Department of Ophthalmology, Loma Linda University, Loma Linda, California.
Wilmer Eye Institute, Johns Hopkins University, Baltimore, Maryland.
Ophthalmol Glaucoma. 2021 May-Jun;4(3):330-335. doi: 10.1016/j.ogla.2020.10.011. Epub 2020 Oct 17.
Intra-Tenon or subconjunctival injection of a solution of mitomycin C (MMC) and 1% preservative-free lidocaine (as an anesthetic) has gained popularity for its use in trabeculectomy, a filtering surgery for glaucoma. To our knowledge, no studies have analyzed the impact of lidocaine on the cytotoxic effects of MMC in this setting. This study was conducted to evaluate in vitro fibroblast cytotoxicity to a solution of MMC (0.2 mg/ml) and 1% preservative-free lidocaine.
Experimental study.
Nonhuman subject research.
Cultured human conjunctival fibroblasts were incubated in phosphate-buffered saline (PBS) (control), MMC (0.2 mg/ml), a mixture of 0.2 mg/ml MMC + 1% preservative-free lidocaine, or 1% preservative-free lidocaine. Samples were taken at 2, 5, 10, 30, and 60 minutes, and a 3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromide (MTT) assay with photoabsorbance testing was used to assess conjunctival cell viability.
Mean photoabsorbance.
Mean photoabsorbance across all time intervals was 0.680 for solutions incubated in PBS, 0.642 for MMC, 0.612 for MMC + 1% preservative-free lidocaine, and 0.605 for 1% preservative-free lidocaine. A 2-way analysis of variance analyzing solution, time, and solution-time interaction on photoabsorbance showed that PBS was least cytotoxic and an optimal control for this study. Tukey post hoc comparisons showed that MMC was more cytotoxic than PBS (P < 0.001). However, both MMC + 1% preservative-free lidocaine and 1% preservative-free lidocaine were more cytotoxic than MMC and PBS (P < 0.01 for all). No significant differences in cytotoxicity comparing lidocaine-containing solutions were observed.
In this in vitro study, we found an increase in cytotoxicity when MMC (0.2 mg/ml) was combined with 1% preservative-free lidocaine. We note that lidocaine did not inhibit MMC cytotoxicity and exhibited a significant cytotoxic effect on its own.
在特伦诺或结膜下注射丝裂霉素 C(MMC)和 1%无防腐剂利多卡因(作为麻醉剂)溶液已在小梁切开术中得到广泛应用,这是一种用于青光眼的滤过性手术。据我们所知,在这种情况下,还没有研究分析利多卡因对 MMC 细胞毒性的影响。本研究旨在评估 MMC(0.2mg/ml)和 1%无防腐剂利多卡因溶液对体外培养的成纤维细胞的细胞毒性。
实验研究。
非人类受试者研究。
将培养的人结膜成纤维细胞在磷酸盐缓冲盐水(PBS)(对照)、MMC(0.2mg/ml)、0.2mg/ml MMC+1%无防腐剂利多卡因混合物或 1%无防腐剂利多卡因中孵育。在 2、5、10、30 和 60 分钟时取样,并使用 3-[4,5-二甲基噻唑-2-基]-2,5-二苯基四唑溴化物(MTT)测定法进行光吸收测试,以评估结膜细胞活力。
平均光吸收值。
在 PBS 孵育的溶液中,所有时间间隔的平均光吸收值为 0.680,MMC 为 0.642,MMC+1%无防腐剂利多卡因为 0.612,1%无防腐剂利多卡因为 0.605。对光吸收值进行的溶液、时间和溶液-时间相互作用的双因素方差分析表明,PBS 的细胞毒性最低,是本研究的最佳对照。Tukey 事后比较显示,MMC 比 PBS 的细胞毒性更强(P<0.001)。然而,MMC+1%无防腐剂利多卡因和 1%无防腐剂利多卡因均比 MMC 和 PBS 的细胞毒性更强(P<0.01)。比较含利多卡因的溶液时,未观察到细胞毒性的显著差异。
在这项体外研究中,我们发现当 MMC(0.2mg/ml)与 1%无防腐剂利多卡因结合时,细胞毒性增加。我们注意到,利多卡因并没有抑制 MMC 的细胞毒性,而且本身就有显著的细胞毒性作用。