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Development and Evaluation of Artemether Taste Masked Rapid Disintegrating Tablets with Improved Dissolution Using Solid Dispersion Technique

机译:固体分散技术改进溶出度的蒿甲醚味掩蔽快速崩解片的研制与评价

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摘要

The purpose of this research was to mask the intensely bitter taste of artemether (ARM) and to formulate a rapid-disintegrating tablet (RDT) of the taste-masked drug. Taste masking was done by solid dispersion with mono amino glycyrrhyzinate pentahydrate (GLY) by solvent evaporation method. To characterize and formulate taste masked rapid disintegrating tablets (RDTs) of ARM, the 1:1M solid dispersion was selected based on bitterness score. Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), and X-ray powder diffraction (XRPD) were performed to identify the physicochemical interaction between drug and carrier, hence its effect on dissolution. RDTs were evaluated for weight variation, disintegration time, hardness and friability. In vitro drug release studies were performed for RDTs at pH 1.2 and 6.8. Bitterness score was evaluated using mini-column method and compared with gustatory sensation test. FTIR spectroscopy and DSC showed no interaction while XRPD showed amorphization of ARM in GLY solid dispersion. RDTs prepared using solid dispersion, (RDT3), showed faster disintegration (within 28 s) and complete bitter taste masking of ARM. In addition, RDT3 exhibited better dissolution profile at both pH 1.2 and 6.8, than RDTs prepared from pure ARM (RDT5). Taste evaluation of RDTs in human volunteers rated tasteless with a score of 0 to RDT3 and 3 to RDT5. Mini-column revealed that RDT5 showed increase in number of persons who sensed bitterness with increased amount of ARM release while RDT3 sensed no bitterness. Thus, results conclusively demonstrated successful masking of taste and rapid disintegration of the formulated tablets in the oral cavity with improved dissolution.
机译:这项研究的目的是掩盖蒿甲醚(ARM)的强烈苦味,并配制掩味药物的快速崩解片(RDT)。通过溶剂蒸发法与单氨基甘草次酸五水合物(GLY)进行固体分散,掩盖味道。为了表征和配制ARM的掩味速崩片(RDT),基于苦味评分选择1:1M固体分散体。进行了傅里叶变换红外光谱(FTIR),差示扫描量热法(DSC)和X射线粉末衍射(XRPD),以鉴定药物与载体之间的物理化学相互作用,从而了解其对溶出度的影响。对RDT的重量变化,崩解时间,硬度和脆性进行了评估。在pH值为1.2和6.8的条件下对RDT进行了体外药物释放研究。使用小柱法评估苦味评分,并与味觉感觉测试进行比较。 FTIR光谱和DSC显示没有相互作用,而XRPD显示GLY固体分散体中ARM的非晶化。使用固体分散体(RDT3)制备的RDT显示出更快的崩解速度(在28秒内),并且完全掩盖了ARM的苦味。此外,与纯ARM(RDT5)制备的RDT相比,RDT3在pH值为1.2和6.8时均表现出更好的溶出度。在无味的人类志愿者中对RDT的味道评估,对RDT3的评分为0,对RDT5的评分为3。迷你专栏显示,随着ARM释放量的增加,RDT5表示感到苦味的人数增加,而RDT3没有感觉到苦味。因此,结果最终证明成功掩盖了味道,并且使配制的片剂在口腔中快速崩解并改善了溶出度。

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