教師資料查詢 | 類別: 期刊論文 | 教師: 董崇民 Don, Trong-ming (瀏覽個人網頁)

標題:Preparation of pH- and thermo-sensitive chitosan-PNIPAAm core–shell nanoparticles and evaluation as drug carriers
學年102
學期1
出版(發表)日期2013/08/01
作品名稱Preparation of pH- and thermo-sensitive chitosan-PNIPAAm core–shell nanoparticles and evaluation as drug carriers
作品名稱(其他語言)
著者Huang, Chih-Hao; Wang, Cheng-Fan; Don, Trong-Ming; Chiu, Wen-Yen
單位淡江大學化學工程與材料工程學系
出版者Dordrecht: Springer Netherlands
著錄名稱、卷期、頁數Cellulose 20(4), pp.1791–1805
摘要Environmentally sensitive polysaccharide nanoparticles (NPs) were prepared by in situ polymerization of N-isopropylacrylamide (NIPAAm) monomer in the presence of chitosan (CS) micelles. First, CS was found to develop a cationic micelle-like structure in the acetic acid solution when its concentration was increased to above the critical micelle concentration, as evidenced by fluorescence and TEM. When the NIPAAm was polymerized in the CS micelle solution by using potassium persulfate as initiator, the produced PNIPAAm with anionic chain end(s) became hydrophobic, as long as the reaction temperature was above its phase transition temperature; and therefore it would diffuse into the hydrophobic core of the CS micelles, producing CS-PNIPAAm core–shell NPs. Increasing the feeding amount of NIPAAm increased the monomer conversion and therefore the particle size; yet it decreased the surface zeta potential. Moreover, the CS-PNIPAAm NPs were sensitive to both pH value and temperature. For the study of drug release properties, doxycycline hyclate was used as a model drug and loaded into the NPs at pH 4.5 and 25 °C. The result illustrated that these NPs had a continuous drug release behavior up to 1 week, depending on the pH value and temperature. In addition, enzyme or hydrogen peroxide capable of degrading CS shell was added in the solution to facilitate the drug release.
關鍵字Chitosan;N-Isopropyl acrylamide;Self-assembly;Micelles;Drug release
語言英文
ISSN0969-0239
期刊性質國外
收錄於SCI;
產學合作
通訊作者Don, Trong-Ming; Chiu, Wen-Yen
審稿制度
國別荷蘭
公開徵稿
出版型式,紙本
相關連結
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