2014
DOI: 10.1002/jbm.a.35106
|View full text |Cite
|
Sign up to set email alerts
|

Sugar-based crosslinker forms a stable atelocollagen hydrogel that is a favorable microenvironment for 3D cell culture

Abstract: We created sugar-based crosslinkers for precise chemical crosslinking of atelocollagen to form a stable hydrogel microenvironment for three-dimensional (3D) cell culture. Crosslinkers were synthesized by partially oxidizing glucose, fructose, maltose, sucrose, or raffinose with periodate. The partial oxidization of sugar generated multiple aldehydes in the molecule, which acted as multifunctional crosslinkers, allowing atelocollagen to form chemical hydrogels. The crosslink reaction of atelocollagen was compet… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3

Citation Types

1
14
0
1

Year Published

2015
2015
2023
2023

Publication Types

Select...
8
1

Relationship

0
9

Authors

Journals

citations
Cited by 16 publications
(16 citation statements)
references
References 19 publications
1
14
0
1
Order By: Relevance
“…There are chemical, physical and biological methods available to improve collagen properties. Chemical crosslinking is mostly accomplished by glutaraldehyde [ 13 , 14 , 15 ], ethyl-3(3-dimethylamino) propyl carbodiimide/ N-hydroxysuccinimide (EDC/NHS) [ 11 , 16 , 17 ], diisocyanates [ 18 , 19 ] or oxidized sugar [ 20 , 21 ]. However, chemical crosslinking is often time consuming due to the required wash steps, potentially leaves toxic residues and may reduce biocompatibility [ 18 , 22 ].…”
Section: Introductionmentioning
confidence: 99%
“…There are chemical, physical and biological methods available to improve collagen properties. Chemical crosslinking is mostly accomplished by glutaraldehyde [ 13 , 14 , 15 ], ethyl-3(3-dimethylamino) propyl carbodiimide/ N-hydroxysuccinimide (EDC/NHS) [ 11 , 16 , 17 ], diisocyanates [ 18 , 19 ] or oxidized sugar [ 20 , 21 ]. However, chemical crosslinking is often time consuming due to the required wash steps, potentially leaves toxic residues and may reduce biocompatibility [ 18 , 22 ].…”
Section: Introductionmentioning
confidence: 99%
“…The molecular size of oxidized oligosaccharides depends on the size of their precursors, so mono- and oligosaccharide-derived ones are reasonably small and could access the deep part of protein hydrogel by free diffusion from a heterogeneous phase. However, to the best of our knowledge, so far this type of compound has only been used in highly dispersed systems by premixing, such as solutions of chitosan [ 12 ], corn starch [ 13 ], atelocollagen [ 14 ] and keratin [ 15 ], but no study on a heterogeneous system has been reported. Furthermore, compared with normal polyaldehydes, oxidized oligosaccharides bear abundant hydroxyl groups which provide higher water solubility and biocompatibility [ 15 , 16 ].…”
Section: Introductionmentioning
confidence: 99%
“…Alternatively, click reactions, formed by the mixing of click group‐modified ECM solutions, can rapidly form drug depots with tunable mechanical properties for in vivo applications . In recent years, click reactions (e.g., copper‐catalyzed azide–alkyne cycloaddition or photoclick reactions) have been used to rapidly form ECM hydrogel depots at physiologically relevant conditions .…”
Section: Introductionmentioning
confidence: 95%