生物利用度差的药物口服隐形脂质体的设计与研制

G. Manisha, G. Sharma, Shraddha Shekar, T. Rao
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摘要

本研究的目的是研制含有姜黄素的隐形脂粒,该脂粒由胆固醇、二硬脂酰磷脂酰胆碱、氢化磷脂酰胆碱组合而成,用于治疗类风湿性关节炎。姜黄,尤其是它最活跃的化合物姜黄素有许多科学证明的健康益处。它是一种有效的抗炎药,有助于改善风湿性关节炎的症状。通过薄膜水化法,以不同比例的胆固醇、二硬脂酰磷脂酰胆碱、氢化硫磷脂酰胆碱开发了总共8种配方,并对包封效率、SEM、粒径和形状、FTIR研究、体外溶出研究进行了评估。体外实验表明,随着胆固醇比的增加,药物释放率增加到一定比例。其中F7制剂24 h释药效果最佳,释药量为92.62%,其他制剂释药量均不超过F7。因此选择F7为优化配方。
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Design and development of stealth liposomes for oral administration of poorly bioavailable drug
The aim of the present study was to formulate Stealth Liposomes containing Curcumin which are formulated by combinations of Cholesterol, Distearoylphosphatidylcholine, hydrogenated soyphosphotidylcholine to treat rheumatoid arthritis. Turmeric and especially its most active compound curcumin have many scientifically-proven health benefits. It's a potent anti-inflammatory and help improve symptoms of Rheumatoid arthritis. Total 8 formulations were developed using Cholesterol, Distearoylphosphatidylcholine, hydrogenated soyphosphotidylcholine in various ratios by thin film hydration method & evaluated for Entrapment Efficiency, SEM, particle size and shape, FTIR studies, invitro dissolution studies. From the invitro studies we can say that as the cholesterol ratio increases, drug release rate is increased upto particular ratio. Among all the fomulations, F7 formulation shows best drug release of 92.62% by the end of 24 hours whereas all the other formulations did not release the drug more than F7. So F7 formulation was choosen as optimized formulation.
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