Review: Solid Dispersion Formulation Methods and Applications in Drug Delivery

About 44% of the active medicinal components in all previously disclosed chemical units are hydrophobic and do not extend shop because of their limited water solubility. One of the factors limiting the rate at which oral medications can reach the appropriate concentration in the systemic circulation for pharmacological action is their solubility. Our medical preparation scientists and researchers are constantly surrounded by issues relating to drug release, drug targeting, solubility, overdosing, permeability and bioavailability. Thus, creating or improving frameworks for drug delivery is a territory of ongoing research. Solid dispersion, micronization, salt formation, are some of the vital methods usually employed to improve the solubility of poorly soluble drugs, but each method has some drawbacks and benefits. This review focuses on different methods of improving drug solubility in order to lower the proportion of medication candidates that are removed from development due to poor solubility. The popular solution for all problems related to aspects of solubility and <i>in vitro</i> release rate of certain poorly watersoluble drugs, is solid dispersion. Solid dispersions smear the standard to drug release via producing a combination of a poorly water-soluble active pharmaceutical ingredients (API) and greatly soluble coformers. The solid dispersion method has been commonly used to increase the <i>in vitro</i> drug release, solubility, and bioavailability of poorly watersoluble drugs. The focus of this review paper is on carriers, BCS classification, and solubility. This page also summarizes some of the most current technological advancements and offers a variety of preparation methods for solid dispersion. The various solid dispersions were highlighted according to their molecular configuration and carrier type. It also provides an overview of the solid dispersion methodologies and their mechanics, as well as the marketed medications that can be made utilizing them.

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Publication Details

Journal
Current Physical Chemistry
Published
2024-12-24
DOI
https://doi.org/10.2174/0118779468337741241126094712
Citations
1
Primary Topic
Drug Solubulity and Delivery Systems
Type
article
Field-Weighted Citation Impact
0.21
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Review: Solid Dispersion Formulation Methods and Applications in Drug Delivery

Kavita Bahmani, Sunita Devi, Nisham Rani, Jyoti Malik et al.
1 citations
Current Physical Chemistry
Drug Solubulity and Delivery Systems
0.21
article

Review: Solid Dispersion Formulation Methods and Applications in Drug Delivery

Kavita Bahmani, Sunita Devi, Nisham Rani, Jyoti Malik, Samiksha Grewal, Rajni Tanwar, Neelam Sihag
article en
1 citations

Abstract

About 44% of the active medicinal components in all previously disclosed chemical units are hydrophobic and do not extend shop because of their limited water solubility. One of the factors limiting the rate at which oral medications can reach the appropriate concentration in the systemic circulation for pharmacological action is their solubility. Our medical preparation scientists and researchers are constantly surrounded by issues relating to drug release, drug targeting, solubility, overdosing, permeability and bioavailability. Thus, creating or improving frameworks for drug delivery is a territory of ongoing research. Solid dispersion, micronization, salt formation, are some of the vital methods usually employed to improve the solubility of poorly soluble drugs, but each method has some drawbacks and benefits. This review focuses on different methods of improving drug solubility in order to lower the proportion of medication candidates that are removed from development due to poor solubility. The popular solution for all problems related to aspects of solubility and <i>in vitro</i> release rate of certain poorly watersoluble drugs, is solid dispersion. Solid dispersions smear the standard to drug release via producing a combination of a poorly water-soluble active pharmaceutical ingredients (API) and greatly soluble coformers. The solid dispersion method has been commonly used to increase the <i>in vitro</i> drug release, solubility, and bioavailability of poorly watersoluble drugs. The focus of this review paper is on carriers, BCS classification, and solubility. This page also summarizes some of the most current technological advancements and offers a variety of preparation methods for solid dispersion. The various solid dispersions were highlighted according to their molecular configuration and carrier type. It also provides an overview of the solid dispersion methodologies and their mechanics, as well as the marketed medications that can be made utilizing them.

Current Physical ChemistryVol. 15(2)
Chaudhary Devi Lal University (IN), Guru Jambheshwar University of Science and Technology (IN), Chaudhary Charan Singh Haryana Agricultural University (IN), GD Goenka University (IN)
Openalex Percentile: Top 48%
Drug Solubulity and Delivery Systems
0.21
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