The high-purity cholesterol (CHO) supplied by V.A.T. is suitable for the preparation of fat emulsions and liposomes. Compared to its role as an emulsifier in fat emulsions, CHO is more widely used in liposome preparation. It has been extensively employed as a membrane material in commercially available liposomal products and liposomal products (such as Lipoplatin, a liposomal cisplatin) at clinical stages.
| Product Name | CHO（plant origin） |
| Chemical Name | / |
| CAS No. | 57-88-5 |
| NMPA CDE registration no. | / |
| USFDA DMF No. | / |
| Quality grade | Injection |
| Quality standards | Manufacturer's standard |
| Molecular Formula | C27H46O |
| Applications and examples | CHO-HP (plant-derived) is high-purity cholesterol used in formulations of emulsions, liposomes, and lipid nanoparticles (LNPs). Compared to its use as an emulsifier for lipid emulsions, it has a broader application in the field of liposomes. |
| Product code | B03001 |
| Package sizes | 5g, 10g, 50g |
| Storage condition | This product should be stored and transported in a sealed and light-protected container at controlled room temperature. Retest annually when stored properly. |
CHO can insert into the phospholipid bilayer of liposomes, interacting with phospholipid molecules to modulate the fluidity of the liposome membrane. Its effect varies with temperature changes;
As CHO is amphiphilic, possessing both hydrophilic and hydrophobic properties, it can enhance the stability of liposomes by regulating the liposome membrane.
Traditional liposomes are primarily composed of phospholipids and cholesterol. Being a key component of the liposomal bilayer, CHO presents in almost all marketed products (refer to Table 1). In Shingrix (Zoster Vaccine Recombinant, Adjuvanted), CHO is used in a 2:1 ratio (CHO:QS21, w/w) to prevent the hydrolysis of the immune-enhancing agent QS21 in the adjuvant AS01B. In AmBisome (Amphotericin B liposome), CHO maintains the stability of the liposome in the bloodstream, preventing drug leakage while also reducing the toxicity of the liposomal formulation.
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