Catalog | ACM9012764-51 |
CAS | 9012-76-4 |
Description | Very High DDA% – High Mol. Wt. |
Molecular Weight | 600 kDa |
Molecular Formula | (C6H11NO4)n |
Appearance | White to light yellow powder, free flowing powder |
Application | Biocompatible, antibacterial and environmentally friendly polyelectrolyte with a variety of applications including water treatment, chromatography, additives for cosmetics, textile treatment for antimicrobial activity, novel fibers for textiles, photographic papers, biodegradable films, biomedical devices, and microcapsule implants for controlled release in drug delivery. |
Storage | <25°C, cool dry environment, well-sealed |
Feature | Degree of Deacetylation (DDA) – 98.2% |
Form | Powder |
Moisture Content | 0.071 |
Packaging | 100g, 250g |
Particle Size | 100% pass 80 mesh |
pH | 8 |
Type | Source: Mushroom - Fungal, Non-Animal, Vegetal, Plant-Based Source |
Li J, et al. Molecules, 2018, 23(10). 2661.
Due to its biocompatibility, biodegradability, low toxicity, and structural variability, chitosan (CS) has long been studied as a therapeutic and diagnostic drug delivery vehicle. Here are some drug delivery research cases based on chitosan nanomaterials based on different administration routes.
· Oral Administration: Medications used for oral administration should be stable and not cause stomach problems. Santos et al designed a multifunctional and customizable composite system based on mucoadhesive chitosan for oral delivery of peptide drugs. Horcajada et al. developed a chitosan-coated mesoporous metal-organic framework (nanoMOF) as a promising oral delivery vehicle.
· Injectable drug delivery: Zhang et al. developed staged pH-responsive nanoparticles that release doxorubicin on demand. The nanoparticles contain pH-responsive dimethylmaleic acid and urocanic acid. In the slightly acidic extracellular environment of tumors, doxorubicin-loaded nanoparticles were significantly taken up by tumor tissues. The acidic environment of the endo/lysosome then triggers the on-demand release of doxorubicin from the nanoparticles.
· Topical delivery: Katsarov et al formulated chemically cross-linked chitosan microparticles for nasal delivery. These particles were shown to have high affinity for mucin in vitro and significantly prolonged drug release.
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