4.5 Article

Manipulations in hydrogel chemistry control photoencapsulated chondrocyte behavior and their extracellular matrix production

期刊

JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A
卷 67A, 期 4, 页码 1430-1436

出版社

WILEY
DOI: 10.1002/jbm.a.20003

关键词

photopolymerization; poly(ethylene glycol); cartilage; tissue engineering; degradation

资金

  1. NIDCR NIH HHS [R01 DE12998] Funding Source: Medline

向作者/读者索取更多资源

In engineering a cell-carrier to support cartilage growth, hydrogels provide a unique, largely aqueous environment for 3-dimensional chondrocyte culture that facilitates nutrient transport yet provides an elastic framework dictating tissue shape and supporting external loads. Although the gel environment is often >90% water, we demonstrate that slight variations in hydrogel chemistry control gel degradation, evolving macroscopic properties, and ultimately the secretion and distribution of extracellular matrix molecules. Specifically, biodegradable poly(ethylene glycol)co-poly(lactic acid) hydrogels were fabricated via photopolymerization. When chondrocytes were photoencapsulated in these gels, changes in the poly(ethylene glycol)-co-poly-(lactic acid) repeat unit ratio from 19 to 7 increased total collagen synthesis 2.5-fold after 6 weeks in vitro. Furthermore, the ratio of collagen to glycosaminoglycans varied from glycosaminoglycan-rich, 0.33 +/- 0.13, to collagen-rich, 4.58 +/- 1.21, depending on gel chemistry and in vitro versus in vivo culture environment. By tuning scaffold chemistry, and subsequently, gel structure and degradation behavior, we can better guide tissue evolution and development. (C) 2003 Wiley Periodicals, Inc.

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