Ferrozine (hydrate)
目录号 : GC49031
A colorimetric reagent for the detection of iron
Cas No.:1266615-85-3
Sample solution is provided at 25 µL, 10mM.
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Quality Control & SDS
- View current batch:
- Purity: >98.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
Ferrozine is a colorimetric reagent commonly used in the detection of iron.1,2 Ferrozine forms a complex with ferrous iron that can be quantified by colorimetric detection at 562 nm as a measure of iron concentration.
1.Stookey, L.L.Ferrozine-A new spectrophotometric reagent for ironAnal. Chem.42(7)779-781(1970) 2.Jeitner, T.M.Optimized ferrozine-based assay for dissolved ironAnal. Biochem.45436-37(2014)
| Cas No. | 1266615-85-3 | SDF | |
| Canonical SMILES | OS(C1=CC=C(C2=C(C3=CC=C(S([O-])(=O)=O)C=C3)N=C(C4=CC=CC=N4)N=N2)C=C1)(=O)=O.[Na+].O | ||
| 分子式 | C20H13N4O6S2·Na [XH2O] | 分子量 | 492.5 |
| 溶解度 | PBS (pH 7.2): 1 mg/ml | 储存条件 | -20°C |
| General tips | 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液；一旦配成溶液，请分装保存，避免反复冻融造成的产品失效。 储备液的保存方式和期限：-80°C 储存时，请在 6 个月内使用，-20°C 储存时，请在 1 个月内使用。 为了提高溶解度，请将管子加热至37℃，然后在超声波浴中震荡一段时间。 |
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| Shipping Condition | 评估样品解决方案：配备蓝冰进行发货。所有其他可用尺寸：配备RT，或根据请求配备蓝冰。 | ||
| 制备储备液 | |||
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1 mg | 5 mg | 10 mg |
| 1 mM | 2.0305 mL | 10.1523 mL | 20.3046 mL |
| 5 mM | 0.4061 mL | 2.0305 mL | 4.0609 mL |
| 10 mM | 0.203 mL | 1.0152 mL | 2.0305 mL |
| 第一步：请输入基本实验信息（考虑到实验过程中的损耗，建议多配一只动物的药量） | ||||||||||
| 给药剂量 | mg/kg |  |
动物平均体重 | g | |
每只动物给药体积 | ul | |
动物数量 | 只 |
| 第二步：请输入动物体内配方组成（配方适用于不溶于水的药物；不同批次药物配方比例不同，请联系GLPBIO为您提供正确的澄清溶液配方） | ||||||||||
| % DMSO % % Tween 80 % saline | ||||||||||
| 计算重置 | ||||||||||
计算结果:
工作液浓度： mg/ml；
DMSO母液配制方法： mg 药物溶于 μL DMSO溶液（母液浓度 mg/mL，
体内配方配制方法：取 μL DMSO母液，加入 μL PEG300，混匀澄清后加入μL Tween 80，混匀澄清后加入 μL saline，混匀澄清。
1. 首先保证母液是澄清的；
2.
一定要按照顺序依次将溶剂加入，进行下一步操作之前必须保证上一步操作得到的是澄清的溶液，可采用涡旋、超声或水浴加热等物理方法助溶。
3. 以上所有助溶剂都可在 GlpBio 网站选购。
N-Acetylcysteine Nanocarriers Protect against Oxidative Stress in a Cellular Model of Parkinson's Disease
Antioxidants (Basel) 2020 Jul 9;9(7):600.PMID:32660079DOI:10.3390/antiox9070600.
Oxidative stress is a key mediator in the development and progression of Parkinson's disease (PD). The antioxidant n-acetylcysteine (NAC) has generated interest as a disease-modifying therapy for PD but is limited due to poor bioavailability, a short half-life, and limited access to the brain. The aim of this study was to formulate and utilise mitochondria-targeted nanocarriers for delivery of NAC alone and in combination with the iron chelator deferoxamine (DFO), and assess their ability to protect against oxidative stress in a cellular rotenone PD model. Pluronic F68 (P68) and dequalinium (DQA) nanocarriers were prepared by a modified thin-film hydration method. An MTT assay assessed cell viability and iron status was measured using a Ferrozine assay and ferritin immunoassay. For oxidative stress, a modified cellular antioxidant activity assay and the thiobarbituric acid-reactive substances assay and mitochondrial hydroxyl assay were utilised. Overall, this study demonstrates, for the first time, successful formulation of NAC and NAC + DFO into P68 + DQA nanocarriers for neuronal delivery. The results indicate that NAC and NAC + DFO nanocarriers have the potential characteristics to access the brain and that 1000 μM P68 + DQA NAC exhibited the strongest ability to protect against reduced cell viability (p = 0.0001), increased iron (p = 0.0033) and oxidative stress (p ≤ 0.0003). These NAC nanocarriers therefore demonstrate significant potential to be transitioned for further preclinical testing for PD.
Chemical differences between long and short amosite asbestos: differences in oxidation state and coordination sites of iron, detected by infrared spectroscopy
Occup Environ Med 1999 Sep;56(9):606-11.PMID:10615293DOI:10.1136/oem.56.9.606.
Objectives: Short fibres of amosite asbestos (SFA), obtained by ball milling of long fibres (LFA), have been shown to be less pathogenic than long fibres. Accumulating evidence suggests an important role for differences in surface chemistry between fibres. Iron has been implicated in the pathogenesis of asbestos fibres. In this study infrared (IR) spectroscopy was used to compare LFA and SFA in terms of the coordination and oxidation state of iron at the three cation sites (M1, M3, M1). Methods: Infrared was used to examine LFA ad SFA, when dry and when hydrated in the presence and absence of the chelators desferroxamine and Ferrozine. With appropriate software the proportions of iron and its oxidation states in the overlapping peaks were resolved and assigned, and the three coordination sites were identified. Data were obtained from 10 samples of both lengths of fibre for each of the four treatments. Iron release was also monitored. Results: Iron was significantly more oxidised in LFA than SFA. Further oxidation of the dry fibres with water, Ferrozine, or desferroxamine tended to abolish these differences. There were also significant differences between the proportions of iron held in the different coordination sites of the fibres. For LFA, a higher proportion of its iron was held in the cation sites coordinating less with iron and more with Mg. Interestingly, the sites coordinating single irons were significantly more oxidised than multiple sites. The single iron sites were more oxidised in LFA than SFA and were more readily oxidised by the treatments. Conclusions: Important chemical differences between LFA and SFA were found. There seemed to be some mobility of iron near the surface. Based on these data it is speculated that the 1 iron surface site may be important in pathogenesis.
Dual-analyte spectroscopic sensing in sol-gel derived polyelectrolyte-silica composite thin films
Talanta 1998 Dec;47(5):1071-6.PMID:18967411DOI:10.1016/s0039-9140(98)00140-4.
Ferrozine (3-(2-pyridyl)-5,6-diphenyl-1,2,4-triazine-p,p'-disulfonic acid, monosodium salt hydrate), an iron indicator, and HTPS (8-hydroxyl-1,3,6-pyrenetrisulfonic acid, trisodium salt), a pH indicator, were immobilized in sol-gel derived PDMDAAC-SiO(2) (where PDMDAAC stands for poly(dimethyldiallylammonium chloride), composite thin films via ion-exchange. The two indicators were immobilized in two adjacent sections of the same PDMDAAC-SiO(2) film which was supported on a glass optical substrate. The spectroscopic response of the film to both Fe(2+) and H(+) in solutions was investigated by attenuated total reflection (ATR) spectrometry at two well-separated wavelengths, 562 nm for Fe(2+) and 460 nm for H(+). The Ferrozine/HPTS immobilized PDMDAAC-SiO(2) films had the following characteristics: linear range, 2.5x10(-6)-5.0x10(-5) M for Fe(2+), pH 4.1-6.8 for H(+); sensitivity, 2.2x10(4) DeltaA/M for Fe(2+), 0.583 DeltaA/pH for H(+).