Design and Development of Solid Self Emulsifying Osmotic Delivery System of Nifedipine

被引:0
作者
Bagul, Nilesh [1 ]
Patel, Vineet [2 ]
Shahiwala, Aliasgar [1 ]
Misra, Manju [1 ]
机构
[1] NIPER, Dept Pharmaceut, BV Patel PERD Ctr,SG Highway, Ahmadabad 380054, Gujarat, India
[2] BV Patel PERD Ctr, Dept Pharmaceut, Ahmadabad 380054, Gujarat, India
关键词
Gelucire; Nifedipine; Osmotic tablet; self emulsifying drug delivery system; zero order release;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objectives: In order to enhance solubility and to obtain controlled release characteristics, preparation of nifedipine has been made into a osmotic pump tablet which includes Gelucire 44/14, Lutrol F127, Transcutol P, silicon dioxide, lactose, mannitol, citric acid, and sodium bicarbonate. Material and methods: The developed dosage form was evaluated for particle size, solid state properties and release profile. Effect of orifice size and amount of plasticizers on drug release was also studied. Results: The results revealed that Self-emulsifying osmotic pump tablet (SEOPT) has not only provided improvement in solubility of nifedipine by self-emulsifying effect (SEDDS) but also controlled release due to elementary osmotic pump system. The particle size analysis revealed no difference in the droplet size of liquid SEDDS & reconstituted SEDDS. Conclusion: Release studies revealed that nifedipine followed zero order release profile for 12 h independent of agitational intensity with cumulative release of 83.85%. The in vitro release profiles of the optimized system & commercialized conventional tablet (Nicardia r Retard 20) in different amount of sodium lauryl sulphate (SLS) were also compared.
引用
收藏
页码:128 / 135
页数:8
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