Product Name | Sucrose (for injection) |
Chemical Name | α-D-Glucopyranoside, β-D-fructofuranosyl-sucrose |
CAS No. | 57-50-1 |
NMPA CDE registration no. | F20200000093 |
USFDA DMF No. | 035209 |
Quality grade | Injection |
Quality standards | Conforms with USP, EP, JP, ChP standards |
Molecular Formula | C12H22O11 |
Applications and examples | Liposome active drug loading novel excipient (Irinotecan liposome) |
Product code | O09001 |
Package sizes | 10kg |
Storage condition | It is valid for three years when used and stored properly. |
High quality: It complies with the ChP, USP, EP and other mainstream pharmacopoeias; Key indicators such as color value, conductivity, bacterial endotoxins and microbial limits are much stricter than the pharmacopoeia requirements; Supporting the product registration abroad.
The product has been certified by a third-party authority, SGS. Stable cooperation with major pharmaceutical companies in China has been achieved;
Adequate production capacity: annual supply of 300 tons +, with the ability of expansion to 1,000 tons +/year;
Ready supply: Sufficient stock, rapid supply;
Controllable cost: significantly reduces procurement costs and improves product competitive advantage.
Sucrose is effective in reducing membrane fusion, protecting liposome particles from rupture and drug leakage during freeze-drying process, and regulating osmotic pressure. Compared with mannitol, glucose, etc., it has a higher glass transition temperature and better viscosity protection. The general dosage is 5%–10%. In addition, sucrose also plays the role of vehicle in lyophilized preparations. Studies have shown that adding sucrose has an impact on the shape, porosity and collapse of the lyophilized preparations.
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