Gelatin methacrylate microspheres for controlled growth factor release.
Gelatin methacrylate microspheres for controlled growth factor release.
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DOI:
10.1016/j.actbio.2014.11.028
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发表时间:
2015-02
影响因子:
9.7
通讯作者:
McDevitt, Todd C.
中科院分区:
文献类型:
--
作者:
Nguyen, Anh H.;McKinney, Jay;Miller, Tobias;Bongiorno, Tom;McDevitt, Todd C.
Gelatin has been commonly used as a delivery vehicle for various biomolecules for tissue engineering and regenerative medicine applications due to its simple fabrication methods, inherent electrostatic binding properties, and proteolytic degradability. Compared to traditional chemical cross-linking methods, such as the use of glutaraldehyde (GA), methacrylate modification of gelatin offers an alternative method to better control the extent of hydrogel cross-linking. Here we examined the physical properties and growth factor delivery of gelatin methacrylate (GMA) microparticles formulated with a wide range of different cross-linking densities (15–90%). Less methacrylated MPs had decreased elastic moduli and larger mesh sizes compared to GA MPs, with increasing methacrylation correlating to greater moduli and smaller mesh sizes. As expected, an inverse correlation between microparticle cross-linking density and degradation was observed, with the lowest cross-linked GMA MPs degrading at the fastest rate, comparable to GA MPs. Interestingly, GMA MPs at lower cross-linking densities could be loaded with up to a 10-fold higher relative amount of growth factor over conventional GA cross-linked MPs, despite an order of magnitude greater gelatin content of GA MPs. Moreover, a reduced GMA cross-linking density resulted in more complete release of bone morphogenic protein 4 (BMP4) and basic fibroblast growth factor (bFGF) and accelerated release rate with collagenase treatment. These studies demonstrate that GMA MPs provide a more flexible platform for growth factor delivery by enhancing the relative binding capacity and permitting proteolytic degradation tunability, thereby offering a more potent controlled release system for growth factor delivery.
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影响因子:
10.8
作者:
Holland, TA;Tabata, Y;Mikos, AG
通讯作者:
Mikos, AG
影响因子:
14
作者:
Nichol, Jason W.;Koshy, Sandeep T.;Bae, Hojae;Hwang, Chang M.;Yamanlar, Seda;Khademhosseini, Ali
通讯作者:
Khademhosseini, Ali
影响因子:
3.4
作者:
Nichol JW;Khademhosseini A
通讯作者:
Khademhosseini A
影响因子:
14
作者:
Carpenedo, Richard L.;Bratt-Leal, Andrs M.;Marklein, Ross A.;Seaman, Scott A.;Bowen, Nathan J.;McDonald, John F.;McDevitt, Todd C.
通讯作者:
McDevitt, Todd C.
影响因子:
4.6
作者:
Hu, Xiaohong;Ma, Lie;Gao, Changyou
通讯作者:
Gao, Changyou