» Articles » PMID: 35566319

Supersaturation-Based Drug Delivery Systems: Strategy for Bioavailability Enhancement of Poorly Water-Soluble Drugs

Overview
Journal Molecules
Publisher MDPI
Specialty Biology
Date 2022 May 14
PMID 35566319
Authors
Affiliations
Soon will be listed here.
Abstract

At present, the majority of APIs synthesized today remain challenging tasks for formulation development. Many technologies are being utilized or explored for enhancing solubility, such as chemical modification, novel drug delivery systems (microemulsions, nanoparticles, liposomes, etc.), salt formation, and many more. One promising avenue attaining attention presently is supersaturated drug delivery systems. When exposed to gastrointestinal fluids, drug concentration exceeds equilibrium solubility and a supersaturation state is maintained long enough to be absorbed, enhancing bioavailability. In this review, the latest developments in supersaturated drug delivery systems are addressed in depth.

Citing Articles

Soluplus-Based Pharmaceutical Formulations: Recent Advances in Drug Delivery and Biomedical Applications.

Guembe-Michel N, Nguewa P, Gonzalez-Gaitano G Int J Mol Sci. 2025; 26(4).

PMID: 40003966 PMC: 11855892. DOI: 10.3390/ijms26041499.


Co-Amorphization, Dissolution, and Stability of Quench-Cooled Drug-Drug Coamorphous Supersaturating Delivery Systems with RT-Unstable Amorphous Components.

Zhang Y, Yao Q, Lin X, Ma Y, Zhang H, Yu H Pharmaceutics. 2025; 16(12.

PMID: 39771470 PMC: 11677066. DOI: 10.3390/pharmaceutics16121488.


Supersaturated Liquid Formulation of Pazopanib Hydrochloride Loaded with Synergistic Precipitation Inhibitors.

Park J, Lee S, Lee J, Jee J, Maeng H, Jang D Molecules. 2024; 29(22).

PMID: 39598656 PMC: 11596717. DOI: 10.3390/molecules29225267.


Nanoformulations in Pharmaceutical and Biomedical Applications: Green Perspectives.

Petrovic S, Bita B, Barbinta-Patrascu M Int J Mol Sci. 2024; 25(11).

PMID: 38892030 PMC: 11172476. DOI: 10.3390/ijms25115842.


Solid dispersion systems for enhanced dissolution of poorly water-soluble candesartan cilexetil: In vitro evaluation and simulated pharmacokinetics studies.

Ali I, Sajad U, Abdul Rasool B PLoS One. 2024; 19(6):e0303900.

PMID: 38843120 PMC: 11156308. DOI: 10.1371/journal.pone.0303900.


References
1.
Agrawal A, Dudhedia M, Zimny E . Hot Melt Extrusion: Development of an Amorphous Solid Dispersion for an Insoluble Drug from Mini-scale to Clinical Scale. AAPS PharmSciTech. 2016; 17(1):133-47. PMC: 4766127. DOI: 10.1208/s12249-015-0425-7. View

2.
Shi Y, Gao P, Gong Y, Ping H . Application of a biphasic test for characterization of in vitro drug release of immediate release formulations of celecoxib and its relevance to in vivo absorption. Mol Pharm. 2010; 7(5):1458-65. DOI: 10.1021/mp100114a. View

3.
Jog R, Burgess D . Pharmaceutical Amorphous Nanoparticles. J Pharm Sci. 2016; 106(1):39-65. DOI: 10.1016/j.xphs.2016.09.014. View

4.
Park K . Drug release mechanisms from amorphous solid dispersions. J Control Release. 2015; 211:171. DOI: 10.1016/j.jconrel.2015.06.027. View

5.
Yang M, Gong W, Wang Y, Shan L, Li Y, Gao C . Bioavailability Improvement Strategies for Poorly Water-Soluble Drugs Based on the Supersaturation Mechanism: An Update. J Pharm Pharm Sci. 2016; 19(2):208-25. DOI: 10.18433/J3W904. View