da Silva Wander José, Seneviratne Jayampath, Parahitiyawa Nipuna, Rosa Edvaldo Antonio Ribeiro, Samaranayake Lakshman Perera, Del Bel Cury Altair Antoninha
Department of Prosthodontics and Periodontology, Dental School of Piracicaba, State University of Campinas, Piracicaba, SP, Brazil.
Braz Dent J. 2008;19(4):364-9. doi: 10.1590/s0103-64402008000400014.
2, 3-bis (2-methoxy-4-nitro-5-sulfophenyl)-5-[(phenylamino) carbonyl]-2H-tetrazolium hydroxide (XTT) reduction assay has been used to study Candida biofilm formation. However, considering that the XTT reduction assay is dependent on cell activity, its use for evaluating mature biofilms may lead to inaccuracies since biofilm bottom cell layers tend to be relatively quiescent at later stages of biofilm formation. The aim of this study was to improve XTT reduction assay by adding glucose supplements to the standard XTT formulation. Candida albicans ATCC 90028 was used to form 24-, 48- and 72-h biofilms. The oxidative activity at 90, 180 and 270 min of incubation was evaluated. The control consisted of standard XTT formulation without glucose supplements, and was modified by the addition of 50, 100 and 200 mM of glucose. The XTT assay with 200 mM glucose showed more accurate and consistent readings correlating with biofilm development at 24, 48 and 72 h. Biofilm growth yield after 180 min incubation, when evaluated with the 200 mM glucose supplemented XTT, produced the most consistent readings on repetitive testing. It may be concluded that glucose supplementation of XTT could minimize variation and produce more accurate data for the XTT assay.
2,3-双(2-甲氧基-4-硝基-5-磺基苯基)-5-[(苯氨基)羰基]-2H-四唑氢氧化合物(XTT)还原试验已用于研究白色念珠菌生物膜的形成。然而,鉴于XTT还原试验依赖于细胞活性,其用于评估成熟生物膜可能会导致不准确,因为在生物膜形成的后期,生物膜底部细胞层往往相对静止。本研究的目的是通过在标准XTT制剂中添加葡萄糖补充剂来改进XTT还原试验。使用白色念珠菌ATCC 90028形成24、48和72小时的生物膜。评估孵育90、180和270分钟时的氧化活性。对照组由不添加葡萄糖补充剂的标准XTT制剂组成,并通过添加50、100和200 mM葡萄糖进行修改。添加200 mM葡萄糖的XTT试验显示出与24、48和72小时生物膜发育相关的更准确和一致的读数。用添加200 mM葡萄糖的XTT评估孵育180分钟后的生物膜生长产量,在重复测试中产生了最一致的读数。可以得出结论,向XTT中添加葡萄糖可以最小化变异,并为XTT试验产生更准确的数据。