环糊精功能化多壁碳纳米管对芒柄花素的装载及其细胞毒性研究
利用羟丙基-β-环糊精(HP-β-CD)修饰羧基化多壁碳纳米管(CD-MWCNTs),通过红外光谱证明了CDMWCNTs的成功合成,并经溶液共混法将CD-MWCNTs装载芒柄花素(FMN)。选用激光粒径仪,X射线衍射、扫描电镜对载药CD-MWCNTs(CD-MWCNTs-FMN)进行表征,并考察其释药特性。采用水溶性四唑盐试剂(WST-1)测定CD-MWCNTs-FMN的抗肿瘤活性。研究结果表明CD-MWCNTs对FMN的包封率为(50.60±1.92)%,载药率为(7.20±0.98)%。FMN在CD-MWCNTs的释放行为具有pH值依赖。细胞毒性结果表明载药CD-MWCNTs的抗肿瘤活性强...
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Published in | 功能材料 Vol. 49; no. 1; pp. 1071 - 1077 |
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Main Author | |
Format | Journal Article |
Language | Chinese |
Published |
广东药科大学 药学院,广州,510006
30.01.2018
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Subjects | |
Online Access | Get full text |
ISSN | 1001-9731 |
DOI | 10.3969/j.issn.1001-9731.2018.01.014 |
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Summary: | 利用羟丙基-β-环糊精(HP-β-CD)修饰羧基化多壁碳纳米管(CD-MWCNTs),通过红外光谱证明了CDMWCNTs的成功合成,并经溶液共混法将CD-MWCNTs装载芒柄花素(FMN)。选用激光粒径仪,X射线衍射、扫描电镜对载药CD-MWCNTs(CD-MWCNTs-FMN)进行表征,并考察其释药特性。采用水溶性四唑盐试剂(WST-1)测定CD-MWCNTs-FMN的抗肿瘤活性。研究结果表明CD-MWCNTs对FMN的包封率为(50.60±1.92)%,载药率为(7.20±0.98)%。FMN在CD-MWCNTs的释放行为具有pH值依赖。细胞毒性结果表明载药CD-MWCNTs的抗肿瘤活性强于游离药物。这说明环糊精修饰的多壁碳纳米管是一种良好的缓释性载药系统,并且能提高芒柄花素的抗肿瘤活性。 |
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Bibliography: | The carboxylic multiwalled carbon nanotubes were modified by hydroxypropyl-β-cyclodextrin to prepare CD-MWCNTs.According to the result of Fourier-transform infrared spectrometry(FT-IR),HP-β-CD has been grafted to MWCNTs-COOH successfully.Then CD-MWCNTs were non-covalently conjugated with FMN,and laser particle size analyzer,X-ray diffractometry(XRD)and scanning electron microscopy(SEM)were used to characterize the compounds.The drug release characteristics were investigated.The anticancer activity of CD-MWCNTs-FMN was determined using a water-soluble tetrazolium salt reagent(WST-1).The results demonstrated that the encapsulation efficiency of CD-MWCNTs for FMN was(50.60±1.92)% and the drug loading capacity was(7.20±0.98)%.In vitro release studies showed that the drug release rate under an acidic condition(pH 5.5)was lower than that under physiological condition(pH 7.4),which indicated a pH dependence.The cytotoxicity assay showed that the anti-cancer activity of CD-MWCNTs-FMN was stronger than that of free dr |
ISSN: | 1001-9731 |
DOI: | 10.3969/j.issn.1001-9731.2018.01.014 |