Quantification of Substitution of Gelatin Methacryloyl: Best Practice and Current Pitfalls

被引:111
作者
Claassen, Christiane [1 ]
Claassen, Marc H. [2 ]
Truffault, Vincent [2 ]
Sewald, Lisa [1 ]
Tovar, Guenter E. M. [1 ,3 ]
Borchers, Kirsten [1 ,3 ]
Southan, Alexander [1 ]
机构
[1] Univ Stuttgart, Inst Interfacial Proc Engn & Plasma Technol IGVP, Nobelstr 12, D-70569 Stuttgart, Germany
[2] Max Planck Inst Dev Biol, Max Planck Ring 5, D-72076 Tubingen, Germany
[3] Fraunhofer Inst Interfacial Engn & Biotechnol IGB, Nobelstr 12, D-70569 Stuttgart, Germany
关键词
DRUG-DELIVERY; CROSS-LINKING; HYDROGELS; RELEASE; MATRIX; FABRICATION;
D O I
10.1021/acs.biomac.7b01221
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cross-linkable gelatin methacryloyl (GM) is widely used for the generation of artificial extracellular matrix (ECM) in tissue engineering. However, the quantification of modified groups in GM is still an unsolved issue, although this is the key factor for tailoring the physicochemical material properties. In this contribution, H-1-C-13-HSQC NMR spectra are used to gain detailed structural information on GMs and of 2-fold modified gelatin containing methacryloyl and acetyl groups (GMAs). Distinctive identification of methacrylate, methacrylamide, and acetyl groups present in GMs and GMAs revealed an overlap of methacrylamide and modified hydroxyproline signals in the H-1 NMR spectrum. Considering this, we suggest a method to quantify methacrylate and methacrylamide groups in GMs precisely based on simple (1) H NMR spectroscopy with an internal standard. Quantification of acetylation in GMAs is also possible, yet, 2D NMR spectra are necessary. The described methods allow direct quantification of modified groups in gelatin derivatives, making them superior to other, indirect methods known so far.
引用
收藏
页码:42 / 52
页数:11
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