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给予米索硝唑、SR - 2508和Ro 03 - 8799后在人类肿瘤中达到的浓度。

Concentrations achieved in human tumors after administration of misonidazole, SR-2508 and Ro 03-8799.

作者信息

Dische S, Saunders M I, Dunphy E P, Bennett M H, Des Rochers C, Stratford M R, Minchinton A I, Orchard R A

出版信息

Int J Radiat Oncol Biol Phys. 1986 Jul;12(7):1109-11. doi: 10.1016/0360-3016(86)90237-3.

DOI:10.1016/0360-3016(86)90237-3
PMID:2943708
Abstract

Misonidazole, SR-2508 and Ro 03-8799 have been given in sequence to patients before tumor sampling. Tumor concentrations of the three drugs have been measured and it has been possible to make prediction as to the likely advantage of the newer drugs over misonidazole. Based upon the three cases described here and 13 others given two drug combination, we suggest that in multifraction radiotherapy, both are likely to prove more than five times more efficient than misonidazole.

摘要

在对患者进行肿瘤采样前,已按顺序给予其灭滴灵、SR - 2508和Ro 03 - 8799。已测量了这三种药物在肿瘤中的浓度,并且能够预测新药相对于灭滴灵可能具有的优势。基于此处描述的3例病例以及其他13例接受两种药物联合治疗的病例,我们认为在多分割放射治疗中,这两种新药可能比灭滴灵有效五倍以上。

相似文献

1
Concentrations achieved in human tumors after administration of misonidazole, SR-2508 and Ro 03-8799.给予米索硝唑、SR - 2508和Ro 03 - 8799后在人类肿瘤中达到的浓度。
Int J Radiat Oncol Biol Phys. 1986 Jul;12(7):1109-11. doi: 10.1016/0360-3016(86)90237-3.
2
The pharmacokinetics and tumor and neural tissue penetrating properties of SR-2508 and SR-2555 in the dog--hydrophilic radiosensitizers potentially less toxic than misonidazole.SR-2508和SR-2555在犬体内的药代动力学以及对肿瘤和神经组织的穿透特性——亲水性放射增敏剂,毒性可能低于甲硝唑。
Radiat Res. 1980 Dec;84(3):542-61.
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A comparison of tumor and normal tissue levels of acidic, basic and neutral 2-nitroimidazole radiosensitizers in mice.
Int J Radiat Oncol Biol Phys. 1986 Jul;12(7):1117-20. doi: 10.1016/0360-3016(86)90239-7.
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A comparison of the tumour concentrations obtainable with misonidazole and Ro 03-8799.米索硝唑与Ro 03 - 8799可达到的肿瘤浓度比较。
Br J Radiol. 1986 Sep;59(705):911-7. doi: 10.1259/0007-1285-59-705-911.
5
Pharmacokinetics of the hypoxic radiosensitizers misonidazole and demethylmisonidazole after intraperitoneal administration in humans.低氧放射增敏剂米索硝唑和去甲基米索硝唑腹腔注射后在人体的药代动力学
Cancer Res. 1983 Feb;43(2):913-6.
6
Pharmacokinetics and toxicology of continuously infused nitroimidazoles.持续输注硝基咪唑类药物的药代动力学与毒理学
Int J Radiat Oncol Biol Phys. 1984 Aug;10(8):1311-4. doi: 10.1016/0360-3016(84)90338-9.
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Comparison of the fate of misonidazole (RO 07-0582) and its metabolite desmethylmisonidazole (RO 05-9963), two hypoxic cell radiosensitizers: penetration properties in tumor bearing rats.两种乏氧细胞放射增敏剂米索硝唑(RO 07-0582)及其代谢产物去甲基米索硝唑(RO 05-9963)的转归比较:在荷瘤大鼠体内的渗透特性
J Pharmacol. 1983 Jan-Mar;14(1):67-77.
8
A phase I study of the combination of two hypoxic cell radiosensitizers, Ro 03-8799 and SR-2508: toxicity and pharmacokinetics.两种低氧细胞放射增敏剂Ro 03-8799与SR-2508联合应用的I期研究:毒性与药代动力学
Int J Radiat Oncol Biol Phys. 1986 Jul;12(7):1113-6. doi: 10.1016/0360-3016(86)90238-5.
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The radiosensitizer Ro 03-8799 and the concentrations which may be achieved in human tumours: a preliminary study.放射增敏剂Ro 03 - 8799及其在人类肿瘤中可能达到的浓度:一项初步研究。
Br J Cancer. 1982 Nov;46(5):706-10. doi: 10.1038/bjc.1982.262.
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A drug for improved radiosensitization in radiotherapy.一种用于改善放射治疗中放射增敏作用的药物。
Br J Cancer. 1980 Jul;42(1):153-5. doi: 10.1038/bjc.1980.213.

引用本文的文献

1
Clinical results of hypoxic cell radiosensitisation from hyperbaric oxygen to accelerated radiotherapy, carbogen and nicotinamide.从高压氧到加速放疗、卡波金和烟酰胺的乏氧细胞放射增敏的临床结果。
Br J Cancer Suppl. 1996 Jul;27:S271-8.
2
Autoradiographic distribution of [14C]-labelled pimonidazole in rhabdomyosarcoma-bearing rats and pigmented mice.[14C]标记的匹莫硝唑在荷横纹肌肉瘤大鼠和有色小鼠体内的放射自显影分布
Cancer Chemother Pharmacol. 1988;22(4):308-15. doi: 10.1007/BF00254237.
3
Distribution of pimonidazole and RSU 1069 in tumour and normal tissues.
匹莫硝唑和RSU 1069在肿瘤组织和正常组织中的分布。
Br J Cancer. 1990 Dec;62(6):915-8. doi: 10.1038/bjc.1990.408.
4
Lack of stereoselectivity in the pharmacokinetics and metabolism of the radiosensitizer Ro 03-8799 in man.放射增敏剂Ro 03-8799在人体药代动力学和代谢过程中缺乏立体选择性。
Cancer Chemother Pharmacol. 1991;28(2):118-22. doi: 10.1007/BF00689700.