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Recent advances in the development of extended-release formulations for oral drug delivery.

Asian Journal of Pharmaceutical Technology and Innovation (ajpti)

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Perspective- Asian Journal of Pharmaceutical Technology and Innovation(2023)

Recent advances in the development of extended-release formulations for oral drug delivery.

Emma Adeleke A*
 
Department of Drug Metabolism, Dalhousie University, Halifax, Canada
 
*Corresponding Author:
Emma Adeleke A, Department of Drug Metabolism, Dalhousie University, Halifax, Canada, Email: em.adeleke@drugmail.org

Received: 21-Jan-2023, Manuscript No. AJPTI-23-92524; Editor assigned: 26-Jan-2023, Pre QC No. AJPTI-23-92524; Reviewed: 16-Feb-2023, QC No. AJPTI-23-92524; Revised: 22-Feb-2023, Manuscript No. AJPTI-23-92524; Published: 28-Feb-2023

Description

Extended-release formulations for oral drug delivery are designed to provide a sustained release of drugs over a prolonged period of time, thereby improving drug efficacy, reducing dosing frequency, and enhancing patient compliance. These formulations offer several advantages over conventional immediate-release formulations, such as reduced side effects, improved therapeutic outcomes, and convenience of use.

The primary goal of extended-release formulations is to maintain a steady-state concentration of the drug in the bloodstream, which is achieved by controlling the rate and extent of drug release. There are several different types of extended-release formulations, including diffusion-controlled systems, matrix systems, osmotic systems, and reservoir systems.

Diffusion-controlled systems are the most common type of extended-release formulation. They work by embedding the drug in a matrix, which slowly releases the drug as it diffuses through the matrix. The matrix may be composed of a polymer or a combination of polymers, and the drug may be incorporated into the matrix as a solid or a solution. The rate of drug release is determined by the diffusion coefficient of the drug through the matrix, as well as the thickness and porosity of the matrix.

Matrix systems work by incorporating the drug into a hydrophilic or hydrophobic matrix, which swells or dissolves in the presence of water. This leads to the formation of channels or pores through which the drug can diffuse. The rate of drug release is determined by the rate of matrix swelling or dissolution, as well as the size and shape of the channels or pores.

Osmotic systems work by producing a pressure gradient across a semipermeable membrane, which allows water to enter the system and push the drug out through a small orifice. The rate of drug release is determined by the osmotic pressure of the drug formulation, as well as the size and shape of the orifice.

Reservoir systems consist of a drug reservoir and a rate- controlling membrane, which separates the drug from the external environment. The drug is released from the reservoir through a small orifice or through diffusion across the membrane. The rate of drug release is determined by the thickness and permeability of the membrane, as well as the size and shape of the orifice.

Extended-release formulations offer several advantages over conventional immediate-release formulations. One of the main advantages is that they can reduce the frequency of dosing, which improves patient compliance and reduces the risk of side effects. They also provide a more consistent drug concentration in the bloodstream, which improves therapeutic outcomes and reduces the risk of toxicity. Extended-release formulations can also improve the convenience of drug administration, which can be particularly beneficial for patients with chronic conditions.

However, extended-release formulations also have some disadvantages. They can be more expensive than conventional immediate-release formulations, and they may require more complex manufacturing processes. They can also be more difficult to swallow or administer, which can be a problem for some patients. In addition, the rate of drug release from extended- release formulations can be affected by various factors, such as the pH of the gastrointestinal tract, the presence of food or other drugs, and individual differences in gastrointestinal motility.

Extended-release formulations for oral drug delivery offer several advantages over conventional immediate-release formulations, including improved drug efficacy, reduced dosing frequency, and enhanced patient compliance. The different types of extended-release formulations, such as diffusion-controlled systems, matrix systems, osmotic systems, and reservoir systems, have different mechanisms of action and advantages and disadvantages. While extended-release formulations can be more expensive and difficult to administer, they provide a more consistent drug concentration in the bloodstream, which can improve therapeutic outcomes and reduce the risk of side effects.

Citation: Adeleke EA. Recent Advances in the Development of Extended-Release Formulations for Oral Drug Delivery AJPTI 2023;11(40):1-2.