Chinese Journal of Tissue Engineering Research ›› 2026, Vol. 30 ›› Issue (31): 8092-8099.doi: 10.12307/2026.450
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Wang Quansheng1, 2, 3, Chen Songtao1, 2, 3, Zhang Yongqing1, 2, 3, Qiao Hua1, 2, 3
Received:2025-12-01
Accepted:2026-02-02
Online:2026-11-08
Published:2026-05-22
Contact:
Qiao Hua, MD, Associate professor, Master’s supervisor, Department of Biochemistry and Molecular Biology, School of Basic Medicine, Shanxi Medical University, Taiyuan 030001, Shanxi Province, China; Ministry of Education Key Laboratory of Coal Environmental Pathogenicity and Prevention, Taiyuan 030001, Shanxi Province, China; Shanxi Key Laboratory of Birth Defect and Cell Regeneration, Taiyuan 030001, Shanxi Province, China
About author:Wang Quansheng, MS candidate, Department of Biochemistry and Molecular Biology, School of Basic Medicine, Shanxi Medical University, Taiyuan 030001, Shanxi Province, China; Ministry of Education Key Laboratory of Coal Environmental Pathogenicity and Prevention, Taiyuan 030001, Shanxi Province, China; Shanxi Key Laboratory of Birth Defect and Cell Regeneration, Taiyuan 030001, Shanxi Province, China
Supported by:CLC Number:
Wang Quansheng, Chen Songtao, Zhang Yongqing, Qiao Hua. Preparation and performance evaluation of essence with mesenchymal stem cell conditioned medium[J]. Chinese Journal of Tissue Engineering Research, 2026, 30(31): 8092-8099.
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2.1 间充质干细胞条件培养基精华液的配方设计 通过L9(33)正交试验优化精华液配方,以感官性能评分为考察指标,筛选黄原胶添加量(A)、间充质干细胞条件培养基添加量(B)和甘油添加量(C)的最优用量和配比。由表6可知,黄原胶添加量对感官性能影响最大,其次是间充质干细胞条件培养基,影响最小的是甘油。根据极差分析,以感官性能为评分标准时,3个因素的最优组合为A2B1C3,即间充质干细胞条件培养基添加量为5%,甘油添加量为5%,黄原胶添加量为0.25%。在最优组合下,重复配制间充质干细胞条件培养基精华液多次,发现此配方重复性高,操作简易,感官评分高。最终间充质干细胞条件培养基精华液成品见图1。 "
2.2 间充质干细胞条件培养基精华液的稳定性 精华液在4 ℃下放置1,3,6,12个月后,无沉淀产生,未出现分层,说明4 ℃条件下贮存12个月该精华液稳定性良好。冷热循环方面,48 ℃下存放12 h,精华液无沉淀产生,无分层现象;再放入-16 ℃冰箱中存放12 h后,亦无沉淀产生,也未出现分层,说明该精华液在冷热循环条件下稳定。精华液3 750 r/min离心5 h (相当于地心重力作用1年的结果),无沉淀产生和分层、变色、浮油现象,提示该精华液具有良好的离心稳定性,在地心重力作用1年的条件下稳定。 2.3 间充质干细胞条件培养基精华液的pH值 用pH计测得精华液的pH值为6.50±0.10,符合《化妆品通用检测法》所规定的要求[29],可以避免刺激皮肤或破坏活性成分。 2.4 间充质干细胞条件培养基精华液的失水率 37 ℃恒温5 h,精华液的失水率较低,仅为(5.09±0.46)%,结果见表7。该结果与同类型精华液的失水率相当[30],表明该精华液具有良好的保湿性能,为精华液中活性物质发挥功能提供了可能。 "
2.6.2 衰老人皮肤成纤维细胞中活性氧水平 如图6所示,与模型组相比,其他组细胞活性氧水平显著下调(P < 0.05)。5%,10%空白精华液组活性氧水平分别为(47.49±1.29)%,(49.55±3.15)%,5%,10%间充质干细胞条件培养基精华液组活性氧水平分别为(36.05±1.35)%和(25.17±1.66)%,空白精华液组与间充质干细胞条件培养基精华液组细胞内活性氧水平均有显著性差异(P < 0.05)。10%间充质干细胞条件培养基精华液组细胞内活性氧的清除效果最强(P < 0.001)。这些结果表明空白精华液及间充质干细胞条件培养基精华液均能对衰老人皮肤成纤维细胞内活性氧有一定的清除作用,但间充质干细胞条件培养基精华液抑制细胞内活性氧生成能力更强,同时随着精华液浓度增加清除活性氧能力增强。 "
2.6.3 衰老斑马鱼胚胎活性氧水平 见图7。 如图7所示,当设置空白组荧光强度为1,模型组绿色荧光水平为2.185±0.215,相较空白组显著提高(P < 0.001),说明H2O2诱导斑马鱼胚胎体内活性氧水平升高。1%,2%空白精华液组荧光强度分别为2.09±0.18和2.03±0.06,与模型组无显著性差异。1%,2%间充质干细胞条件培养基精华液组荧光强度分别为1.28±0.55和1.13±0.10,均较模型组显著下降(P < 0.05,P < 0.01),且呈现出浓度依赖性。在相同浓度下,间充质干细胞条件培养基精华液组与空白精华液组活性氧水平均有显著性差异(P < 0.05),说明加入间充质干细胞条件培养基成分的精华液可显著抑制H2O2诱导的衰老斑马鱼胚胎体内活性氧产生。 "
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