Electrospinning Nanofibers from Chitosan/Hyaluronic Acid Complex Coacervates

凝聚 纳米纤维 静电纺丝 壳聚糖 化学工程 溶剂 材料科学 生物高聚物 水溶液 乙烯醇 高分子化学 化学 纳米技术 聚合物 复合材料 有机化学 工程类
作者
Juanfeng Sun,Sarah L. Perry,Jessica D. Schiffman
出处
期刊:Biomacromolecules [American Chemical Society]
卷期号:20 (11): 4191-4198 被引量:94
标识
DOI:10.1021/acs.biomac.9b01072
摘要

Electrospun biopolyelectrolyte nanofibers hold potential for use in a range of biomedical applications, but eliminating toxic chemicals involved in their production remains a key challenge. In this study, we successfully electrospun nanofibers from an aqueous complex coacervate solution composed of chitosan and hyaluronic acid. Experimentally, we investigated the effect of added salt and electrospinning apparatus parameters, such as how applied voltage affected fiber formation. We also studied how the addition of alcohol cosolvents affected the properties of the coacervate solution and the resulting nanofibers. Overall, we observed a trade-off in how the addition of salt and alcohol affected the phase behavior and rheology of the coacervates and, consequently, the size of the resulting fibers. While salt served to weaken electrostatic associations within the coacervate and decrease the precursor solution viscosity, the addition of alcohol lowered the dielectric constant of the system and strengthened these interactions. We hypothesize that the optimized concentration of alcohol accelerated the solvent evaporation during the electrospinning process to yield desirable nanofiber morphology. The smallest average nanofiber diameter was determined to be 115 ± 30 nm when coacervate samples were electrospun using an aqueous solvent containing 3 wt % ethanol and an applied voltage of 24 kV. These results demonstrate a potentially scalable strategy to manufacture electrospun nanofibers from biopolymer complex coacervates that eliminate the need for toxic solvents and could enable the use of these materials across a range of biomedical applications.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
agony发布了新的文献求助10
刚刚
1秒前
2秒前
3秒前
ding应助SIXGOD采纳,获得10
5秒前
王天翔完成签到,获得积分10
6秒前
小蘑菇应助liuwei采纳,获得10
7秒前
ZOE应助Cindy采纳,获得30
7秒前
8秒前
长孙若灵发布了新的文献求助20
8秒前
楠楠发布了新的文献求助10
8秒前
hdh发布了新的文献求助10
9秒前
柒号完成签到,获得积分10
10秒前
10秒前
脑洞疼应助沈阳四季采纳,获得10
10秒前
科研通AI6.2应助星期八采纳,获得10
11秒前
炫远完成签到,获得积分10
11秒前
snjxh发布了新的文献求助10
13秒前
14秒前
14秒前
星辰大海应助科研通管家采纳,获得10
14秒前
14秒前
Akim应助科研通管家采纳,获得10
14秒前
14秒前
Cm666应助科研通管家采纳,获得10
14秒前
科研通AI6.2应助Ma采纳,获得10
14秒前
完美世界应助科研通管家采纳,获得10
14秒前
15秒前
搜集达人应助科研通管家采纳,获得10
15秒前
小二郎应助科研通管家采纳,获得30
15秒前
CodeCraft应助科研通管家采纳,获得10
15秒前
小二郎应助科研通管家采纳,获得10
15秒前
molihuakai应助科研通管家采纳,获得10
15秒前
Lucas应助科研通管家采纳,获得10
15秒前
Owen应助科研通管家采纳,获得10
15秒前
SIXGOD发布了新的文献求助10
15秒前
16秒前
18秒前
18秒前
corainder发布了新的文献求助10
19秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
The Cambridge History of China: Volume 4, Sui and T'ang China, 589–906 AD, Part Two 1500
Cowries - A Guide to the Gastropod Family Cypraeidae 1200
Quality by Design - An Indispensable Approach to Accelerate Biopharmaceutical Product Development 800
Pulse width control of a 3-phase inverter with non sinusoidal phase voltages 777
The Cambridge Handbook of Second Language Acquisition (2nd)[第二版] 666
Signals, Systems, and Signal Processing 610
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6402995
求助须知:如何正确求助?哪些是违规求助? 8221181
关于积分的说明 17424054
捐赠科研通 5455619
什么是DOI,文献DOI怎么找? 2883183
邀请新用户注册赠送积分活动 1859451
关于科研通互助平台的介绍 1700935