聚合物链包装和结晶对黄素嵌入的聚L-乳酸的排放行为的影响
G Virat1,2, Kaustabh Kumar Maiti3,2, R B Amal Raj1
1Materials Science and Technology Division CSIR-National Institute for Interdisciplinary Science and Technology, Trivandrum 695 019, Kerala, India. bhojegowd@niist.res.in.
Soft matter
|August 23, 2023
概括
研究人员通过控制结晶条件和聚合物形式,在可生物降解的聚酸中调整了生物活性黄素的固态光. 这为智能包装和生物医学用途提供了潜力.
科学领域:
- 材料科学 材料科学 材料科学
- 聚合物化学 聚合物化学
- 生物医学工程 生物医学工程
背景情况:
- 可生物降解和生物相容的光材料对于智能包装和生物医学应用至关重要.
- 分子包装和构造显著影响光材料的固态光物理性质.
研究的目的:
- 为了实现可调节的生物活性黄素的固态排放在聚L-乳化物 (PLLA) 中.
- 为了研究结晶条件和PLLA多态形式对黄素光的影响.
主要方法:
- 在不同异热温度下,黄素嵌入PLLA (黄素-PLLA) 的化结晶.
- 用溶剂诱导的黄素-PLLA单晶和凝的制备.
- 研究PLLA多态形式对黄素-PLLA排放的影响.
主要成果:
- 增加的异热结晶温度诱导了库尔库-PLLA光的巴托克罗姆变化,这是由于分子内结合的改变造成的.
- 结晶温度的变化导致黄素的环旋转,受螺旋式PLLA链的影响.
- 不同的PLLA多态形式 (晶体,凝) 影响了黄素-PLLA的排放行为.
结论:
- 聚合物链包装,结晶条件,形态和多态形态是控制光嵌聚合物的光特性的关键因素.
- 本研究展示了一种用于先进应用的可生物降解聚合物的固态光调节方法.
相关概念视频
Polymer Classification: Crystallinity
2.9K
Unlike ionic or small covalent molecules, polymers do not form crystalline solids due to the diffusion limitations of their long-chain structures. However, polymers contain microscopic crystalline domains separated by amorphous domains.
Crystalline domains are the regions where polymer chains are aligned in an orderly manner and held together in proximity by intermolecular forces. For example, chains in the crystalline domains of polyethylene and nylon are bound together by van der Waals...
Crystalline domains are the regions where polymer chains are aligned in an orderly manner and held together in proximity by intermolecular forces. For example, chains in the crystalline domains of polyethylene and nylon are bound together by van der Waals...
2.9K
Polymer Classification: Stereospecificity
2.5K
Polymerization generates chiral centers along the entire backbone of a polymer chain. Accordingly, the stereochemistry of the substituent group has a significant effect on polymer properties. Polymers formed from monosubstituted alkene monomers feature chiral carbons at every alternate position in the polymer backbone. Relative to the predominant orientation of substituents at the adjacent chiral carbons, the polymer can exist in three different configurations: isotactic, syndiotactic, and...
2.5K
Polymer Classification: Architecture
2.8K
Polymers are classified as linear or branched on the basis of their chain architecture. The polymer chains in linear polymers have a long chain-like structure with minimal to no branching at all. Even if a polymer features large substituent groups on the monomer, which appear as branches to the skeleton, it is not considered a branched polymer. A branched polymer contains secondary polymer chains that arise from the main polymer chain. The branching occurs when the polymer growth shifts from...
2.8K
Anionic Chain-Growth Polymerization: Overview
2.1K
The polymerization process that involves carbanion as an intermediate is called anionic polymerization. It is also a type of addition or chain-growth polymerization. Anionic polymerization gets initiated by a strong nucleophile such as an organolithium or a Grignard reagent. The most commonly used initiator for anionic polymerization is butyl lithium. Monomers involved in anionic polymerization must possess a vinyl group bonded to one or two electron-withdrawing groups. For instance,...
2.1K
Anionic Chain-Growth Polymerization: Mechanism
2.1K
The mechanism for anionic chain-growth polymerization involves initiation, propagation, and termination steps. In the initiation step, a nucleophilic anion, such as butyl lithium, initiates the polymerization process by attacking the π bond of the vinylic monomer. As a result, a carbanion, stabilized by the electron‐withdrawing group, is generated. The resulting carbanion acts as a Michael donor in the propagation step and attacks the second vinylic monomer, which acts as a Michael...
2.1K
Cationic Chain-Growth Polymerization: Mechanism
2.4K
The cationic polymerization mechanism consists of three steps: initiation, propagation, and termination. In the initiation step of the polymerization process, the π bond of a monomer gets protonated by the Lewis acid catalyst, which is formed from boron trifluoride and water. The protonation of the π bond generates a carbocation stabilized by the electron‐donating group. In the propagation step, the π bond of the second monomer acts as a nucleophile and attacks the...
2.4K


