摘要
背景:葡聚糖/聚乳酸-乙醇酸微球药物缓释系统可使药物在作用部位维持有效药物浓度。目的:探讨携载粒细胞集落刺激因子、促红细胞生成素或血管内皮生长因子葡聚糖/聚乳酸-乙醇酸微球对缺血下肢血管再生的影响。方法:制备分别携载粒细胞集落刺激因子、促红细胞生成素与血管内皮生长因子的葡聚糖/聚乳酸-乙醇酸微球,通过扫描电镜观察其表面形态,利用ELISA法检测其包封率和累积释放率。将3种携载生长因子的微球与纤维蛋白胶混合,制备携载生长因子葡聚糖/聚乳酸纤维蛋白胶复合物。取24只雄性SD大鼠(江西省中医学院实验动物中心提供),制作右下肢缺血模型,随机分成2组干预,每组12只:观察组大腿肌肉内侧分5点注射携载3种生长因子葡聚糖/聚乳酸-乙醇酸微球的纤维蛋白胶复合物,对照组大腿肌肉内侧注射葡聚糖/聚乳酸-乙醇酸微球纤维蛋白凝胶复合物。术后第1周取注射部位肌肉组织,免疫组织化学染色观察增殖细胞核抗原、Bcl-2、基质细胞衍生因子1和趋化因子基质细胞衍生因子4的表达;术后第4周取注射部位肌肉组织,碱性磷酸酶与免疫组织化学染色观察毛细血管密度。实验方案经南昌大学医学院动物实验伦理委员会批准。结果与结论:(1)葡聚糖/聚乳酸-乙醇酸微球呈球形,表面光滑,直径40-120μm;搭载粒细胞集落刺激因子、促红细胞生成素与血管内皮生长因子葡聚糖/聚乳酸-乙醇酸微球的包封率分别为84%,85%,82%,4周的累积释放率分别为89.5%,90.3%,91.2%;(2)观察组增殖细胞核抗原、Bcl-2、基质细胞衍生因子1和趋化因子基质细胞衍生因子4阳性表达高于对照组;(3)观察组毛细血管密度与α-平滑肌肌动蛋白阳性血管密度高于对照组(P <0.05);(4)结果表明利用葡聚糖/聚乳酸-乙醇酸微球联合多种血管再生因子治疗下肢缺血,是一种有前途的血管再生方法。
BACKGROUND: The dextran/poly(lactic-co-glycolic acid)(PLGA) microspheres as a sustained release drug delivery system enables the drug to maintain an effective concentration at the site of action.OBJECTIVE: To investigate the effects of dextran/PLGA microspheres carrying granulocyte colony-stimulating factor, erythropoietin and vascular endothelial growth factor on the neovascularization of ischemic lower limb of rats.METHODS: Dextran/PLGA microspheres carrying granulocyte colony-stimulating factor, erythropoietin, and vascular endothelial growth factor were prepared and their surface morphology was observed by scanning electron microscopy. The encapsulation efficiency and cumulative release rate were detected by ELISA method. Dextran/PLGA microspheres carrying three growth factors were mixed with fibrin glue to prepare a growth factor dextran/PLGA/fibrin glue complex. Right lower limb ischemia models were produced in 24 male Sprague-Dawley rats(Laboratory Animal Center, Jiangsu University of Traditional Chinese Medicine, China). These animal models were randomly divided into two groups(n = 12/group). In the experimental group, dextran/PLGA/fibrin glue complex carrying three growth factors was injected into the inner thigh muscle at 5 points. In the control group, dextran/PLGA/fibrin glue complex without growth factors was identically injected. At 1 week after surgery, the muscle tissue around the injection site was harvested for immunohistochemistry to detect the expression of proliferating cell nuclear antigen, Bcl-2, stromal cell-derived factor 1, and C-X-C chemokine receptor type 4. At 4 weeks after surgery, the muscle tissue around the injection site was harvested for histological and immunohistochemical examination to measure capillary density. This study was approved by Animal Ethics Committee of Nanchang University School of Medicine, China.RESULTS AND CONCLUSION: The dextran/PLGA microspheres were spherical and had a smooth surface with a diameter of 40-120 μm.The encapsulation efficiency of dextran/PLGA microspheres carrying granulocyte colony-stimulating factor, erythropoietin, and vascular endothelial growth factor was 84%, 85%, and 82%, respectively. The 4-week cumulative release rate was 89.5%, 90.3%, 91.2%, respectively.The expression of proliferating cell nuclear antigen, Bcl-2, stromal cell-derived factor 1, and C-X-C chemokine receptor type 4 in the experimental group was significantly higher than that in the control group. Capillary density and α-smooth muscle actin-positive vascular density in the experimental group were significantly higher than those in the control group(P < 0.05). These results suggest that dextran/PLGA microspheres carrying multiple growth factors for treatment of lower limb ischemia is a promising therapeutic method.
作者
朱仙花
陈锋
刘崇栋
周卫
唐新华
Zhu Xianhua;Chen Feng;Liu Chongdong;Zhou Wei;Tang Xinhua(Department of Vascular Surgery, Second Affiliated Hospital of Nanchang University, Nanchang 330006, Jiangxi Province, China)
出处
《中国组织工程研究》
CAS
北大核心
2019年第26期4142-4147,共6页
Chinese Journal of Tissue Engineering Research
基金
国家自然科学基金项目(81460083):复合促血管再生因子/葡聚糖/PLGA纳米微球纤维蛋白胶的血管再生鸡尾酒疗法研究,项目负责人:陈锋
江西省科技厅青年科学基金项目(20142BAB215034):复合血管再生细胞因子-PLGA纳米微球纤维蛋白胶治疗下肢慢性缺血的实验研究,项目负责人:陈锋
江西省科技厅科技计划一般项目(20141BBG70032):葡聚糖-PLGA纳米微球携载复合血管生成细胞因子的血管再生治疗研究,项目负责人:陈锋
江西省科技厅青年科学基金重大项目(20151522070093):动静脉短路法抑制动脉支架内再狭窄的机制研究,项目负责人:陈锋~~