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Clodronate liposomes

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Catalog No. TCL-00390

Clodronate liposomes are composed of chlorophosphate salts encapsulated within phospholipid bilayer liposomes, which are selectively ingested by macrophages following systemic administration. Within macrophage lysosomes, phosphatases gradually release the chlorophosphate salts from the liposomal vesicles, leading to their intracellular accumulation. Once a threshold concentration is reached, the accumulation results in irreversible damage to the macrophages and induces apoptosis, making clodronate liposomes a useful research tool for investigating macrophage depletion and immune modulation.

Clodronate liposomes

Clodronate liposomes

😃Good
Catalog No. TCL-00390
Clodronate liposomes are composed of chlorophosphate salts encapsulated within phospholipid bilayer liposomes, which are selectively ingested by macrophages following systemic administration. Within macrophage lysosomes, phosphatases gradually release the chlorophosphate salts from the liposomal vesicles, leading to their intracellular accumulation. Once a threshold concentration is reached, the accumulation results in irreversible damage to the macrophages and induces apoptosis, making clodronate liposomes a useful research tool for investigating macrophage depletion and immune modulation.
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Description
Clodronate liposomes are composed of chlorophosphate salts encapsulated within phospholipid bilayer liposomes, which are selectively ingested by macrophages following systemic administration. Within macrophage lysosomes, phosphatases gradually release the chlorophosphate salts from the liposomal vesicles, leading to their intracellular accumulation. Once a threshold concentration is reached, the accumulation results in irreversible damage to the macrophages and induces apoptosis, making clodronate liposomes a useful research tool for investigating macrophage depletion and immune modulation.
In vivo
Methods for Macrophage Depletion by Clodronate liposomes in Different Tissues (For reference only; specific experimental protocols should be determined and optimized based on literature):
1. Depletion of splenic/red pulp macrophages:
Single dose: 200 μL/mouse (intravenous or intraperitoneal injection).
Long-term administration: Initial dose of 200 μL/mouse, followed by 200 μL/mouse every 2-3 days.
2. Depletion of liver/Kupffer cells:
Single dose: 200 µL/mouse (intravenous or intraperitoneal injection).
Long-term administration: Initial dose of 200 µL/mouse, followed by 200 µL/mouse every 2-3 days.
3. Depletion of alveolar macrophages:
Optimal effect achieved by intravenous injection (150-200 μL) combined with intratracheal or intranasal administration (50 μL).
4. Depletion of brain/microglia:
Intracerebroventricular or cerebrospinal fluid injection: 10 μL for mice, 50 μL for rats.
Chemical Properties
ColorWhite
AppearanceLiquid
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year

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Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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