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基于β-环糊精-生物素共轭物的鬼臼毒素复合物的制备、表征及生物学评价

Preparation, characterization and biological evaluation of β-cyclodextrin-biotin conjugate based podophyllotoxin complex.

作者信息

Zhao Xiu, Qiu Neng, Ma Yingyu, Liu Junda, An Lianying, Zhang Teng, Li Ziqin, Han Xu, Chen Lijuan

机构信息

Department of Chemical & Pharmaceutical Engineering, College of Materials and Chemistry and Chemical Engineering, Chengdu University of Technology, Chengdu 610059, China.

Department of Chemical & Pharmaceutical Engineering, College of Materials and Chemistry and Chemical Engineering, Chengdu University of Technology, Chengdu 610059, China.

出版信息

Eur J Pharm Sci. 2021 May 1;160:105745. doi: 10.1016/j.ejps.2021.105745. Epub 2021 Feb 5.

Abstract

Podophyllotoxin is a natural occurring aryltetralin lignin with pronounced cytotoxic activity. However, its clinical application for cancer treatment has been blocked due to its poor water solubility and selectivity. In this work, biotin as a tumor specific ligand was coupled with β-cyclodextrin and the resulting biotin modified β-cyclodextrin was used to complex with podophyllotoxin to improve its aqueous solubility and tumor selectivity. The solubility of β-cyclodextrin was greatly enhanced(>16 times) by conjugating with biotin. podophyllotoxin/ mono-6-biotin-amino-6-deoxy-β-cyclodextrin inclusion complex was prepared by freeze-drying method and the complex behavior between mono-6-biotin-amino-6-deoxy-β-cyclodextrin and podophyllotoxin was studied by water solubility, phase solubility, Job's plot, UV spectroscopy, Proton Nuclear Magnetic Resonance, Rotating-frame Overhauser Effect Spectroscopy, Powder X-ray diffraction and Scanning electron microscopy. The solubility of podophyllotoxin/ mono-6-biotin-amino-6-deoxy-β-cyclodextrin complex was greatly improved(9 times) compared with Podophyllotoxin. The stability constant of podophyllotoxin/ mono-6-biotin-amino-6-deoxy-β-cyclodextrin complex (K= 415.29 M) was 3.2 times that of podophyllotoxin/β-cyclodextrin complex. The possible inclusion mode of podophyllotoxin/mono-6-biotin-amino-6-deoxy-β-cyclodextrin complex was inferred from the Proton Nuclear Magnetic Resonance and Rotating-frame Overhauser Effect Spectroscopy. The cellular uptake study showed that the introduction of biotin increased the cellular uptake of rhodamine-B/mono-6-biotin-amino-6-deoxy-β-cyclodextrin complex. Moreover, cell cytotoxicity study showed that the antitumor activity of podophyllotoxin/ mono-6-biotin-amino-6-deoxy-β-cyclodextrin complex was more potent than podophyllotoxin/β-cyclodextrin complex and free podophyllotoxin. The superior water solubility and enhanced cytotoxicity suggested that the mono-6-biotin-amino-6-deoxy-β-cyclodextrin associated inclusion complex might be a potential and promising delivery system for hydrophobic chemotherapeutics such as podophyllotoxin.

摘要

鬼臼毒素是一种天然存在的芳基四氢萘木脂素,具有显著的细胞毒性活性。然而,由于其水溶性差和选择性低,其在癌症治疗中的临床应用受到了阻碍。在这项工作中,将生物素作为肿瘤特异性配体与β-环糊精偶联,所得的生物素修饰的β-环糊精用于与鬼臼毒素络合,以提高其水溶性和肿瘤选择性。通过与生物素共轭,β-环糊精的溶解度大大提高(>16倍)。采用冷冻干燥法制备了鬼臼毒素/单-6-生物素-氨基-6-脱氧-β-环糊精包合物,并通过水溶性、相溶解度、Job曲线、紫外光谱、质子核磁共振、旋转框架Overhauser效应光谱、粉末X射线衍射和扫描电子显微镜研究了单-6-生物素-氨基-6-脱氧-β-环糊精与鬼臼毒素之间的络合行为。与鬼臼毒素相比,鬼臼毒素/单-6-生物素-氨基-6-脱氧-β-环糊精复合物的溶解度大大提高(9倍)。鬼臼毒素/单-6-生物素-氨基-6-脱氧-β-环糊精复合物的稳定常数(K = 415.29 M)是鬼臼毒素/β-环糊精复合物的3.2倍。通过质子核磁共振和旋转框架Overhauser效应光谱推断了鬼臼毒素/单-6-生物素-氨基-6-脱氧-β-环糊精复合物可能的包合模式。细胞摄取研究表明,生物素的引入增加了罗丹明-B/单-6-生物素-氨基-6-脱氧-β-环糊精复合物的细胞摄取。此外,细胞毒性研究表明,鬼臼毒素/单-6-生物素-氨基-6-脱氧-β-环糊精复合物的抗肿瘤活性比鬼臼毒素/β-环糊精复合物和游离鬼臼毒素更强。优异的水溶性和增强的细胞毒性表明,单-6-生物素-氨基-6-脱氧-β-环糊精相关包合物可能是一种潜在且有前景的疏水性化疗药物如鬼臼毒素的递送系统。

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