新型不对称AB(n)型两亲性聚乙二醇-b-[聚(l-丙交酯)](n)(n = 2、4、8),通过树枝状酯键连接:I. 合成及其表征。

New asymmetric AB(n)-shaped amphiphilic poly(ethylene glycol)-b-[poly(l-lactide)](n) (n = 2, 4, 8) bridged with dendritic ester linkages: I. Syntheses and their characterization.

作者信息

Li Qiaobo, Li Faxue, Jia Lin, Li Yang, Liu Yanchun, Yu Jianyong, Fang Qiang, Cao Amin

机构信息

Laboratory for Polymer Materials, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Road, Shanghai 200032, China.

出版信息

Biomacromolecules. 2006 Aug;7(8):2377-87. doi: 10.1021/bm060372l.

Abstract

This study presents new investigations on chemical syntheses and characterization of new asymmetric AB(n)-shaped amphiphilic diblock methoxy poly(ethylene glycol)-b-poly(l-lactide), MPEG-b-(PLLA)(n) (n = 2, 4, and 8), bridged with dendritic ester linkages. First, a new series of A(OH)(n)-shaped hydroxy end-capped MPEG-(OH)(2), MPEG-(OH)(4), and MPEG-(OH)(8) bearing corresponding one- to three-generation dendritic ester moieties were efficiently derived from the starting MPEG (M(n) = 2 KDa) and 2,2'-bis(hydroxymethyl)propionic acid (Bis-HMPA) via ester coupling and a facile hydroxy protection-deprotection cycle, and then, chemical structures of these functional MPEG-(OH)(n) were characterized by nuclear magnetic resonance spectrometry (NMR) and MALDI-FTMS. Subsequently, by employing these MPEG-(OH)(n) as functional macroinitiators, new asymmetric AB(n)()-shaped amphiphilic MPEG-b-(PLLA)(2) S1, MPEG-b-(PLLA)(4) S2, and MPEG-b-(PLLA)(8) S3 bridged with dendritic Bis-HMPA ester linkages of L1-L3 as well as linear structural MPEG-b-PLLA references (R1-R3) were synthesized through the SnOct(2)-catalyzed ring-opening polymerization (ROP) of l-lactide at 130 degrees C in m-xylene solution, and their structures were further examined by NMR and gel permeation chromatography (GPC). It was demonstrated that the functional MPEG-(OH)(n) efficiently initiated the ROP of LLA, finally leading to successful formation of the AB(n)-shaped amphiphilic MPEG-b-(PLLA)(n) (n = 2, 4, and 8) with each PLLA arm weight close to 2 KDa and very narrow molecular weight distribution. Moreover, thermal history, crystallization, and spherulite morphologies were studied by means of differential scanning calorimeter (DSC), thermal gravimetric analyzer (TGA), and polarized microscope (POM) for these new structural amphiphilic S1-S3 as well as the linear R1-R3, intriguingly indicating a strong molecular architecture dependence of segmental crystallizability, spherulite morphology, and apparent crystal growth rate. Due to the favorable biodegradability and biocompatibility of the PLLA and MPEG, these results may therefore create new possibilities for these novel structural AB(n)-shaped amphiphilic MPEG-b-(PLLA)(n) as potential biomaterials.

摘要

本研究针对新型不对称AB(n)型两亲性二嵌段甲氧基聚(乙二醇)-b-聚(l-丙交酯),即MPEG-b-(PLLA)(n)(n = 2、4和8),通过树枝状酯键连接进行了化学合成及表征方面的新研究。首先,通过酯偶联以及简便的羟基保护-脱保护循环,从起始原料甲氧基聚乙二醇(M(n) = 2 KDa)和2,2'-双(羟甲基)丙酸(双羟甲基丙酸,Bis-HMPA)高效衍生出一系列新型的A(OH)(n)型羟基封端的MPEG-(OH)(2)、MPEG-(OH)(4)和MPEG-(OH)(8),它们带有相应的一至三代树枝状酯基,然后通过核磁共振光谱法(NMR)和基质辅助激光解吸电离飞行时间质谱(MALDI-FTMS)对这些功能性MPEG-(OH)(n)的化学结构进行了表征。随后,以这些MPEG-(OH)(n)作为功能性大分子引发剂,通过l-丙交酯在130℃下于间二甲苯溶液中由辛酸亚锡(SnOct(2))催化的开环聚合(ROP)反应,合成了新型不对称AB(n)型两亲性的、通过L1-L3的树枝状双羟甲基丙酸酯键连接的MPEG-b-(PLLA)(2) S1、MPEG-b-(PLLA)(4) S2和MPEG-b-(PLLA)(8) S3,以及线性结构的MPEG-b-PLLA参比物(R1-R3),并通过NMR和凝胶渗透色谱法(GPC)进一步研究了它们的结构。结果表明,功能性MPEG-(OH)(n)能够有效地引发丙交酯的ROP反应,最终成功形成AB(n)型两亲性MPEG-b-(PLLA)(n)(n = 2、4和8),每个聚丙交酯臂的重量接近2 KDa,且分子量分布非常窄。此外,借助差示扫描量热仪(DSC)、热重分析仪(TGA)和偏光显微镜(POM)对这些新型结构的两亲性物质S1-S3以及线性物质R1-R3的热历史、结晶和球晶形态进行了研究,有趣的是,研究表明链段结晶性、球晶形态和表观晶体生长速率强烈依赖于分子结构。由于聚丙交酯(PLLA)和甲氧基聚乙二醇(MPEG)具有良好的生物降解性和生物相容性,因此这些结果可能为这些新型结构的AB(n)型两亲性MPEG-b-(PLLA)(n)作为潜在生物材料创造新的可能性。

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