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作 者:孙辉[1] 高萌[2] 蒋妮 鲍旭[2] 李磊[2] 李镇[2] 田燕[2]
机构地区:[1]解放军210医院药剂科,辽宁大连116001 [2]大连医科大学药学院,辽宁大连116044 [3]大连儿童医院药剂科,辽宁大连116001
出 处:《大连医科大学学报》2013年第5期438-441,共4页Journal of Dalian Medical University
摘 要:目的制备姜黄素乳酸羟基乙酸共聚物-水溶性维生素E纳米粒(CM-PLGA-TPGS-NPs,简称CPTN)并评价其质量。方法用自制的PLGA-TPGS为载体材料,采用超声乳化-溶剂挥发法制备CPTN,通过粒径、Zeta电位、载药量、包封率和体外释放度控制其质量。采用RP-HPLC法,色谱柱为KROMASIL柱(4.6 mm×250 mm,5μm),用乙腈-2%冰醋酸溶液(58∶42)为流动相,检测波长为430 nm。结果自制CPTN的平均粒径为(197.9±6.2)nm,Zeta电位为(-22.3±1.8)mV,载药量为(13.2±0.9)%和包封率为(79.3±1.6)%。体外姜黄素在含0.5%十二烷基硫酸钠的磷酸盐缓冲液(pH7.4)中呈两相释放,30 d时累积释放率为91.3%。结论 CPTN质量稳定可控,体外试验显示具有明显的缓释作用。Objective To prepare Curcumin - loaded polylactic - co - glycolic acid - D - α - tocopherol polyethylene glycol 1000 succinate nanoparticles (CM -PLGA- TPGS- NPs, namely CPTN) and evaluate their quality. Methods CPTN were prepared by ultrasonication emulsion/solvent evaporation technique using PLGA -TPGS made by ourselves, its mean size, Zeta potential, drug - loading, encapsulation efficiency and in vitro release rate of CPTN were determined. The condi- tion was checked by RP - HPLC on KROM ASIL C18 column (4.6 mm ×250 mm, 5 μm) with acetonitrile and 2% acetic acid (58: 42) as mobile phase, and the detective wavelength was 430 nm. Results CPTN was sphere -like with mean particle size of (197.9± 6.2) nm, Zeta potential of ( -22.3 ± 1.8) mV, drugloading of (13.2±0.9) % and encapsula- tion efficiency of (79.3± 1.6) %. The in vitro drug release profile in phosphate buffer solution of pH 7.4 containing 0.5% w/v Sodium dodecyl sulfate showed diphasic release pattern, the cumulative release rate was 91.3% at 30 d. Conclusion CPTN is stable and controllable in quality, in vitro release rate shows obvious sustained release.
关 键 词:姜黄素 乳酸羟基乙酸共聚物-水溶性维生素E 纳米粒 RP-HPLC法 体外释放度
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