欢迎访问《日用化学工业(中英文)》,今天是

日用化学工业 ›› 2022, Vol. 52 ›› Issue (7): 710-716.doi: 10.3969/j.issn.1001-1803.2022.07.004

• 开发与应用 • 上一篇    下一篇

PR-CS/γ-PGA纳米胶囊的制备和表征

张婉萍1,2,吴凯翔1,2,蒋汶1,2,张冬梅1,2,*()   

  1. 1.上海应用技术大学 香料香精技术与工程学院,上海 201418
    2.香料香精化妆品省部共建协同创新中心,上海 201418
  • 收稿日期:2021-10-17 修回日期:2022-06-24 出版日期:2022-07-22 发布日期:2022-07-21
  • 通讯作者: 张冬梅

Preparation and characterization of PR-CS/γ-PGA nanocapsules

Zhang Wanping1,2,Wu Kaixiang1,2,Jiang Wen1,2,Zhang Dongmei1,2,*()   

  1. 1. School of Perfume and Aroma Technology, Shanghai Institute of Technology, Shanghai 201418, China
    2. Collaborative Innovation Center of Fragrance Flavour and Cosmetics, Shanghai 201418, China
  • Received:2021-10-17 Revised:2022-06-24 Online:2022-07-22 Published:2022-07-21
  • Contact: Dongmei Zhang

摘要:

以壳聚糖(CS)和聚谷氨酸(γ-PGA)为壁材,采用离子凝胶法制备包覆苯乙基间苯二酚(PR)壳聚糖/聚谷氨酸(PR-CS/γ-PGA)纳米胶囊,提高PR的稳定性。研究了γ-PGA质量浓度、CS溶液pH以及PR质量浓度对包覆PR-CS/γ-PGA纳米胶囊粒径大小、Zeta电位和包覆率的影响。研究结果表明,体系中CS质量浓度为1.33 mg/mL时,制备PR-CS/γ-PGA的最佳条件:CS溶液pH为4.5,γ-PGA质量浓度为0.27 mg/mL,PR质量浓度为0.4 mg/mL,反应时磁力搅拌速度为400 r/min,γ-PGA滴加速度为0.5 mL/min,反应时间为1 h。通过对PR-CS/γ-PGA纳米胶囊进行系统表征:TEM扫描表明,PR-CS/γ-PGA纳米胶囊呈球形。FT-IR分析表明,CS与γ-PGA之间发生静电相互作用形成CS/γ-PGA纳米胶囊,且PR-CS/γ-PGA纳米胶囊中含有PR。TGA曲线表明,CS/γ-PGA纳米胶囊可以提高PR的热稳定性,PR-CS/γ-PGA纳米胶囊成功包覆了PR。

关键词: 壳聚糖, 聚谷氨酸, 苯乙基间苯二酚, 离子凝胶法, 纳米胶囊

Abstract:

Encapsulated phenylethyl resorcinol chitosan/polyglutamic acid (PR-CS/γ-PGA) nanocapsules were prepared by ionic gelation method with chitosan (CS) and polyglutamic acid (γ-PGA) as wall materials. The effects of the mass concentration of γ-PGA, the pH of the CS solution and the mass concentration of PR on the particle size, Zeta potential and encapsulation rate of PR-CS/γ-PGA nanocapsules were studied. The results showed that, with the increase of γ-PGA concentration, the particle size of the suspension of PR-CS/γ-PGA nanocapsules was decreased, and the Zeta potential was also decreased. The encapsulation rate of PR-CS/γ-PGA nanocapsules was first decreased and then increased (the encapsulation rate was the largest when the mass concentration of γ-PGA was 0.27 mg/mL), and if the mass concentration of γ-PGA was further increased, the encapsulation rate was not significantly changed. With the increase of PR mass concentration, the particle size of the suspension of PR-CS/γ-PGA nanocapsules was increased and the Zeta potential was decreased. The encapsulation rate of PR-CS/γ-PGA nanocapsules was reduced. As the pH of the CS solution was increased, the particle size of the suspension of PR-CS/γ-PGA nanocapsules was first decreased and then increased (the particle size was the smallest when pH=4.5), and the Zeta potential was decreased. The encapsulation rate of PR-CS/γ-PGA nanocapsules was not significantly changed. When the CS concentration in the system was 1.33 mg/mL, the optimized conditions for preparing PR-CS/γ-PGA nanocapsules were as follows: the pH of CS solution was 4.5, the mass concentration of γ-PGA was 0.27 mg/mL, the mass concentration of PR was 0.4 mg/mL, the magnetic stirring speed was 400 r/min during the reaction, the speed of adding γ-PGA was 0.5 mL/min, and the reaction time was 1 h. Systematic characterization of the PR-CS/γ-PGA nanocapsules was made. TEM results showed that the PR-CS/γ-PGA nanocapsules were spherical. FT-IR analysis showed that the electrostatic interaction between CS and γ-PGA formed CS/γ-PGA nanocapsules, and the PR-CS/γ-PGA nanocapsules contained PR. The TGA curve showed that CS/γ-PGA nanocapsules could improve the thermal stability of PR, and PR-CS/γ-PGA nanocapsules successfully encapsulated PR.

Key words: chitosan, polyglutamic acid, phenethyl resorcinol, ionic gelation method, nanocapsule

中图分类号: 

  • TQ658