CN114134108A - 一种干细胞生物活性组合物及其制备方法 - Google Patents
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Abstract
本发明公开了一种干细胞生物活性组合物及其制备方法,具体涉及医疗领域,包括12.36‑55.86pg/ml 1‑Octacosanol、5.63‑20.14pg/ml EPO、10.36‑36.45pg/ml醋酸钠,本发明通过在组合物中添加醋酸钠,提高干细胞的本身活性,并在组合物中添加1‑Octacosanol,此时在向组合物中添加EPO,红细胞生成的一种糖蛋白,添加的1‑Octacosanol会加快酯化反应,加快形成糖蛋白,形成质量良好的干细胞生物活性组合物。
Description
技术领域
本发明涉及医疗领域,具体涉及一种干细胞生物活性组合物及其制备方法。
背景技术
多年来对干细胞的定义不断进行修正,并从不同的层面上来进行定义。大多数生物学家和医学家认为干细胞是来自于胚胎、胎儿或成人体内具有在一定条件下无限制自我更新与增殖分化能力的一类细胞,能够产生表现型与基因型和自己完全相同的子细胞,也能产生组成机体组织、器官的已特化的细胞,同时还能分化为祖细胞,同时干细胞在存储是需要使用干细胞生物活性组合物。
但是现如今的干细胞生物活性组合物及其制备方法在对干细胞进行存储是,活性不高,而且生产的干细胞生物活性组合物质量不高。
发明内容
为此,本发明提供一种干细胞生物活性组合物及其制备方法,以解决现有技术中的问题。
为了实现上述目的,本发明实施例提供如下技术方案:一种干细胞生物活性组合物,包括1.69-22.24pg/ml EGF、2443.17-4459.43pg/ml bFGF、1.44-134.36pg/ml beta-NGF、1.55-355.14pg/ml VEGF、11.87-159.70pg/ml PDGF-DD、135.79-688.13pg/ml KGF、1176.99-3825.79pg/ml TGF-β1、12.36-55.86pg/ml 1-Octacosanol、5.63-20.14pg/mlEPO、10.36-36.45pg/ml醋酸钠。
进一步地,所述12.36pg/ml 1-Octacosanol、5.63pg/ml EPO、36.45pg/ml醋酸钠。
进一步地,所述55.86pg/ml 1-Octacosanol、20.14pg/ml EPO、10.36pg/ml醋酸钠。
进一步地,所述55.86pg/ml 1-Octacosanol、20.14pg/ml EPO、36.45pg/ml醋酸钠。
进一步地,所述检测方法基于权利要求1-4任一项的***,步骤如下:
S1:利用培养基,对间充质干细胞和脂肪基质细胞进行非接触式共培养;
S2:并收集间充质干细胞液进行收集,并使用离心机收集上清液;
S3:向上清液中逐次添加EGF、bFGF、beta-NGF、VEGF、PDGF-DD、KGF、TGF-β1、1-Octacosanol、EPO、醋酸钠;
S4:使用RT-PCR检测TPX2基因在乳腺癌组织及癌旁组织中的表达差异使用慢病毒干扰载体建立稳定低表达TPX2蛋白的乳腺癌细胞平板克隆、MTT试验验证TPX2对乳腺癌细胞生长能力的影响流式细胞仪检测敲除TPX2之后对乳腺癌细胞凋亡比率的影响;
S5:之后使用微型振动机将混合液进行性震动混合得到组合物。
本发明实施例具有如下优点:
本发明通过在组合物中添加醋酸钠,提高干细胞的本身活性,并在组合物中添加1-Octacosanol,此时在向组合物中添加EPO,红细胞生成的一种糖蛋白,添加的1-Octacosanol会加快酯化反应,加快形成糖蛋白,形成质量良好的干细胞生物活性组合物。
说明
为了更清楚地说明本发明的实施方式或现有技术中的技术方案,下面将对实施方式或现有技术描述中所需要使用的作简单地介绍。显而易见地,下面描述中的仅仅是示例性的,对于本领域普通技术人员来讲,在不付出创造性劳动的前提下,还可以根据提供的引伸获得其它的实施。
本说明书所绘示的结构、比例、大小等,均仅用以配合说明书所揭示的内容,以供熟悉此技术的人士了解与阅读,并非用以限定本发明可实施的限定条件,故不具技术上的实质意义,任何结构的修饰、比例关系的改变或大小的调整,在不影响本发明所能产生的功效及所能达成的目的下,均应仍落在本发明所揭示的技术内容得能涵盖的范围内。
具体实施方式
以下由特定的具体实施例说明本发明的实施方式,熟悉此技术的人士可由本说明书所揭露的内容轻易地了解本发明的其他优点及功效,显然,所描述的实施例是本发明一部分实施例,而不是全部的实施例。基于本发明中的实施例,本领域普通技术人员在没有做出创造性劳动前提下所获得的所有其他实施例,都属于本发明保护的范围。
一种干细胞生物活性组合物,包括1.69-22.24pg/ml EGF、2443.17-4459.43pg/mlbFGF、1.44-134.36pg/ml beta-NGF、1.55-355.14pg/m lVEGF、11.87-159.70pg/ml PDGF-DD、135.79-688.13pg/ml KGF、1176.99-3825.79pg/ml TGF-β1、12.36-55.86pg/ml 1-Octacosanol、5.63-20.14pg/ml EPO、10.36-36.45pg/ml醋酸钠。
本发明通过在组合物中添加醋酸钠,提高干细胞的本身活性,并在组合物中添加1-Octacosanol,此时在向组合物中添加EPO,红细胞生成的一种糖蛋白,添加的1-Octacosanol会加快酯化反应,加快形成糖蛋白,形成质量良好的干细胞生物活性组合物。
12.36pg/ml 1-Octacosanol、5.63pg/ml EPO、36.45pg/ml醋酸钠。
该种干细胞生物活性组合物的活性较高,能够匀速产生糖蛋白加快,增加干细胞的存活率。
55.86pg/ml 1-Octacosanol、20.14pg/ml EPO、10.36pg/ml醋酸钠。
该种干细胞生物活性组合物活性较低,干细胞存活率较高。
55.86pg/ml 1-Octacosanol、20.14pg/ml EPO、36.45pg/ml醋酸钠。
该种干细胞生物活性组合物活性较高,干细胞存活率较高。
检测方法基于权利要求1-4任一项的***,步骤如下:
S1:利用培养基,对间充质干细胞和脂肪基质细胞进行非接触式共培养;
S2:并收集间充质干细胞液进行收集,并使用离心机收集上清液;
S3:向上清液中逐次添加EGF、bFGF、beta-NGF、VEGF、PDGF-DD、KGF、TGF-β1、1-Octacosanol、EPO、醋酸钠;
S4:使用RT-PCR检测TPX2基因在乳腺癌组织及癌旁组织中的表达差异使用慢病毒干扰载体建立稳定低表达TPX2蛋白的乳腺癌细胞平板克隆、MTT试验验证TPX2对乳腺癌细胞生长能力的影响流式细胞仪检测敲除TPX2之后对乳腺癌细胞凋亡比率的影响;
S5:之后使用微型振动机将混合液进行性震动混合得到组合物。
虽然,上文中已经用一般性说明及具体实施例对本发明作了详尽的描述,但在本发明基础上,可以对之作一些修改或改进,这对本领域技术人员而言是显而易见的。因此,在不偏离本发明精神的基础上所做的这些修改或改进,均属于本发明要求保护的范围。
Claims (5)
1.一种干细胞生物活性组合物,包括1.69-22.24pg/ml EGF、2443.17-4459.43pg/mlbFGF、1.44-134.36pg/ml beta-NGF、1.55-355.14pg/ml VEGF、11.87-159.70pg/ml PDGF-DD、135.79-688.13pg/ml KGF、1176.99-3825.79pg/ml TGF-β1、12.36-55.86pg/ml 1-Octacosanol、5.63-20.14pg/ml EPO、10.36-36.45pg/ml醋酸钠。
2.根据权利要求1所述的一种干细胞生物活性组合物及其制备方法,其特征在于:所述12.36pg/ml 1-Octacosanol、5.63pg/ml EPO、36.45pg/ml醋酸钠。
3.根据权利要求1所述的一种干细胞生物活性组合物及其制备方法,其特征在于:所述55.86pg/ml 1-Octacosanol、20.14pg/ml EPO、10.36pg/ml醋酸钠。
4.根据权利要求1所述的一种干细胞生物活性组合物及其制备方法,其特征在于:所述55.86pg/ml 1-Octacosanol、20.14pg/ml EPO、36.45pg/ml醋酸钠。
5.一种干细胞生物活性组合物的制备方法,其特征在于:所述检测方法基于权利要求1-4任一项的***,步骤如下:
S1:利用培养基,对间充质干细胞和脂肪基质细胞进行非接触式共培养;
S2:并收集间充质干细胞液进行收集,并使用离心机收集上清液;
S3:向上清液中逐次添加EGF、bFGF、beta-NGF、VEGF、PDGF-DD、KGF、TGF-β1、1-Octacosanol、EPO、醋酸钠;
S4:使用RT-PCR检测TPX2基因在乳腺癌组织及癌旁组织中的表达差异使用慢病毒干扰载体建立稳定低表达TPX2蛋白的乳腺癌细胞平板克隆、MTT试验验证TPX2对乳腺癌细胞生长能力的影响流式细胞仪检测敲除TPX2之后对乳腺癌细胞凋亡比率的影响;
S5:之后使用微型振动机将混合液进行性震动混合得到组合物。
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