Comparison Between Moxifloxacin and Chloramphenicol for the Treatment of Bacterial Eye Infections

IF 1.6 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Current Therapeutic Research-clinical and Experimental Pub Date : 2024-01-01 DOI:10.1016/j.curtheres.2024.100740
Valentina Gentili PhD , Giovanni Strazzabosco MS , Rossella Spena MD , Sabrina Rizzo MS , Silvia Beltrami MS , Giovanna Schiuma MS , Andrea Alogna MS , Roberta Rizzo PhD
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Abstract

Background

Moxifloxacin is a bactericidal methoxyquinolone used for the treatment of conjunctivitis and prophylactic therapy in cataract and refractive surgeries. Chloramphenicol is a bacteriostatic organochlorine introduced into clinical practice in 1948 and used mainly in topical preparations because of its known toxicity.

Objectives

The study aimed to evaluate the in vitro antibacterial effect and the ocular cytotoxicity of these broad-spectrum antibiotics.

Methods

Antimicrobic activity was tested on 4 bacteria strains (Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, and Staphylococcus epidermidis), and determined through calculation of MIC and half inhibitory concentration for each microorganism. Antibacterial activity was determined by microdilution method after 24 hours’ incubation with 2-fold serial dilutions (2.5 mg/mL to 4.883 µg/mL) of moxifloxacin and chloramphenicol. Disk diffusion test were performed according to European Committee on Antimicrobial Susceptibility Testing methodology. Biofilm formation inhibition and biofilm eradication concentration assay were conducted for P aeruginosa and S epidermidis using the microdilution method. Cytotoxicity of antibiotics was evaluated by MTT (3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromide) colorimetric assay on human corneal cell.

Results

Cytotoxicity of antibiotics was evaluated on human epithelial corneal cells after 4 hours treatment by viability assay. Results showed that corneal cell viability was significantly higher after moxifloxacin treatment compared with chloramphenicol (P < 0.01). Moxifloxacin is characterized by a significantly lower MIC and half inhibitory concentration values and a larger inhibition zone for all the strain tested, with high performance in controlling gram-negative growth, compared with chloramphenicol. Moreover, moxifloxacin showed higher activity compared with chloramphenicol in the inhibition of biofilm formation and in the disruption of biofilm, especially against S epidermidis biofilm.

Conclusions

The lower corneal cell toxicity and the broader spectrum of antibacterial activity observed with moxifloxacin suggests its use in ophthalmic solution for the treatment of bacterial eye infections.

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莫西沙星与氯霉素治疗眼部细菌感染的比较
背景莫西沙星是一种杀菌甲氧基喹诺酮,用于治疗结膜炎以及白内障和屈光手术的预防性治疗。氯霉素是一种具有抑菌作用的有机氯,于 1948 年引入临床,由于其已知的毒性,主要用于局部制剂。方法对 4 种菌株(大肠杆菌、铜绿假单胞菌、金黄色葡萄球菌和表皮葡萄球菌)进行抗菌活性测试,并通过计算每种微生物的 MIC 和半数抑制浓度来确定抗菌活性。用莫西沙星和氯霉素的 2 倍序列稀释液(2.5 毫克/毫升至 4.883 微克/毫升)培养 24 小时后,采用微量稀释法测定抗菌活性。根据欧洲抗菌药物敏感性测试委员会的方法进行了盘扩散测试。采用微量稀释法对铜绿假单胞菌和表皮葡萄球菌进行了生物膜形成抑制和生物膜根除浓度检测。用 MTT(3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide)比色法评估抗生素对人类角膜细胞的细胞毒性。结果表明,与氯霉素相比,莫西沙星处理后的角膜细胞存活率明显更高(P < 0.01)。与氯霉素相比,莫西沙星对所有受试菌株的 MIC 值和半数抑制浓度值都明显较低,抑制区也更大,在控制革兰氏阴性菌生长方面具有很高的性能。此外,与氯霉素相比,莫西沙星在抑制生物膜形成和破坏生物膜方面表现出更高的活性,尤其是对表皮葡萄球菌生物膜。
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来源期刊
CiteScore
3.50
自引率
0.00%
发文量
31
审稿时长
3 months
期刊介绍: We also encourage the submission of manuscripts presenting preclinical and very preliminary research that may stimulate further investigation of potentially relevant findings, as well as in-depth review articles on specific therapies or disease states, and applied health delivery or pharmacoeconomics. CTR encourages and supports the submission of manuscripts describing: • Interventions designed to understand or improve human health, disease treatment or disease prevention; • Studies that focus on problems that are uncommon in resource-rich countries; • Research that is "under-published" because of limited access to monetary resources such as English language support and Open Access fees (CTR offers deeply discounted English language editing); • Republication of articles previously published in non-English journals (eg, evidence-based guidelines) which could be useful if translated into English; • Preclinical and clinical product development studies that are not pursued for further investigation based upon early phase results.
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