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CN1119172C - Chitosan/gelatin network modification on surface of aliphatic polyester - Google Patents

Chitosan/gelatin network modification on surface of aliphatic polyester Download PDF

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CN1119172C
CN1119172C CN 00134077 CN00134077A CN1119172C CN 1119172 C CN1119172 C CN 1119172C CN 00134077 CN00134077 CN 00134077 CN 00134077 A CN00134077 A CN 00134077A CN 1119172 C CN1119172 C CN 1119172C
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polylactic acid
gelatin
chitosan
film
acid film
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CN1296852A (en
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姚康德
沈锋
崔元璐
成国祥
蔡开勇
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Tianjin University
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Tianjin University
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Abstract

一种以N-羧甲基壳聚糖和明胶为修饰剂,采用碱性直接活化法对聚乳酸表面进行修饰,在聚乳酸表面引入细胞活性基团,制备软骨细胞支架材料的方法,由于壳聚糖是一种碱性多糖,它与聚乳酸同时降解,还可以对聚乳酸降解过程中对环境产生pH脉冲作用起到抑制作用,提高了聚乳酸材料表面的细胞亲和性。A method of using N-carboxymethyl chitosan and gelatin as modifiers, modifying the surface of polylactic acid by an alkaline direct activation method, introducing cell active groups on the surface of polylactic acid, and preparing a chondrocyte scaffold material. Glycan is a kind of basic polysaccharide, it degrades with polylactic acid at the same time, and can also inhibit the pH pulse effect on the environment during the degradation of polylactic acid, and improve the cell affinity of the surface of polylactic acid materials.

Description

脂肪族聚酯表面的壳聚糖/明胶网络修饰方法Modification method of chitosan/gelatin network on the surface of aliphatic polyester

                           技术领域Technical field

本发明属于生物医学工程。The invention belongs to biomedical engineering.

                           技术背景 technical background

组织工程学是运用工程科学与生命科学的基本原理和方法,研究与开发生物学替代物来恢复、维持和改进组织功能的一门新兴学科。是在体外分离、培养细胞,将一定量的细胞种植到具有一定形状的三维生物材料支架内,并加以持续培养,最终形成具有一定结构的组织和器官并回植体内达到修复和/或重建的目的。目前的工作多以合成材料为主,尤其是以聚乳酸类为基材制作支架材料。研究表明,聚乳酸类材料表面缺乏细胞结合位点[Rouhi A M,Contemporary biomaterials,Understanding surfaces is key to the design of clinically useful materials,Chem EngNews,1999,77(3):51-59],且其降解产物呈酸性,产物的pH脉冲作用在一定程度上造成无菌炎症[Peppas H A,Langer R,New challenges in biomaterials,Science,1994,263:1715-1720;Lam K,Esselbrugge H,Schakenrad J,Biodegradable of porousversus non-porous poly(L-lactic acid)film,J Mater Sci:Mater Med,1994,5(2):101-110]。大内辰郎等以聚[(乳酸-共-羟基乙酸)-赖氨酸]微球表面官能团经化学修饰引入糖链,赋予其细胞识别功能[大矢裕一,大内辰郎,生分解性バイオマテリアルとしての新しいポリ乳酸系高分子,高分子加工,1999,48(12):530-534]。其缺点为:反应过程中容易残留细胞毒性试剂,且步骤烦琐,难于操作;另一方面,没有考虑对聚乳酸降解过程中的pH脉冲加以抑制。山冈哲二等以碱性条件下直接活化法用明胶修饰聚乳酸表面,效果良好[山冈哲二,竹部羲之,木村良晴,高分子论文集,1998,55(6),328-333]。然而,山冈等同样没有考虑对聚乳酸酸性降解产物对周围环境的影响加以抑制。上述方法的缺陷在于:没有从复合的仿生角度出发,同时考虑采用避免高毒试剂化学表面修饰和抑制聚乳酸降解产生的pH脉冲作用。Tissue engineering is an emerging discipline that uses the basic principles and methods of engineering science and life science to research and develop biological substitutes to restore, maintain and improve tissue functions. It is to separate and cultivate cells in vitro, plant a certain amount of cells into a three-dimensional biomaterial scaffold with a certain shape, and continue to cultivate them, and finally form tissues and organs with a certain structure and implant them back into the body to achieve repair and/or reconstruction. Purpose. The current work is mostly based on synthetic materials, especially polylactic acid as the base material to make scaffold materials. Studies have shown that the surface of polylactic acid materials lacks cell binding sites [Rouhi A M, Contemporary biomaterials, Understanding surfaces is key to the design of clinically useful materials, Chem EngNews, 1999, 77(3): 51-59], and its The degradation product is acidic, and the pH pulse action of the product causes sterile inflammation to a certain extent [Peppas H A, Langer R, New challenges in biomaterials, Science, 1994, 263: 1715-1720; Lam K, Esselbrugge H, Schakenrad J, Biodegradable of porousversus non-porous poly(L-lactic acid) film, J Mater Sci: Mater Med, 1994, 5(2): 101-110]. Ouchi Tatsuro et al. introduced sugar chains through chemical modification of poly[(lactic acid-co-glycolic acid)-lysine] microsphere surface functional groups to endow them with cell recognition function [Ouchi Yuichi, Ouchi Tatsuro, Biodegradable biomaterialsの新しいポリ Lactic acid-based polymers, Polymer Processing, 1999, 48(12): 530-534]. Its disadvantages are: cytotoxic reagents are easy to remain in the reaction process, and the steps are cumbersome and difficult to operate; on the other hand, the pH pulse in the degradation process of polylactic acid is not considered to be suppressed. Tetsuji Yamaoka et al used direct activation method under alkaline conditions to modify the surface of polylactic acid with gelatin. However, Yamaoka et al. also did not consider to suppress the impact of the acidic degradation products of PLA on the surrounding environment. The disadvantage of the above method is that it does not consider the use of chemical surface modification of highly toxic reagents and the pH pulse effect of inhibiting the degradation of polylactic acid from the perspective of composite bionics.

                         发明内容Contents of invention

本发明的目的是以N-羧甲基壳聚糖和明胶为修饰剂,采用碱性直接活化法对聚乳酸表面进行修饰。不但可以用相对简单的方法在聚乳酸表面引入细胞活性基团,而且壳聚糖是一种碱性多糖,它与聚乳酸同时降解,还可以对聚乳酸降解过程中对环境产生pH脉冲作用起到抑制作用,克服已有技术存在的问题。The object of the invention is to use N-carboxymethyl chitosan and gelatin as modifiers, and adopt an alkaline direct activation method to modify the surface of polylactic acid. Not only can a relatively simple method be used to introduce cell active groups on the surface of polylactic acid, but also chitosan is an alkaline polysaccharide, which can be degraded simultaneously with polylactic acid, and can also play a role in the pH pulse of the environment during the degradation of polylactic acid. To the inhibitory effect, overcome the problems existing in the prior art.

本发明脂肪族聚酯表面的壳聚糖/明胶网络修饰方法的内容为:配制浓度为1~10重量%聚乳酸的氯仿溶液,将其流延成膜,然后用去离子水冲洗后,在40℃条件下烘干,得到聚乳酸薄膜。以浓度为0.1~2mol/L的NaOH水溶液配制2~7重量%的N-羧甲基壳聚糖水溶液,按壳聚糖与明胶重量比1∶5至5∶1的比例加入明胶,在45℃条件下微搅拌2~4小时,得到N-羧甲基壳聚糖-明胶的碱性溶液。将聚乳酸膜浸入N-羧甲基壳聚糖-明胶的碱性溶液中,在45℃条件下搅拌0.5~4小时。将薄膜取出,用去离子水冲洗3~10次,在40℃条件下干燥1~3小时。再将改性后的薄膜采用60Co射线进行2~10小时处理,累计10~80万拉德剂量的照射以达到灭菌,用聚乙烯薄膜将薄膜密封后待用。The content of the chitosan/gelatin network modification method on the surface of aliphatic polyester of the present invention is: preparation concentration is the chloroform solution of polylactic acid of 1~10% by weight, casts it into film, after washing with deionized water then, in Dry at 40°C to obtain a polylactic acid film. Be that the NaOH aqueous solution preparation 2~7 weight % of N-carboxymethyl chitosan aqueous solution with concentration is 0.1~2mol/L, add gelatin by the ratio of chitosan and gelatin weight ratio 1:5 to 5:1, at 45 Stir slightly under the condition of ℃ for 2-4 hours to obtain an alkaline solution of N-carboxymethyl chitosan-gelatin. The polylactic acid film is immersed in the alkaline solution of N-carboxymethyl chitosan-gelatin, and stirred at 45 DEG C for 0.5-4 hours. The film is taken out, rinsed with deionized water for 3 to 10 times, and dried at 40° C. for 1 to 3 hours. Then, the modified film is treated with 60 Co rays for 2-10 hours, with a cumulative dose of 100,000-800,000 rads to achieve sterilization. The film is sealed with a polyethylene film before use.

本发明采用细胞相容性良好的天然可降解生物材料修饰合成生物材料聚乳酸表面。其突出优点是一方面为材料表面引入细胞结合位点;另一方面可以通过反应程度调整聚乳酸材料表面的亲/疏水平衡性;而且壳聚糖的引入可以抑制聚乳酸降解过程中对环境产生的pH脉冲效应,该改性手段能提高聚乳酸材料表面的细胞亲和性。The invention adopts the natural degradable biological material with good cell compatibility to modify the surface of the synthetic biological material polylactic acid. Its outstanding advantages are that on the one hand, it introduces cell binding sites for the surface of the material; on the other hand, it can adjust the hydrophilic/hydrophobic balance of the surface of the polylactic acid material through the degree of reaction; and the introduction of chitosan can inhibit the environment during the degradation of polylactic acid. The pH pulse effect, the modification method can improve the cell affinity of the surface of the polylactic acid material.

                         具体实施方式 Detailed ways

取分子量10.8×104,左旋度98%的医用聚乳酸0.5g置入三角烧瓶中,加入10ml氯仿,室温下放置12小时,使聚乳酸完全溶解。将溶液移入120cm玻璃培养皿中,放入真空干燥箱,维持干燥室气压小于50μatm,保持12小时。流延成膜后,用去离子水冲洗,然后在40℃条件下烘干,得到聚乳酸薄膜。将流延形成的薄膜取下,用去离子水反复冲洗,置入烘箱,在40℃下保持4小时,得到不含溶剂的聚乳酸薄膜。以50ml浓度为1mol/L的NaOH水溶液配制2重量%的N-羧甲基壳聚糖水溶液,按壳聚糖与明胶重量比1∶1的比例加入明胶,在45℃条件下轻微搅拌4小时,得到N-羧甲基壳聚糖-明胶的碱性溶液。将聚乳酸薄膜浸入N-羧甲基壳聚糖-明胶的碱性溶液中,在45℃条件下搅拌4小时。将处理后的薄膜取出,用去离子水冲洗3次,在40℃条件下干燥3小时。再将改性后的薄膜采用60Co射线进行2~10小时,累计10~80万拉德剂量的照射以达到灭菌,即得到经N-羧甲基壳聚糖和明胶改性的聚乳酸薄膜,用聚乙烯薄膜将制备的聚乳酸薄膜密封后待用。Take 0.5 g of medical polylactic acid with a molecular weight of 10.8×10 4 and a degree of left-handedness of 98%, and put it into an Erlenmeyer flask, add 10 ml of chloroform, and place it at room temperature for 12 hours to completely dissolve the polylactic acid. Transfer the solution into a 120cm glass petri dish, put it into a vacuum drying oven, and keep the air pressure in the drying room less than 50μatm for 12 hours. After casting into a film, it was rinsed with deionized water, and then dried at 40° C. to obtain a polylactic acid film. The film formed by casting was removed, washed repeatedly with deionized water, placed in an oven, and kept at 40° C. for 4 hours to obtain a solvent-free polylactic acid film. Prepare 2% by weight of N-carboxymethyl chitosan aqueous solution with 50ml concentration of 1mol/L NaOH aqueous solution, add gelatin according to the ratio of chitosan and gelatin weight ratio 1: 1, stir slightly under 45 ℃ for 4 hours , to obtain an alkaline solution of N-carboxymethyl chitosan-gelatin. The polylactic acid film was immersed in the alkaline solution of N-carboxymethyl chitosan-gelatin, and stirred at 45°C for 4 hours. The treated film was taken out, rinsed three times with deionized water, and dried at 40° C. for 3 hours. Then, the modified film is irradiated with 60 Co rays for 2 to 10 hours, with a cumulative dose of 100,000 to 800,000 rads to achieve sterilization, and the polylactic acid modified by N-carboxymethyl chitosan and gelatin is obtained. Film, the prepared polylactic acid film is sealed with a polyethylene film for use.

Claims (3)

1, the chitosan/gelatin network modification method on a kind of aliphatic polyester surface is characterized in that the aqueous slkali that polylactic acid film is immersed N-carboxymethyl chitosan-gelatin is handled, and the polylactic acid film after the modification is adopted again 60The Co ray carries out handling in 2~10 hours, and the irradiation of accumulative total 10~800,000 rad doses is to reach sterilization, and is with polyethylene film that this polylactic acid film sealing back is stand-by.
2, chitosan according to claim 1/gelatin network modification method is characterized in that, the preparation of polylactic acid film is that first compound concentration is the chloroformic solution of 1~10 weight % polylactic acid, behind the casting film-forming, use deionized water rinsing, under 40 ℃ of conditions, dry, make polylactic acid film.
3, chitosan according to claim 1/gelatin network modification method, it is characterized in that, it is to be the N-carboxymethyl chitosan sugar aqueous solution of NaOH aqueous solution preparation 2~7 weight % of 0.1~2mol/L with concentration that the aqueous slkali of polylactic acid film immersion N-carboxymethyl chitosan-gelatin is handled, add gelatin in chitosan and 1: 5 to 5: 1 ratio of gelatin weight ratio, gentle agitation is 2~4 hours under 45 ℃ of conditions, obtain the alkaline solution of N-carboxymethyl chitosan-gelatin, polylactic acid film is immersed in the aqueous slkali of this N-carboxymethyl chitosan-gelatin, under 45 ℃ of conditions, stirred 0.5~4 hour, thin film is taken out, with deionized water rinsing 3~10 times, what dry 1~3 hour carried out under 40 ℃ of conditions.
CN 00134077 2000-12-12 2000-12-12 Chitosan/gelatin network modification on surface of aliphatic polyester Expired - Fee Related CN1119172C (en)

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Publication number Priority date Publication date Assignee Title
CN1328316C (en) * 2004-03-26 2007-07-25 杨晓霞 Prepn process of degradable bioactive film
JP2008530206A (en) * 2005-02-17 2008-08-07 メディバス エルエルシー Polymer particle delivery compositions and methods of use
CN102010513B (en) * 2010-10-12 2013-01-23 中南大学 Stable polysaccharide modified gelatin nano particle and preparation method and application thereof
EP4406558A3 (en) 2011-06-23 2024-10-23 DSM IP Assets B.V. New biodegradable polyesteramide copolymers for drug delivery
US9873765B2 (en) 2011-06-23 2018-01-23 Dsm Ip Assets, B.V. Biodegradable polyesteramide copolymers for drug delivery
CN103721293A (en) * 2013-07-25 2014-04-16 天津大学 Photo-crosslinking multilayer gradient hydrogel capable of controllably releasing active factors and preparation method of hydrogel
AU2015366355B2 (en) 2014-12-18 2020-05-28 Dsm Ip Assets B.V. Drug delivery system for delivery of acid sensitive drugs
CN109771695A (en) * 2018-02-09 2019-05-21 河北工业大学 A kind of preparation method of bioactive surface with antibacterial properties
CN110373743A (en) * 2019-07-17 2019-10-25 东华大学 A method of alleviating aliphatic polyester Acid Materials Acidic catabolite
CN114099791B (en) * 2021-11-03 2022-10-14 西南交通大学 Method for constructing ionic gel drug-loaded coating on biodegradable metal surface

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