Quantitative chemical mapping of sodium acrylate- and N-vinylpyrrolidone-enhanced alginate microcapsules

被引:13
作者
Araki, T
Hitchcock, AP
Shen, F
Chang, PL
Wang, M
Childs, RF
机构
[1] McMaster Univ, Dept Pediat, Hlth Sci Ctr, Hamilton, ON L8N 3Z5, Canada
[2] McMaster Univ, Dept Chem, Hamilton, ON L8N 3Z5, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
molecular imaging; co-polymer; hydrogel; image analysis; photopolymerization;
D O I
10.1163/1568562053783687
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
Alginate microcapsules enclosing recombinant cells secreting therapeutic products have been used successfully to treat several murine models of human diseases. The mechanical and chemical properties of these alginate capsules can be improved by the addition and in situ photopolymerization of sodium acrylate and N-vinylpyrrolidone in the alginate capsule. The purpose of this modification was to form additional covalent cross-links. In this work we have used scanning transmission X-ray microscopy (STXM) to probe the nature and location of the chemical modifications in the modified capsules by comparison with unmodified capsules. Analysis of X-ray image sequences and selected area spectra has been used to map the calcium gradient in capsules, to identify the presence of polyacrylate throughout the capsules and the localization of poly-N-vinylpyrrolidone in the outer regions of the alginate capsules. The differences in the spatial distributions of these species have led to better understanding of the chemical modifications that provide a mechanically more stable capsule structure.
引用
收藏
页码:611 / 627
页数:17
相关论文
共 42 条
[1]
X-RAY MICROSCOPY IN POLYMER SCIENCE - PROSPECTS OF A NEW IMAGING TECHNIQUE [J].
ADE, H ;
SMITH, AP ;
CAMERON, S ;
CIESLINSKI, R ;
MITCHELL, G ;
HSIAO, B ;
RIGHTOR, E .
POLYMER, 1995, 36 (09) :1843-1848
[2]
CHEMICAL CONTRAST IN X-RAY MICROSCOPY AND SPATIALLY RESOLVED XANES SPECTROSCOPY OF ORGANIC SPECIMENS [J].
ADE, H ;
ZHANG, X ;
CAMERON, S ;
COSTELLO, C ;
KIRZ, J ;
WILLIAMS, S .
SCIENCE, 1992, 258 (5084) :972-975
[3]
Ade H., 2002, CHEM APPL SYNCHROTRO, P285
[4]
Ade H., 1998, EXPT METHODS PHYS SC, V32, P225
[5]
Intrathecal delivery of CNTF using encapsulated genetically modified xenogeneic cells in amyotrophic lateral sclerosis patients [J].
Aebischer, P ;
Schluep, M ;
Deglon, N ;
Joseph, JM ;
Hirt, L ;
Heyd, B ;
Goddard, M ;
Hammang, JP ;
Zurn, AD ;
Kato, AC ;
Regli, F ;
Baetge, EE .
NATURE MEDICINE, 1996, 2 (06) :696-699
[6]
Gene therapy for amyotrophic lateral sclerosis (ALS) using a polymer encapsulated xenogenic cell line engineered to secrete hCNTF [J].
Aebischer, P ;
Pochon, NAM ;
Heyd, B ;
Deglon, N ;
Joseph, JM ;
Zurn, AD ;
Baetge, EE ;
Hammang, JP ;
Goddard, M ;
Lysaght, M ;
Kaplan, F ;
Kato, AC ;
Schluep, M ;
Hirt, L ;
Regli, F ;
Porchet, F ;
DeTribolet, N .
HUMAN GENE THERAPY, 1996, 7 (07) :851-860
[7]
MACROENCAPSULATION OF DOPAMINE-SECRETING CELLS BY COEXTRUSION WITH AN ORGANIC POLYMER-SOLUTION [J].
AEBISCHER, P ;
WAHLBERG, L ;
TRESCO, PA ;
WINN, SR .
BIOMATERIALS, 1991, 12 (01) :50-56
[8]
CORRECTION OF THE GROWTH DEFECT IN DWARF MICE WITH NONAUTOLOGOUS MICROENCAPSULATED MYOBLASTS - AN ALTERNATE APPROACH TO SOMATIC GENE-THERAPY [J].
ALHENDY, A ;
HORTELANO, G ;
TANNENBAUM, GS ;
CHANG, PL .
HUMAN GENE THERAPY, 1995, 6 (02) :165-175
[9]
Becker TA, 2001, J BIOMED MATER RES, V54, P76, DOI 10.1002/1097-4636(200101)54:1<76::AID-JBM9>3.0.CO
[10]
2-V