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Forced degradation of tacrolimus and the development of a UHPLC method for impurities determination.
Acta Pharm. 2019 Sep 1;69(3):363-380. doi: 10.2478/acph-2019-0025.
Acta Pharm. 2019.
PMID: 31259735
Free article.
Using different experimental designs in drug-excipient compatibility studies during the preformulation development of a stable solid dosage formulation.
Bohanec S, Peterka TR, Blažič P, Jurečič R, Grmaš J, Krivec A, Zakrajšek J.
Bohanec S, et al. Among authors: peterka tr.
Acta Chim Slov. 2010 Dec;57(4):895-903.
Acta Chim Slov. 2010.
PMID: 24061893
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