Wednesday, 18 January 2023

Development and Validation of a Stability Indicating Related Substances of Atenolol and Nitrendipine by RP-HPLC| Chapter 6 | Current Overview on Pharmaceutical Science Vol. 3

 The present inquiry analyzed a validated strength-indicating RP-HPLC pattern for Atenolol and Nitrendipine was developed by separating allure related impurities. Atenolol is a discriminating beta 1 blocker that maybe used alone or together with hydrochlorothiazide or with chlorthalidone for the situation of hypertension and prevention from a heart failure.By using Waters HPLC e-2695 quaternary push with a PDA detector of 2998 tool, the chromatographic separation of Atenolol, Nitrendipine and allure related impurities was realized on the column of Agilent eclipse C18 (150x4.6 mm, 3.5 µ) using slope elution with a safeguard containing 0.1percent formic acid and acetonitrile as a mobile aspect with a flow rate of 1 ml/min at atmosphere temperature. A indicator wavelength of 218 nm utilizing the PDA indicator was given in the instrumental backgrounds. Validation of the proposed arrangement was carried out according to an International Conference on Harmonization (ICH) directions.In relation to the test concentration, LOD and LOQ were established for Atenolol and allure impurities. The reversion coefficient for the plotted measurement curves was R2>0.999, indicating that the linearity was inside the limit. The results were raise to be within the permissible limit as a result of determining limits like specificity, time, accuracy, ruggedness, and strength as part of means validation.  With a runtime of 40 minutes, extreme efficiency, and compliance accompanying the USP's modified SST requirements, the developed method created positive results for Atenolol, Nitrendipine, and their associated pollutions. The current work's use of an Agilent eclipse C18 column has created better analyte elution with good resolution, revised plate count, and reduced tailing.The grown method was establish to be useful for weighing active pharmaceutical elements and to be appropriate to routine analysis (i. e, Atenolol, Nitrendipine and their related contaminations). Since Atenolol, Nitrendipine, and their related impurities have no HPLC plan reported in the drama, it is necessary to develop determinable methods under various degree to improve precision, selectivity, etc.

Author(s) Details:

Karunasree Merugu,
Department of Chemistry, GITAM (Deemed to be University), Bengaluru-560034, Karnataka, India.

Thulaseedhar Alumuri,
Department of Chemistry, GITAM (Deemed to be University), Bengaluru-560034, Karnataka, India.

Aravind Kurnool,
Department of Chemistry, Osmania University, Hyderabad 500007, Telangana, India.

Please see the link here: https://stm.bookpi.org/COPS-V3/article/view/9111

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