Solid Dispersion Technology: A Review of Recent Advances and Applications

Authors

  • Himabindu A.V.S. Department of Pharmaceutics, Vijaya Institute of Pharmaceutical Sciences for Women, Enikepadu, Vijayawada – 521108.
  • U. Vimala Kumari
  • K. Kavya
  • T. Mounika
  • K. Lakshmi Prasanna
  • D. Deepthi Akshay
  • K. Padmalatha

Keywords:

Bioavailability enhancement, Drug solubility, Hot-melt extrusion, Polymer carriers, Solid dispersion

Abstract

Solid dispersion technology is a well-established and widely used method for enhancing the solubility and bioavailability of poorly water-soluble drugs. The technique involves the dispersion of the drug in an inert matrix or carrier material, thereby improving the dissolution rate, which is often a limitation for many pharmacologically active compounds. Over the past few years, advances in solid dispersion systems have made them a promising approach for drug development, especially for the formulation of oral dosage forms. Various methods, including solvent evaporation, fusion, and hot-melt extrusion, are employed to prepare solid dispersions, each with its own advantages and challenges. Additionally, a wide range of carriers, such as polymers, surfactants, and lipids, have been explored to optimize the performance of solid dispersions. Recent research highlights the importance of understanding the physical characteristics and stability of these systems to ensure their efficacy in clinical applications. Despite their significant potential, challenges related to stability, scale-up production, and regulatory considerations remain. This review article aims to present a comprehensive analysis of the recent advancements in solid dispersion technology, focusing on its formulation strategies, applications, and future perspectives. Moreover, it will also examine the potential for overcoming the challenges associated with these systems to enhance their commercialization prospects in the pharmaceutical industry.

References

Albetawi S, Abdalhafez A, Abu-Zaid A. Recent solubility and dissolution enhancement techniques for repaglinide a BCS class II drug: a review. Pharmacia. 2021;68(3):573–583. https://doi.org/10.3897/pharmacia.68.e66586

Patel K, Shah S, Patel J. Solid dispersion technology as a formulation strategy for the fabrication of modified release dosage forms: A comprehensive review. DARU J. Pharm. Sci. 2022;3 0(1):165-89. https://doi.org/10.1007/s40199-022-00440-0

Saboo S, Mugheirbi NA, Zemlyanov DY, Kestur US, Taylor LS. Congruent release of drug and polymer: A “sweet spot” in the dissolution of amorphous solid dispersions. J. Control. Release. 2019; 298:68-82. https://doi.org/10.1016/j.jconrel.2019.01.039

Tran P, Pyo YC, Kim DH, Lee SE, Kim JK, Park JS. Overview of the Manufacturing Methods of Solid Dispersion Technology for Improving the Solubility of Poorly Water-Soluble Drugs and Application to Anticancer Drugs. Pharmaceutics. 2019;11(3):132. https://doi.org/10.3390%2Fpharmaceutics11030132

Kumar A, Kumar K. Solid dispersion – strategy to enhance solubility and dissolution of poorly water-soluble drugs. Univ. J. Pharm. Res. 2017; 2(5): 50-54. http://doi.org/10.22270/ujpr.v2i5.RW4

Malkawi R, Malkawi WI, Al-Mahmoud Y, Tawalbeh J. Current Trends on Solid Dispersions: Past, Present, and Future. Mutalik S, editor. Adv. Pharmacol. Pharm. Sci. 2022; 2022:1–17. https://doi.org/10.1155%2F2022%2F5916013

Li J, Li C, Zhang H, Gao X, Wang T, Wang Z, et al. Preparation of Azithromycin Amorphous Solid Dispersion by Hot-Melt Extrusion: An Advantageous Technology with Taste Masking and Solubilization Effects. Polymers. 2022;14(3):495. https://doi.org/10.3390/polym14030495

Wang H, Li R, Rao Y, Liu S, Hu C, Zhang Y, et al. Enhancement of the Bioavailability and Anti-Inflammatory Activity of Glycyrrhetinic Acid via Novel Soluplus® A Glycyrrhetinic Acid Solid Dispersion. Pharmaceutics. 2022;14(9):1797–7. https://doi.org/10.3390%2Fpharmaceutics14091797

Fouad AS et al. Preparation of solid dispersion systems for enhanced dissolution of poorly water soluble diacerein: in vitro evaluation, optimization and physiologically based pharmacokinetic modeling. PloS One. 2021;16(1): 1-26. https://doi.org/10.1371/journal.pone.0245482

Giri BR et al. Hot-melt extruded amorphous solid dispersion for solubility, stability, and bioavailability enhancement of telmisartan. Pharmaceuticals. 2021;14(73):1-18. https://doi.org/10.3390%2Fph14010073

Kim SJ, Lee HK, Na YG, Bang KH, Lee HJ, Wang M, et al. A novel composition of ticagrelor by solid dispersion technique for increasing solubility and intestinal permeability. Int. J. Pharm. 2019; 555:11–8. https://doi.org/10.1016/j.ijpharm.2018.11.038

Raj AL, Kumar YS. Preparation and Evaluation of Solid Dispersion of Nebivolol Using Solvent Evaporation Method. Int. J. Pharm. Sci. Drug. Res. 2018;10(4): 322-328. https://doi.org/10.25004/Ijpsdr.2018.100418

Kaur S, Jena SK, Samal SK, Saini V, Sangamwar AT. Freeze dried solid dispersion of exemestane: A way to negate an aqueous solubility and oral bioavailability problems. Eur. J. Pharm. Sci. 2017; 107:54–61. https://doi.org/10.1016/j.ejps.2017.06.032

Pinho LA, Lima SG, Malaquias LF, Pires FD, Sá-Barreto LL, Cardozo-Filho L, Gratieri T, Gelfuso GM, Cunha-Filho M. Improvements of theobromine pharmaceutical properties using solid dispersions prepared with newfound technologies. Chem. Eng. Res. Des. 2018; 132:1193-201.

Published

2025-04-21