Paper Details 
Original Abstract of the Article :
A rapid and selective LC-MS/MS method is described for the simultaneous assay of Avanafil and Dapoxetine in human plasma <i>via</i> a protein precipitation (PP) sample preparation technique. Tadalafil was chosen as the internal standard reaching good recovery and reproducibility while diminishing th...See full text at original site
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引用元:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9040755/

データ提供:米国国立医学図書館(NLM)

A New Oasis in the Desert of Erectile Dysfunction Treatment

Erectile dysfunction (ED) can be a challenging condition, often leading to a search for effective treatment options. This study explores a new analytical method for simultaneously measuring two medications, Avanafil and Dapoxetine, in human plasma. The researchers developed a rapid and selective liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for quantifying these drugs, which are used to treat ED and premature ejaculation, respectively. This method provides a more precise and efficient way to monitor drug levels in patients undergoing treatment.

Precise Measurement for Enhanced Treatment

This study offers a significant improvement in the analysis of Avanafil and Dapoxetine in human plasma. The developed LC-MS/MS method is more rapid, selective, and accurate than previous methods, providing a more robust tool for monitoring drug levels and optimizing treatment regimens.

Navigating the Desert of ED Treatment

This research highlights the ongoing quest for better and more precise methods to manage ED and premature ejaculation. The development of this analytical method could contribute to a more individualized and effective approach to treatment.

Dr. Camel's Conclusion

This study, like a skilled navigator charting a course through the desert of ED treatment, introduces a new and precise tool for monitoring drug levels. This method offers a promising path towards more effective and personalized treatment strategies, bringing a glimmer of hope to the desert of ED management.

Date :
  1. Date Completed n.d.
  2. Date Revised 2022-07-16
Further Info :

Pubmed ID

35479534

DOI: Digital Object Identifier

PMC9040755

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Languages

English

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