1)Hematoporphyrin derivative血卟啉衍生物
1.Comparative study on the killing effect between hypocrellins B-photodynamic therapy and hematoporphyrin derivative-photodynamic therapy on human lung cancer cells;竹红菌乙素-PDT与血卟啉衍生物-PDT对人肺癌细胞杀伤效应的比较研究
2.Objective To investigate the killing effect of photodynamic therapy(PDT)mediated by hematoporphyrin derivative(HpD)on human colon carcinoma LoVo and CoLo205 cells in vitro.目的探讨血卟啉衍生物(HpD)光动力学效应(PDT)对体外培养人结肠癌细胞株LoVo和CoLo205的生物作用。
3.Objective To investigate biological effect of hematoporphyrin derivative (HpD) photodynamic therapy (PDT) on in vitro cultured nasopharyngeal carcinoma (NPC) cell lines CNE2 and C666-1.目的探讨血卟啉衍生物(HpD)光动力学效应(PDT)对体外培养人鼻咽癌细胞株CNE2和C666-1的生物作用。
英文短句/例句
1.Ultrastructural Studies on Effect of HpD on Carcinoma Cell Line血卟啉衍生物对癌细胞作用的超微结构研究
2.Affinity of Different Cell Lines for HpD in vitro不同细胞系对血卟啉衍生物亲和力的初步研究
3.Treatment of Superficial Bladder Tumor by Phototherapy with Hematoporphyrin Derivatives Argon Ion Laser: A Preliminary Report of 31 Cases血卟啉衍生物-氩激光治疗浅表性膀胱肿瘤31例
4.Preparation, Phototoxicity and Mechanism Studies of Anticarcinoembryonic Antigen Monoclonal Antibody-HPD Conjugates;血卟啉衍生物—癌胚抗原单抗偶联物抗肿瘤特性的研究
5.A total fo 31 patients with superficial bladder tumor have undergone photodynamic therapy with hematoporphyrin derivatives (HpD) argon ion laser since 1985. A modified high power interstitial irradiation of argon ion laser was used to destroy the visible tumor.1985年以来,用血卟啉衍生物-氩激光治疗浅表性膀胱肿瘤31例。
6.Haematoporphyrin derivative destruct laryngeal carcinoma cell line Hep-2 in vitro by photodynamic therapy血卟啉衍生物光动力学疗法体外杀伤人喉癌细胞株Hep-2的实验研究
7.Study on Synthesis of Porphryin Derivatives and Their Anti-tumor Activities;卟啉衍生物的合成及抗肿瘤活性研究
8.Synthesis of Novel Porphyrin Derivatives with Peripheral Ligands带侧基配体的新型卟啉衍生物的合成
9.Synthesis and characterization of porphyrin-5-fluorouracil compounds卟啉-5-氟尿嘧啶衍生物的合成与表征
10.Interfacial Supramolecular Assembly of Achiral Phthalocyanine and Porphyrin Derivatives;非手性酞菁和卟啉衍生物界面超分子组装
11.Synthesis and Properties of Naphthylporphyrin Compounds and Their Anthraquinone Derivatives;萘基卟啉及其蒽醌衍生物的合成及性能研究
12.The Linear and Nonlinear Spectral Properties Study of Several Porphyrin Derivatives;几种卟啉衍生物的线性和非线性光谱性质研究
13.Synthesis and Properties of Asymmetric Porphyrins and Their Anthraquinone Derivatives;不对称卟啉及其蒽醌衍生物的合成和性能研究
14.Synthesis, Mesomorphic Behavior and Catalytic Polymerization Studies of Porphyrin Derivatives;卟啉衍生物的合成与液晶行为及催化聚合研究
15.Study on the Synthesis and Interaction with DNA of a Series of Novel Porphyrin Derivate卟啉衍生物的合成及其与DNA相互作用的研究
16.Photophysical Properties of Meso-positions Zn(Ⅱ) Porphyrins:A Density Functional Theory StudyMeso取代Zn(Ⅱ)卟啉衍生物的光电性质的理论研究
17.New Fluorescent Probes for Cation Detection Based on Porphrin, Naphthalimide and Quinoline Derivatives基于卟啉、萘酰亚胺和喹啉衍生物的新型阳离子荧光探针的研究
18.Synthesis and Characterization of Porphyrins Containing Nitrogen Mustard and Piperazine Derivatives Substituents and Investigation on Their Biological Activities;氮芥和哌嗪衍生物卟啉的合成、表征及生物活性研究
相关短句/例句
Porphyrin derivatives卟啉衍生物
1.Photoelectrochemical study of nanoporous TiO_2 electrodes sensitized by porphyrin derivatives;卟啉衍生物敏化纳米TiO_2多孔膜电极的光电性质研究
2.Particularly the synthesis of 5,10,15,20-tetraphenylporphyrin derivatives are most studied.人们采用各种方法合成了具有各种取代基的卟啉化合物,其中以5,10,15,20-四苯基卟啉衍生物的合成尤为普遍。
3)porphyrin derivative卟啉衍生物
1.Some new progresses (including the author's own work) in the syntheses of NADH (nicotinamide adenine dinucleotide hydrogen) models, carotenoid related compounds and porphyrin derivatives are introduced.对一些生物活性分子的合成研究进展 ,如NADH (nicotinamideadeninedinucleotidehydrogen)模型、类胡萝卜素相关分子、卟啉衍生物的合成研究作了简要的概
2.Three novel porphyrin derivatives,meso-tetrakis[4-(nicotinoyloxy)phenyl]porphyrin,meso-tetrakis[4-(isonicotinoyloxy)phenyl]porphyrin and meso-tetrakis[4-(nicotinoyloxypropoxy)phenyl]porphyrin,were sythesized from meso-tetrakis[4-(hydroxy)phenyl]porphyrin.由四[4-(羟基)苯基]卟啉出发,合成了三种带吡啶侧基的新型卟啉衍生物——四[4-(烟酸酰氧基)苯基]卟啉,四[4-(异烟酸酰氧基)苯基]卟啉和四[4-(烟酸酰氧基丙氧基)苯基]卟啉,其结构经UV,1H NMR,IR和MS表征。
4)porphyrin[英]['p?:f?rin][美]['p?rf?r?n]卟啉衍生物
1.Reverse saturable absorption of porphyrin-like complexes;新型卟啉衍生物反饱和吸收研究
2.Nonlinear Absorption Study of a New Porphyrin Ramification (9, 9-bis (2-ethylhexyl)-2, 7-fluorene Ethynylene) (FE);新型卟啉衍生物（9，9-bis（2-ethylhexyl）-2，7-fluorene-ethynylene）（FE）的非线性吸收的研究
3.n this paper the relationship between structure of porphyrin derivatives and its R_f values in TLC is stud-ied.卟啉衍生物的结构与其薄层色谱Ｒ＿ｆ值的关系杨文炳，韩士田，刘彦钦，王继业，谢虹（河北师范学院化学系石家庄０５００９１）１前言有机化合物的分子结构与其薄层色谱比移值Ｒ＿ｆ之间有着密切关系，研究两者的关系将有助于由相应Ｒ＿ｆ值去推测同类化。
5)hematoporphyrin and its derivatives血卟啉及其衍生物(HPD)
6)Liposome hematoporphyrin derivatives血卟啉衍生物脂质体
延伸阅读
血卟啉注射液药物名称：血卟啉注射液英文名：Hematoporphyrine Injection汉语拼音：主要成分：血卟啉钠、双血卟啉醚和原卟啉等多种卟啉化合物的钠盐性状：暗红色的溶液。药理作用：在动物和人体内或体外细胞试验中都证明荧光效果明显。和激光联合应用，能增强杀伤癌细胞的作用，动物试验证明本品安全、毒性低。药代动力学：正常小鼠静脉注射本品经同位素3H标记的样品溶液，1小时后，各组织中放射性含量达到高峰，组织分布顺序为肺＞肝＞肾＞血＞胃＞肠＞脾＞心＞肌肉＞胸腺＞脑＞骨。S180荷瘤小鼠的组织分布顺序与正常鼠大致相同。在组织中放射性最高的第1小时，肿瘤中的含量为以上12种组织中的第8～9位，放射性下降较慢，到72小时，肿瘤组织的含量上升到第5位。注射本品5小时后，粪尿总排泄量占注射剂量的73.29%。第11天是91%。适应症：定位诊断和治疗口腔、膀胱、支气管等部位的表浅癌症及白斑等癌前病变。用法与用量：用药前先在病人前臂作皮肤划痕试验，观察15分钟，如无红肿硬结，则以每公斤体重5mg加生理盐水250ml静脉滴注。48～72小时，观察荧光并进行激光治疗。如须进行第二次治疗，应相隔一个月。不良反应：个别患者可出现暴露部位红肿，严重恶心。部分病人可出现一过性肝、肾功能损伤。禁忌症： 1.皮肤划痕试验阳性者。 2.肿瘤晚期，井有扩散至其他部位者。 3.光导纤维不能到达的深部肿瘤。注意事项：只能在有条件的医疗单位内使用。用药后患者应避光一个月。以免在暴光部位产生红肿色素沉着等光敏副作用。一旦发生，可给予抗过敏药物和外用皮质激素搽剂。 临床用药时必须注意控制给药剂量和次数，密切观察肝、肾功能及红细胞系的变化。规格：（1）5ml∶25mg （2）20ml∶0.1g贮藏：密闭，低温（-5～-8℃）冷藏保存。有效期：暂定一年。处方药：是
