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For: Matsumura N, Ono A, Akiyama Y, Fujita T, Sugano K. Bottom-Up Physiologically Based Oral Absorption Modeling of Free Weak Base Drugs. Pharmaceutics 2020;12:E844. [PMID: 32899235 DOI: 10.3390/pharmaceutics12090844] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
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1 Ashkar A, Sosnik A, Davidovich-Pinhas M. Structured edible lipid-based particle systems for oral drug-delivery. Biotechnol Adv 2021;:107789. [PMID: 34186162 DOI: 10.1016/j.biotechadv.2021.107789] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
2 Gonzalez-Alvarez I, Bermejo M, Tsume Y, Ruiz-Picazo A, Gonzalez-Alvarez M, Hens B, Garcia-Arieta A, Amidon GE, Amidon GL. An In Vivo Predictive Dissolution Methodology (iPD Methodology) with a BCS Class IIb Drug Can Predict the In Vivo Bioequivalence Results: Etoricoxib Products. Pharmaceutics 2021;13:507. [PMID: 33917118 DOI: 10.3390/pharmaceutics13040507] [Reference Citation Analysis]
3 Uekusa T, Avdeef A, Sugano K. Is equilibrium slurry pH a good surrogate for solid surface pH during drug dissolution? Eur J Pharm Sci 2021;168:106037. [PMID: 34637897 DOI: 10.1016/j.ejps.2021.106037] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
4 Price E, Kalvass JC, DeGoey D, Hosmane B, Doktor S, Desino K. Global Analysis of Models for Predicting Human Absorption: QSAR, In Vitro, and Preclinical Models. J Med Chem 2021;64:9389-403. [PMID: 34152772 DOI: 10.1021/acs.jmedchem.1c00669] [Reference Citation Analysis]
5 Aishwarya R, Murthy A, Ahmed T, Chachad S. A Novel Approach to Justify Dissolution Differences in an Extended Release Drug Product Using Physiologically Based Biopharmaceutics Modeling and Simulation. J Pharm Sci 2022:S0022-3549(22)00071-5. [PMID: 35217007 DOI: 10.1016/j.xphs.2022.02.007] [Reference Citation Analysis]
6 Yoshikawa T, Oki J, Ichikawa N, Yamashita S, Sugano K. Small differences in acidic pH condition significantly affect dissolution equivalence between drug products of acidic drug salt. Journal of Drug Delivery Science and Technology 2021;63:102546. [DOI: 10.1016/j.jddst.2021.102546] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]