Pharmacokinetic evaluation of poorly soluble compounds formulated as nano- or microcrystals after intraperitoneal injection to mice
Keywords
Drug delivery
Lymphatics
Parenteral
Preformulation
Suspension
Intraperitoneal administration
Microparticles
Nanoparticles
AbbreviationsCmax
Maximum plasma concentration
AUC
Area under the plasma concentration-time profile
Data availability
No data was used for the research described in the article.
© 2023 Elsevier B.V. All rights reserved.
留言 (0)