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Heparin sodium
- 1. Meng Ren, et al. "Gut microbial co-metabolite 2-methylbutyrylcarnitine exacerbates thrombosis via binding to and activating integrin α2β1." Cell Metab. 2024 Mar 5;36(3):598-616.e9. PMID: 38401546
- 2. Xiaomeng Li, et al. "Genotoxic mode of action and threshold exploration of 2-methyl furan under 120-day sub-chronic exposure in male Sprague-Dawley rats." Ecotoxicol Environ Saf. 2024 Mar 15:273:116125. PMID: 38394755
- 3. Yiyi Chen, Jiao Huo, et al. "Development of a novel flow cytometry‐based approach for reticulocytes micronucleus test in rat peripheral blood." J Appl Toxicol. 2021 Apr;41(4):595-606. PMID: 33067908
Physical Appearance | A solid |
Storage | Store at -20°C |
M.Wt | 50000 |
Cas No. | 9041-08-1 |
Solubility | insoluble in EtOH; insoluble in DMSO; ≥12.75 mg/mL in H2O |
Shipping Condition | Small Molecules with Blue Ice, Modified Nucleotides with Dry Ice. |
General tips | We do not recommend long-term storage for the solution, please use it up soon. |
Animal experiment:[1] | |
Animal models |
Male New Zealand rabbits with a mean body weight of 2300 ± 300 g |
Dosage form |
2000 IU heparin Administered by the intravenous route (i.v.) |
Applications |
Heparin increased both anti-factor Xa activity and activated partial thromboplastin time (aPTT). Heparin (2000 IU, i.v.) showed an AUC0→24/kg value of 3.30 ± 0.59 IU·h-1·mL-1·kg-1, with 100% absolute bioavailability. Apart from the parenteral route, heparin could also be administered by the oral route when incorporated into polymeric nanoparticles which were able to maintain the anti-Xa activity of heparin for a longer period. |
Note |
The technical data provided above is for reference only. |
References: 1. Jiao Y, Ubrich N, Marchand-Arvier M, et al. In vitro and in vivo evaluation of oral heparin-loaded polymeric nanoparticles in rabbits. Circulation, 2002, 105(2): 230-235. |
Quality Control & MSDS
- View current batch:
-
Purity = 98.00%
- COA (Certificate Of Analysis)
- MSDS (Material Safety Data Sheet)
- Datasheet