Kawano Yayoi, Ito Akihiko, Sasatsu Masanaho, Machida Yoshiharu
Department of Drug Delivery Research, Hoshi University, Tokyo, Japan.
Yakugaku Zasshi. 2010 Jan;130(1):81-6. doi: 10.1248/yakushi.130.81.
We investigated several methods of taste masking in the preparation of orally disintegrating tablets (ODTs), using furosemide (FU) as a model drug. Four types of FU preparations were prepared: granules with maltitol (MA), granules with yogurt powder (YO), a physical mixture of FU and MA, and a physical mixture of FU and YO. All taste-masking granules were prepared using the dry granulation method. The taste of each type of preparation was evaluated. All four preparations markedly improved the taste of the FU tablets, but the mixing ratios of the correctives did not affect the masking effect. No difference in masking effect was found between MA and YO in the physical mixtures, but the masking effect in the granules with YO was superior to that of the granules with MA. Taste-masked FU tablets were prepared using the direct compression method; crystalline cellulose (Avicel PH-302) and mannitol were added as excipients at the mixing ratio of 1/1. All four types of tablets displayed sufficient hardness, but MA-containing tablets were harder than YO-containing tablets. The hardness of the tablets prepared from YO granules increased as the YO content increased. The most rapidly disintegrating tablets were those of YO granules prepared at a mixing ratio of FU/YO=1/1, which disintegrated within 20 s, followed by the tablets of MA granules prepared at a mixing ratio of FU/MA=1/1. The disintegration times of the tablets made from physical mixtures, in contrast, were longer than 200 s. Disintegration time lengthened as the mixing ratio of YO or MA increased. The hardness and disintegration time of these tablets could be controlled by varying the compression pressure. We found that YO is more useful than MA in masking unpleasant tastes and confirmed that orally disintegrating tablets with taste-masking function can be prepared using granules of YO prepared using the dry granulation method as a new corrective.
我们以呋塞米(FU)为模型药物,研究了口腔崩解片(ODT)制备过程中的几种掩味方法。制备了四种类型的FU制剂:含麦芽糖醇(MA)的颗粒剂、含酸奶粉(YO)的颗粒剂、FU与MA的物理混合物以及FU与YO的物理混合物。所有掩味颗粒均采用干法制粒法制备。对每种制剂的味道进行了评估。所有四种制剂均显著改善了FU片剂的味道,但矫味剂的混合比例不影响掩味效果。物理混合物中MA和YO的掩味效果无差异,但含YO颗粒剂的掩味效果优于含MA颗粒剂。采用直接压片法制备了掩味FU片剂;以1/1的混合比例加入微晶纤维素(Avicel PH - 302)和甘露醇作为辅料。所有四种类型的片剂均表现出足够的硬度,但含MA的片剂比含YO的片剂更硬。由YO颗粒制备的片剂硬度随着YO含量的增加而增加。崩解最快的片剂是FU/YO = 1/1混合比例制备的YO颗粒片剂,在20秒内崩解,其次是FU/MA = 1/1混合比例制备的MA颗粒片剂。相比之下,由物理混合物制成的片剂崩解时间超过200秒。崩解时间随着YO或MA混合比例的增加而延长。这些片剂的硬度和崩解时间可通过改变压片压力来控制。我们发现YO在掩蔽不良味道方面比MA更有用,并证实可以使用干法制粒法制备的YO颗粒作为新型矫味剂来制备具有掩味功能的口腔崩解片。