首页> 外文期刊>Journal of Applied Polymer Science >Syntheses of poly(lactic acid)-poly(ethylene glycol) serial biodegradable polymer materials via direct melt polycondensation and their characterization
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Syntheses of poly(lactic acid)-poly(ethylene glycol) serial biodegradable polymer materials via direct melt polycondensation and their characterization

机译:直接熔融缩聚法合成聚乳酸-聚乙二醇系列可生物降解高分子材料及其表征

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摘要

Directly starting from lactic acid (LA) and poly(ethylene glycol) (PEG), biodegradable material polylactic acid-polyethylene glycol (PLEG) was synthesized via melt copolycondensation. The optimal synthetic conditions, including prepolymerization method, catalyst kinds and quantity, copolymerization temperature and time, LA stereochemical configuration, feed weight ratio M-LA/M-PEG and M,, of PEG, were all discussed in detail. When D,L-LA and PEG (M-n = 1000 Da) prepolymerized together as feed weight ratio M-D,M-L-LA/M-PEG = 90/10, 15 h copolycondensation under 165 degrees C and 70 Pa, and 0.5 wt % SnO as catalyst, gave D,L-PLEG1000 with the highest [eta] of 0.40 dL/g, and the corresponding MW was 41,700 Da. Using L-LA instead of D,L-LA, 10 h polymerization under 165 degrees C and 70 Pa, and 0.5 wt % SnO as catalyst, gave L-PLEG1000 with the highest [eta] of 0.21 dL/g and MW of 15,600 Da. Serial D,L-PLEG with different feed weight ratio and M, of PEG were synthesized via the simple and practical direct melt copolycondensation, and characterized with FTIR, H-1 NMR, GPC, DSC, XRD, and contact angle testing. D,L-PELG not only had higher MW than PDLLA, PLLA and L-PELG, but also better hydrophilicity than PDLLA. The novel one-step method could be an alternative route to the synthesis of hydrophilic drug delivery carrier PLEG instead of the traditional two-step Method using lactide as intermediate. (c) 2006 Wiley Periodicals,, Inc.
机译:直接从乳酸(LA)和聚乙二醇(PEG)开始,通过熔融共缩聚法合成了可生物降解的材料聚乳酸-聚乙二醇(PLEG)。详细讨论了PEG的最佳合成条件,包括预聚方法,催化剂种类和数量,共聚温度和时间,LA立体化学构型,进料重量比M-LA / M-PEG和M。当D,L-LA和PEG(Mn = 1000 Da)以进料重量比MD,ML-LA / M-PEG = 90/10一起预聚合时,在165摄氏度和70 Pa下与0.5 wt%的SnO共聚15 h作为催化剂,得到D,L-PLEG1000,其最高η为0.40dL / g,相应的MW为41,700Da。使用L-LA代替D,L-LA,在165℃和70Pa下10小时聚合,以及0.5wt%的SnO作为催化剂,得到具有最大η为0.21dL / g和MW为15,600的L-PLEG1000。大。通过简单实用的直接熔融共聚法合成了具有不同进料重量比和M的PEG系列D,L-PLEG,并通过FTIR,H-1 NMR,GPC,DSC,XRD和接触角测试对其进行了表征。 D,L-PELG不仅具有比PDLLA,PLLA和L-PELG更高的MW,而且比PDLLA具有更好的亲水性。新颖的一步法可以替代亲水性药物递送载体PLEG的替代方法,而不是使用丙交酯作为中间体的传统两步法。 (c)2006年Wiley Periodicals,Inc.

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