In-Vitro Degradation and Cytotoxicity of Gelatin/Chitosan Microspheres for Drug Controlled Release

被引:9
作者
Peng, Zhiyuan [1 ]
Li, Zhiping [1 ]
Zhang, Fan [1 ]
Peng, Xiaochun [1 ]
机构
[1] Jishou Univ, Coll Chem & Chem Engn, Jishou, Peoples R China
来源
JOURNAL OF MACROMOLECULAR SCIENCE PART A-PURE AND APPLIED CHEMISTRY | 2014年 / 51卷 / 08期
关键词
Gelatin; chitosan; composite microspheres; in-vitro degradation; cytotoxicity; CHITOSAN MICROSPHERES; FABRICATION; BIOCOMPATIBILITY; 5-FLUOROURACIL; APOPTOSIS; CELLS;
D O I
10.1080/10601325.2014.925262
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The composite microspheres based on gelatin (Gel) and chitosan (Cs) loaded with 5-fluorouracil (5-FU) were fabricated using glutaraldehyde (GA) as a crosslinker. The in-vitro degradation behaviors of the Gel / Cs microspheres, including the changes of pH value, mass loss and microsphere morphology, were studied. The in-vitro cytotoxicites of Gel / Cs microspheres loaded and unloaded with 5-FU were carried out with MCF-7 breast cancer cell line. The empty Gel / Cs microspheres showed a smooth surface and were evenly distributed; however, there was much aggregation observed for the microspheres loaded with 5-FU. The degradation results showed that the pH values of both PBS and PBS-lysozyme solutions increased with increasing degradation time but the increase of pH value of PBS-lysozyme solution was quicker than that of PBS solution. The aggregated Gel / Cs microspheres lose their shape and many fibers were found after 21 days in PBS solution; while the Gel / Cs microsphere disappeared in PBS-lysozyme solution. The mass loss of the Gel / Cs microspheres in PBS-lysozyme solution was larger than that of the Gel / Cs in PBS solution. The results indicated that lysozyme can accelerate the degradation of Gel / Cs microspheres. The cytotoxicity results showed that the cell viability decreased with increasing glutaraldehyde content for the empty Gel / Cs microspheres; however, the cell viability increased with increasing glutaraldehyde content for the Gel / Cs microspheres loaded with 5-FU. Therefore, the Gel / Cs microspheres can be offered as drug carrier candidates for long-term applications of anti-cancer drugs.
引用
收藏
页码:646 / 652
页数:7
相关论文
共 22 条
[1]   Gelatin microspheres cross-linked with EDC as a drug delivery system for doxycyline: Development and characterization [J].
Adhirajan, N. ;
Shanmugasundaram, N. ;
Babu, Mary .
JOURNAL OF MICROENCAPSULATION, 2007, 24 (07) :659-671
[2]   Porous Three-Dimensional PVA/Gelatin Sponge for Skin Tissue Engineering [J].
Choi, Soon Mo ;
Singh, Deepti ;
Kumar, Ashok ;
Oh, Tae Hwan ;
Cho, Yong Woo ;
Han, Sung Soo .
INTERNATIONAL JOURNAL OF POLYMERIC MATERIALS AND POLYMERIC BIOMATERIALS, 2013, 62 (07) :384-389
[3]   Properties and biocompatibility of chitosan films modified by blending with PVA and chemically crosslinked [J].
Costa, Ezequiel de Souza, Jr. ;
Pereira, Marivalda M. ;
Mansur, Herman S. .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2009, 20 (02) :553-561
[4]  
Denkbas EB, 2000, J APPL POLYM SCI, V76, P1637, DOI 10.1002/(SICI)1097-4628(20000613)76:11<1637::AID-APP4>3.0.CO
[5]  
2-Q
[6]   Polymer microspheres for controlled drug release [J].
Freiberg, S ;
Zhu, X .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2004, 282 (1-2) :1-18
[7]   Sequence-dependent antagonism between fluorouracil and paclitaxel in human breast cancer cells [J].
Grem, JL ;
Nguyen, D ;
Monahan, BP ;
Kao, V ;
Geoffroy, FJ .
BIOCHEMICAL PHARMACOLOGY, 1999, 58 (03) :477-486
[8]   Preparation and Properties of Drug-Loaded Chitosan-Sodium Alginate Complex Membrane [J].
Ke, Guizhen ;
Xu, Weilin ;
Yu, Weidong .
INTERNATIONAL JOURNAL OF POLYMERIC MATERIALS, 2010, 59 (03) :184-191
[9]   The Properties of Chitosan-Gelatin Scaffolds by Once or Twice Vacuum Freeze-Drying Methods [J].
Liu, Yang ;
An, Meiwen ;
Qiu, Hai-Xia ;
Wang, Li .
POLYMER-PLASTICS TECHNOLOGY AND ENGINEERING, 2013, 52 (11) :1154-1159
[10]   Micro and nano-fabrication of biodegradable polymers for drug delivery [J].
Lu, Y ;
Chen, SC .
ADVANCED DRUG DELIVERY REVIEWS, 2004, 56 (11) :1621-1633