Fast disintegrating buccal film is a new type of solid immediate-release formulation that can be disintegrated quickly in saliva only and is used for convenient drug delivery through rapid delivery, a fast and effective way of drug delivery. Due to its unique properties, more and more studies on fast-dissolving buccal films have been conducted in recent years and have become a major hotspot. The development of fast-dissolving buccal films has great prospects in the pharmaceutical field.
CD Formulation's fast disintegrating buccal film development services offer an effective alternative to traditional drug delivery methods. Our rapid disintegrating buccal films offer a fast, efficient, and patient-friendly alternative. Our commitment to excellence ensures that our fast disintegrating buccal film development process and services meet the highest standards, contributing to advancing pharmaceutical solutions for diverse therapeutic needs.
Formulation Design Phase
We achieve the desired buccal film properties by selecting the right polymer, plasticizer, and active pharmaceutical ingredient (API). At the same time, factors such as drug solubility, stability, and bioavailability need to be considered. The choice of polymer plays a key role in characterizing the mechanical and drug release properties of the buccal membrane, while the plasticizer enhances flexibility and prevents brittleness.
Development phase
During the drug development phase, we actually produce the buccal film by using appropriate manufacturing techniques to ensure uniform drug distribution and consistent film thickness. For example, during the cast film process, we form a thin, pliable film by applying the formulation to the substrate and subsequently drying it to form a thin, pliable film. In addition, we need to repeatedly tune to determine accuracy in order to obtain reproducible results.
Pilot stage
In this phase, we focus on the critical phase of rapid disintegration of buccal mucosal performance testing and safety assessment. In performance testing, we perform various tests including disintegration time, tensile strength, and drug release studies to evaluate the performance of the buccal mucosa. Safety assessment involves a thorough examination of the buccal mucosa for potential adverse reactions.
Upon completion of the above development phases, we scale up the manufacturing process to commercial production, through which we finally deliver satisfactory project development results to our customers.
Figure 1. Photos of the disintegration of (a) blank fibers, and (b) drug-loaded fibers. (Alkahtani ME, et al,. 2021)
CD Formulation has grown to be an industry leader in oral thin films drug delivery R&D, which greatly assists our clients in accomplishing difficult drug discovery and development services. If you are interested in us, please feel free to contact us.
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