J Drugs Dermatol. 2024 Nov 1;23(11):986-991. doi: 10.36849/JDD.7985.
Tyrosinase is the rate-limiting enzyme of melanogenesis and thus an ideal inhibitory target for treating hyperpigmentation. There are many commercially available tyrosinase inhibitors with limited clinical efficacy. A recent screen of 50,000 compounds found isobutylamido thiazolyl resorcinol (ITR) to be the most potent inhibitor of human tyrosinase.
To summarize the current evidence on the efficacy and adverse effects of ITR in treating hyperpigmentation.
A literature search was conducted using PubMed and Google Scholar databases in June 2022. Fourteen clinical studies investigating the use of topical ITR in hyperpigmentation treatment or prevention were identified.
Most studies (n=13) investigated topical ITR as a treatment, while only one investigated ITR as a preventative measure against hyperpigmentation. All studies (n=14) found ITR to provide statistically significant improvements to hyperpigmentation conditions, including facial hyperpigmentation (n=3), melasma (n=5), post-inflammatory hyperpigmentation (PIH) (n=3), and UV-induced hyperpigmentation (n=3). Evidence suggests that the effective dosage and duration of topical ITR appears to be 0.1% to 0.2% ITR 2 to 4 times daily for 12 to 24 weeks. Successful prevention of UVB-induced hyperpigmentation has been seen following twice-daily topical ITR application for 3 weeks (P<0.001).
Topical ITR can significantly reduce hyperpigmentation, however, the evidence for its use is limited. Further investigation is warranted to identify the optimal dosage and application schedule of ITR, as well as compare the efficacy of ITR vs hydroquinone to determine if ITR is superior to the current standard of care. J Drugs Dermatol. 2024;23(11):986-991. doi:10.36849/JDD.7985.
酪氨酸酶是黑色素生成的限速酶,因此是治疗色素沉着过度的理想抑制靶点。有许多市售的酪氨酸酶抑制剂,但临床疗效有限。最近对 50,000 种化合物进行筛选发现,异丁酰胺噻唑基间苯二酚(ITR)是对人酪氨酸酶最有效的抑制剂。
总结 ITR 治疗色素沉着过度的疗效和不良反应的现有证据。
2022 年 6 月,使用 PubMed 和 Google Scholar 数据库进行文献检索。确定了 14 项关于局部使用 ITR 治疗色素沉着过度或预防色素沉着过度的临床研究。
大多数研究(n=13)将局部 ITR 作为治疗方法进行了研究,而只有一项研究将 ITR 作为预防色素沉着过度的措施进行了研究。所有研究(n=14)均发现 ITR 可显著改善色素沉着过度的情况,包括面部色素沉着过度(n=3)、黄褐斑(n=5)、炎症后色素沉着过度(PIH)(n=3)和紫外线诱导的色素沉着过度(n=3)。证据表明,局部 ITR 的有效剂量和持续时间似乎为 0.1%至 0.2% ITR,每日 2 至 4 次,持续 12 至 24 周。每日两次局部 ITR 应用 3 周可成功预防 UVB 诱导的色素沉着过度(P<0.001)。
局部 ITR 可显著减少色素沉着过度,但目前对其使用的证据有限。需要进一步研究以确定 ITR 的最佳剂量和应用方案,并比较 ITR 与氢醌的疗效,以确定 ITR 是否优于当前的标准治疗。J 皮肤病学杂志。2024;23(11):986-991.