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Metronidazole 是一種硝基咪唑類(lèi)抗生素,具有口服活性。Metronidazole 能夠穿過(guò)血腦屏障。Metronidazole 可用于厭氧微生物感染的研究。
生物活性
Metronidazole is an orally active nitroimidazole antibiotic. Metronidazole can cross blood brain barrier. Metronidazole can be used for the research of anaerobic infections[1][2][3][4].
體外研究(In Vitro)
Metronidazole displays inhibitory activity towards anaerobic protozoa Trichomonas vaginalis, Entamoeba histolytica, Giardia lamblia, and Balantidium coli[1].
Metronidazole (4-8 μg/mL) inhibits anaerobic bacteria and shows good bactericidal activity[1].
Metronidazole (0.1 μg/mL-0.01 mg/mL; 12-96 h) induces granular formation and triggers apoptosis in Blastocystis sp[2].
Apoptosis Analysis[2]
Cell Line: | Blastocystis sp. Cells |
Concentration: | 0.1 μg/mL-0.01 mg/mL |
Incubation Time: | 12, 24, 48, 60, 72, 84, 96 hours |
Result: | Decreased cell diameter, as a hallmark of an apoptotic cell, and resulted cell shrinkage. |
體內(nèi)研究(In Vivo)
Metronidazole (135 mg/kg/d; p.o.; 28 d) can cross the blood brain barrier, and exhibits neurotoxicity under long term administration in rats[3].
Metronidazole (1 g/L; p.o.; 4 weeks) results skeletal muscle atrophy and changes the expression of genes involved in the muscle peripheral circadian rhythm machinery and metabolic regulation[4].
Animal Model: | Sprague-Dawley (SD) rats (200-220 g)[3] |
Dosage: | 135 mg/kg |
Administration: | Oral gavage; once daily; 28 days |
Result: | Caused inflammatory markers increasing, including iNOS, eNOS, Bax and caspase 3 protein expressions increasing and caused oxidative stress damage in brain tissue, with MDA content rising. |
分子量:171.15
Formula:C6H9N3O3
CAS 號(hào):443-48-1
中文名稱:甲硝唑
來(lái)源:Gram-negative and Gram-positive anaerobic
運(yùn)輸條件:Room temperature in continental US; may vary elsewhere.
儲(chǔ)存方式:
4°C, protect from light
*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
溶解性數(shù)據(jù)
DMSO : 35 mg/mL (204.50 mM; Need ultrasonic and warming)
H2O : 16.67 mg/mL (97.40 mM; Need ultrasonic)
濃度溶劑體積質(zhì)量 | 1 mg | 5 mg | 10 mg |
---|
1 mM | 5.8428 mL | 29.2141 mL | 58.4283 mL |
5 mM | 1.1686 mL | 5.8428 mL | 11.6857 mL |
10 mM | 0.5843 mL | 2.9214 mL | 5.8428 mL |
請(qǐng)根據(jù)產(chǎn)品在不同溶劑中的溶解度選擇合適的溶劑配制儲(chǔ)備液;一旦配成溶液,請(qǐng)分裝保存,避免反復(fù)凍融造成的產(chǎn)品失效。
儲(chǔ)備液的保存方式和期限:-80°C, 6 months; -20°C, 1 month (protect from light)。-80°C 儲(chǔ)存時(shí),請(qǐng)?jiān)?6 個(gè)月內(nèi)使用,-20°C 儲(chǔ)存時(shí),請(qǐng)?jiān)?1 個(gè)月內(nèi)使用。
以下溶解方案都請(qǐng)先按照 In Vitro 方式配制澄清的儲(chǔ)備液,再依次添加助溶劑:
——為保證實(shí)驗(yàn)結(jié)果的可靠性,澄清的儲(chǔ)備液可以根據(jù)儲(chǔ)存條件,適當(dāng)保存;體內(nèi)實(shí)驗(yàn)的工作液,建議您現(xiàn)用現(xiàn)配,當(dāng)天使用; 以下溶劑前顯示的百
分比是指該溶劑在您配制終溶液中的體積占比;如在配制過(guò)程中出現(xiàn)沉淀、析出現(xiàn)象,可以通過(guò)加熱和/或超聲的方式助溶
請(qǐng)依序添加每種溶劑: 10% DMSO 90% (20% SBE-β-CD in saline)
Solubility: ≥ 2.08 mg/mL (12.15 mM); Clear solution
參考文獻(xiàn)
Metronidazole 是一種硝基咪唑類(lèi)抗生素,具有口服活性。Metronidazole 能夠穿過(guò)血腦屏障。Metronidazole 可用于厭氧微生物感染的研究。
生物活性
Metronidazole is an orally active nitroimidazole antibiotic. Metronidazole can cross blood brain barrier. Metronidazole can be used for the research of anaerobic infections[1][2][3][4].
體外研究(In Vitro)
Metronidazole displays inhibitory activity towards anaerobic protozoa Trichomonas vaginalis, Entamoeba histolytica, Giardia lamblia, and Balantidium coli[1].
Metronidazole (4-8 μg/mL) inhibits anaerobic bacteria and shows good bactericidal activity[1].
Metronidazole (0.1 μg/mL-0.01 mg/mL; 12-96 h) induces granular formation and triggers apoptosis in Blastocystis sp[2].
Apoptosis Analysis[2]
Cell Line: | Blastocystis sp. Cells |
Concentration: | 0.1 μg/mL-0.01 mg/mL |
Incubation Time: | 12, 24, 48, 60, 72, 84, 96 hours |
Result: | Decreased cell diameter, as a hallmark of an apoptotic cell, and resulted cell shrinkage. |
體內(nèi)研究(In Vivo)
Metronidazole (135 mg/kg/d; p.o.; 28 d) can cross the blood brain barrier, and exhibits neurotoxicity under long term administration in rats[3].
Metronidazole (1 g/L; p.o.; 4 weeks) results skeletal muscle atrophy and changes the expression of genes involved in the muscle peripheral circadian rhythm machinery and metabolic regulation[4].
Animal Model: | Sprague-Dawley (SD) rats (200-220 g)[3] |
Dosage: | 135 mg/kg |
Administration: | Oral gavage; once daily; 28 days |
Result: | Caused inflammatory markers increasing, including iNOS, eNOS, Bax and caspase 3 protein expressions increasing and caused oxidative stress damage in brain tissue, with MDA content rising. |
分子量:171.15
Formula:C6H9N3O3
CAS 號(hào):443-48-1
中文名稱:甲硝唑
來(lái)源:Gram-negative and Gram-positive anaerobic
運(yùn)輸條件:Room temperature in continental US; may vary elsewhere.
儲(chǔ)存方式:
4°C, protect from light
*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
溶解性數(shù)據(jù)
DMSO : 35 mg/mL (204.50 mM; Need ultrasonic and warming)
H2O : 16.67 mg/mL (97.40 mM; Need ultrasonic)
濃度溶劑體積質(zhì)量 | 1 mg | 5 mg | 10 mg |
---|
1 mM | 5.8428 mL | 29.2141 mL | 58.4283 mL |
5 mM | 1.1686 mL | 5.8428 mL | 11.6857 mL |
10 mM | 0.5843 mL | 2.9214 mL | 5.8428 mL |
請(qǐng)根據(jù)產(chǎn)品在不同溶劑中的溶解度選擇合適的溶劑配制儲(chǔ)備液;一旦配成溶液,請(qǐng)分裝保存,避免反復(fù)凍融造成的產(chǎn)品失效。
儲(chǔ)備液的保存方式和期限:-80°C, 6 months; -20°C, 1 month (protect from light)。-80°C 儲(chǔ)存時(shí),請(qǐng)?jiān)?6 個(gè)月內(nèi)使用,-20°C 儲(chǔ)存時(shí),請(qǐng)?jiān)?1 個(gè)月內(nèi)使用。
以下溶解方案都請(qǐng)先按照 In Vitro 方式配制澄清的儲(chǔ)備液,再依次添加助溶劑:
——為保證實(shí)驗(yàn)結(jié)果的可靠性,澄清的儲(chǔ)備液可以根據(jù)儲(chǔ)存條件,適當(dāng)保存;體內(nèi)實(shí)驗(yàn)的工作液,建議您現(xiàn)用現(xiàn)配,當(dāng)天使用; 以下溶劑前顯示的百
分比是指該溶劑在您配制終溶液中的體積占比;如在配制過(guò)程中出現(xiàn)沉淀、析出現(xiàn)象,可以通過(guò)加熱和/或超聲的方式助溶
請(qǐng)依序添加每種溶劑: 10% DMSO 90% (20% SBE-β-CD in saline)
Solubility: ≥ 2.08 mg/mL (12.15 mM); Clear solution
參考文獻(xiàn)