Cardiogreen (Foxgreen)
(Synonyms: 吲哚菁绿; Foxgreen; IC Green; Cardiogreen) 目录号 : GC30003Cardiogreen (Foxgreen, indocyanine green) 是一种两亲性碘化三碳菁染料,可与蛋白质结合形成非共价荧光复合物,用于蛋白质测定。
Cas No.:3599-32-4
Sample solution is provided at 25 µL, 10mM.
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Cardiogreen 在细胞中的摄取试验: |
Cardiogreen (Foxgreen, indocyanine green)是一种无毒的生物染料,只有经静脉注射后才能被肝细胞吸收,然后由肝细胞分泌。在无血清培养基中培养时,肝细胞摄取 Cardiogreen,细胞质呈绿色。血清恢复后, Cardiogreen从细胞质中分泌出来。 1. 将Cardiogreen加入终浓度为1mg /mL的无血清肝细胞培养基中,在37℃下培养1小时。 2. 除去无血清培养基,用PBS洗涤细胞三次。 3. 用显微镜对细胞检查和成像。 |
研究Cardiogreen脂质体对小鼠尿路的成像 [1]: |
0 ~ 0.8 μM Cardiogreen分别与1%脂质体和20 μM或200 μM pyrene孵育,评估极性和流动性。用荧光分光光度计测定激发波长335 nm处的荧光光谱。
研究Liposomal Cardiogreen 在泌尿系统积累:
仅供参考,请根据您的实验具体需要进行修改。 |
References: [1].Portnoy E, Nizri E, et,al. Imaging the urinary pathways in mice by liposomal indocyanine green. Nanomedicine. 2015 Jul;11(5):1057-64. doi: 10.1016/j.nano.2015.02.019. Epub 2015 Mar 16. PMID: 25791809. |
Cardiogreen (Foxgreen, indocyanine green) is an amphiphilic iodized tricarbocyanine dye (mass = 751.4 Da) that can be reconstituted in aqueous solutions at pH 6.5. It is negatively charged and binds to proteins to form non-covalent fluorescent complexes that can be used in capillary electrophoresis semiconductor laser-induced fluorescence detection for protein determination[1-3].
Cardiogreen can be used to isolate several labeled proteins, including human blood harmless protein, nuclease a, transferrin, and cytochrome C. Used intravenously in patients, within the blood vessels, the compound binds to plasma proteins that confine most of the drug to the blood vessels until it is taken up by the liver and excreted into the bile. Cardiogreen is also widely applied in off-label use for real-time imaging for abdominal surgery, plastic surgery, and in oncologic staging and treatment[4-7].
References:
[1]. Alander JT, Kaartinen I, et,al.A review of indocyanine green fluorescent imaging in surgery. Int J Biomed Imaging. 2012;2012:940585. doi: 10.1155/2012/940585. Epub 2012 Apr 22. PMID: 22577366; PMCID: PMC3346977.
[2]. Alander JT, Kaartinen I, et,al. A review of indocyanine green fluorescent imaging in surgery. Int J Biomed Imaging. 2012;2012:940585. doi: 10.1155/2012/940585. Epub 2012 Apr 22. PMID: 22577366; PMCID: PMC3346977.
[3]. Engel E, Schraml R, et,al.Light-induced decomposition of indocyanine green. Invest Ophthalmol Vis Sci. 2008 May;49(5):1777-83. doi: 10.1167/iovs.07-0911. PMID: 18436812.
[4]. Portnoy E, Nizri E, et,al. Imaging the urinary pathways in mice by liposomal indocyanine green. Nanomedicine. 2015 Jul;11(5):1057-64. doi: 10.1016/j.nano.2015.02.019. Epub 2015 Mar 16. PMID: 25791809.
[5]. Petrut B, Bujoreanu CE, et,al.Indocyanine green use in Urology. J BUON. 2021 Jan-Feb;26(1):266-274. PMID: 33721461.
[6]. Maarek JM, Holschneider DP. Estimation of indocyanine green concentration in blood from fluorescence emission: application to hemodynamic assessment during hemodialysis. J Biomed Opt. 2009 Sep-Oct;14(5):054006. doi: 10.1117/1.3233652. PMID: 19895108.
[7]. Pollack GM, Brouwer KL, et,al. Determination of hepatic blood flow in the rat using sequential infusions of indocyanine green or galactose. Drug Metab Dispos. 1990 Mar-Apr;18(2):197-202. PMID: 1971573.
Cardiogreen (Foxgreen, indocyanine green) 是一种两亲性碘化三碳菁染料(质量= 751.4 Da),可在pH 6.5的水溶液中重构。它带负电荷,与蛋白质结合形成非共价荧光复合物,可用于毛细管电泳半导体激光诱导荧光检测,用于蛋白质测定[1-3]。
Cardiogreen可用于分离几种标记蛋白,包括人血无害蛋白、核酸酶a、转铁蛋白和细胞色素C。患者静脉注射时,在血管内,该化合物与血浆蛋白结合,将大部分药物限制在血管内,直到被肝脏吸收并排泄到胆汁中。Cardiogreen还广泛应用于非适应症下的腹部手术、整形手术、肿瘤分期和治疗的实时成像[4-7]。
Cas No. | 3599-32-4 | SDF | |
别名 | 吲哚菁绿; Foxgreen; IC Green; Cardiogreen | ||
Canonical SMILES | O=S(CCCC[N+]1=C(/C=C/C=C/C=C/C=C2N(CCCCS(=O)([O-])=O)C3=C(C4=CC=CC=C4C=C3)C/2(C)C)C(C)(C)C5=C1C=CC6=CC=CC=C56)([O-])=O.[Na+] | ||
分子式 | C43H47N2NaO6S2 | 分子量 | 774.96 |
溶解度 | DMF: 10 mg/ml; DMSO: 10 mg/ml; Ethanol: 1 mg/ml; ddH2O:1mg/ml | 储存条件 | Store at -20°C ,protect from light |
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。 |
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1 mg | 5 mg | 10 mg | |
1 mM | 1.2904 mL | 6.4519 mL | 12.9039 mL |
5 mM | 0.2581 mL | 1.2904 mL | 2.5808 mL |
10 mM | 0.129 mL | 0.6452 mL | 1.2904 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 | |||
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% DMSO % % Tween 80 % saline | ||||||||||
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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。
Indocyanine Green: Historical Context, Current Applications, and Future Considerations
Background: Indocyanine green (ICG) is a dye used in medicine since the mid-1950s for a variety of applications in in cardiology, ophthalmology, and neurosurgery; however, its fluorescent properties have only recently been used in the intraoperative evaluation of tissue perfusion. Method: A literature review was conducted on the characterization and employment of ICG within the medical field. Historical and current context of ICG was examined while also considering implications for its future use. Results: ICG is a relatively nontoxic, unstable compound bound by albumin in the intravascular space until rapid clearance by the liver. It has widespread uses in hepatic, cardiac, and ophthalmologic studies, and its use in analyzing tissue perfusion and identifying sentinel lymph nodes in cancer staging is gaining popularity. Conclusions: ICG has myriad applications and poses low risk to the patient. Its historical uses have contributed to medical knowledge, and it is now undergoing investigation for quantifying tissue perfusion, providing targeted therapies, and intraoperative identification of neurovascular anatomy, ophthalmic structures, and sentinel lymph nodes. New applications of ICG may lead to reduction in postoperative wound-related complications, more effective ophthalmologic procedures, and better detection and treatment of cancer cells.
NIR fluorescence-guided tumor surgery: new strategies for the use of indocyanine green
Surgery is the frontline treatment for a large number of cancers. The objective of these excisional surgeries is the complete removal of the primary tumor with sufficient safety margins. Removal of the entire tumor is essential to improve the chances of a full recovery. To help surgeons achieve this objective, near-infrared fluorescence-guided surgical techniques are of great interest. The concomitant use of fluorescence and indocyanine green (ICG) has proved effective in the identification and characterization of tumors. Moreover, ICG is authorized by the Food and Drug Administration and the European Medicines Agency and is therefore the subject of a large number of studies. ICG is one of the most commonly used fluorophores in near-infrared fluorescence-guided techniques. However, it also has some disadvantages, such as limited photostability, a moderate fluorescence quantum yield, a high plasma protein binding rate, and undesired aggregation in aqueous solution. In addition, ICG does not specifically target tumor cells. One way to exploit the capabilities of ICG while offsetting these drawbacks is to develop high-performance near-infrared nanocomplexes formulated with ICG (with high selectivity for tumors, high tumor-to-background ratios, and minimal toxicity). In this review article, we focus on recent developments in ICG complexation strategies to improve near-infrared fluorescence-guided tumor surgery. We describe targeted and nontargeted ICG nanoparticle models and ICG complexation with targeting agents.
Comparison of indocyanine green dye fluorescent cholangiography with intra-operative cholangiography in laparoscopic cholecystectomy: a meta-analysis
Objective: To compare indocyanine green dye fluorescence cholangiography (ICG-FC) with intra-operative cholangiography (IOC) in minimal access cholecystectomy for visualization of the extrahepatic biliary tree.
Background: Although studies have shown that ICG-FC is safe, feasible, and comparable to IOC to visualize the extrahepatic biliary tree, there is no comparative review.
Methods: We searched The Embase, PubMed, Cochrane Library, and Web of Science databases up to 8 April 2020 for all studies comparing ICG-FC with IOC in patients undergoing minimal access cholecystectomy. The primary outcomes were percentage visualization of the cystic duct (CD), common bile duct (CBD), CD-CBD junction, and the common hepatic duct (CHD). We used RevMan v5.3 software to analyze the data.
Results: Seven studies including 481 patients were included. Five studies, comprising 275 patients reported higher CD (RR = 0.90, p = 0.12, 95% CI 0.79-1.03, I2 = 74%) and CBD visualization rates (RR = 0.82, p = 0.09, 95% CI 0.65-1.03, I2 = 87%) by ICG-FC. Four studies, comprising 223 patients, reported higher CD-CBD junction visualization rates using ICG-FC compared to IOC (RR = 0.68, p = 0.06, 95% CI = 0.45-1.02, I2 = 94%). Four studies, comprising 210 patients, reported higher CHD visualization rates using ICG-FC compared to IOC (RR = 0.58, p = 0.03, 95% CI 0.35-0.93, I2 = 91%).
Conclusion: ICG-FC is safe, and it improves visualization of CHD.
The Future Is Bright Green
Self-assembled nanoparticles containing photosensitizer and polycationic brush for synergistic photothermal and photodynamic therapy against periodontitis
Background: Periodontitis is a chronic inflammatory disease in oral cavity owing to bacterial infection. Photothermal therapy (PTT) and photodynamic therapy (PDT) have many advantages for antibacterial treatment. As an excellent photosensitizer, indocyanine green (ICG) shows prominent photothermal and photodynamic performances. However, it is difficult to pass through the negatively charged bacterial cell membrane, thus limiting its antibacterial application for periodontitis treatment.
Results: In this work, self-assembled nanoparticles containing ICG and polycationic brush were prepared for synergistic PTT and PDT against periodontitis. First, a star-shaped polycationic brush poly(2-(dimethylamino)ethyl methacrylate) (sPDMA) was synthesized via atom transfer radical polymerization (ATRP) of DMA monomer from bromo-substituted β-cyclodextrin initiator (CD-Br). Next, ICG was assembled with sPDMA to prepare ICG-loaded sPDMA (sPDMA@ICG) nanoparticles (NPs) and the physicochemical properties of these NPs were characterized systematically. In vitro antibacterial effects of sPDMA@ICG NPs were investigated in porphyromonas gingivalis (Pg), one of the recognized periodontitis pathogens. A ligature-induced periodontitis model was established in Sprague-Dawley rats for in vivo evaluation of anti-periodontitis effects of sPDMA@ICG NPs. Benefiting from the unique brush-shaped architecture of sPDMA polycation, sPDMA@ICG NPs significantly promoted the adsorption and penetration of ICG into the bacterial cells and showed excellent PTT and PDT performances. Both in vitro and in vivo, sPDMA@ICG NPs exerted antibacterial and anti-periodontitis actions via synergistic PTT and PDT.
Conclusions: A self-assembled nanosystem containing ICG and polycationic brush has shown promising clinical application for synergistic PTT and PDT against periodontitis.