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载银及重组人碱性成纤维细胞生长因子的甲基丙烯酸酐明胶水凝胶对兔深Ⅱ度烧伤创面的影响

[Effects of methacrylic anhydride gelatin hydrogel loaded with silver and recombinant human basic fibroblast growth factor on deep partial-thickness burn wounds in rabbits].

作者信息

Chen X J, Wu X, Lin H H, Liu Z X, Liu S

机构信息

Department of Burn Orthopaedics, the 969th Hospital of PLA Joint Logistic Support Force, Hohhot 010051, China.

出版信息

Zhonghua Shao Shang Yu Chuang Mian Xiu Fu Za Zhi. 2022 Jul 20;38(7):640-649. doi: 10.3760/cma.j.cn501120-20210726-00260.

Abstract

To investigate the effects of methacrylic anhydride gelatin (GelMA) hydrogel loaded with silver and recombinant human basic fibroblast growth factor (rh-bFGF) on deep partial-thickness burn wounds in rabbits. The experimental research method was adopted. Low-concentration GelMA materials, medium-concentration GelMA materials and high-concentration GelMA materials containing different concentrations of methacrylic anhydride (MA) were prepared, after adding photoinitiator, low-concentration GelMA hydrogels, medium-concentration GelMA hydrogels, and high-concentration GelMA hydrogels were obtained, respectively. The nuclear magnetic resonance spectroscopy was performed to detect the hydrogen nuclear magnetic resonance spectra of the above-mentioned three concentrations of GelMA materials, and to calculate the degree of substitution according to the spectrum diagram. The three-dimensional microstructure and pore size of 3 types of above-mentioned GelMA hydrogels were detected by field emission scanning electron microscopy (FESEM), with 9 samples measured. According to the selected concentration of MA, ten kinds of solutions of GelMA with different concentration of silver (silver-containing GelMA) were synthesized, and the silver-containing GelMA solution of each concentration was divided into three parts, and then exposed to ultraviolet light lasting for 20, 25, and 35 s, respectively. After adding photoinitiator,the corresponding silver-containing GelMA hydrogels were obtained. The residual degradation rate of silver-containing GelMA hydrogel with different photocrosslinking times was detected by collagenase degradation method at degradation of 12, 24, 36, and 48 h; and the time required for complete degradation was detected, and the sample number was 5. The inhibition zone diameter of GelMA hydrogel under above screened photocrosslinking times containing 10 concentrations of silver against was measured to reflect its antibacterial ability, and the sample numbers were all 5. The silver-containing GelMA hydrogel with statistical significance compared with the antibacterial circle diameter of the silver-containing GelMA hydrogel containing the lowest concentration (no silver) was considered as having antibacterial activity. The three-dimensional microstructure and pore size of the silver-containing GelMA hydrogels with antibacterial activity and the lowest drug concentration selected were detected by FESEM, and the sample numbers were all 9. The freeze-dried alone GelMA hydrogel and the freeze-dried silver-containing GelMA hydrogel were soaked in phosphate buffer solution for 24 h, respectively, then the swelling rate of the two GelMA hydrogel were calculated and compared by weighing method, and the sample number was 5. GelMA hydrogel containing silver and rh-bFGF, namely compound hydrogel for short, was prepared according to the preliminary experiment and the above experimental results. The appearance of the composite hydrogel was observed in general, and its three-dimensional microstructure and pore size were detected by FESEM. The deep partial-thickness burn wound was made on the back of 30 rabbits (aged 4-6 months, female half and half). Meanwhile, with the rabbit head as the benchmark, the wounds on the left side of the spine were treated as composite hydrogel treatment group, and the wounds on the right side were treated as gauze control group, and which were treated accordingly. On post injury day (PID) 3, 7, 14, 21, and 28, the healing of wounds in the two groups was observed. On PID 7, 14, 21, and 28, the wound healing area was recorded and the healing rate was calculated, with a sample number of 30. Data were statistically analyzed with analysis of variance for repeated measurement, one-way analysis of variance, and independent sample test. The substitution degree among low-concentration GelMA materials, medium-concentration GelMA materials, and high-concentration GelMA materials was significantly different (=1 628.00, <0.01). The low-concentration GelMA hydrogel had a loose and irregular three-dimensional spatial network structure with a pore size of (60±17) μm; the medium-concentration GelMA hydrogel had a relatively uniform three-dimensional spatial network and pore size with a pore size of (45±13) μm; the high-concentration GelMA hydrogel had the dense and disordered three-dimensional spatial network with a pore size of (25±15) μm, the pore sizes of 3 types of GelMA hydrogels were significantly differences (=12.20, <0.01), and medium concentration of MA was selected for the concentration of subsequent materials. The degradability of silver-containing GelMA hydrogels with different concentrations of the same photocrosslinking time was basically same. The degradation residual rates of silver-containing GelMA hydrogels with 20, 25, and 35 s crosslinking time at 12 h were (74.2±1.7)%, (85.3±0.9)%, and (93.2±1.2)%, respectively; the residual rates of degradation at 24 h were (58.3±2.1)%, (65.2±1.8)%, and (81.4±2.6)%, respectively; the residual rates of degradation at 36 h were (22.4±1.9)%, (45.2±1.7)%, and (68.1±1.4)%, respectively; the residual rates of degradation at 48 h were (8.2±1.7)%, (32.4±1.3)%, and (54.3±2.2)%, respectively, and 20, 25, and 30 s photocrosslinking time required for complete degradation of silver-containing GelMA hydrogels were (50.2±2.4), (62.4±1.4), and (72.2±3.2) h, and the difference was statistically significant (=182.40, <0.01), 25 s were selected as the subsequent photocrosslinking time. The antibacterial diameters of 10 types of silver-containing GelMA hydrogels against from low to high concentrations were (2.6±0.4), (2.5±0.4), (3.2±0.4), (12.1±0.7), (14.8±0.7), (15.1±0.5), (16.2±0.6), (16.7±0.5), (16.7±0.4), and (16.7±0.6) mm, respectively, and which basically showed a concentration-dependent increasing trend, and the overall difference was statistically significant (=428.70, <0.01). Compared with the silver-containing GelMA hydrogel with the lowest concentration, the antibacterial circle diameters of other silver-containing GelMA hydrogels with antibacterial ability from low to high concentration were significantly increased (with values of 26.35, 33.84, 43.65, 42.17, 49.24, 55.74, and 43.72, respectively, <0.01). The silver-containing GelMA hydrogel with the antibacterial diameter of (12.1±0.7) mm had the lowest antibacterial activity against and the lowest drug loading concentration, and the concentration of silver was selected for the concentration of subsequent materials. The microscopic morphology of the silver-containing GelMA hydrogel containing silver element with a pore size of (45±13) μm had a regular and linear strip-like structure. After soaking for 24 h, the swelling ratio of silver-containing GelMA hydrogel was similar to that of alone GelMA hydrogel. The composite hydrogel was colorless, clear and transparent, and its three-dimensional microstructure was a regular and uniform grid, with a filament network structure inside, and the pore size of (40±21) μm. On PID 3, a large amount of necrotic tissue and exudate of rabbit wound in composite hydrogel group were observed, and scattered scabs, a small amount of necrotic tissue and exudate of rabbit wound in gauze control group were observed. On PID 7, the area of rabbit wound in composite hydrogel group was significantly reduced, and adhesion of rabbit wound and gauze in gauze control group was observed. On PID 14, In composite hydrogel group, the rabbit wound surface was ruddy, and the growth of granulation tissue was observed, and in gauze control group, the rabbit wound base was pale, and the blood supply was poor. On PID 21, the rabbit wounds in composite hydrogel group healed completely, and rabbit wound in gauze control group had healing trend. On PID 28, new hair could be seen on rabbit wound surface in composite hydrogel group; oval wound of rabbit in gauze control group still remained. On PID 7, 14, 21, and 28, the wound healing areas of rabbit in composite hydrogel group were significantly larger than those in gauze control group (with values of 2.24, 4.43, 7.67, and 7.69, respectively, 0.05 or <0.01). The medium-concentration GelMA hydrogel has good physical and chemical properties in terms of swelling and degradability. The screened silver-containing GelMA hydrogels had the lowest antibacterial activity and the lowest drug loading concentration. Composite hydrogel can significantly shorten the healing time of deep partial-thickness burn wounds in rabbits.

摘要

探讨载银及重组人碱性成纤维细胞生长因子(rh-bFGF)的甲基丙烯酸酐明胶(GelMA)水凝胶对兔深Ⅱ度烧伤创面的影响。采用实验研究方法。制备含不同浓度甲基丙烯酸酐(MA)的低浓度GelMA材料、中浓度GelMA材料和高浓度GelMA材料,加入光引发剂后,分别得到低浓度GelMA水凝胶、中浓度GelMA水凝胶和高浓度GelMA水凝胶。进行核磁共振波谱分析,检测上述三种浓度GelMA材料的氢核磁共振谱,并根据谱图计算取代度。用场发射扫描电子显微镜(FESEM)检测上述3种GelMA水凝胶的三维微观结构和孔径,共检测9个样本。根据选定的MA浓度,合成10种不同银浓度的GelMA溶液(含银GelMA),将每种浓度的含银GelMA溶液分为三份,分别进行20、25和35 s的紫外线照射。加入光引发剂后,得到相应的含银GelMA水凝胶。采用胶原酶降解法在降解12、24、36和48 h时检测不同光交联时间的含银GelMA水凝胶的残余降解率;检测完全降解所需时间,样本数为5。测量上述筛选出的光交联时间下含10种银浓度的GelMA水凝胶对 的抑菌圈直径,以反映其抗菌能力,样本数均为5。将含银GelMA水凝胶的抑菌圈直径与含最低浓度(无银)的含银GelMA水凝胶的抑菌圈直径进行比较,具有统计学意义的视为具有抗菌活性。用场发射扫描电子显微镜检测具有抗菌活性且所选药物浓度最低的含银GelMA水凝胶的三维微观结构和孔径,样本数均为9。将冻干的单纯GelMA水凝胶和冻干的含银GelMA水凝胶分别在磷酸盐缓冲液中浸泡24 h,然后采用称重法计算并比较两种GelMA水凝胶的溶胀率,样本数为5。根据前期实验及上述实验结果制备含银和rh-bFGF的GelMA水凝胶,简称复合水凝胶。观察复合水凝胶的外观,用场发射扫描电子显微镜检测其三维微观结构和孔径。在30只4~6月龄的兔背部制作深Ⅱ度烧伤创面。同时,以兔头部为基准,将脊柱左侧创面作为复合水凝胶治疗组,右侧创面作为纱布对照组,并进行相应处理。于伤后第3、7、14、21和28天观察两组创面愈合情况。在伤后第7、14、21和28天记录创面愈合面积并计算愈合率,样本数为30。采用重复测量方差分析、单因素方差分析和独立样本检验进行统计学分析。低浓度GelMA材料、中浓度GelMA材料和高浓度GelMA材料之间的取代度差异有统计学意义( =1 628.00, <0.01)。低浓度GelMA水凝胶具有疏松不规则的三维空间网络结构,孔径为(60±17)μm;中浓度GelMA水凝胶具有相对均匀的三维空间网络和孔径,孔径为(45±13)μm;高浓度GelMA水凝胶具有致密无序的三维空间网络,孔径为(25±15)μm,3种GelMA水凝胶的孔径差异有统计学意义( =12.20, <0.01),后续材料浓度选用中浓度MA。相同光交联时间下不同浓度含银GelMA水凝胶的降解性能基本相同。交联时间为20、25和35 s的含银GelMA水凝胶在12 h时的降解残余率分别为(74.2±1.7)%、(85.3±0.9)%和(93.2±1.2)%;24 h时的降解残余率分别为(58.3±2.1)%、(65.2±1.8)%和(81.4±2.6)%;36 h时的降解残余率分别为(22.4±1.9)%、(45.2±1.7)%和(68.1±1.4)%;48 h时的降解残余率分别为(8.2±1.7)%、(32.4±1.3)%和(54.3±2.2)%,含银GelMA水凝胶完全降解所需的20、25和30 s光交联时间分别为(50.2±2.4)、(62.4±1.4)和(72.2±3.2)h,差异有统计学意义( =182.40, <0.01),后续光交联时间选用25 s。10种不同浓度含银GelMA水凝胶对 的抑菌圈直径由低到高分别为(2.6±0.4)、(2.5±0.4)、(3.2±0.4)、(12.1±0.7)、(14.8±0.7)、(15.1±0.5)、(16.2±0.6)、(16.7±0.5)、(16.7±0.4)和(16.7±0.6)mm,基本呈浓度依赖性增加趋势,总体差异有统计学意义( =428.70, <0.01)。与最低浓度含银GelMA水凝胶相比,其他具有抗菌活性的不同浓度含银GelMA水凝胶的抑菌圈直径均显著增大( 值分别为26.35、33.84、43.65、42.17、49.24、55.74和43.72,均<0.01)。抑菌圈直径为(

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