Preparation of chitosan capsule materials and its sustained release properties

被引:0
|
作者
Liu Q. [1 ,2 ,3 ]
Xie W. [1 ]
Jia Z. [1 ,2 ,3 ]
Zhu X. [2 ]
Wang R. [2 ]
机构
[1] College of Chemistry and Chemical Engineering, Zhongkai University of Agriculture and Engineering, Guangzhou
[2] Zhanjiang Botai Bio-Chemical Technology Industrial Co., Ltd., Zhanjiang
[3] Guangdong Weiqian Technology Co., Ltd., Foshan
关键词
Capsule material; Carrageenan; Chitosan; Pectin; Sustained release;
D O I
10.16085/j.issn.1000-6613.2020-0568
中图分类号
学科分类号
摘要
Films material was prepared through crosslinking of chitosan and pectin. The effects of carrageenan and starch as additives on the mechanical properties of the films were investigated. The results showed that the pectin-chitosan composite membrane material without carrageenan and starch was not suitable to be used as sustained-release capsule material alone because it was insoluble in simulated gastric solution and intestinal solution. When carrageenan and starch were added, the flexibility, gelatinization, transparency and mechanical properties of the films were further improved, and the solubility of the films in simulated intestinal and gastric solution was increased. When chitosan-pectin: carrageenan: starch had a mass ratio of 2: 1: 1, the film material not only had good formability and elasticity, but also had moderate solubility in gastric solution and intestinal solution. The results of the capsule degradation showed that the capsule dissolution was a slow process in the simulated gastric solution and intestinal solution, and the sustained release rate of the capsule was about 93% after 6h immersion. © 2021, Chemical Industry Press Co., Ltd. All right reserved.
引用
收藏
页码:339 / 345
页数:6
相关论文
共 9 条
  • [1] DEORE K L, THOMBRE N A, GIDE P S., Formulation and development of tinidazole microspheres for colon targeted drug delivery system, Journal of Pharmacy Research, 6, 1, pp. 158-165, (2013)
  • [2] DAS S, CHAUDHURY A, NG K Y., Preparation and evaluation of zinc-pectin-chitosan composite particles for drug delivery to the colon: Role of chitosan in modifying in vitro and in vivo drug release, International Journal of Pharmaceutics, 406, 1, pp. 11-20, (2011)
  • [3] BAGLIOTTI M, ANDREIA, BEATRIZ S F C, Et al., Films from resistant starch-pectin dispersions intended for colonic drug delivery, Carbohydrate Polymers, 99, 1, pp. 140-149, (2014)
  • [4] HIORTH M, SKOLEN T, SANDE S A., Immersion coating of pellet cores consisting of chitosan and calcium intended for colon drug delivery, European Journal of Pharmaceutics and Biopharmaceutics, 75, 2, pp. 245-253, (2010)
  • [5] WANG M J, XIE Y L, CHEN Z J, Et al., Optimizing preparation of NaCS-chitosan complex to form a potential material for the colon-specific drug delivery system, Journal of Applied Polymer Science, 117, 5, pp. 3001-3012, (2010)
  • [6] HAMMAN J H., Chitosan based polyelectrolyte complexes as potential carrier materials in drug delivery systems, South Africa Mar. Drugs, 8, pp. 1305-1322, (2010)
  • [7] MORRIS, KOK G A, HARDING M S, Et al., Polysaccharide drug delivery systems based on pectin and chitosan, Biotechnol. Genet. Eng. Rev, 27, pp. 257-283, (2010)
  • [8] BHATTARAI N N, GUNN J, ZHANG M Q., Chitosan-based hydrogels for controlled, localized drug delivery, Advanced Drug Delivery Reviews, 9, 1, pp. 83-99, (2010)
  • [9] PARK J H, SARAVANAKUMAR G, KIM K, Et al., Targeted delivery of low molecular drugs using chitosan and its derivatives, Advanced Drug Delivery Reviews, 62, 1, pp. 28-41, (2009)