Sao Carlos Institute of Physics, University of Sao Paulo, Brazil.
Sao Carlos Institute of Physics, University of Sao Paulo, Brazil.
J Photochem Photobiol B. 2020 Dec;213:112071. doi: 10.1016/j.jphotobiol.2020.112071. Epub 2020 Nov 2.
Photosensitization of all tissue in sufficient quantity to generate damage is one of the limiting factors for Photodynamic Therapy (PDT) efficiency. Methyl nicotinate (MN) is a thermogenic and vasodilating substance that facilitates the topical tissue penetration of some compounds. The topical MAL (methyl aminolevulinate) PDT is commonly used as a precursor of protoporphyrin IX (PpIX). This study investigates the safety of topical use in NM, as well as its ability to improve the efficiency of topical PDT. For this, we investigate the cytotoxicity of MN, as well as its actions in increasing cellular metabolism and vasodilation. Besides, its ability to optimize the formation of PpIX in the tissue when associated with MAL cream was investigated, besides assessing the severity of necrosis obtained by treatments. The cytotoxicity of MN was tested for concentrations of 0, 0.1, 0.25, 0.5, 0.75 and 1% in cell culture. For the concentration of 0.5%, the cellular metabolism was evaluated using confocal microscopy to calculate the redox rate. In the Chorioallantoic Membrane Model, vasodilation was evaluated for concentrations of 0.5 and 1% MN during 1 h of incubation. In the animal model, the healthy skin of Wistar rat was used to evaluate the production of PpIX in the tissue and the degree of necrosis obtained by Photodynamic therapy when using NM associated with methyl aminolevulinate. It was observed the non-cytotoxicity in vitro of MN in the concentration used (0.5%) and its ability to increase cellular metabolism. In a chorioallantoic model, the MN vasodilation power was demonstrated for different caliber of vessels. In vivo studies are showing that the incorporation of MN in the MAL cream increases the amount of PpIX produced in the tissue causing a higher effect on the epidermis after PDT. This improvement of the protocol may make the procedure more effective both in the destruction of tumor tissue and in the treatment of deeper cells decreasing possible recurrence, in addition to allowing improvements in the protocol, such as reducing the cream's incubation time.
足够数量的所有组织的光敏化以产生损伤是光动力疗法(PDT)效率的限制因素之一。烟碱酸甲酯(MN)是一种产热和血管扩张物质,可促进某些化合物的局部组织穿透。局部 MAL(甲基氨基酮戊酸)PDT 通常用作原卟啉 IX(PpIX)的前体。本研究调查了 NM 的局部使用安全性,以及其提高局部 PDT 效率的能力。为此,我们研究了 MN 的细胞毒性及其增加细胞代谢和血管扩张的作用。此外,还研究了其与 MAL 乳膏联合使用时在组织中优化 PpIX 形成的能力,以及评估通过治疗获得的坏死的严重程度。MN 的细胞毒性在细胞培养物中测试了 0、0.1、0.25、0.5、0.75 和 1%的浓度。对于 0.5%的浓度,使用共聚焦显微镜评估细胞代谢以计算氧化还原率。在鸡胚绒毛尿囊膜模型中,评估了 0.5 和 1%MN 孵育 1 小时时的血管扩张。在动物模型中,使用 Wistar 大鼠的健康皮肤评估组织中 PpIX 的产生以及在使用 MN 时通过光动力疗法获得的坏死程度与甲基氨基酮戊酸相关联。观察到在使用浓度(0.5%)时 MN 的体外非细胞毒性及其增加细胞代谢的能力。在鸡胚绒毛尿囊膜模型中,证明了 MN 的血管扩张能力适用于不同口径的血管。体内研究表明,MN 掺入 MAL 乳膏可增加组织中产生的 PpIX 量,在 PDT 后对表皮产生更高的作用。该方案的改进可能会使该程序在破坏肿瘤组织和治疗深层细胞方面更加有效,从而降低可能的复发,同时还允许改进该方案,例如减少乳膏的孵育时间。