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灯盏花素载于超变形纳米脂质体灯盏花素 EDTMP(S-UNL-E)的制备及表征及其成骨作用的体外研究。

Preparation and characterization of scutellarin loaded on ultradeformable nano-liposomes scutellarin EDTMP (S-UNL-E) and in vitro study of its osteogenesis.

机构信息

Department of Oral Implantology, The Affiliated Hospital of Qingdao University, Qingdao, China.

School of Stomatology, Qingdao University, Qingdao, China.

出版信息

Bioengineered. 2022 Jan;13(1):1013-1024. doi: 10.1080/21655979.2021.2016095.

DOI:10.1080/21655979.2021.2016095
PMID:34974800
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8805926/
Abstract

The present research aimed to elucidate a convenient, safe and economic approach to induce the growth of endogenous bone tissue and bone regeneration. S-UNL-E was prepared using reverse-phase evaporation, and scutellarin encapsulation was subsequently compared. Meanwhile, the optimal preparation scheme was developed using an orthogonal method, and the particle size was determined using laser light scattering. In osteoblasts cultured in vitro, methyl thiazolyl tetrazolium (MTT), alkaline phosphatase (ALP) staining and alizarin red staining were used to detect the osteogenic effects of S-UNL-E. The results indicated that the optimal process conditions for S-UNL-E included mass ratios of phospholipid-cholesterol, phospholipid-breviscapine, phospholipid-sodium cholate, and phospholipid-stearamide were 2:1, 15:1, 7:1 and 7:1, respectively, and the mass of ethylenediamine tetramethylphosphonic acid (EDTMP) was 30 mg. The average particle size of S-UNL-E was 156.67 ± 1.76 nm, and Zeta potential was -28.77 ± 0.66 mv. S-UNL-E substantially increased the expression of ALP osteoblasts, elevated the content of osteocalcin protein and promoted the formation of mineralized nodules. Cells in the S-UNL-E group were densely distributed with integrated cell structure, and the actin filaments were clear and obvious. The findings demonstrated that S-UNL-E greatly promoted the differentiation and maturation of osteoblasts, and S-UNL-E (2.5 × 10) produced the most favorable effect in differentiation promotion. In conclusion, the present study successfully constructed an S-UNL-E material characterized by high encapsulation and high stability, which could effectively promote osteogenic differentiation and bone formation.

摘要

本研究旨在阐明一种方便、安全和经济的方法,以诱导内源性骨组织的生长和骨再生。采用反相蒸发法制备 S-UNL-E,并对灯盏乙素包封进行了比较。同时,采用正交法制定了最佳制备方案,并采用激光光散射法测定了粒径。在体外培养的成骨细胞中,采用甲基噻唑基四唑(MTT)、碱性磷酸酶(ALP)染色和茜素红染色检测 S-UNL-E 的成骨作用。结果表明,S-UNL-E 的最佳工艺条件为:磷脂-胆固醇、磷脂-灯盏乙素、磷脂-胆酸钠、磷脂-硬脂酰胺的质量比分别为 2:1、15:1、7:1 和 7:1,乙二胺四甲叉膦酸(EDTMP)的质量为 30mg。S-UNL-E 的平均粒径为 156.67±1.76nm,Zeta 电位为-28.77±0.66mv。S-UNL-E 可显著增加 ALP 成骨细胞的表达,提高骨钙蛋白含量,促进矿化结节的形成。S-UNL-E 组细胞分布密集,细胞结构完整,肌动蛋白丝清晰明显。结果表明,S-UNL-E 能显著促进成骨细胞的分化成熟,S-UNL-E(2.5×10)在促进分化方面效果最佳。综上所述,本研究成功构建了一种 S-UNL-E 材料,其具有高包封率和高稳定性,能有效促进成骨分化和骨形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fd/8805926/afdfd67ee820/KBIE_A_2016095_F0006_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fd/8805926/a87080fa36a9/KBIE_A_2016095_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fd/8805926/01722cdc7df2/KBIE_A_2016095_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fd/8805926/6d38ff0e94f8/KBIE_A_2016095_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fd/8805926/6efa0ef15944/KBIE_A_2016095_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fd/8805926/b682004f1a47/KBIE_A_2016095_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fd/8805926/afdfd67ee820/KBIE_A_2016095_F0006_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fd/8805926/a87080fa36a9/KBIE_A_2016095_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fd/8805926/01722cdc7df2/KBIE_A_2016095_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fd/8805926/6d38ff0e94f8/KBIE_A_2016095_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fd/8805926/6efa0ef15944/KBIE_A_2016095_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fd/8805926/b682004f1a47/KBIE_A_2016095_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fd/8805926/afdfd67ee820/KBIE_A_2016095_F0006_OC.jpg

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