Cross-linked nanoparticles of cytarabine: encapsulation, storage and in-vitro release

被引:0
|
作者
Joseph, Nisha Mary [1 ]
Sharma, Pramod Kumar [2 ]
机构
[1] Mekelle Univ, Sch Pharm, Mekelle, Ethiopia
[2] Bundelkhand Univ, Inst Pharm, Jhansi, Uttar Pradesh, India
来源
关键词
Cytarabine; nanoparticles; in-vitro release; sodium tripolyphosphate;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This work presents results of the preparation and characterization of nanoparticles for entrapping cytarabine, a chemotherapeutic agent. The particle size analysis indicated a uniform particle size. The study of the release of drug from nanoparticles exhibited a prolonged release profile as studied over a period of 16 hours. The drug release was constant from the 10(th) to the 16(th) hours, which showed that the formulation was successful for long-term treatment. The drug entrapment efficiency of the nanoparticles having the same ratio of polymer and drug was about 90.2%. The physical stability of the nanoparticles was good as studied over a period of 4 weeks. These results are promising for producing nanoparticles by entrapping cytarabine, which can be useful for cancer therapy.
引用
收藏
页码:10 / 13
页数:4
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