Valacyclovir - NDSRI's
References
FAQ's
References
- Krenitsky, Thomas Anthony; Beauchamp, Lilia Marie, Therapeutic nucleosides, Wellcome Foundation Ltd., United Kingdom, EP308065B1, January 4, 1995
- Pham-Huy, C.; Stathoulopoulou, F.; Sandouk, P.; Scherrmann, J.-M.; Palombo, S.; Girre, C., Rapid determination of valaciclovir and acyclovir in human biological fluids by high-performance liquid chromatography using isocratic elution, Journal of Chromatography B: Biomedical Sciences and Applications, Volume: 732, Issue: 1, Pages: 47-53, 1999
Frequently Asked Questions
Why is it vital to analyze Valacyclovir impurities?
Analysis of Valacyclovir impurities helps assess the purity profile and identify potentially harmful substances.
Which solvent helps in analyzing Valacyclovir impurities?
Dimethyl sulfoxide (DMSO) is a common solvent for analyzing many Valacyclovir impurities.
What analytical methods are used for Valacyclovir impurities?
High-performance liquid chromatography (HPLC) is employed to separate and analyze the impurities of Valacyclovir.
How should Valacyclovir impurities be stored in terms of temperature?
The recommendation is to store Valacyclovir impurities at room temperature, within 2-8 °C.
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