利用固体分散技术提高兰索拉唑的溶解度

Rohit S. Bhamare, Rajendra K. Surawase, Jayshree S. Bhadane
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引用次数: 0

摘要

现有研究的重点是利用固体分散技术提高兰索拉唑的溶解度。兰索拉唑是质子泵抑制剂(PPI)。兰索拉唑用于治疗胃溃疡。兰索拉唑是生物制药分类系统中的第二类药物。通过使用新型固体分散方法来提高水溶性差的药物的口服溶解度。兰索拉唑具有低溶解度和高渗透性的特点。因此,为了提高兰索拉唑的溶解度,我们用 PVP K30、聚乙二醇 6000(PEG 6000)和 Poloxamer 407 制备了兰索拉唑固体分散体(SD)。兰索拉唑溶片是用各种超崩解剂(如克罗波维酮和淀粉乙醇酸钠)通过直接压片法配制而成的。对所制备的片剂进行了各种参数的评估,如重量变化、硬度、易碎性、崩解时间、药物含量均匀性和体外溶解度。固体分散体 SD6 的体外药物释放研究表明,药物释放率高达 98.93%。总之,在所有配方中,F12(含有 6%、3.75% 和 10%的氯磺丙酮)、SSG 和 MCC 的药物释放率最高,达到 98.93%。
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Solubility Enhancement of Lansoprazole by using Solid Dispersion Technique
In the existing study focused on the solubility enhancement of lansoprazole by using solid dispersion technique. Lansoprazole is proton pump inhibitor (PPI). Lansoprazole is used for the treatment of gastric ulcer. Lansoprazole is the Class II Drug of Biopharmaceutical Classification system. By using novel solid dispersion methods to enhance the oral solubility of poor water-soluble drug. Lansoprazole has the low solubility and high permeability. Hence to enhance the solubility of lansoprazole we prepared the Lansoprazole solid dispersion (SD) with PVP K30, Poly Ethylene Glycol 6000 (PEG 6000) and Poloxamer 407. Lansoprazoledissolving tablet were formulated using various superdisintegrants like Crospovidone and Sodium Starch Glycolate by Direct compression. The prepared the tablet is evaluated at various parameters like weight variation, hardness, friability, disintegration time, drug content uniformity and In-vitro dissolution. The In-vitro Drug release study of solid dispersions SD6 show the high drug release around 98.93%. Overall, in the all formulations F12 which contains 6%, 3.75% and 10% of Crospovidone, SSG and MCC release the 98.93% drug is the best formulation.
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