首页> 外文会议>Annual meeting exposition of the Controlled Release Society >Formulation And Evaluation Of Sustained Release Orally Disintegrating Tablets OfMetoclopramide Hydrochloride Intended For Gastro retention
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Formulation And Evaluation Of Sustained Release Orally Disintegrating Tablets OfMetoclopramide Hydrochloride Intended For Gastro retention

机译:胃胃retention留用盐酸甲氧氯普胺缓释口腔崩解片的研制与评价

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Metoclopramide Hydrochloride is used for themanagement of nausea and vomiting due to migraine,cancer chemotherapy, tardive dyskinesia and gastroesophageal reflux disorders. The drug has a shortbiological half-life and is administered in a dose of 10–15mg q.I.dd1. Also the drug finds applicability in pediatricand geriatric patients who prefer patient compliantproducts. Patients who have difficulty in swallowingcannot swallow a sustained release tablet or capsule as theformulation is required to be taken intact. Also thepatients who are suffering from emesis would prefer aformulation to be consumed without water. Hence anorally disintegrating sustained release gastro retentivetype of dosage form was formulated so as to get asustained effect by means of gastro retention as well asprovide the ease of administration.. 2-4 Taste masking of thedrug was carried out to mask the bitter taste. Sustainedrelease floating pellets were formulated and compressedto form orally disintegrating tablets. In vitro evaluationwas carried out to assess disintegration, wetting, drugrelease, buoyancy and assay. In vivo evaluation wascarried out to confirm the taste masking, oraldispersibility, buoyancy and gastro retention. Theformulated tablet produced a very short disintegrationtime in oral cavity and showed buoyancy and drug releasefor period of 12 hrs. Also the gamma scintigraphy studiesconfirmed the gastro retention.
机译:盐酸甲氧氯普胺用于 处理偏头痛引起的恶心和呕吐, 癌症化疗,迟发性运动障碍和胃 食道反流疾病。该药有一个短 生物半衰期,剂量为10–15 毫克q.I.d d1。该药物也可用于儿科 和老年患者更喜欢患者依从性 产品。吞咽困难的患者 不能吞咽缓释片剂或胶囊剂,因为 要求保持原样。还有 呕吐的患者更喜欢 无需水即可食用的配方。因此, 口腔崩解缓释型胃滞留剂 配制剂型的类型以获得 通过胃retention留以及 提供易于管理的功能。 。 2-4掩味 进行药物掩盖苦味。持续 配制释放的浮粒并压制 形成口腔崩解片。体外评估 进行了评估崩解,润湿,药物 释放,浮力和化验。体内评估为 进行掩味确认,口服 分散性,浮力和胃retention留性。这 配制片剂产生了非常短的崩解 在口腔中停留时间并显示浮力和药物释放 持续12小时。也是伽玛闪烁显像的研究 确认胃保留。

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