Fabrication of nano-fibrous collagen microspheres for protein delivery and effects of photochemical crosslinking on release kinetics

光敏剂 化学 动力学 药物输送 生物物理学 化学工程 光化学 有机化学 量子力学 生物 物理 工程类
作者
Oliver Chan,Kwok‐Fai So,Barbara Pui Chan
出处
期刊:Journal of Controlled Release [Elsevier]
卷期号:129 (2): 135-143 被引量:76
标识
DOI:10.1016/j.jconrel.2008.04.011
摘要

Protein compatibility is important for protein drug delivery using microsphere-based devices. Collagen has excellent protein compatibility but has poor mechanical stability for microsphere fabrication and open meshwork for controlled release. In this study, a protein-compatible fabrication method for injectable collagen microspheres has been developed. The surface morphology, interior microstructure and protein release characteristics of collagen microspheres were investigated. Moreover, effects of photochemical crosslinking on these characteristics were also studied. Finally, the mechanisms governing the protein release and the retention of protein bioactivity were studied. Stable and injectable collagen microspheres consisting of nano-fibrous meshwork were successfully fabricated under ambient conditions in an organic solvent and crosslinking reagent-free manner. These microspheres have open meshwork and showed large initial burst and rapid release of proteins. Photochemical crosslinking significantly reduced the initial burst effect and controlled the protein release in a photosensitizer dose-dependent manner without significantly altering the mesh size. We further demonstrated that there was significantly higher protein retention within the photochemically crosslinked collagen microspheres as compared with the uncrosslinked, suggesting a secondary retention mechanism. Lastly, both surfactant treatment and photochemical crosslinking did not compromise the bioactivity of the encapsulated proteins. In summary, this study reports a novel collagen microsphere-based protein delivery system and demonstrates the possibility to use photochemical crosslinking as the secondary retention mechanism for proteins.
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
更新
大幅提高文件上传限制,最高150M (2024-4-1)

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
聪明短靴完成签到,获得积分10
1秒前
宁羽完成签到,获得积分10
2秒前
2秒前
拼搏的青雪完成签到,获得积分10
3秒前
kannar完成签到,获得积分10
4秒前
羽言完成签到,获得积分10
4秒前
Jesica完成签到,获得积分10
4秒前
EYRE完成签到,获得积分10
6秒前
6秒前
N维度完成签到,获得积分10
7秒前
顺利毕业完成签到,获得积分10
7秒前
Chenmengyi发布了新的文献求助10
7秒前
跟屁虫完成签到,获得积分10
8秒前
Ava应助azj采纳,获得10
8秒前
9秒前
霸气雪珊发布了新的文献求助80
9秒前
难过冷玉完成签到,获得积分10
9秒前
天tian完成签到,获得积分10
9秒前
谢会会完成签到 ,获得积分10
10秒前
迷你的百川完成签到,获得积分10
10秒前
harper完成签到 ,获得积分10
10秒前
11秒前
科研顺风发布了新的文献求助10
11秒前
执笔完成签到,获得积分10
11秒前
Chao完成签到,获得积分10
12秒前
义气的身影完成签到,获得积分10
12秒前
yyh完成签到,获得积分10
12秒前
忽忽完成签到,获得积分10
12秒前
whisper完成签到,获得积分10
13秒前
sevenlalala完成签到,获得积分10
13秒前
小熊猫发布了新的文献求助10
14秒前
wshwx完成签到 ,获得积分10
14秒前
优美的元瑶完成签到,获得积分10
14秒前
15秒前
科研君不爱科研完成签到,获得积分10
16秒前
lcsolar完成签到,获得积分10
16秒前
16秒前
孤岛完成签到,获得积分10
16秒前
pb完成签到,获得积分10
16秒前
阳光盼山完成签到 ,获得积分10
16秒前
高分求助中
Evolution 2024
Experimental investigation of the mechanics of explosive welding by means of a liquid analogue 1060
Die Elektra-Partitur von Richard Strauss : ein Lehrbuch für die Technik der dramatischen Komposition 1000
How to Create Beauty: De Lairesse on the Theory and Practice of Making Art 1000
Gerard de Lairesse : an artist between stage and studio 670
大平正芳: 「戦後保守」とは何か 550
LNG地下タンク躯体の構造性能照査指針 500
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3004872
求助须知:如何正确求助?哪些是违规求助? 2664288
关于积分的说明 7221177
捐赠科研通 2300923
什么是DOI,文献DOI怎么找? 1220238
科研通“疑难数据库(出版商)”最低求助积分说明 594615
版权声明 593226