Peptide Hydrogel for Sustained Release of Recombinant Human Bone Morphogenetic Protein-2 In Vitro

被引:0
|
作者
Wang, Dalin [1 ]
Qi, Guangyan [2 ,3 ]
Zhang, Mingcai [1 ]
Carlson, Brandon [1 ]
Gernon, Matthew [1 ]
Burton, Douglas [1 ]
Sun, Xiuzhi Susan [2 ,3 ]
Wang, Jinxi [1 ]
机构
[1] Univ Kansas, Med Ctr, Dept Orthoped Surg, 3901 Rainbow Blvd, Kansas City, KS 66160 USA
[2] Kansas State Univ, Dept Biol & Agr Engn, Seaton Hall,919 Mid Campus Dr North, Manhattan, KS 66506 USA
[3] Wake Forest Univ, Sch Med, Wake Forest Inst Regenerat Med, Winston Salem, NC 27101 USA
关键词
peptide hydrogel; bone morphogenetic protein; drug delivery; controlled release; biomaterials; LUMBAR INTERBODY FUSION; DRUG-DELIVERY; RESORPTION; CARRIER; ENCAPSULATION; REGENERATION; DEGRADATION; FABRICATION; PARAMETERS; SCAFFOLDS;
D O I
10.3390/jfb15120369
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
This study aimed to investigate the impact of varying the formulation of a specific peptide hydrogel (PepGel) on the release kinetics of rhBMP-2 in vitro. Three PepGel formulations were assessed: (1) 50% v/v (peptides volume/total volume) PepGel, where synthetic peptides were mixed with crosslinking reagents and rhBMP-2 solution; (2) 67% v/v PepGel; (3) 80% v/v PepGel. Each sample was loaded with 12 mu g of rhBMP-2 and incubated in PBS. Released rhBMP-2 was quantified by ELISA at 1 h, 6 h, and 1, 2, 4, 7, 10, 14, and 21 days. To explore how PepGel formulations influence rhBMP-2 release, the gel porosities, swelling ratios, and mechanical properties of the three PepGel formulations were quantitatively analyzed. The results showed that rhBMP-2 encapsulated with 50% v/v PepGel exhibited a sustained release over the 21-day experiment, while the 67% and 80% v/v PepGels demonstrated significantly lower rhBMP-2 release rates compared to the 50% formulation after day 7. Higher histological porosity of PepGel was significantly correlated with increased rhBMP-2 release rates. Conversely, the swelling ratio and elastic modulus of the 50% v/v PepGel were significantly lower than that of the 67% and 80% v/v formulations. In conclusion, this study indicates that varying the formulation of crosslinked PepGel can control rhBMP-2 release rates in vitro by modulating gel porosity, swelling ratio, and mechanical properties. Encapsulation with 50% v/v PepGel offers a sustained rhBMP-2 release pattern in vitro; if replicated in vivo, this could mitigate the adverse effects associated with burst release of rhBMP-2 in clinical applications.
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页数:13
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