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DOI 10.1007/s40620-023-01769-8

Медицинская библиотека · Journal of nephrology · 2023

Spectrophotometric analysis of purple urine secondary to methylene blue and hydroxocobalamin co-administration.

Hardin Jeremy, Galust Henrik, Clark Richard Franklin, Ly Binh, Suhandynata Raymond Theodore

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Аннотация

BACKGROUND

The development of purple urine after methylene blue (methylthioninium chloride) and hydroxocobalamin co-administration is a rare clinical entity that has not been fully elucidated. A 47-year-old male presented to the emergency department with hypotension, cyanosis, and depressed mental status. The patient was noted to have profound peripheral and central cyanosis, as well as chocolate-colored arterial blood. He was treated with both methylene blue and hydroxocobalamin and developed purple urine for approximately 1 week.

METHODS

Color chromatography was performed by placing the patient's urine directly onto absorbent filter paper. Urine spectrophotometry was performed utilizing the NanoDrop One/One C UV-Vis Spectrophotometer.

RESULTS

Color chromatography of the urine was demonstrated clear separation of distinct red and blue phases. Urine spectrophotometry demonstrated near perfect overlap between the methylene blue + hydroxocobalamin absorbance spectrum and the patient's purple urine absorbance spectrum.

CONCLUSION

Purple urine secondary to methylene blue and hydroxocobalamin co-administration is due to combined urinary excretion of methylene blue (blue) and hydroxocobalamin (red), and not a novel purple metabolite. We anticipate that this is going to be an increasingly common clinical entity as the roles of both hydroxocobalamin and methylene blue expand from toxicologic antidotes to adjunct therapies for vasoplegia, poor cardiac output, and sepsis.

Для цитирования: Hardin Jeremy, Galust Henrik, Clark Richard Franklin, Ly Binh, Suhandynata Raymond Theodore. Spectrophotometric analysis of purple urine secondary to methylene blue and hydroxocobalamin co-administration.. Journal of nephrology. 2023. DOI: 10.1007/s40620-023-01769-8.

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