Quantitative Investigation of Intestinal Drug Absorption Enhancement by Drug-Rich Nanodroplets Generated via Liquid–Liquid Phase Separation
Author:
Affiliation:
1. Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba 260-8675, Japan
Funder
Japan Society for the Promotion of Science
Over-the-counter Drug Self-Medication Promotion Foundation
KOS? Cosmetology Research Foundation
Publisher
American Chemical Society (ACS)
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.molpharmaceut.3c01078
Reference62 articles.
1. The Role of BCS (Biopharmaceutics Classification System) and BDDCS (Biopharmaceutics Drug Disposition Classification System) in Drug Development
2. Advances in Polymer Design for Enhancing Oral Drug Solubility and Delivery
3. Liquid–liquid phase separation drug aggregate: Merit for oral delivery of amorphous solid dispersions
4. Characteristics and Significance of the Amorphous State in Pharmaceutical Systems
5. Amorphous pharmaceutical solids: preparation, characterization and stabilization
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1. Amorphous Solubility Advantage: Theoretical Considerations, Experimental Methods, and Contemporary Relevance;Journal of Pharmaceutical Sciences;2024-09
2. Impact of Colloidal Drug-Rich Droplet Size and Amorphous Solubility on Drug Membrane Permeability: A Comprehensive Analysis;Journal of Pharmaceutical Sciences;2024-06
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