IMMEDIATE RELEASE ORAL SOLID DOSAGE FORMS: A REVIEW

被引:0
作者
Pawar, Dinesh Chhotu [1 ]
Kale, Vrushali Rajkumar
Ige, Pradyumna P. [1 ]
机构
[1] RC Patel Inst Pharmaceut Educ & Res, Dept Pharmaceut, Shirpur 425405, Dhule Maharastr, India
来源
INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES | 2019年 / 6卷 / 05期
关键词
Immediate release dosage form; tablet; polymer; superdisintegrants; etc; DELIVERY;
D O I
暂无
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Recently, Immediate release dosage form have taken over an important position in the market by overcoming previously administration problems and contributing to extension of patient life, which have difficulty in swallowing tablets and capsules. Many drugs belongs to BCS class2 having poor solubility in water need to be improvement in solubility and dissolution rate for enhancing its oral bioavailability, Although in many cases immediate onset of action is required than conventional therapy. Immediate release dosage form includes tablets, capsule, pellets, microsphere, granules, etc, among all these dosage from Tablet is more widespread dosage form. The basic approached of development of tablet use of superdisintegrants like cross linked carboxymelhyl cellulose (Croscarmeliose), Sodium starch glycolate (Primogel, Explotab), Polyvinylpyrrolidone (Polyplasdone) etc. which provide instantaneous disintegration of tablet after administration. Various techniques are implemented to developed immediate release dosage form. The present review highlights on the prospective advantages, design and development of robust, stable, and orally immediate release as a pharmaceutical dosage form.
引用
收藏
页码:10595 / 10610
页数:16
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