Photodynamic therapeutic effect of iminodiacetic acid modified tetraphenylporphyrin in mice bearing H22 liver cancer
10.3760/cma.j.issn.1673-4181.2013.03.003
- VernacularTitle:亚氨基二乙酸修饰四苯基卟啉光敏剂介导的光动力疗法对H22肝癌小鼠体内抗肿瘤作用的研究
- Author:
Ge HONG
;
Jianghong GUO
;
Xiaojiao YANG
;
Tianjun LIU
- Publication Type:Journal Article
- Keywords:
Iminodiacetic acid modified tetraphenylporphyrin;
Photodynamic therapy;
H22 liver cancer;
Octanol-water partition coefficient;
Singlet oxygen
- From:
International Journal of Biomedical Engineering
2013;36(3):139-142,164,封3
- CountryChina
- Language:Chinese
-
Abstract:
Objective To explore the physical/chemical properties and effect of photodynamic therapy (PDT) of iminodiacetic acid modified tetraphenylporphyrin on mice bearing H22 liver cancer.Methods The UV absorbance spectrum,singlet oxygen yield and lipid-water partition coefficient were measured by UV spectrophotometry.Mice bearing H22 liver cancer as animal model were divided into control group (no drug,no light),light treated group (no drug,only light),drug treated group (only drug,no light),experimental once group (with drug and light,once) and experimental twice group (with drug and light,twice,PDT twice).Tumor inhibition rate and index of liver,spleen,lung,thymus of the mice were calculated to evaluate the antitumor activity of iminodiacetic acid modified tetraphenyl porphyrin-PDT.Results The iminodiacetic acid modified tetraphenylporphyrin had absorption at 650 nm,while its singlet oxygen yield and lipid-water partition coefficient were 2.30 and 0.52,respectively.No antitumor effect on mice bearing H22liver cancer for light treated group and drug treated group respectively.However,significant antitumor effect (P＜0.001)was found at experimental group.The maximum tumor inhibition rate could be 95.15％ for PDT twice group.No significant differences were observed on weight gain and liver,lung,spleen,thymus index in each group.Conclusion Iminodiacetic acid modified tetraphenylporphyrin with high singlet oxygen yield,low toxicity and significant in vivo anti-tumor activity,is suitable to be developed as an anti-tumor drug candidate for photodynamic therapy.
