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Preparation of Microcrystalline Cellulose from Cotton and its Evaluation as Direct Compressible Excipient in the Formulation of Naproxen Tablets

机译:棉花微晶纤维素的制备及其在萘普生片中的直接压制赋形剂的评价

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Microcrystalline cellulose (MCC) was prepared by acid hydrolysis from the cellulose purified from the cotton. Chemical assay, determination of degree of polymerization (DP) and FT-IR confirm the identification of prepared microcrystalline cellulose. The FT-IR spectrum of synthesized MCC is very similar to that of Avicel? PH- 102, a commercial direct compression excipient, at consideration of both band position and intensity. The degree of polymerization (DP) of prepared MCC and Avicel PH102, determined from the value of intrinsic viscosity, were 210 and 240, respectively. The tableting properties of prepared MCC was excellent while formulating naproxen tablet. The hardness and friability of the tablets prepared from MCC was 5.33 ± 0.45 kg and 0.077%, respectively which were comparable to the tablets prepared from marketed Avicel PH102 having hardness and friability 7.35 ± 0.41 kg and 0.063%, respectively. The disintegration time of tablet prepared from MCC and Avicel PH102 was 8.25 ± 0.41 min and 4.50 ±0.28 min, respectively. Again, the tablets prepared from MCC and Avicel PH102 showed more than 90% and 98% dissolution, respectively as per the USP specified medium. All these data indicate that the hardness, friability, disintegration and dissolution properties of tablets prepared by using our MCC comply with the USP specifications. This makes the prepared MCC as a promising candidate for direct compressible excipient of tablet. DOI: http://dx.doi.org/10.3329/dujps.v13i2.21899 Dhaka Univ. J. Pharm. Sci. 13(2): 187-192, 2014 (December)
机译:微晶纤维素(MCC)是通过酸水解从棉制纤维素中制得的。化学测定,聚合度(DP)的测定和FT-IR证实了所制备微晶纤维素的鉴定。合成的MCC的FT-IR光谱与Avicel?的光谱非常相似。考虑到条带的位置和强度,PH-102是一种商用直接压缩赋形剂。由特性粘度的值确定的所制备的MCC和Avicel PH102的聚合度(DP)分别为210和240。配制萘普生片剂时,制得的MCC的压片性能优异。由MCC制备的片剂的硬度和脆性分别为5.33±0.45kg和0.077%,这与由市售的具有硬度和脆性的Avicel PH102制成的片剂相当,其硬度和脆性分别为7.35±0.41kg和0.063%。由MCC和Avicel PH102制备的片剂的崩解时间分别为8.25±0.41分钟和4.50±0.28分钟。同样,按照美国药典规定的介质,从MCC和Avicel PH102制备的片剂分别显示出超过90%和98%的溶出度。所有这些数据表明,使用我们的MCC制备的片剂的硬度,易碎性,崩解和溶解特性符合USP规范。这使得制备的MCC成为片剂的直接可压缩赋形剂的有前途的候选者。 DOI:http://dx.doi.org/10.3329/dujps.v13i2.21899达卡大学。 J.药物科学13(2):187-192,2014(12月)

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