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Fabrication of agar‐gelatin hybrid scaffolds using a novel entrapment method for in vitro tissue engineering applications
Author(s) -
Verma Vipin,
Verma Poonam,
Kar Santosh,
Ray Pratima,
Ray Alok R.
Publication year - 2006
Publication title -
biotechnology and bioengineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.136
H-Index - 189
eISSN - 1097-0290
pISSN - 0006-3592
DOI - 10.1002/bit.21111
Subject(s) - gelatin , glutaraldehyde , agar , kinetics , tissue engineering , self healing hydrogels , chemistry , materials science , swelling , chemical engineering , chromatography , biomedical engineering , polymer chemistry , biochemistry , composite material , bacteria , biology , genetics , engineering , medicine , physics , quantum mechanics
Scaffolds of agar and gelatin were developed using a novel entrapment method where agar and gelatin molecules mutually entrapped one another forming stable cell adhesive matrices. Glutaraldehyde was used as a crosslinking agent for gelatin. Three types of hybrid matrices were prepared using agar and gelatin in different proportions in the weight ratio of 1:1, 2:1, and 3:1. Surface characterization of dry scaffolds was carried out by scanning electron microscope. Swelling studies were carried out in phosphate buffer saline (PBS) at physiological pH 7.4. The integral stability of the scaffolds was evaluated by estimating the released disintegrated gelatin from them in PBS at pH 7.4. The attachment kinetics of the cells was evaluated by culturing mouse fibroblast cell line NIH 3T3 on films. The cytocompatibility of these matrices was determined by studying growth kinetics of NIH 3T3 cells on them and morphology of cells was observed through optical photographs taken at various days of culture. It was found that the matrices containing agar and gelatin in 2:1 weight ratio exhibited best growth kinetics. The results obtained from these studies have suggested that the above‐described method is a cheap and easy way to fabricate agar‐gelatin hybrid scaffolds to grow cells which can be used in various in vitro tissue engineering applications like screening of drugs. Biotechnol. Bioeng. 2007;96: 392–400. © 2006 Wiley Periodicals, Inc.