Amphiphilic sodium alginate-vinyl acetate microparticles for drug delivery | |
Yu Weiting1; Zhang Demeng2,4; Liu Xiudong3; Wang Yunhong3; Tong Jun3; Zhang Mengxue4; Ma Xiaojun5 | |
刊名 | JOURNAL OF OCEANOLOGY AND LIMNOLOGY |
2019-05-01 | |
卷号 | 37期号:3页码:855-862 |
关键词 | hydrophobic modification sodium alginate-vinyl acetate amphiphilic Alg-g-PVAc/chitosan microcapsules drug delivery |
ISSN号 | 2096-5508 |
DOI | 10.1007/s00343-019-8127-8 |
通讯作者 | Yu Weiting(yuwt@dicp.ac.cn) ; Zhang Demeng(zdm@bmscn.com) |
英文摘要 | To overcome the fast or burst release of hydrophilic drugs from hydrophilic alginate-based carriers, hydrophobic molecule (vinyl acetate, VAc) was grafted on alginate (Alg), which was further used to prepare drug carriers. Amphiphilic Alg-g-PVAc hydrogel beads were firstly prepared by emulsification/internal gelation technique for the loading of bovine serum albumin (BSA). Then, chitosan was coated on the surface of beads to form novel amphiphilic Alg-g-PVAc/chitosan (Alg-g-PVAc/CS) microcapsules. The BSA-loading amphiphilic Alg-g-PVAc/chitosan (Alg-g-PVAc/CS) microcapsules display similar morphology and size to the hydrophilic alginate/chitosan (AC) microcapsules. However, the drug loading and loading efficiency of BSA in Alg-g-PVAc/CS microcapsules are higher, and the release rate of BSA from Alg-g-PVAc/CS microcapsules is slower. The results demonstrate that the introduction of hydrophobic PVAc on alginate can effectively help retard the release of BSA, and the higher degree of substitution is, the slower the release rate is. In addition, the complex membrane can also be adjusted to delay the release of BSA. As a whole, amphiphilic sodium alginate-vinyl acetate/CS microparticles could be developed for macromolecular drug delivery. |
资助项目 | National Natural Science Foundation of China[21276033] ; Open Foundation of the State Key Laboratory of Bioactive Seaweed Substances[SKL-BASS1711] ; Open Foundation of the State Key Laboratory of Bioactive Seaweed Substances[SKL-BASS1707] ; National Undergraduates Innovation and Entrepreneurship Training Program of China[201711258000001] |
WOS研究方向 | Marine & Freshwater Biology ; Oceanography |
语种 | 英语 |
出版者 | SCIENCE PRESS |
WOS记录号 | WOS:000469401600009 |
内容类型 | 期刊论文 |
源URL | [http://ir.qdio.ac.cn/handle/337002/161568] |
专题 | 中国科学院海洋研究所 |
通讯作者 | Yu Weiting; Zhang Demeng |
作者单位 | 1.Dalian Univ, Affiliated Zhongshan Hosp, Dalian 116001, Peoples R China 2.Chinese Acad Sci, Inst Oceanol, Qingdao 266071, Shandong, Peoples R China 3.Dalian Univ, Coll Environm & Chem Engn, Dalian Econ Technol Dev Zone, Dalian 116622, Peoples R China 4.Qingdao Brightmoon Seaweed Grp Co Ltd, State Key Lab Bioact Seaweed Subst, Qingdao 266400, Shandong, Peoples R China 5.Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China |
推荐引用方式 GB/T 7714 | Yu Weiting,Zhang Demeng,Liu Xiudong,et al. Amphiphilic sodium alginate-vinyl acetate microparticles for drug delivery[J]. JOURNAL OF OCEANOLOGY AND LIMNOLOGY,2019,37(3):855-862. |
APA | Yu Weiting.,Zhang Demeng.,Liu Xiudong.,Wang Yunhong.,Tong Jun.,...&Ma Xiaojun.(2019).Amphiphilic sodium alginate-vinyl acetate microparticles for drug delivery.JOURNAL OF OCEANOLOGY AND LIMNOLOGY,37(3),855-862. |
MLA | Yu Weiting,et al."Amphiphilic sodium alginate-vinyl acetate microparticles for drug delivery".JOURNAL OF OCEANOLOGY AND LIMNOLOGY 37.3(2019):855-862. |
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