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1
Pharmacokinetics and renal elimination of desferrioxamine and ferrioxamine in healthy subjects and patients with haemochromatosis.去铁胺和铁胺在健康受试者及血色素沉着症患者中的药代动力学及肾脏清除情况。
Br J Clin Pharmacol. 1987 Aug;24(2):207-12. doi: 10.1111/j.1365-2125.1987.tb03163.x.
2
Pharmacokinetics of aluminoxamine and ferrioxamine and dose finding of desferrioxamine in haemodialysis patients.
Nephrol Dial Transplant. 1992;7(9):931-8. doi: 10.1093/ndt/7.9.931.
3
Low percentage of aluminoxamine and ferrioxamine in uremic serum after desferrioxamine administration.去铁胺给药后尿毒症血清中铝去铁胺和铁去铁胺的比例较低。
Clin Chem. 1998 Jun;44(6 Pt 1):1262-8.
4
Pharmacokinetics of desferrioxamine and of its iron and aluminum chelates in patients on peritoneal dialysis.去铁胺及其铁和铝螯合物在腹膜透析患者中的药代动力学。
Clin Chim Acta. 1988 Apr 29;173(3):313-6. doi: 10.1016/0009-8981(88)90019-8.
5
Kinetics of aluminoxamine and feroxamine chelates in dialysis patients.
Nephron. 1992;60(4):411-7. doi: 10.1159/000186800.
6
Urinary and biliary excretion of aluminoxamine and ferrioxamine in dogs with various renal function.
Kidney Int. 1994 Jan;45(1):76-84. doi: 10.1038/ki.1994.9.
7
Studies in desferrioxamine and ferrioxamine metabolism in normal and iron-loaded subjects.
Br J Haematol. 1979 Aug;42(4):547-55. doi: 10.1111/j.1365-2141.1979.tb01167.x.
8
Deferoxamine pharmacokinetics.
Semin Hematol. 2001 Jan;38(1 Suppl 1):63-8. doi: 10.1016/s0037-1963(01)90061-7.
9
Effect of aluminum and deferoxamine on biliary iron elimination in the rat.铝和去铁胺对大鼠胆汁铁排泄的影响。
Proc Soc Exp Biol Med. 1988 Sep;188(4):471-3. doi: 10.3181/00379727-188-42762.
10
Estimation of aluminoxamine and ferrioxamine in plasma by high performance liquid chromatography.
Clin Chim Acta. 1986 May 30;157(1):115-20. doi: 10.1016/0009-8981(86)90325-6.

引用本文的文献

1
Deferoxamine Intradermal Delivery Patch for Treatment of a Beta-Thalassemia Wound.用于治疗β地中海贫血伤口的去铁胺皮内给药贴片
Ann Surg Open. 2024 Jan 11;5(1):e372. doi: 10.1097/AS9.0000000000000372. eCollection 2024 Mar.
2
Targeting Pro-Oxidant Iron with Deferoxamine as a Treatment for Ischemic Stroke: Safety and Optimal Dose Selection in a Randomized Clinical Trial.以去铁胺靶向促氧化铁作为缺血性中风的治疗方法:一项随机临床试验中的安全性和最佳剂量选择
Antioxidants (Basel). 2021 Aug 10;10(8):1270. doi: 10.3390/antiox10081270.
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Protective Effects of Deferoxamine on Vestibulotoxicity in Gentamicin-Induced Bilateral Vestibulopathy Rat Model.去铁胺对庆大霉素诱导的双侧前庭病大鼠模型前庭毒性的保护作用
Front Neurol. 2021 Mar 24;12:650752. doi: 10.3389/fneur.2021.650752. eCollection 2021.
4
Potential Anti-SARS-CoV-2 Therapeutics That Target the Post-Entry Stages of the Viral Life Cycle: A Comprehensive Review.潜在的针对病毒生命周期进入后阶段的抗 SARS-CoV-2 治疗药物:全面综述。
Viruses. 2020 Sep 26;12(10):1092. doi: 10.3390/v12101092.
5
Nanogel-DFO conjugates as a model to investigate pharmacokinetics, biodistribution, and iron chelation in vivo.纳米凝胶-DFO 缀合物作为研究体内药代动力学、生物分布和铁螯合的模型。
Int J Pharm. 2018 Mar 1;538(1-2):79-86. doi: 10.1016/j.ijpharm.2018.01.004. Epub 2018 Jan 16.
6
Visualization of Inflammation at Early Stage of Lung Cancer in Xenografted Temporally Immunosuppression Rats by Ferrioxamine Magnetic Resonance Imaging.去铁胺磁共振成像对异种移植的短期免疫抑制大鼠肺癌早期炎症的可视化研究
Int J Mol Imaging. 2016;2016:8434308. doi: 10.1155/2016/8434308. Epub 2016 Dec 15.
7
Iron homeostasis and eye disease.铁稳态与眼部疾病
Biochim Biophys Acta. 2009 Jul;1790(7):637-49. doi: 10.1016/j.bbagen.2008.11.001. Epub 2008 Nov 14.
8
Conjugation of hydroxyethyl starch to desferrioxamine (DFO) modulates the dual role of DFO in Yersinia enterocolitica infection.将羟乙基淀粉与去铁胺(DFO)结合可调节去铁胺在小肠结肠炎耶尔森菌感染中的双重作用。
Clin Diagn Lab Immunol. 2000 May;7(3):457-62. doi: 10.1128/CDLI.7.3.457-462.2000.
9
Response of rat model of Pneumocystis carinii pneumonia to continuous infusion of deferoxamine.卡氏肺孢子虫肺炎大鼠模型对持续输注去铁胺的反应。
Antimicrob Agents Chemother. 1995 Jul;39(7):1442-4. doi: 10.1128/AAC.39.7.1442.
10
Deferoxamine (desferrioxamine). New toxicities for an old drug.去铁胺(去铁敏)。一种老药的新毒性。
Drug Saf. 1991 Jan-Feb;6(1):37-46. doi: 10.2165/00002018-199106010-00004.

本文引用的文献

1
STRIPE: an interactive computer program for the analysis of drug pharmacokinetics.STRIPE:一款用于药物药代动力学分析的交互式计算机程序。
J Pharmacol Methods. 1983 May;9(3):193-9. doi: 10.1016/0160-5402(83)90038-4.
2
High-performance liquid chromatography of deferoxamine and ferrioxamine: interference by iron present in the chromatographic system.去铁胺和铁去铁胺的高效液相色谱法:色谱系统中存在的铁的干扰
J Chromatogr. 1984 Jul 20;295(2):405-11. doi: 10.1016/s0021-9673(01)87642-1.
3
The metabolism of desferrioxamine B and ferrioxamine B.去铁胺B和铁胺B的代谢
Biochem Pharmacol. 1967 Mar;16(3):527-35. doi: 10.1016/0006-2952(67)90100-1.
4
Indirect micro-scale method for the determination of desferrioxamine and its aluminium and iron chelated forms in biological samples by atomic absorption spectrometry with electrothermal atomisation.间接微量法:采用电热原子化原子吸收光谱法测定生物样品中的去铁胺及其铝和铁螯合形式
Analyst. 1986 May;111(5):531-3. doi: 10.1039/an9861100531.
5
Studies in desferrioxamine and ferrioxamine metabolism in normal and iron-loaded subjects.
Br J Haematol. 1979 Aug;42(4):547-55. doi: 10.1111/j.1365-2141.1979.tb01167.x.

去铁胺和铁胺在健康受试者及血色素沉着症患者中的药代动力学及肾脏清除情况。

Pharmacokinetics and renal elimination of desferrioxamine and ferrioxamine in healthy subjects and patients with haemochromatosis.

作者信息

Allain P, Mauras Y, Chaleil D, Simon P, Ang K S, Cam G, Le Mignon L, Simon M

出版信息

Br J Clin Pharmacol. 1987 Aug;24(2):207-12. doi: 10.1111/j.1365-2125.1987.tb03163.x.

DOI:10.1111/j.1365-2125.1987.tb03163.x
PMID:3620295
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1387751/
Abstract

1 Desferrioxamine mesylate (DM) (10 mg kg-1 = 15.24 mumol kg-1) was given by intramuscular injection to five healthy subjects and to six patients with haemochromatosis, after informed consent. 2 Desferrioxamine (DFA), ferrioxamine (FeA), aluminoxamine (AlA), aluminium (Al) and iron (Fe) were measured in plasma, before and 10, 20, 30, 60 min and 2, 4, 6, 8, 12 h after DM injection and in urine collected over a 6 h period the day before and the day of administration. 3 The predominant form in plasma from control subjects was DFA whereas FeA predominated in plasma from patients. In controls, rapid and slow phases of decline in plasma DFA concentrations were found, with half-lives of 1.0 h and 6.1 h, respectively. In the patients, only a single phase of decline was observed, with a half-life of 5.6 h. Total clearances of DFA were 296 ml h-1 kg-1 in controls and 239 ml h-1 kg-1 in patients. 4 The amount of FeA eliminated in urine during 6 h was significantly lower in controls (8.0 +/- 4.6 mumol) than in patients (129.2 +/- 40.0 mumol), with respective renal clearances estimated over 6 h of 516 ml h-1 kg-1 and 1,716 ml h-1 kg-1. DFA elimination was similar in both groups and its renal clearance estimated over 6 h was 91 ml h-1 kg-1 in controls and 85 ml h-1 kg-1 in patients. 5 Since there was no overlap in the 1 h DFA/FeA plasma ratio between controls and patients, this might be useful as an index of iron overload.

摘要

1 在获得知情同意后,对5名健康受试者和6名血色素沉着症患者进行肌肉注射甲磺酸去铁胺(DM)(10 mg kg-1 = 15.24 μmol kg-1)。2 在注射DM前以及注射后10、20、30、60分钟和2、4、6、8、12小时,测定血浆中的去铁胺(DFA)、铁胺(FeA)、铝胺(AlA)、铝(Al)和铁(Fe),并在给药前一天和给药当天收集6小时的尿液进行检测。3 对照受试者血浆中的主要形式是DFA,而患者血浆中FeA占主导。在对照组中,发现血浆DFA浓度下降有快速和缓慢两个阶段,半衰期分别为1.0小时和6.1小时。在患者中,仅观察到一个下降阶段,半衰期为5.6小时。对照组中DFA的总清除率为296 ml h-1 kg-1,患者为239 ml h-1 kg-1。4 对照组6小时内尿中排出的FeA量(8.0±4.6 μmol)明显低于患者(129.2±40.0 μmol),6小时内各自的肾清除率估计分别为516 ml h-1 kg-1和1716 ml h-1 kg-1。两组中DFA的清除情况相似,6小时内其肾清除率估计在对照组中为91 ml h-1 kg-1,在患者中为85 ml h-1 kg-1。5 由于对照组和患者之间1小时的DFA/FeA血浆比值没有重叠,这可能作为铁过载的一个指标。