{"title":"体外和体内5-ALA在血管内皮细胞中的光敏能力。","authors":"C J Chang, S F Ma, F C Wei","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>The object of our study is to evaluate the feasibility of photodynamic therapy for complicated hemangiomas. We studied the effect of the photosensitizing agent 5-aminolevulinic acid (5-ALA) in both in vitro and in vivo models.</p><p><strong>Methods: </strong>The in vitro photosensitizing activity of 5-ALA was examined in a microvascular endothelial cell (MEC) culture system. 5-ALA was added in various concentrations and the cells were illuminated at 630 nm. The percentage of MEC killed was measured by either a Live/Dead assay or an lactate dehydrogenase (LDH) assay. The effect of varying the light energy dose delivered at 630 nm after the administration of 5-ALA was studied by determining the amount of necrosis produced in chicken combs.</p><p><strong>Results: </strong>The combination of 5-ALA at a concentration of 35 micrograms/ml, and illumination by 100 mW/cm2 of laser light at 630 nm wavelength, caused 50% cell kill in the MEC culture system. Chicken combs of animals that received 200 mg/kg of 5-ALA and illumination at a power density of 80 mW/cm2 had a depth of injury of 362.5 +/- 27.6 microns upon histological examination. Those combs that received 100 or 120 mW/cm2 showed a depth of injury of 732.5 +/- 29.1 and 792.5 +/- 36.0 microns respectively.</p><p><strong>Conclusion: </strong>5-ALA is effective in sensitizing human MEC to laser illumination. However, the degree of absorption and tissue destruction in different anatomical structures should be considered in future clinical studies.</p>","PeriodicalId":77066,"journal":{"name":"Changgeng yi xue za zhi","volume":"22 2","pages":"181-8"},"PeriodicalIF":0.0000,"publicationDate":"1999-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"In vitro and in vivo photosensitizing capabilities of 5-ALA in vascular endothelial cells.\",\"authors\":\"C J Chang, S F Ma, F C Wei\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>The object of our study is to evaluate the feasibility of photodynamic therapy for complicated hemangiomas. We studied the effect of the photosensitizing agent 5-aminolevulinic acid (5-ALA) in both in vitro and in vivo models.</p><p><strong>Methods: </strong>The in vitro photosensitizing activity of 5-ALA was examined in a microvascular endothelial cell (MEC) culture system. 5-ALA was added in various concentrations and the cells were illuminated at 630 nm. The percentage of MEC killed was measured by either a Live/Dead assay or an lactate dehydrogenase (LDH) assay. The effect of varying the light energy dose delivered at 630 nm after the administration of 5-ALA was studied by determining the amount of necrosis produced in chicken combs.</p><p><strong>Results: </strong>The combination of 5-ALA at a concentration of 35 micrograms/ml, and illumination by 100 mW/cm2 of laser light at 630 nm wavelength, caused 50% cell kill in the MEC culture system. Chicken combs of animals that received 200 mg/kg of 5-ALA and illumination at a power density of 80 mW/cm2 had a depth of injury of 362.5 +/- 27.6 microns upon histological examination. Those combs that received 100 or 120 mW/cm2 showed a depth of injury of 732.5 +/- 29.1 and 792.5 +/- 36.0 microns respectively.</p><p><strong>Conclusion: </strong>5-ALA is effective in sensitizing human MEC to laser illumination. However, the degree of absorption and tissue destruction in different anatomical structures should be considered in future clinical studies.</p>\",\"PeriodicalId\":77066,\"journal\":{\"name\":\"Changgeng yi xue za zhi\",\"volume\":\"22 2\",\"pages\":\"181-8\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1999-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Changgeng yi xue za zhi\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Changgeng yi xue za zhi","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
In vitro and in vivo photosensitizing capabilities of 5-ALA in vascular endothelial cells.
Background: The object of our study is to evaluate the feasibility of photodynamic therapy for complicated hemangiomas. We studied the effect of the photosensitizing agent 5-aminolevulinic acid (5-ALA) in both in vitro and in vivo models.
Methods: The in vitro photosensitizing activity of 5-ALA was examined in a microvascular endothelial cell (MEC) culture system. 5-ALA was added in various concentrations and the cells were illuminated at 630 nm. The percentage of MEC killed was measured by either a Live/Dead assay or an lactate dehydrogenase (LDH) assay. The effect of varying the light energy dose delivered at 630 nm after the administration of 5-ALA was studied by determining the amount of necrosis produced in chicken combs.
Results: The combination of 5-ALA at a concentration of 35 micrograms/ml, and illumination by 100 mW/cm2 of laser light at 630 nm wavelength, caused 50% cell kill in the MEC culture system. Chicken combs of animals that received 200 mg/kg of 5-ALA and illumination at a power density of 80 mW/cm2 had a depth of injury of 362.5 +/- 27.6 microns upon histological examination. Those combs that received 100 or 120 mW/cm2 showed a depth of injury of 732.5 +/- 29.1 and 792.5 +/- 36.0 microns respectively.
Conclusion: 5-ALA is effective in sensitizing human MEC to laser illumination. However, the degree of absorption and tissue destruction in different anatomical structures should be considered in future clinical studies.