个人信息Personal Information
副教授
硕士生导师
任职 : 功能弹性体材料课题组组长
性别:男
毕业院校:中科院长春应化所
学位:博士
所在单位:化工学院
学科:高分子材料. 高分子化学与物理. 凝聚态物理
办公地点:化工实验楼A303
联系方式:0412-84986101,13842631065(微信同步)
电子邮箱:zfzhao@dlut.edu.cn
Hot-melt pressure-sensitive adhesives based on SIS-g-PB copolymer for transdermal delivery of hydrophilic drugs
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论文类型:期刊论文
发表时间:2019-06-01
发表刊物:INTERNATIONAL JOURNAL OF ADHESION AND ADHESIVES
收录刊物:SCIE、EI
卷号:91
页面范围:72-76
ISSN号:0143-7496
关键字:Hot-melt pressure-sensitive adhesives; SIS-g-PB copolymers; In vitro drug release; Adhesive performance
摘要:SIS-g-PB copolymers were successfully synthesized by grafting living polybutadiene (PB) lithium macroanions onto epoxidized SIS copolymers. Their molecular structures and thermal properties were characterized by TGA, H-1-NMR and DSC, respectively. SIS, epoxidized SIS (ESIS) and SIS-g-PB copolymers were melt-blended with tackifiers to develop hot-melt pressure-sensitive adhesives (HMPSAs), respectively (named of H-SIS, H-ESIS and H-SIS-g-PB). Their adhesive performances were measured in terms of 180 degrees peel strength and holding power. A modified Franz type horizontal diffusion cell was used to carry out In vitro drug release experiments, in which geniposides were chosen as hydrophilic model drugs. The results showed that H-SIS-g-PB has two times as high a 180 degrees peel strength as H-SIS. Meanwhile H-SIS-g-PB has a slightly lower drug cumulative release rate than H-ESIS. It is indicated that the PB branches not only could impart good adhesive performance to H-SIS-g-PB via improving the compatibility between the epoxidized main chains and tackifier resins but also provide release channels to hydrophilic drugs by retaining most of the epoxide groups in the SIS-g-PB copolymers.