Drastic difference in porous structure of calcium alginate microspheres prepared with fresh or hydrolyzed sodium alginate

被引:28
作者
Akamatsu, Kazuki [1 ]
Maruyama, Kaho [1 ]
Chen, Wei [2 ]
Nakao, Aiko [3 ]
Nakao, Shin-ichi [1 ]
机构
[1] Kogakuin Univ, Fac Engn, Dept Environm & Energy Chem, Hachioji, Tokyo 1920015, Japan
[2] Univ Tokyo, Dept Chem Syst Engn, Bunkyo Ku, Tokyo 1138656, Japan
[3] RIKEN, Cooperat Support Team, ASI, Wako, Saitama 3510198, Japan
关键词
Alginate; Membrane emulsification; Microsphere; Porous structure; SPG membrane; Hydrolysis; SPG MEMBRANE EMULSIFICATION; EMULSION; RELEASE; CELLS;
D O I
10.1016/j.jcis.2011.08.014
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Fresh or hydrolyzed sodium alginate was used as a material for preparing calcium alginate microspheres, and a drastic difference in porous structure was observed between them, even though the other materials and the preparation method except for the sodium alginate were exactly the same. When fresh sodium alginate was used, nonporous microspheres were obtained. In contrast, when 82-day-hydrolyzed sodium alginate, whose molecular weight became 7% of the molecular weight of the fresh sodium alginate, was used, porous microspheres with 6.5 times larger BET surface area were obtained. XPS studies indicated that the atomic ratio of Ca, the crosslinker of the alginic acid polymer, was almost the same in both cases. Therefore, the difference in porous structure was not attributed to the amount of crosslinking points, but to the low-molecular-weight compounds formed by hydrolysis, and they would work as pore-generating agents. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:707 / 710
页数:4
相关论文
共 30 条
[11]   Immobilized metal affinity chromatography without chelating ligands: Purification of soybean trypsin inhibitor on zinc alginate beads [J].
Gupta, MN ;
Jain, S ;
Roy, I .
BIOTECHNOLOGY PROGRESS, 2002, 18 (01) :78-81
[12]   Preparation of porous scaffolds by using freeze-extraction and freeze-gelation methods [J].
Ho, MH ;
Kuo, PY ;
Hsieh, HJ ;
Hsien, TY ;
Hou, LT ;
Lai, JY ;
Wang, DM .
BIOMATERIALS, 2004, 25 (01) :129-138
[13]   Characterization of the block structure and molecular weight of sodium alginates [J].
Johnson, FA ;
Craig, DQM ;
Mercer, AD .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1997, 49 (07) :639-643
[14]   Continuous release of endostatin from microencapsulated engineered cells for tumor therapy [J].
Joki, T ;
Machluf, M ;
Atala, A ;
Zhu, JH ;
Seyfried, NT ;
Dunn, IF ;
Abe, T ;
Carroll, RS ;
Black, PM .
NATURE BIOTECHNOLOGY, 2001, 19 (01) :35-39
[15]   Preparation of silver nanoparticles using the SPG membrane emulsification technique [J].
Kakazu, Emiri ;
Murakami, Takuya ;
Akamatsu, Kazuki ;
Sugawara, Takashi ;
Kikuchi, Ryuji ;
Nakao, Shin-ichi .
JOURNAL OF MEMBRANE SCIENCE, 2010, 354 (1-2) :1-5
[16]   Regular-sized cell creation in microchannel emulsification by visual microprocessing method [J].
Kawakatsu, T ;
Kikuchi, Y ;
Nakajima, M .
JOURNAL OF THE AMERICAN OIL CHEMISTS SOCIETY, 1997, 74 (03) :317-321
[17]  
LARSEN B, 1989, CARBOHYD RES, V338, P2325
[18]   Controlled growth factor release from synthetic extracellular matrices [J].
Lee, KY ;
Peters, MC ;
Anderson, KW ;
Mooney, DJ .
NATURE, 2000, 408 (6815) :998-1000
[19]   Shape-controlled production of biodegradable calcium alginate gel microparticles using a novel microfluidic device [J].
Liu, Kan ;
Ding, Hui-Jiang ;
Liu, Jing ;
Chen, Yong ;
Zhao, Xing-Zhong .
LANGMUIR, 2006, 22 (22) :9453-9457
[20]   ALGINATE AS IMMOBILIZATION MATERIAL .3. DIFFUSIONAL PROPERTIES [J].
MARTINSEN, A ;
STORRO, I ;
SKJAKBRAEK, G .
BIOTECHNOLOGY AND BIOENGINEERING, 1992, 39 (02) :186-194