Development of Discriminatory Method for Dissolution of Carvedilol Marketed Formulations

نویسندگان

  • T.E.G.K Murthy
  • G. Sowjanya
چکیده

Carvedilol (BCS Class II drug) is a nonselective β-adrenergic blocking agent with α1-blocking activity and it is mainly used in the management of hypertension. Two commercial brands of carvedilol drug, of strength 12.5mg were used for the Invitro dissolution studies. In the present study four dissolution media [pH 1.2 (0.1 N Hcl), pH 4.5 Acetate buffer, pH 6.8 phosphate buffer, and Distilled water] with different agitation speeds (50, 75 and 100 rpm) were employed. An agitation speed of 100 rpm showed more drug release profile than 50 and 75 rpm. The dissolution rate was found to be influenced by the dissolution medium and paddle speed. The dissolution studies conducted with water in presence of paddle set at 50 rpm is more suitable for discrimination of marketed formulations of Carvedilol.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Development and Validation of New Discriminative Dissolution Method for Carvedilol Tablets

The objective of the present study was to develop and validate a discriminative dissolution method for evaluation of carvedilol tablets. Different conditions such as type of dissolution medium, volume of dissolution medium and rotation speed of paddle were evaluated. The best in vitro dissolution profile was obtained using Apparatus II (paddle), 50 rpm, 900 ml of pH 6.8 phosphate buffer as diss...

متن کامل

Role of Cogrinding in Enhancing the In vitro Dissolution Characteristics of Carvedilol

In the present study, an attempt was made to increase the in vitro dissolution rate of carvedilol (antihypertensive) by cogrinding technique using various carriers, namely lactose, corn starch, treated agar, microcrystalline cellulose. The coground mixtures were prepared using the above excipients in four drug-carrier ratios, viz., 1:1, 1:3, 1:4 and 1:9. The prepared coground mixtures were eval...

متن کامل

Formulation and Evaluation of Liquisolid Compacts of Carvedilol P.Sandhya

The purpose of this study is to develop a novel liquisolid technique to enhance the dissolution rate of poorly water soluble drug Carvedilol, a BCS class II drug, which is a β-blocker, by using different excipients. The main components of a liquisolid system are a non volatile solvent, carrier and coating materials and a disintegrant. Liquisolid system refers to the formulations that are formed...

متن کامل

Development and validation of dissolution method for carvedilol compression-coated tablets

The present study describes the development and validation of a dissolution method for carvedilol compression-coated tablets. Dissolution test was performed using a TDT-06T dissolution apparatus. Based on the physiological conditions of the body, 0.1N hydrochloric acid was used as dissolution medium and release was monitored for 2 hours to verify the immediate release pattern of the drug in aci...

متن کامل

Dissolution Profile Evaluation of Solid Pharmaceutical Forms Containing Chloramphenicol Marketed in Brazil

The dissolution profile for solid pharmaceutical forms containing chloramphenicol 250 mg available in Brazil was determined using a method from the American Pharmacopoeia (United States Pharmacopoeia, 2004) and then compared. Two different methods of dissolution profile comparison were used: ANOVA, and an independent model. Differences between the formulations were reflected in the dissolution ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2003