JP2006111867A5 - - Google Patents

Info

Publication number

JP2006111867A5

JP2006111867A5 JP2005263042A JP2005263042A JP2006111867A5 JP 2006111867 A5 JP2006111867 A5 JP 2006111867A5 JP 2005263042 A JP2005263042 A JP 2005263042A JP 2005263042 A JP2005263042 A JP 2005263042A JP 2006111867 A5 JP2006111867 A5 JP 2006111867A5

Authority

JP

Japan

Prior art keywords

polysaccharide

photoreactive

photocrosslinked

gel

ultraviolet

Prior art date

2005-09-09

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Pending

Links

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• 150000004676 glycans Chemical class 0.000 description 21
• 229920001282 polysaccharide Polymers 0.000 description 21
• 239000005017 polysaccharide Substances 0.000 description 21
• 239000002131 composite material Substances 0.000 description 7
• 239000010408 film Substances 0.000 description 7
• 238000000034 method Methods 0.000 description 5
• 238000004132 cross linking Methods 0.000 description 4
• 230000001678 irradiating effect Effects 0.000 description 4
• 239000000243 solution Substances 0.000 description 4
• 230000004888 barrier function Effects 0.000 description 3
• 230000000694 effects Effects 0.000 description 3
• 238000004519 manufacturing process Methods 0.000 description 3
• KIUKXJAPPMFGSW-DNGZLQJQSA-N (2S,3S,4S,5R,6R)-6-[(2S,3R,4R,5S,6R)-3-Acetamido-2-[(2S,3S,4R,5R,6R)-6-[(2R,3R,4R,5S,6R)-3-acetamido-2,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-2-carboxy-4,5-dihydroxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid Chemical group CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@H](O3)C(O)=O)O)[C@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](C(O)=O)O1 KIUKXJAPPMFGSW-DNGZLQJQSA-N 0.000 description 2
• 238000006243 chemical reaction Methods 0.000 description 2
• 150000001875 compounds Chemical class 0.000 description 2
• 229920002674 hyaluronan Polymers 0.000 description 2
• 229960003160 hyaluronic acid Drugs 0.000 description 2
• 238000011907 photodimerization Methods 0.000 description 2
• 239000010409 thin film Substances 0.000 description 2
• WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
• WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 description 1
• 238000007605 air drying Methods 0.000 description 1
• 239000007864 aqueous solution Substances 0.000 description 1
• 229930016911 cinnamic acid Natural products 0.000 description 1
• 235000013985 cinnamic acid Nutrition 0.000 description 1
• 239000011248 coating agent Substances 0.000 description 1
• 238000000576 coating method Methods 0.000 description 1
• 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
• -1 glycidyl ester Chemical class 0.000 description 1
• 239000000463 material Substances 0.000 description 1
• QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
• 229910052753 mercury Inorganic materials 0.000 description 1
• 229910001507 metal halide Inorganic materials 0.000 description 1
• 150000005309 metal halides Chemical class 0.000 description 1
• WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
• 239000000758 substrate Substances 0.000 description 1