Formulation and evaluation of Metoprolol succinate buccal tablets in hypertension treatment

Kishore Bandarapalle, Rajasekhar Kk, Teja Sri Kamasani, Sangeetha Mohanrao, Neeraja Boyalapalli, Likhitha Chejarla, Bhargavi Cy, Chaitanya Krishna
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引用次数: 0

Abstract

The research aims to formulate and evaluate the Metoprolol succinate buccal tablets in hypertension treatment. The Fourier transform infrared (FTIR) results depict no incompatibility between the drug and excipients. The study results of pre-compression parameters have excellent flow qualities and compressibility. The post-compression parameters show that the results are within the specified standard deviations. The swelling index reveals that the formulation F6 shows that the complete drug was released and the tablet integrity was maintained during the expected duration. Formulation F6 chitosan and Carbopol 934 were used in a ratio of 1:1, resulting in the release of the drug up to the 10th hour and completely. Therefore, formulation F6 was optimized and compared with the marketed product. Formulation F6 exhibited better drug release performance than the marketed product.
琥珀酸美托洛尔口腔片在高血压治疗中的配制和评估
该研究旨在配制和评估用于治疗高血压的琥珀酸美托洛尔口含片。傅立叶变换红外光谱(FTIR)结果表明,药物与辅料之间没有不相容性。压缩前参数的研究结果表明,片剂具有良好的流动性和可压缩性。压缩后参数显示结果在规定的标准偏差范围内。膨胀指数显示,配方 F6 在预期的时间内释放了全部药物并保持了片剂的完整性。配方 F6 中壳聚糖和 Carbopol 934 的使用比例为 1:1,结果表明药物在第 10 小时内完全释放。因此,对配方 F6 进行了优化,并与市售产品进行了比较。配方 F6 的药物释放性能优于市售产品。
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