Photoinduced nitroso crosslinked hydrogel material and preparation method and application thereof

A technology of alkylene and o-nitrobenzyl, applied in the field of photo-induced nitroso cross-linked hydrogel materials and its preparation, can solve unfavorable clinical operations, limit the clinical transformation of non-free radical photo-coupling cross-linking technology, Problems such as slowing down of cross-linking speed

Active Publication Date: 2018-05-04
ZHONGSHAN GUANGHE MEDICAL TECH CO LTD
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  • Abstract
  • Description
  • Claims
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Problems solved by technology

However, compared with the free radical crosslinking mode, the crosslinking speed of aldehyde groups and amine groups is greatly slowed down (the initial gelation time is about 30s, and th

Method used

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  • Photoinduced nitroso crosslinked hydrogel material and preparation method and application thereof
  • Photoinduced nitroso crosslinked hydrogel material and preparation method and application thereof
  • Photoinduced nitroso crosslinked hydrogel material and preparation method and application thereof

Examples

Experimental program
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Example Embodiment

[0180] Example 1: Synthesis of component A-1

[0181]

[0182] (1) Synthesis of compound 1: According to the referenced literature Yunlong Yang; Jieyuan Zhang; Zhenzhen Liu; Qiuning Lin; Xiaolin Liu; Chunyan Bao; Yang Wang; Linyong Zhu. Adv. Mater. 2016, 28, 2724. . 1 H NMR(400MHz, CDCl 3 ): δ=7.71(s,1H),7.22(s,1H), 4.96(s,2H), 4.13(t, J=6.1Hz,2H), 3.99(s,3H), 3.32(dd,J= 11.6,5.7Hz,2H),2.82(t,J=5.9Hz,2H),2.44(t,J =7.2Hz,2H),2.26-2.17(m,2H).MS(ESI):[M+H ]328.1507.

[0183] (2) Synthesis of component A-1: ​​Dissolve Hyaluronic acid (2g, 340kDa) in 100mL0.01mol / L 2-(N-morpholine)ethanesulfonic acid MES buffer solution (pH=5.2), stir To completely dissolve, weigh compound 1 (65mg, 0.2mmol) dissolved in 10mL dimethyl sulfoxide DMSO, add the above reaction solution, weigh 4-(4,6-dimethoxytriazin-2-yl)- 4-Methylmorpholine hydrochloride DMTMM (0.4g, 1.5mmol) was dissolved in 3mL MES buffer solution and added to the above reaction solution three times (every 1h) and reacted at 35°C for 2...

Example Embodiment

[0184] Example 2: Synthesis of component A-2

[0185]

[0186] (1) Synthesis of compound 2: According to the method disclosed in the references James F. Cameron.; Jean M.J. Frechet. J. Am. Chem. Soc. 1991, 113, 4303.

[0187] (2) Synthesis of compound 3: Dissolve compound 2 (1g, 3.2mmol) and ethylenediamine (1.1mL) in methanol (50mL), reflux for overnight reaction, and rotatory evaporation under reduced pressure, and dissolve the crude product in methanol , Reprecipitated in ethyl acetate. After multiple dissolution-reprecipitation, filtration and vacuum drying, compound 3 (0.89 g, yield 82%) can be obtained. 1 H NMR (400MHz, CDCl 3 ): δ=7.71(s,1H),7.22(s,1H), 4.96(m,1H), 4.13(t,J=6.1Hz,2H), 3.99(s, 3H), 3.32(dd,J= 11.6,5.7Hz,2H), 2.82(t,J=5.9Hz,2H), 2.44(t,J=7.2Hz,2H),2.26- 2.17(m,2H),1.33(d,J=6.9Hz, 3H).MS(ESI):[M+H]342.1624.

[0188] (3) Synthesis of component A-2: Dissolve Hyaluronic acid (2g, 340kDa) in 100mL0.01mol / L 2-(N-morpholine)ethanesulfonic acid MES buffer solution (p...

Example Embodiment

[0189] Example 3: Synthesis of component A-3

[0190]

[0191] (1) Synthesis of compound 4: According to the published method of Michael C. Pirrung.; Yong Rok Lee.; Kaapjoo.; James B. Springer. J. Org. Chem. 1999, 64, 5042.

[0192] (2) Synthesis of compound 5: Dissolve compound 4 (1g, 2.7mmol) and ethylenediamine (1.1mL) in methanol (50mL), reflux for overnight reaction, and rotatory evaporation under reduced pressure, and dissolve the crude product in methanol , Reprecipitated in ethyl acetate. After multiple dissolution-reprecipitation, filtration and vacuum drying, compound 5 (0.80 g, yield 74%) can be obtained. 1 H NMR (400MHz, CDCl 3 ): δ = 7.71 (s, 1H), 7.22 (s, 1H), 6.35 (dd, J = 10.0, 15.0 Hz, 1H), 6.04 (m, 1H), 5.8 (m, 1H), 5.4 (m, 1H), 4.96 (m, 1H), 4.13 (t, J = 6.1Hz, 2H), 3.99 (s, 3H), 3.32 (dd, J = 11.6, 5.7 Hz, 2H), 2.82 (t, J = 5.9 Hz,2H),2.44(t,J=7.2Hz,2H),2.26-2.17(m,2H),1.75(d, J=6.5Hz,3H).MS(ESI):[M+H]394.1908.

[0193] (3) Synthesis of component A-3: Dissolve ...

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Abstract

The invention relates to a photoinduced nitroso crosslinked hydrogel material and a preparation method and application thereof. The preparation method comprises the following steps of dissolving a macromolecular derivative which is modified by an o-nitrobenzyl photo trigger in a component A into a biocompatible medium, so as to obtain a solution A; uniformly mixing the solution A, or adding a solution B containing a component B, so as to obtain a hydrogel precursor solution; under the condition of using light source to radiate the hydrogel precursor solution, enabling the o-nitrobenzyl photo trigger in the component A to produce nitroso groups through photo-inducing, and enabling the nitroso group to generate dimerization crosslinking by self to form the hydrogel, or generate addition crosslinking with nucleophile or electrophile in the component B to form the hydrogel. The invention also provides a kit for preparing the hydrogel, and application of the hydrogel in tissue engineering,regeneration medicines, 3D (three-dimensional) printing or cell, protein or drug carriers. The photoinduced nitroso crosslinked hydrogel material has the advantages that the hydrogel precursor solution can be sprayed or smeared onto the surface of the tissue, so as to realize the in-situ gelling under the condition of light radiation; the photoinduced nitroso crosslinked hydrogel material is especially suitable for the post-operation wound sealing and the tissue liquid leakage blockage.

Description

technical field [0001] The invention belongs to the technical field of biological materials, and in particular relates to a photo-induced nitroso-crosslinked hydrogel material and a preparation method and application thereof. Background technique [0002] Hydrogel is a kind of highly water-containing polymer material with a three-dimensional network cross-linked structure. Due to its excellent biocompatibility and certain mechanical strength, it can highly fit the microenvironment of biological tissues, so it is widely used in tissue fields of engineering and regenerative medicine. In situ cured hydrogels have excellent tissue shaping properties in clinical applications. Currently, in-situ curable hydrogels mainly include thermosensitive type (such as LeGoo, hydroxybutyl chitosan, etc.), two-component injection type (such as Fibrin Glue, Adherus AutoSpray, etc.), photosensitive Type (such as FocalSeal, ChonDux, etc.), etc. [0003] Among them, photosensitive hydrogel mate...

Claims

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Application Information

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IPC IPC(8): C08J3/075C08J3/24C08B37/08C08B37/04C08B37/02C08H1/00C08G69/48C08G65/333C08B11/12A61L24/04A61L26/00A61L27/18A61K47/34C09D11/14C09D11/102C09D11/04B33Y70/00C08L5/08C08L5/04C08L77/04C08L77/02C08L71/02C08L89/00C08L1/28
CPCA61K47/34A61L24/046A61L26/0019A61L27/18A61L2430/02A61L2430/06B33Y70/00C08B11/12C08B37/0009C08B37/003C08B37/0069C08B37/0072C08B37/0084C08G65/33396C08G69/48C08H1/00C08J3/075C08J3/246C08J2301/28C08J2305/04C08J2305/08C08J2371/02C08J2377/02C08J2377/04C08J2389/00C09D11/04C09D11/102C09D11/14
Inventor 林秋宁朱麟勇华宇杰张依晴包春燕钟学鹏
Owner ZHONGSHAN GUANGHE MEDICAL TECH CO LTD
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