A Stability Indicating UPLC Method for Finasteride and Its Related Impurities

نویسندگان
چکیده

برای دانلود باید عضویت طلایی داشته باشید

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

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

A Stability Indicating UPLC Method for Finasteride and Its Related Impurities

The objective of the present research work is to develop a gradient, reversed-phase liquid chromatographic (RP-UPLC) method for the determination of Finasteride in pharmaceutical bulk drugs for assay and its related impurities. The chromatographic separation was achieved on a Waters ACQUITY UPLC BEH Phenyl Column (150 mm × 2.1 mm, 1.7 μm), The gradient LC method employs solutions A and B as mob...

متن کامل

A validated stability-indicating UPLC method for desloratadine and its impurities in pharmaceutical dosage forms.

A novel stability-indicating gradient reverse phase ultra-performance liquid chromatographic (RP-UPLC) method was developed for the determination of purity of desloratadine in presence of its impurities and forced degradation products. The method was developed using Waters Aquity BEH C18 column with mobile phase containing a gradient mixture of solvents A and B. The eluted compounds were monito...

متن کامل

A validated stability-indicating UPLC method for the determination of impurities in Maraviroc.

Maraviroc is an antiretroviral drug in the CCR5 receptor antagonist class, which is used in the treatment of HIV. Maraviroc has six impurities. A novel, stability-indicating reversed-phase ultra-performance liquid chromatography (RP-UPLC) method has been developed for the quantitative determination of maraviroc in active pharmaceutical ingredients, along with its six impurities. The method is a...

متن کامل

A Validated Stability Indicating RP-UPLC Method for Atrovastain Calcium

The present paper describes stability indicating reverse phase Ultra performance liquid chromatographic (RPLC) assay method for Atrovastatin Calcium in bulk drugs. The developed method is also applicable for the related substance determination and degradation products generated from forced decomposition studies. The drug substance was subjected to stress conditions of acid hydrolysis, base hydr...

متن کامل

Development and Validation of a Stability-Indicating RP-UPLC Method for the Quantitative Analysis of antiparkinson drug and its related impurities

High efficiency, cost effectiveness and short run time are the basic requirements of high-speed chromatographic separations. To fulfill these requirements, an advanced separation technique, ultraperformance liquid chromatography (UPLC), has shown promising developments. A rapid, specific, sensitive, and precise reverse-phase UPLC method was developed for the determination of antiparkinson drug ...

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

ژورنال

عنوان ژورنال: American Journal of Analytical Chemistry

سال: 2012

ISSN: 2156-8251,2156-8278

DOI: 10.4236/ajac.2012.311098