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引用本文:闻真,郭桂萍,谢鑫鑫,王俊腾,秦利芳,林东海.细胞膜红色荧光探针PLGA纳米粒的制备及表征[J].中国现代应用药学,21013,(3):280-284.
WEN Zhen,GUO Guiping,XIE Xinxin,WANG Junteng,QIN Lifang,LIN Donghai .Preparation and Characterization of DiI Loaded PLGA Nanoparticles[J].Chin J Mod Appl Pharm(中国现代应用药学),21013,(3):280-284.
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细胞膜红色荧光探针PLGA纳米粒的制备及表征
闻真, 郭桂萍, 谢鑫鑫, 王俊腾, 秦利芳, 林东海
烟台大学药学院,山东 烟台 264005
摘要:
目的 以聚乳酸-羟基乙酸共聚物(PLGA)和单甲氧基聚乙二醇聚乳酸-羟基乙酸共聚物(MePEG-PLGA)为材料,制备包载细胞膜红色荧光探针(DiI)的纳米粒,为后续的细胞实验奠定基础。方法 采用自乳化溶剂扩散法制备纳米粒;超滤法分离纯化纳米粒,紫外可见分光光度法测定DiI的含量,并计算包封率。结果 DiI用量为0.5 mg,PLGA或MePEG- PLGA投入量为50 mg,PVA浓度为0.5%,可制得粒径较合适的纳米粒。DiI-PLGA-NP平均粒径为(280.7±3.6)nm,Zeta电位为(-2.98±0.47)mV,包封率可达88.0%; DiI-MePEG-PLGA-NP平均粒径为(157.2±3.2)nm,Zeta电位为(-4.90±0.54)mV,包封率可达87.1%。结论 DiI作为脂溶性良好的示踪剂,用其制得的荧光素纳米粒可为后续的体外实验奠定良好的基础。
关键词:  细胞膜红色荧光探针  聚乳酸-羟基乙酸共聚物纳米粒  单甲氧基聚乙二醇聚乳酸-羟基乙酸共聚物纳米粒  自乳化溶剂扩散法  超滤法  紫外可见分光光度法
DOI:
分类号:
基金项目:国家自然科学基金资助项目(30973949);山东省自然科学基金资助项目(ZR2009CM012)
Preparation and Characterization of DiI Loaded PLGA Nanoparticles
WEN Zhen, GUO Guiping, XIE Xinxin, WANG Junteng, QIN Lifang, LIN Donghai
Department of Pharmacy, Yantai University, Yantai 264005, China
Abstract:
OBJECTIVE To prepare DiI loaded nanoparticles using PLGA and MePEG-PLGA as carriers. METHODS Spontaneous emulsion solvent diffusion method(SESD) was adopt to prepare nanoparticles. Ultrafiltration-UV-visible spectrophotometry was used for the determination of DiI-NP' encapsulation efficiency. RESULTS When DiI’s dosage was 0.5 mg, PLGA’s or MePEG-PLGA’s dosage was 50 mg, PVA’s content was 0.5%, the suitable nanoparticles were obtained. DiI-PLGA-NP’ average diameter was (280.7±3.6)nm, DiI-PLGA-NP’ Zeta potential was (-2.98±0.47)mV, DiI-PLGA-NP’ encapsulation efficiency was 88.0%; DiI-MePEG-PLGA-NP’ average diameter was (157.2±3.2)nm, DiI-MePEG-PLGA-NP’ Zeta potential was (-4.90±0.54)mV, DiI-MePEG-PLGA-NP’ encapsulation efficiency was 87.1%. CONCLUSION As a liposoluble long-term tracer, DiI-NP can lay the foundation for subsequent in vitro tests.
Key words:  fluorescent probe(DiI)  PLGA nanoparticles  MePEG-PLGA nanoparticles  spontaneous emulsion solvent diffusion method  ultrafiltration  UV-visible spectrophotometry
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