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制备及表征作为 FGF-2 载体的低分子量肝素/鱼精蛋白纳米粒(LMW-H/P NPs)。

Preparation and characterization of low-molecular-weight heparin/protamine nanoparticles (LMW-H/P NPs) as FGF-2 carrier.

机构信息

Research Institute, National Defense Medical College, Tokorozawa, Saitama, Japan.

出版信息

Int J Nanomedicine. 2010 Apr 7;5:147-55. doi: 10.2147/ijn.s8692.

Abstract

We produced low-molecular-weight heparin/protamine nanoparticles (LMW-H/P NPs) as a carrier for heparin-binding growth factors, such as fibroblast growth factor-2 (FGF-2). A mixture of low-molecular-weight heparin (MW: about 5000 Da, 6.4 mg/mL) and protamine (MW: about 3000 Da, 10 mg/mL) at a ratio of 7:3 (vol:vol) yields a dispersion of microparticles (1-6 microm in diameter). In this study, diluted low-molecular-weight heparin solution in saline (0.32 mg/mL) mixed with diluted protamine (0.5 mg/mL) at a ratio at 7:3 (vol:vol) resulted in soluble nanoparticles (112.5 +/- 46.1 nm in diameter). The generated NPs could be then stabilized by adding 2 mg/mL dextran (MW: 178-217 kDa) and remained soluble after lyophilization of dialyzed LMW-H/P NP solution. We then evaluated the capacity of LMW-H/P NPs to protect activity of FGF-2. Interaction between FGF-2 and LMW-H/P NPs substantially prolonged the biological half-life of FGF-2. Furthermore, FGF-2 molecules were protected from inactivation by heat and proteolysis in the presence of LMW-H/P NPs.

摘要

我们制备了低分子量肝素/鱼精蛋白纳米颗粒(LMW-H/P NPs)作为肝素结合生长因子(如成纤维细胞生长因子-2(FGF-2))的载体。将低分子量肝素(MW:约 5000 Da,6.4 mg/mL)和鱼精蛋白(MW:约 3000 Da,10 mg/mL)以 7:3(体积比)的比例混合得到微粒分散体(直径为 1-6 微米)。在这项研究中,将生理盐水中稀释的低分子量肝素溶液(0.32 mg/mL)与稀释的鱼精蛋白(0.5 mg/mL)以 7:3(体积比)的比例混合得到可溶性纳米颗粒(直径为 112.5 +/- 46.1 nm)。然后通过添加 2 mg/mL 葡聚糖(MW:178-217 kDa)可以稳定生成的 NPs,并且在透析 LMW-H/P NP 溶液的冻干后仍然保持可溶性。然后我们评估了 LMW-H/P NPs 保护 FGF-2 活性的能力。FGF-2 与 LMW-H/P NPs 的相互作用大大延长了 FGF-2 的生物学半衰期。此外,在 LMW-H/P NPs 的存在下,FGF-2 分子免受热和蛋白水解的失活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ad/2865009/5f5b7c901822/ijn-5-147f1.jpg

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