高血压用硝苯地平脉动微球的研制与表征。

Q3 Pharmacology, Toxicology and Pharmaceutics Recent Patents on Drug Delivery and Formulation Pub Date : 2017-03-31 DOI:10.2174/1872211311666170213104321
R. Taneja, G. Gupta
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引用次数: 3

摘要

背景:开发聚合物Carbopol 971P和Eudragit RS100的Nifedipine混合物的脉动微球,用于降压,以在特定的滞后时间释放药物。方法采用Carbopol 971P和Eudragit RS100在不同比例的混合溶剂中制备硝苯地平缓释微球。根据粒径、产率和药物包封率制备并优化了制剂。通过光学显微镜、扫描电子显微镜(SEM)、体外溶出度研究和动力学模型,以每分钟不同的分辨率(rpm)进一步分析优化的制剂。将最有前景的配方与市场上的产品进行了比较。近年来,用于高血压药物的微球的专利为连心碱(CN104757561)。多巴胺拮抗剂(US20030069232A1)、人血清白蛋白(EP19990304616)和奥美拉唑(IN2107/DEL/2014)有助于选择药物和聚合物。结果配制的微球的平均粒径范围为177.31至277.48µm。配方F83最初显示药物缓慢释放4小时,6小时后药物在特定的滞后时间急剧释放增强(显示脉冲释放)。然而,常规上市产品最初在1小时显示最大释放,并逐渐减少,而对照上市产品显示持续模式。结论在数据的基础上,配方F83表现出缓慢的释放和特定的滞后时间,随后是脉动释放模式,并遵循一级动力学模型。结论:复方硝苯地平脉冲剂型可用于治疗高血压。
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Development and Characterization Pulsatile Microspheres of Nifedipine for Hypertension.
BACKGROUND To develop pulsatile microspheres of Nifedipine blend of polymers Carbopol 971P and Eudragit RS100 for antihypertensive to release the drug at a particular lag time. METHODS Pulsatile nifedipine microspheres were prepared using the blend of Carbopol 971P and Eudragit RS100 at different ratios in a mixture of solvents. Formulations were prepared and optimized on the basis of particle size, percentage yield and drug entrapment efficiency. Optimized formulations were further analyzed at different resolutions per minute (rpm) by optical microscopy, scanning electron microscopy (SEM), in-vitro dissolution studies and kinetics model. The most promising formulation was compared with the marketed products. The recent patents on microsphere used for hypertension for drug used Liensinine (CN104757561). Dopamine antagonist (US20030069232A1), Human Serum Albumin (EP19990304616) and Omeprazole (IN2107/DEL/2014) helped in selecting the drug and polymers. RESULTS The formulated microspheres had mean particle size ranging from 177.31 to 277.48 µm. Formulation F83 showed slow release of drug initially for 4 h and drastically release of drug enhanced at a particular lag time (Showed pulsatile release) after 6 h. However, conventional marketed products showed maximum release initially at 1 h and decreased gradually while controlled released marketed product showed sustained pattern. CONCLUSION On the basis of data formulation F83 showed slow release and at a particular lag time followed by pulsatile release pattern and followed first order kinetics model. It was concluded that the formulated nifedipine pulsatile dosage form could be useful in the treatment of hypertension.
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来源期刊
Recent Patents on Drug Delivery and Formulation
Recent Patents on Drug Delivery and Formulation Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
2.30
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期刊介绍: Recent Patents on Drug Delivery & Formulation publishes review and research articles, drug clinical trial studies and guest edited thematic issues on recent patents on drug delivery and formulation. A selection of important and recent patents on drug delivery and formulation is also included in the journal. The journal is essential reading for all researchers involved in the fields of drug delivery and formulation. The journal also covers recent research (where patents have been registered) in fast emerging therapeutic areas/targets & therapeutic agents related to drug delivery and formulations.
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