Efficient Evaluation of In Vivo Performance in Human for Generic Formulation by Novel Dissolution-Absorption Prediction (DAP) Workflow
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Organic Chemistry,Pharmaceutical Science,Pharmacology,Molecular Medicine,Biotechnology
Link
https://link.springer.com/content/pdf/10.1007/s11095-022-03337-4.pdf
Reference41 articles.
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3. Tanaka Y, Kubota A, Matsuo A, Kawakami A, Kamizi H, Mochigoe A, et al. Effect of absorption behavior of solubilizers on drug dissolution in the gastrointestinal tract: evaluation based on in vivo luminal concentration-time profile of cilostazol, a poorly soluble drug, and solubilizers. J Pharm Sci. 2016;105(9):2825–31. https://doi.org/10.1016/j.xphs.2016.02.026.
4. Bonferoni CM, Ferrari F, Rossi S, Caramella CM. The role of particle size in drug release and absorption. Particulate Products. 2014; p. 323–41. https://doi.org/10.1007/978-3-319-00714-4_11.
5. Jinno J, Kamada N, Miyake M, Yamada K, Mukai T, Odomi M, et al. Effect of particle size reduction on dissolution and oral absorption of a poorly water-soluble drug, cilostazol, in beagle dogs. J Control Release. 2006;111(1–2):56–64. https://doi.org/10.1016/j.jconrel.2005.11.013.
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