聚乳酸-羟基乙酸共聚物载肝细胞生长因子纳米粒的构建及生物学活性评价 |
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引用本文: | 冼文娇,王雪儿,张琳.聚乳酸-羟基乙酸共聚物载肝细胞生长因子纳米粒的构建及生物学活性评价[J].南方医科大学学报,2018,38(2):217. |
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作者姓名: | 冼文娇 王雪儿 张琳 |
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摘 要: | 目的探究制备聚乳酸-羟基乙酸共聚物(PLGA)纳米粒的优化条件,构建肝细胞生长因子(HGF)纳米粒,评价其包封率、
载药量、回收率、释放度和生物学活性。方法采用复乳溶剂挥发法制备牛血清白蛋白(BSA)PLGA纳米粒,通过正交试验设计,
以粒径较小,包封率、载药量和回收率较高为考察指标,优化纳米粒的制备条件;选取优化条件制备HGF纳米粒,分别采用BCA
试剂盒和HGF-ELISA试剂盒检测BSA纳米粒和HGF纳米粒的包封率、载药量和释放度,通过CCK8增殖实验评价HGF纳米粒
的生物活性。结果优化条件下制备的HGF 纳米粒大小均匀,粒径234.4±4.8 nm,包封率(77.75±3.04)%,回收率(49.33±
9.34)%,体外释放度曲线表现为先突释,后缓释;HGF纳米粒可以促进角质形成细胞的增殖。结论复乳溶剂挥发法-优化条件
下制备的HGF纳米粒具有较高包封率,良好的缓释效果和生物学活性。
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Construction and bioactivity evaluation of hepatocyte growth factor-loaded poly (lacticco-
glycolic acid) nanoparticles |
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Abstract: | Objective To explore the optimum conditions for preparing poly(lactic-co-glycolic) acid (PLGA) nanoparticles and
evaluate the bioactivity of hepatocyte growth factor (HGF)-loaded PLGA nanoparticles. Methods Bovine serum albumin
(BSA)-loaded PLGA nanoparticles were prepared using a double emulsion-solvent evaporation method. The preparation
process of nanoparticles was optimized by orthogonal test with the particle size, encapsulation efficiency (EE), drug loading
(DD), and recovery as the indexes. HGF-loaded nanoparticles were then prepared under the optimized conditions. The EE, DD
and release characteristics of BSA-loaded nanoparticles and HGF-loaded nanoparticles were evaluated using a BCA kit and
HGF ELISA kit. The bioactivity of HGF-loaded nanoparticles was evaluated using CCK8 proliferation assay. Results The
HGF-loaded nanoparticles prepared under the optimized conditions had a uniform size with a mean diameter of 234.4±4.8 nm,
an EE of (77.75±3.04)% and a recovery rate of (49.33±9.34)%. The in vitro release curve highlighted an initial burst drug release
followed by sustained release from the nanoparticles. HGF-loaded nanoparticles obviously promoted the proliferation of
Hacat keratinocytes in vitro. Conclusion HGF-loaded nanoparticles prepared using double emulsion-solvent evaporation
method under optimized conditions possesses a high EE with a good sustained drug release profile and a good bioactivity. |
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