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不同链长聚乙二醇修饰的香豆素6脂质纳米粒对口服吸收的影响

戴江东, 李会鹏, 孙敏捷

戴江东, 李会鹏, 孙敏捷. 不同链长聚乙二醇修饰的香豆素6脂质纳米粒对口服吸收的影响[J]. 中国药科大学学报, 2021, 52(3): 293-300. DOI: 10.11665/j.issn.1000-5048.20210305
引用本文: 戴江东, 李会鹏, 孙敏捷. 不同链长聚乙二醇修饰的香豆素6脂质纳米粒对口服吸收的影响[J]. 中国药科大学学报, 2021, 52(3): 293-300. DOI: 10.11665/j.issn.1000-5048.20210305
DAI Jiangdong, LI Huipeng, SUN Minjie. Effects of polyethylene glycol length on oral absorption of coumarin 6-loaded nanostructured lipid carrier[J]. Journal of China Pharmaceutical University, 2021, 52(3): 293-300. DOI: 10.11665/j.issn.1000-5048.20210305
Citation: DAI Jiangdong, LI Huipeng, SUN Minjie. Effects of polyethylene glycol length on oral absorption of coumarin 6-loaded nanostructured lipid carrier[J]. Journal of China Pharmaceutical University, 2021, 52(3): 293-300. DOI: 10.11665/j.issn.1000-5048.20210305

不同链长聚乙二醇修饰的香豆素6脂质纳米粒对口服吸收的影响

基金项目: 国家自然科学基金资助项目(No.81872817);中国药科大学“双一流”大学建设资助项目(No.CPU2018GY07)

Effects of polyethylene glycol length on oral absorption of coumarin 6-loaded nanostructured lipid carrier

Funds: This study was supported by the National Natural Science Foundation of China (No.81872817) and the "Double First-Class" University Project of China Pharmaceutical University (No. CPU2018GY07)
  • 摘要: 通过制备不同链长聚乙二醇(PEG)修饰的纳米脂质载体(NLCs)考察PEG链长对其口服吸收的影响。使用聚乙二醇(100)单硬脂酸酯(S100)、聚乙二醇(55)单硬脂酸酯(S55)、聚乙二醇(40)单硬脂酸酯(S40)3种不同链长的PEG通过薄膜分散法制备NLCs,以香豆素6 (coumarin 6)作为荧光探针,对修饰不同链长PEG的NLCs进行理化性质表征。考察了不同链长PEG修饰的NLCs在模拟缓冲液中的稳定性以及体外释药行为。同时对NLCs的细胞毒性、细胞摄取动力学以及摄取机制进行了考察。结果表明,随着PEG链段长度的增加,其水化层厚度不断增大。与其他NLCs相比,S100修饰的NLCs(pNLC-EG100)具有更好的细胞摄取效率,证明S100的链段长度是用于口服NLCs给药的最佳长度。
    Abstract: Polyethylene glycol (PEG) of different lengths were prepared to investigate their effects on oral absorption of nanostructured lipid carrier (NLCs).Three kinds of PEG-modified NLCs with different chain lengths, including polyethylene glycol (100) monostearate (S100), polyethylene glycol (55) monostearate (S55), polyethylene glycol (40) monostearate (S40), were prepared by film dispersion method.Coumarin 6 was chosen as a fluorescent probe to characterize the physicochemical properties of NLCs with different lengths.Meanwhile, the stability of NLCs in simulate buffer, the release behavior, cytotoxicity of NLCs, the uptake kinetics and cellular uptake mechanisms were evaluated. This work demonstrated that the thickness of the hydrated layer increased with the increase of PEG length. Of note, S100-modified NLCs (pNLC-EG100) exhibited higher cellular uptake efficiency compared with other formulations. Thus, S100 was optimized as the best molecular weight for PEG-modified NLCs on oral drug delivery system.
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出版历程
  • 收稿日期:  2020-07-14
  • 修回日期:  2021-05-25
  • 刊出日期:  2021-06-24

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