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基于取代和未取代内酯合成共聚酯以控制其结晶度及其在软性医疗设备设计中对水解降解的潜在影响。

Synthesis of copolyesters based on substituted and non-substituted lactones towards the control of their crystallinity and their potential effect on hydrolytic degradation in the design of soft medical devices.

作者信息

Ramos-Durán Gabriela, González-Zarate Aracely Del Carmen, Enríquez-Medrano Francisco Javier, Salinas-Hernández Myrna, De Jesús-Téllez Marco A, Díaz de León Ramon, López-González Hector Ricardo

机构信息

Centro de Investigación en Química Aplicada Blvd. Enrique Reyna Hermosillo #140, San José de los Cerritos 25294 Saltillo Coahuila Mexico

出版信息

RSC Adv. 2022 Jun 21;12(28):18154-18163. doi: 10.1039/d2ra01861f. eCollection 2022 Jun 14.

Abstract

A series of copolymers based on ε-caprolactone (ε-CL) in combination with lactone monomers substituted with alkyl groups (4 and 6 carbon atoms), specifically δ-decalactone (δ-DL), ε-decalactone (ε-DL) and δ-dodecalactone (δ-DD), as well as a copolymer using two substituted lactone monomers with alkyl groups (ε-DL and δ-DD) were synthesized in different molar ratios. The objective of the synthesis of these copolymers was to evaluate the effects of branching in the polymer backbone on the crystallinity and the thermal properties of the synthesized materials. All copolymers were obtained ring-opening polymerization with high conversion values for both comonomers using neodymium isopropoxide (Nd(i-Pr)) as the initiator, and their compositions were determined by H NMR and C NMR. The molar masses ( and ) and distributions were obtained by GPC measurements. Such measurements showed that a majority of the copolymers exhibited dispersities () in the range of 1.2-1.6 and in the range of 15-40 kDa. First- and second-order transitions such as melting, crystallization and glass transition, as well as the crystallization degree (melting enthalpy), were determined by DSC analysis. Copolymers based on ε-CL developed interesting behaviors, wherein the copolymers with higher percentages of this monomer exhibited semicrystalline behavior, while the copolymers with a higher percentage of the comonomers ε-DL, δ-DL or δ-DD showed amorphous behavior. In contrast, the copolymers synthesized using both monomers from the alkyl group-substituted lactone developed fully amorphous features, regardless of their composition. These changes in the crystalline features of the synthesized copolymers suggest that the content of short branchings on the copolymer backbone will significantly modify their rates of hydrolytic degradation and their potential use in the development of different soft medical devices.

摘要

合成了一系列基于ε-己内酯(ε-CL)与被烷基(4个和6个碳原子)取代的内酯单体的共聚物,具体为δ-癸内酯(δ-DL)、ε-癸内酯(ε-DL)和δ-十二内酯(δ-DD),以及使用两种被烷基取代的内酯单体(ε-DL和δ-DD)的共聚物,它们具有不同的摩尔比。合成这些共聚物的目的是评估聚合物主链中的支化对合成材料的结晶度和热性能的影响。所有共聚物均通过以异丙醇钕(Nd(i-Pr))为引发剂的开环聚合反应获得,两种共聚单体的转化率都很高,并且通过氢核磁共振(H NMR)和碳核磁共振(C NMR)确定了它们的组成。通过凝胶渗透色谱(GPC)测量获得了摩尔质量(数均分子量和重均分子量)及其分布。这些测量表明,大多数共聚物的分散度在1.2 - 1.6范围内,数均分子量在15 - 40 kDa范围内。通过差示扫描量热法(DSC)分析确定了诸如熔融、结晶和玻璃化转变等一级和二级转变,以及结晶度(熔融焓)。基于ε-CL的共聚物表现出有趣的行为,其中该单体百分比更高的共聚物表现出半结晶行为,而ε-DL、δ-DL或δ-DD共聚单体百分比更高的共聚物表现出无定形行为。相反,使用两种来自烷基取代内酯的单体合成的共聚物,无论其组成如何,都呈现出完全无定形的特征。合成共聚物结晶特征的这些变化表明,共聚物主链上短支链的含量将显著改变其水解降解速率及其在不同软质医疗器械开发中的潜在用途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bc4/9210866/1c2d3f703aca/d2ra01861f-s1.jpg

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