Response of intestinal cells and macrophages to an orally administered cellulose-PEG based polymer as a potential treatment for intractable edemas

被引:23
作者
Esposito, A
Sannino, A
Cozzolino, A
Quintiliano, SN
Lamberti, M
Ambrosio, L
Nicolais, L
机构
[1] Univ Lecce, Dept Engn Innovat, I-73100 Lecce, Italy
[2] Univ Naples 2, Dept Expt Med, I-80138 Naples, Italy
[3] Univ Naples, Dept Food Sci, I-80055 Portici, Italy
[4] Univ Naples 2, Dept Biochem & Biophys, I-80138 Naples, Italy
[5] CNR, Inst Composite & Biomed Mat, Naples, Italy
关键词
hydrogels; cross-linking; swelling; macrophage; intestinal cells; biocompatibility;
D O I
10.1016/j.biomaterials.2004.10.023
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The elimination of water from the body represents a fundamental therapeutic goal in those diseases in which oedemas occur. Aim of this work is the design of a material able to absorb large amount of water to be used, by oral administration, in those cases in which resistance to diuretics appears. Sorption and mechanical properties of the cellulose based superabsorbent hydrogel acting as a water elimination system have been modulated through the insertion of molecular spacers between the crosslinks. Starting polymers are the sodium salt of carboxymethylcellulose (CMCNa), a polyelectrolyte cellulose derivative, and the hydroxyethylcellulose (HEC), a non-polyelectrolyte derivative. Polyethyleneglycol (PEG) with various molecular weights, has been linked by its free ends at two divinylsulfone (DVS) crosslinker molecules, in order to increase the average distance between two crosslinking sites and thus acting as spacer. Both the effect of concentration and molecular weight of the spacer resulted to significantly affect the hydrogel final sorption properties and thus the efficiency of the body water elimination system. Biocompatibility studies have been performed to test the hydrogel compatibility with respect to intestinal and macrophages cell lines. To investigate the effects of intestinal cells conditioned media after the contact with the gel on macrophages nitric oxide release tests have been carried out. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4101 / 4110
页数:10
相关论文
共 34 条
[1]  
ANDERSON JM, 1984, BIOMATERIALS, V5, P5, DOI 10.1016/0142-9612(84)90060-7
[2]  
Arvanitidou M, 1999, J NEPHROL, V12, P32
[3]   iNOS upregulation mediates oxidant-induced disruption of F-actin and barrier of intestinal monolayers [J].
Banan, A ;
Fields, JZ ;
Zhang, Y ;
Keshavarzian, A .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2001, 280 (06) :G1234-G1246
[4]   The pathophysiological mechanism of fluid retention in advanced cancer patients treated with docetaxel, but not receiving corticosteroid comedication [J].
Behar, A ;
PujadeLauraine, E ;
Maurel, A ;
Brun, MD ;
Lagrue, G ;
DeChauvin, FF ;
OulidAissa, D ;
Hille, D .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1997, 43 (06) :653-658
[5]  
Boynton EL, 2000, J BIOMED MATER RES, V52, P239, DOI 10.1002/1097-4636(200011)52:2<239::AID-JBM1>3.0.CO
[6]  
2-R
[7]   DYNAMIC AND EQUILIBRIUM SWELLING BEHAVIOR OF PH-SENSITIVE HYDROGELS CONTAINING 2-HYDROXYETHYL METHACRYLATE [J].
BRANNONPEPPAS, L ;
PEPPAS, NA .
BIOMATERIALS, 1990, 11 (09) :635-644
[8]   13C solid-state NMR determination of cross-linking degree in superabsorbing cellulose-based networks [J].
Capitani, D ;
Del Nobile, MA ;
Mensitieri, G ;
Sannino, A ;
Segre, AL .
MACROMOLECULES, 2000, 33 (02) :430-437
[9]  
DELNOBILE MA, Patent No. 9858686
[10]  
DORKOOSH SA, 2002, INT J PHARM, V241, P34