933597
Poly(Guluronate)
low endotoxin
Synonym(s):
Alginate, Bioink, Bioprinting, Guluronic Acid, Hydrogel, Ionic, Sodium Alginate
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About This Item
Linear Formula:
(C6H8O6)n
UNSPSC Code:
12352201
NACRES:
NA.21
Recommended Products
description
GPC 5-15 kDa
Quality Level
form
(Solid chunks, fibres or powder)
impurities
<125 EU/g Endotoxin
<5 CFU/g Bioburden(Total aerobic)
<5 CFU/g Bioburden(fungal)
color
white to off-white
storage temp.
2-8°C
Related Categories
General description
Sodium alginate is a natural linear polysaccharide derived from brown algae made up of blocks of B-D-mannuronate (M) and a-L-guluronate (G). Guluronate blocks that bind Ca2+ cations to form ionic bonds. Poly(guluronate) is isolated from alginate which can be used alone as a stabilizer or further modified to create additional functional groups.
Application
Sodium Alginate based hydrogels are widely used in tissue engineering, 3D bioprinting, and drug delivery applications.
Features and Benefits
- Sterile, low endotoxin
- Batch control offers reproducible models for preclinical toxicology testing and drug screening
- Extended shelf-life & stability
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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K Y Lee et al.
Journal of biomedical materials research, 56(2), 228-233 (2001-05-08)
Degradable and injectable hydrogels may be ideal for bone-tissue engineering, especially in the craniofacial region because of the ease of access for injection. Alginate hydrogels potentially could be used as injectable cell delivery vehicles, but they exhibit a limited range
David Leal et al.
Carbohydrate polymers, 92(1), 157-166 (2012-12-12)
Graft copolymers were prepared by formation of an amide bond between poly-α-L-guluronic acid (MW 24,000), isolated from sodium alginate and the free amino group of PNIPAAm-NH(2). SEM micrographs revealed the formation of a macroscopic network on the surface of the
Kuen Yong Lee et al.
Biomaterials, 25(13), 2461-2466 (2004-01-31)
Hydrogels, chemically cross-linked or physically entangled, have found a number of applications as novel delivery vehicles of drugs and cells. However, the narrow ranges of degradation rates and mechanical strength currently available from many hydrogels limits their applications. We have
K H Bouhadir et al.
Journal of pharmaceutical sciences, 89(7), 910-919 (2000-06-22)
We have incorporated daunomycin, an antineoplastic agent, into a biodegradable hydrogel through a labile covalent bond. In brief, sodium alginate was chemically broken down to low molecular weight and followed by oxidation to prepare poly(aldehyde guluronate). Adipic dihydrazide was used
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