Immobilization of Coacervate Microcapsules in Multilayer Sodium Alginate Beads for Efficient Oral Anticancer Drug Delivery

被引:83
作者
Feng, Chao [1 ]
Song, Ruixi [1 ]
Sun, Guohui [1 ]
Kong, Ming [1 ]
Bao, Zixian [1 ]
Li, Yang [1 ]
Cheng, Xiaojie [1 ]
Cha, Dongsu [2 ]
Park, Hyunjin [2 ]
Chen, Xiguang [1 ]
机构
[1] Ocean Univ China, Coll Marine Life Sci, Qingdao 266003, Shandong, Peoples R China
[2] Korea Univ, Grad Sch Biotechnol, Seoul 136701, South Korea
基金
中国国家自然科学基金;
关键词
IN-VITRO; CHITOSAN NANOPARTICLES; CARBOXYMETHYL CHITOSAN; OPTIMIZATION; FORMULATION; DOXORUBICIN; SYSTEMS;
D O I
10.1021/bm401890x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
We have designed and evaluated coacervate microcapsules-immobilized multilayer sodium alginate beads (CMs-M-ALG-Beads) for oral drug delivery. The CMs-M-ALG-Beads were prepared by immobilization of doxorubicin hydrochloride (DOX) loaded chitosan/carboxymethyl coacervate microcapsules (DOX:CS/CMCS-CMs) in the core and layers of the multilayer sodium alginate beads. The obtained CMs-M-ALG-beads exhibited layer-by-layer structure and rough surface with many nanoscale particles. The swelling characteristic and drug release results indicated that 4-layer CMs-M-ALG-Beads possessed favorable gastric acid tolerance (the swelling rate <5%, the cumulative drug release rate <3.8%). In small intestine, the intact DOX:CS/CMCS-CMs were able to rapidly release from CMs-M-ALG-Beads with the dissolution of ALG matrix. Ex vivo intestinal mucoadhesive and permeation showed that CMs-M-ALG-Beads exhibited continued growth for P-app values of DOX, which was 1.07-1.15 folds and 1.28-1.38 folds higher than DOX:CS:CMCS-CMs in rat jejunum and ileum, respectively, demonstrating that CMs-M-ALG-Beads were able to enhance the absorption of DOX by controlled releasing DOX:CS/CMCS-CMs and prolonging the contact time between the DOX:CS/CMCS-CMs and small intestinal mucosa.
引用
收藏
页码:985 / 996
页数:12
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