A Brief Review of Analytical Methods for the Estimation of Allopurinol in Pharmaceutical Formulation and Biological Matrices

Sharma, H. R.; Sapkota, Hari Prasad; Dangi, Nim Bahadur

doi:10.1155/2021/5558651

Cited by 3 publications

(1 citation statement)

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“…The culmination of these analytical techniques culminates in robust statistical data analysis, which serves as the foundation for determining the extent to which generic drugs are bioequivalent to their reference counterparts. This intricate analytical process ensures that generic drugs are indeed equivalent in delivering the same therapeutic benefits, thus enabling cost-effective and accessible healthcare for patients [4,5].…”

Section: Review Open Accessmentioning

confidence: 99%

A Brief Review on Analytical Techniques in Bioequivalence Studies

Kosuru,

Jyothi

et al. 2024

J Cli Pharm Res

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In the pharmaceutical research and development, bioequivalence studies hold a critical position, serving as a vital component in evaluating the equivalence of generic drugs with their reference counterparts. These studies, which examine the interchangeability between generic and brand-name medications, depend heavily on a range of analytical techniques to measure the presence and concentration of a drug's active pharmaceutical ingredient (API) within the human body. The comprehensive use of these analytical methods ensures the confidence of healthcare providers and regulatory bodies in the effectiveness, quality and safety of generic medications. The field of pharmaceutical analysis is dynamic and forward-looking, with analysts, researchers and scientists energetically engaged in forging a future characterized by ground breaking discoveries and refined pharmaceutical solutions. This is a realm where scientific excellence and innovation harmonize, ultimately benefiting the health and welfare of individuals and societies across the globe. The key takeaways underscore the field's resilience and its unwavering commitment to upholding the highest standards in drug development and quality control while pioneering cutting-edge technologies with the promise of safer, more effective pharmaceuticals for all.

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Section: Review Open Accessmentioning

confidence: 99%