首页> 外文期刊>Journal of Drug Delivery and Therapeutics >Formulation and Evaluation of Glucosamine Sulphate Potassuim Chloride 1500 Mg and Methyl Sulphonyl Methene 200 Mg Film Coated Tablet
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Formulation and Evaluation of Glucosamine Sulphate Potassuim Chloride 1500 Mg and Methyl Sulphonyl Methene 200 Mg Film Coated Tablet

机译:氨基葡萄糖硫酸盐氯化钾1500 Mg和甲基磺酰甲烷200 Mg薄膜衣片的研制与评价

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Methyl Sulphonyl methane (MSM) is an organ sulfur compound with the formula (CHsub3/sub)sub2/subSOsub2/sub. Glucosamine is naturally hygroscopic is nature when exposed to air and moisture and degradable whether in the form of tablet or raw material. To overcome this problem Glucosamine needs to bond with suitable stabilizer. Glucosamine Sulphate in the form of Salt i.e. Sodium chloride and potassium chloride are stable. The normal dose of Glucosamine is 500-1500 mg TID. It is very difficult to compress the tablet at the label claim 1500 mg because some additives are also required in the formulation and the average weight is 1800 mg. As per the pre formulation studies it is concluded that tablet average weight less than 70 mg are very difficult to compress and more than 1500 mg are difficult to swallow in adult patient. Glucosamine stimulates the formation or manufacture of collagen, the protein portion of the fibrous substance that holds joints together and provides a shock-absorbing cushion, as a person ages, the cartilage that cushions the joints often loses its ability to support healthy cellular growth. This condition, called osteoarthritis, often leads to rough bones that rub together and cause distress with every twist or bend. In this condition patient regularly required the Glucosamine tablet in 1500 mg three times a day. But it’s very difficult to compress the tablet at huge weight because D tooling compression machine have maximum limit is 1500 mg. For such critical formulation weight cam is adjusted in lower direction to increase the weight and feeding of granules in feed frame through force feeder resolve the dissolution problem. This tablet is prepared by wet granulation method by using Non Aqueous binding showed good results physical evaluation parameters and chemical parameters such as Assay, and Dissolution values. The granules are lubricated using suitable lubricants / Glidant / Antiadhrants were good in their flow properties. Assay and dissolution studies were conducted by the HPLC method.
机译:甲基磺酰甲烷(MSM)是一种具有式(CH 3 2 SO 2 的有机硫化合物。当暴露于空气和湿气中时,葡萄糖胺具有天然吸湿性,无论是片剂还是原料形式,均可降解。为了克服这个问题,葡糖胺需要与合适的稳定剂结合。盐形式的氨基葡萄糖硫酸盐,即氯化钠和氯化钾是稳定的。葡萄糖胺的正常剂量为500-1500 mg TID。以1500mg的标签要求压制片剂是非常困难的,因为在制剂中还需要一些添加剂并且平均重量是1800mg。根据预制剂研究,得出的结论是,成年患者的片剂平均重量小于70 mg非常难以压缩,大于1500 mg则难以吞咽。葡萄糖胺刺激胶原蛋白的形成或制造,胶原蛋白是将关节固定在一起的纤维状物质的蛋白质部分,并提供减震垫,随着年龄的增长,缓冲关节的软骨通常会失去支持健康细胞生长的能力。这种情况称为骨关节炎,通常会导致粗糙的骨头相互摩擦,每次扭曲或弯曲都会引起不适。在这种情况下,患者通常每天需要服用1500毫克葡萄糖胺片,每次3次。但是,以巨大的重量压缩平板电脑非常困难,因为D工具压缩机的最大限制为1500 mg。对于这样的关键配方,重量凸轮在较低的方向上被调节以增加重量,并且通过力进料器在进料框架中进料颗粒解决了溶解问题。该片剂通过湿法制粒法制备,使用非水结合法显示出良好的结果,其物理评价参数和化学参数如含量测定和溶出度值。使用合适的润滑剂对颗粒进行润滑/助流剂/抗粘剂的流动性良好。通过HPLC方法进行测定和溶解研究。

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