的氨基糖苷类修饰酶。ABK不仅对包括耐甲氧西林金黄色葡萄球菌(MRSA)在内的革兰氏阳性菌具有广泛的抗菌活性,而且对大肠杆菌、铜绿假单胞菌和肺炎克雷伯菌等革兰氏阴性菌也有抗菌活性。自1990年以来,ABK在日本已被批准作为注射剂使用,商品名为Habekacin,用于治疗由MRSA引起的肺炎和败血症患者。该药物已在超过25万名患者中使用,其临床疗效和安全性在二十多年来已得到证实。由于ABK与β-内酰胺类药物联合使用具有协同作用,目前它在治疗多重耐药革兰氏阴性菌感染(如多重耐药铜绿假单胞菌和鲍曼不动杆菌菌株)方面显示出应用前景。