Showing posts with label disintegration time. Show all posts
Showing posts with label disintegration time. Show all posts

Friday, 11 April 2025

Patient-Centric Design in Orodispersible Films: Balancing Efficacy and Acceptability | Chapter 3 | Pharmaceutical Research: Recent Advances and Trends Vol. 8

Objective: This review paper aims to provide details on the preparation, characterization and evaluation of orodispersible films (ODFs). This review also aims to focus on the merit and demerits that affect film formulation and give an insight into potential drug candidates, and polymers used in ODFs.

 

Background: According to the ninth edition of the European Pharmacopoeia (Ph. Eur.), ODFs films are formulations that are intended for the delivery of drugs by oral administration via the oral cavity. From the past few decades, researchers and companies trying toward novel drug delivery systems to ensure safety, efficacy, compliance, and patient acceptability. Nowadays drug discovery and development are an expensive, complex, and time-consuming process but trends are now moving toward novel drug delivery systems. This delivery system helps to get drug response by local and systemic action through different routes. This novel approach of preparing ODFs provides ease to pediatrics, geriatrics, and bedridden patients.

 

Findings: Regarding formulation, ODFs must have a pleasant taste, be of appropriate size, and be packed in suitable packing material. To ensure all these properties, drugs and excipients must have good stability, the required solubility and permeability, and the dose of the incorporated drug must be small dose with a low molecular weight (MW). The manufacturing of ODFs is not an easy process and a number of techniques have been developed to manufacture them which have been discusses here. The characterization and evaluation of prepared ODFs is important, and numerous methods have been developed to assess prepared ODFs according to desired aims and objectives. Packaging of films is important to maintain stability during storage and retain the mechanical properties of ODF formulations.

 

Conclusion: ODFs are effective, safe, and bioavailable as compared to fast disintegrating tablets. The novel approach has various advantages because it provides effect instantly during the emergency condition and in schizophrenic and dysphasic patients without taking water and disintegrates within a few seconds in the oral cavity.  Solvent casting method is the most frequently used technique to develop ODFs by using film-forming polymers having fast disintegration time, improved drug dissolution and better drug content.

 

Author (s) Details

Ahmad Salawi
Department of Pharmaceutics, College of Pharmacy, Jazan University, Jazan 45142, Saudi Arabia.

 

Please see the book here:- https://doi.org/10.9734/bpi/prrat/v8/2531

Sunday, 30 January 2022

Formulation and Evaluation of Captopril Mouth Dissolving Film: A Recent Study | Chapter 07 | Current Aspects in Pharmaceutical Research and Development Vol. 7

 Fast dissolving films are now favoured over traditional tablets and capsules for disguising the taste of bitter medications and increasing patient compliance. When placed on the tongue, fast dissolving films consist of a very thin oral strip that dissolves in less than one minute. The purpose of this study is to create captopril mouth dissolving films and assess the effects of various formulation parameters on the films' physical and mechanical properties, as well as drug release behaviour. The film forming polymer was hydroxypropyl methyl cellulose (HPMC E15 and K4M) in various grades. In addition, the discussion goes over the various manufacturing procedures for film preparation. The disintegration times of formulations were found to be in the range of (52 2.5 to 125.6 2.02 s). Formula F2 had the quickest in vitro disintegration time (52 2.5 s) and was found to be suitable for film production due to its perfect physicochemical properties, rapid disintegration, and optimal in vitro release. It is possible to conclude that the solvent casting method can be used to produce captopril mouth dissolving films with a higher dissolution rate and better patient compliance.


Author(S) Details

V. T. Iswariya
Department of Pharmaceutics CMR College of Pharmacy, Hyderabad, Telangana, India.

P. Deepika
Department of Pharmaceutics CMR College of Pharmacy, Hyderabad, Telangana, India.

Sowjanya Battu
Department of Pharmaceutics CMR College of Pharmacy, Hyderabad, Telangana, India.

View Book:- https://stm.bookpi.org/CAPRD-V7/article/view/5416