Evaluation of the stability of hydrocortisone sodium succinate in solutions for parenteral use by a validated HPLC-UV method

URN:NBN:SI:doc-CLL7FYH32022Gaál, Enikő ÉvaMihovec, KatjaRoškar, RobertTemova Rakuša, Žanedocuments/doc/C/URN_NBN_SI_doc-CLL7FYH3_001.pdfdocuments/doc/C/URN_NBN_SI_doc-CLL7FYH3_001.txt469articlestr. 796–80210.17344/acsi.2022.75391255751711580-3155URN:NBN:SI:doc-CLL7FYH3engSlovensko kemijsko društvoActa chimica slovenicaBYforced degradation studyinfusioninfuzijainjectioninjekcijain-use stabilityKromatografska analizaRaztopinerok uporabnosti po odprtjuSolu-Cortefstabilnost med uporaboštudija prisilne razgradnjeEvaluation of the stability of hydrocortisone sodium succinate in solutions for parenteral use by a validated HPLC-UV method