GASTRORETENTIVE EFFERVESCENT FLOATING TABLETS (GREFT) OF DRUGS ACTING ON CARDIOVASCULAR DISEASES

S. Majee, Trisha Mishra, Souvik Gupti
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Abstract

Incidences of Cardio Vascular Diseases (CVDs) are increasing in an alarming proportion in India. Conventional oral dosage forms cannot be retained in the stomach for long owing to gastric emptying. Moreover, drugs which are commonly employed in management of chronic CVDs either have reduced solubility at alkaline pH, undergo colonic degradation, exhibit site-specific absorption or varying bioavailability with combination therapy. Gastro-retentive drug delivery systems (GRDDS) are designed to overcome these challenges. Since 2006, Food and Drug Administration has approved only few GRDDS for treating CVDs. The aim of the present review is to summarize the outcomes of research carried on GRRDS with drugs for CVDs since last 15 y and comprehensive analysis of limitations of such studies due to which no product has been approved or commercialized in over last 18 y. Literature survey includes single unit, multi-particulate, monolayer and bilayer dosage forms with or without effervescence-inducing agents and made of natural and/or synthetic polymers like hydroxypropylmethyl cellulose, natural gums etc. Efforts have been made to compile in vitro buoyancy data such as floating lag time, total floating time, swelling index, release profile and release kinetics. Among various studies reported on monolayer and bilayer Gastro-Retentive Effervescent Floating Tablets, only 3 involved bioavailability studies in human volunteers. Toxicity studies in animals or stability studies are totally lacking. Observation with floating-type multi-particulate GRDDS is more disappointing. lack of safety, efficacy data, stability data, in vivo imaging studies and in vitro-in vivo correlation data might be actually responsible for lack of commercialization of any GRDDS for drugs acting on CVDs in 21st century.
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治疗心血管疾病药物的胃复安泡腾片(GREFT)
在印度,心血管疾病(CVDs)的发病率正在以惊人的比例上升。由于胃排空的原因,传统口服剂型无法在胃中保留很长时间。此外,通常用于治疗慢性心血管疾病的药物要么在碱性 pH 值下溶解度降低,要么在结肠中降解,要么表现出特定部位的吸收,要么在联合治疗时生物利用度不同。胃肠保留给药系统(GRDDS)就是为了克服这些难题而设计的。自 2006 年以来,美国食品和药物管理局仅批准了少数几种胃肠保留给药系统用于治疗心血管疾病。本综述旨在总结自过去 15 年以来有关胃复安给药系统与治疗心血管疾病药物的研究成果,并全面分析此类研究的局限性,由于这些局限性,过去 18 年中没有任何产品获得批准或实现商业化。文献调查包括单体、多颗粒、单层和双层剂型,无论是否使用了起泡剂,也无论是否由羟丙基甲基纤维素、天然胶等天然和/或合成聚合物制成。人们一直在努力汇编体外浮力数据,如漂浮滞后时间、总漂浮时间、膨胀指数、释放曲线和释放动力学。在报告的有关单层和双层胃复安泡腾片的各种研究中,只有 3 项涉及在人类志愿者中进行的生物利用度研究。完全缺乏动物毒性研究或稳定性研究。缺乏安全性、疗效数据、稳定性数据、体内成像研究和体外-体内相关性数据,可能是 21 世纪针对心血管疾病药物的胃药泡腾片商业化不足的真正原因。
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KNOWLEDGE, ATTITUDE AND APPLICATION OF HEMOVIGILANCE BY POSTGRADUATES AND INTERNS IN A TERTIARY CARE HOSPITAL GENERIC DRUG REGISTRATION AND COUNTRY-SPECIFIC REQUIREMENTS IN SAUDI ARABIA, QATAR, BAHRAIN, AND OMAN GASTRORETENTIVE EFFERVESCENT FLOATING TABLETS (GREFT) OF DRUGS ACTING ON CARDIOVASCULAR DISEASES REVIEW ON CHEMICAL CONSTITUENTS AND BIOLOGICAL ACTIVITIES OF GENUS JUNIPER A SIMULATION APPROACH FOR NOVEL 1,3,4 THIADIAZOLE ACETAMIDE MOIETIES AS POTENT ANTIMYCOBACTERIAL AGENTS
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