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首页> 外文期刊>Journal of applied science & environmental management: JASEM >An investigation of the direct compression properties of pre-gelatinized African bitter yam and cassava starches in acetylsalicylic acid tablet formulations
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An investigation of the direct compression properties of pre-gelatinized African bitter yam and cassava starches in acetylsalicylic acid tablet formulations

机译:乙酰水杨酸片剂中预糊化的非洲苦山药和木薯淀粉的直接压缩特性研究

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The direct compression ability of pre-gelatinized African bitter yam and cassava starches in acetylsalicylic acid tablet formulation was investigated. Starches from the African bitter yam and cassava tubers were extracted following standard procedures. The starch powders were subjected to some physicochemical evaluations and pre-gelatinized. Batches of acetylsalicylic acid granules and tablets were formulated with the native and pregelatinized forms of both the test and maize starches and microcrystalline cellulose at 5.0 and 10 %w/w by direct compression. Granules were evaluated for their flow properties and drug-excipient compatibility using DSC and FTIR while the tablets were investigated for their tablet parameters. The extracted starches were off-white to white in colour, insoluble in water, smooth in texture with particle sizes ranging from 5.0-10 μm that are oval to elliptical in shapes. The powders showed a swelling capacity ≤ 2.15, hydration capacity ≥ 1.20 and a moisture content ≤ 14.3 %. The granules exhibited good to fair flowability. Only tablets formulated with 10 %w/w of the pre-gelatinized starches and MCC met compendial requirements in their crushing strengths and friability. All the tablets disintegrated within 15 min with the pre-gelatinized cassava starches giving the shortest times of < 1.0 min. The 10 %w/w pre-gelatinized starches tablets compared favourably with MCC in their drug release profiles. Compatibility studies revealed no interaction between drug and excipients. The study show that the pre-gelatinized test starches compared favourably with MCC, a known direct compression excipient in their direct compression ability and drug release profiles especially at a concentration of 10 %w/w.
机译:研究了预糊化的非洲苦山药和木薯淀粉在乙酰水杨酸片剂中的直接压缩能力。按照标准程序从非洲苦瓜和木薯块茎中提取淀粉。对淀粉粉末进行一些理化评估并预糊化。通过直接压片,分别以5.0%和10%w / w的天然淀粉和预糊化形式的测试淀粉和玉米淀粉以及微晶纤维素配制批次的乙酰水杨酸颗粒和片剂。使用DSC和FTIR评估颗粒的流动性质和药物-赋形剂相容性,同时研究片剂的片剂参数。提取的淀粉为灰白色至白色,不溶于水,质地光滑,粒径为5.0-10μm,呈椭圆形至椭圆形。粉末的溶胀能力≤2.15,水合能力≥1.20,水分≤14.3%。颗粒表现出良好至中等的流动性。仅含10%w / w的预糊化淀粉和MCC的片剂的抗碎强度和易碎性符合药典要求。所有片剂均在15分钟内崩解,而预糊化的木薯淀粉的最短时间少于1.0分钟。 10%w / w的预糊化淀粉片在药物释放方面优于MCC。相容性研究表明,药物和赋形剂之间没有相互作用。研究表明,预糊化的测试淀粉与MCC相比具有优势,MCC的直接压缩能力和药物释放曲线尤其是浓度为10%w / w时是已知的直接压缩赋形剂。

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