OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Rate- and Extent-Limiting Factors of Oral Drug Absorption: Theory and Applications
Kiyohiko Sugano, Katsuhide Terada
Journal of Pharmaceutical Sciences (2015) Vol. 104, Iss. 9, pp. 2777-2788
Closed Access | Times Cited: 61

Showing 1-25 of 61 citing articles:

Engineering Cocrystals of Poorly Water-Soluble Drugs to Enhance Dissolution in Aqueous Medium
Indumathi Sathisaran, Sameer V. Dalvi
Pharmaceutics (2018) Vol. 10, Iss. 3, pp. 108-108
Open Access | Times Cited: 182

A Refined Developability Classification System
Julian Rosenberger, James Butler, Jennifer B. Dressman
Journal of Pharmaceutical Sciences (2018) Vol. 107, Iss. 8, pp. 2020-2032
Closed Access | Times Cited: 73

Physiologically Based Biopharmaceutics Modeling to Demonstrate Virtual Bioequivalence and Bioequivalence Safe-space for Ribociclib which has Permeation Rate-controlled Absorption
Marc Laisney, Tycho Heimbach, Martin Mueller‐Zsigmondy, et al.
Journal of Pharmaceutical Sciences (2021) Vol. 111, Iss. 1, pp. 274-284
Open Access | Times Cited: 42

Current perspective on veterinary drug and chemical residues in food of animal origin
Attia H. Atta, Shimaa Atta, Soad M. Nasr, et al.
Environmental Science and Pollution Research (2022) Vol. 29, Iss. 11, pp. 15282-15302
Closed Access | Times Cited: 33

Parameterization of Physiologically Based Biopharmaceutics Models: Workshop Summary Report
Xavier Pépin, Sumit Arora, Luiza Borges, et al.
Molecular Pharmaceutics (2024)
Open Access | Times Cited: 7

The role of pH and dose/solubility ratio on cocrystal dissolution, drug supersaturation and precipitation
Tatiane Cogo Machado, Gislaine Kuminek, Simone Gonçalves Cardoso, et al.
European Journal of Pharmaceutical Sciences (2020) Vol. 152, pp. 105422-105422
Closed Access | Times Cited: 41

Celecoxib Nanoformulations with Enhanced Solubility, Dissolution Rate, and Oral Bioavailability: Experimental Approaches over In Vitro/In Vivo Evaluation
Aslıhan Arslan, Barbaros Yet, Emirhan Nemutlu, et al.
Pharmaceutics (2023) Vol. 15, Iss. 2, pp. 363-363
Open Access | Times Cited: 15

Statistical investigation of simulated fed intestinal media composition on the equilibrium solubility of oral drugs
Zhou Zhou, Claire Dunn, Ibrahim Khadra, et al.
European Journal of Pharmaceutical Sciences (2016) Vol. 99, pp. 95-104
Open Access | Times Cited: 43

Discovery and Characterization of Potent, Efficacious, Orally Available Antimalarial Plasmepsin X Inhibitors and Preclinical Safety Assessment of UCB7362
Martin A. Lowe, Á. de Pablo Cárdenas, Jean‐Pierre Valentin, et al.
Journal of Medicinal Chemistry (2022) Vol. 65, Iss. 20, pp. 14121-14143
Open Access | Times Cited: 21

Supramolecular delivery systems for polyphenols: A green approach to predict in vivo permeability through an in vitro setup
Maddalena Sguizzato, Federica Agosta, Antonella Ciancetta, et al.
International Journal of Pharmaceutics (2025) Vol. 670, pp. 125170-125170
Open Access

Improving accuracy in food effect Predictions: Application of In-Vitro absorption experiments as a useful tool for the evaluation of ten drug products
Gobardhan Bal, Cornelius Harlacher, Dominic Werthmueller, et al.
European Journal of Pharmaceutics and Biopharmaceutics (2025), pp. 114722-114722
Closed Access

Prediction of Bioequivalence and Food Effect Using Flux- and Solubility-Based Methods
Enikő Borbás, Szabina Kádár, Konstantin Tsinman, et al.
Molecular Pharmaceutics (2019) Vol. 16, Iss. 10, pp. 4121-4130
Open Access | Times Cited: 35

An Environmentally Sensitive Silk Fibroin/Chitosan Hydrogel and Its Drug Release Behaviors
Zhangpeng Xu, Erni Tang, Huijing Zhao
Polymers (2019) Vol. 11, Iss. 12, pp. 1980-1980
Open Access | Times Cited: 33

Design and Characterization of Phosphatidylcholine-Based Solid Dispersions of Aprepitant for Enhanced Solubility and Dissolution
Sooho Yeo, Ji‐Eun An, Changhee Park, et al.
Pharmaceutics (2020) Vol. 12, Iss. 5, pp. 407-407
Open Access | Times Cited: 31

Novel High-Drug-Loaded Amorphous Dispersion Tablets of Posaconazole; In Vivo and In Vitro Assessment
Deanna M. Mudie, Aaron M. Stewart, Nishant Biswas, et al.
Molecular Pharmaceutics (2020) Vol. 17, Iss. 12, pp. 4463-4472
Open Access | Times Cited: 28

Lost in modelling and simulation?
Kiyohiko Sugano
ADMET & DMPK (2021) Vol. 9, Iss. 2, pp. 75-109
Open Access | Times Cited: 25

Application of a Refined Developability Classification System
Julian Rosenberger, James Butler, Uwe Muenster, et al.
Journal of Pharmaceutical Sciences (2018) Vol. 108, Iss. 3, pp. 1090-1100
Closed Access | Times Cited: 30

In vivo dissolution of poorly water-soluble drugs: Proof of concept based on fluorescence bioimaging
Yinqian Yang, Yongjiu Lv, Chengying Shen, et al.
Acta Pharmaceutica Sinica B (2020) Vol. 11, Iss. 4, pp. 1056-1068
Open Access | Times Cited: 26

Projection of Target Drug Particle Size in Oral Formulations Using the Refined Developability Classification System (rDCS)
Kristian Beran, Eline Hermans, René Holm, et al.
Pharmaceutics (2023) Vol. 15, Iss. 7, pp. 1909-1909
Open Access | Times Cited: 9

The Discriminatory Power of the BCS-Based Biowaiver: A Retrospective With Focus on Essential Medicines
Martin A. Hofsäss, Jennifer B. Dressman
Journal of Pharmaceutical Sciences (2019) Vol. 108, Iss. 9, pp. 2824-2837
Closed Access | Times Cited: 22

Studying the effect of solubilizing agents on drug diffusion through the unstirred water layer (UWL) by localized spectroscopy
Massimiliano Pio di Cagno, Paul C. Stein
European Journal of Pharmaceutics and Biopharmaceutics (2019) Vol. 139, pp. 205-212
Open Access | Times Cited: 21

FaSSIF-V3, but not compendial media, appropriately detects differences in the peak and extent of exposure between reference and test formulations of ibuprofen
Rodrigo Cristofoletti, Jennifer B. Dressman
European Journal of Pharmaceutics and Biopharmaceutics (2016) Vol. 105, pp. 134-140
Closed Access | Times Cited: 20

Ocular biopharmaceutics: impact of modeling and simulation on topical ophthalmic formulation development
Hovhannes J. Gukasyan, Shumet Hailu, Thomas K. Karami, et al.
Drug Discovery Today (2019) Vol. 24, Iss. 8, pp. 1587-1597
Closed Access | Times Cited: 19

Prediction of negative food effect induced by bile micelle binding on oral absorption of hydrophilic cationic drugs
Yoshiyuki Akiyama, Soichiro Ito, Takuya Fujita, et al.
European Journal of Pharmaceutical Sciences (2020) Vol. 155, pp. 105543-105543
Closed Access | Times Cited: 18

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