以刺槐豆胶为天然超崩解剂的速溶片的配方与评价及与市售制剂的比较

Namrata S. Mane, Namrata A Muddalwar, Priya V. Nikam, N. Dighade
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引用次数: 1

摘要

目的是制定和评价双氯芬酸钠速溶片,以提高药物的生物利用度和患者的依从性。以槐豆胶为强力崩解剂,浓度分别为2%、3%、4%、5%、6%,采用直接压缩法制备双氯芬酸钠速溶片。采用天然强力崩解剂刺槐豆胶(LBG)配制片剂。该制剂混合物,即药物和LBG与其他辅料混合,片剂通过直接压缩进行压缩。采用红外光谱(FTIR)、压缩前后参数对制剂进行表征。在pH为6.8的磷酸盐缓冲液中进行体外药物释放研究。用红外光谱对制剂进行表征,红外光谱研究结果表明,超崩解剂与纯药物无相互作用,红外光谱研究结果表明,制剂中药物稳定。用测定法测定药物含量。对5种配方(F1-F5)进行了预压缩和后压缩参数评价,结果均在标准范围内。配制剂型可以是常规剂型的有效替代剂型,可以有效地用于治疗炎症,特别是在急性疼痛的情况下。
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FORMULATION AND EVALUATION OF FAST DISSOLVING TABLET USING LOCUST BEAN GUM AS A NATURAL SUPERDISINTEGRANT AND COMPARISON WITH THE MARKETED PREPARATION
The aim was to formulate and evaluate fast dissolving tablets of diclofenac sodium to improve the bioavailability of the drug and patient compliance. Fast dissolving tablets of diclofenac sodium were prepared by direct compression method by using superdisintegrants (locust bean gum) in 2%, 3%, 4% 5% & 6% concentration respectively. Tablets were formulated by using natural superdisintegrants locust bean gum (LBG). This formulated mixture i.e., drug and LBG was mixed with other excipients and the tablets were compressed by direct compression. Formulated tablets were characterized by FTIR, pre-compression and post-compression parameters. The In vitro drug release studies were performed in pH 6.8 phosphate buffer. Formulated tablets were characterized by FTIR, the results of IR study showed that there was no interaction between superdisintegrant and pure drug, the results of FTIR study showed that drug was stable in the final formulated tablet. The drug content was evaluated with the help of assay. Five (F1-F5) formulations were evaluated for pre-compression and post-compression parameters and all the results were in the standard limits. Formulated dosage form may be an effective alternative to conventional dosage form which can be effectively used in the treatment of inflammation specially in cases of acute pain.
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