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Cytotoxicity of five fluoroquinolone and two nonsteroidal anti-inflammatory benzalkonium chloride-free ophthalmic solutions in four corneoconjunctival cell lines

机译:五种氟喹诺酮和两种非类固醇消炎无苯扎氯铵的滴眼液对四种角结膜细胞系的细胞毒性

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Purpose: Epithelial disorders after eye surgery can result in visual deterioration and patient discomfort. Such disorders may be caused by drug toxicity. In the present study, we evaluated the toxicity of ophthalmic solutions, with or without benzalkonium chloride (BAK) as the preservative, used for postoperative care.Methods: A range of commercially available antibiotic and anti-inflammatory ophthalmic solutions used postoperatively (ie, levofloxacin, moxifloxacin, gatifloxacin, norfloxacin, tosufloxacin, dibekacin, cefmenoxime, diclofenac, bromfenac, pranoprofen, betamethasone, and fluoromethorone) were assessed in three corneal cell lines and one conjunctival cell line. All antibiotic solutions were BAK free. Cell viability was determined with the 3-(4,5-dimethyl-2 thiazoyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay after cells had been exposed to the drugs for 48 h. The effects of preservatives on cell viability were also determined. Toxicity was compared using the cell viability score (CVS).Results: Based on results of the MTT assay and CVS, the order of cell viability after exposure to the antibiotic solutions was cefmenoxime ≥ tosufloxicin ≥ dibekacin ≥ levofloxacin ≥ norfloxacin = gatifloxacin = moxifloxacin. For the anti-inflammatory solutions, the order of cell viability was betamethasone ≥ betamethasone + fradiomycin > preservative-free diclofenac ≥ preservative-free bromfenac 0.02% fluoromethorone ≥ 0.1% fluoromethorone = diclofenac + preservative = bromfenac + preservative = pranoprofen. The anti-inflammatory drugs were more toxic than the antibiotics. The toxicity of antibiotic drugs against ocular surface cells was dependent on the pharmaceutical components of the solution, whereas that of the anti-inflammatory drugs was dependent on both the pharmaceutical components and the preservatives.Conclusion: Postoperative drug-induced epitheliopathy may be caused primarily by anti-inflammatory drugs. CVS is useful in comparing the cytotoxicity of different drugs.
机译:目的:眼科手术后的上皮疾病可能导致视力下降和患者不适。此类疾病可能是由药物毒性引起的。在本研究中,我们评估了使用或不使用苯扎氯铵(BAK)作为防腐剂的眼用溶液在术后护理中的毒性。方法:术后广泛使用一系列可商购的抗生素和抗炎眼用溶液(即左氧氟沙星)分别在三种角膜细胞系和一种结膜细胞系中评估了莫西沙星,加替沙星,诺氟沙星,托氟沙星,地贝卡星,头孢甲肟,双氯芬酸,溴芬酸,普罗洛芬,倍他米松和氟美洛酮)。所有抗生素溶液均不含BAK。细胞暴露于药物48小时后,通过3-(4,5-二甲基-2噻唑基)-2,5-二苯基-2H-四唑溴化物(MTT)测定细胞活力。还确定了防腐剂对细胞活力的影响。结果:基于MTT分析和CVS的结果,暴露于抗生素溶液后的细胞生存力顺序为头孢甲肟≥托福洛星≥dibekacin≥左氧氟沙星≥诺氟沙星=加替沙星=加替沙星=莫西沙星。对于抗炎溶液,细胞活力的顺序为倍他米松≥倍他米松+黄曲霉素>不含防腐剂的双氯芬酸≥不含防腐剂的溴芬酸 0.02%氟美洛酮≥0.1%氟美洛酮=双氯芬酸+防腐剂=溴芬酸+防腐剂=普罗洛芬。抗炎药比抗生素更具毒性。抗生素对眼表细胞的毒性取决于溶液的药物成分,而抗炎药的毒性取决于药物成分和防腐剂。结论:术后药物引起的上皮病变可能主要是由于抗炎药。 CVS可用于比较不同药物的细胞毒性。

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