Administration of drugs through the vagina is one of the oldest forms of drug therapy. Vaginal tablets are a form of medication specifically designed for intravaginal administration. They provide a targeted topical approach to address a variety of gynecological conditions and provide therapeutic benefits. Vaginal tablets are formulated to deliver the active pharmaceutical ingredient (API) directly into the vagina, ensuring optimal efficacy and minimal systemic absorption.
Protheragen-ING specializes in developing customized, high-quality vaginal tablets to meet specific therapeutic needs. Our experienced formulation scientists create innovative solutions prioritizing efficacy, patient compliance, and safety. With cutting-edge technology and stringent quality standards, we are committed to delivering superior products contributing to women's health and well-being.
Fig. 1 Vaginal drug delivery route. (Osmałek T, et al. 2021)
The vaginal tablets we have developed consist of carefully selected ingredients. They are designed to ensure stability, controlled release, and compatibility with the vaginal environment. Formulations typically include APIs, excipients, and other ancillary substances.
The most common type of vaginal tablets are polymer-based tablets, in which the active substance is uniformly distributed in a hydrophilic polymer backbone. When hydrophilic polymers interact with vaginal fluids, they create an in situ gelling effect through which the drug diffuses.
Following are some of the polymers that we commonly use for vaginal drug delivery systems:
Natural polymers | Polymers of plant origin | Cellulose and its derivatives |
Pectin | ||
Alginates | ||
Starch | ||
Carrageenan | ||
Polymers of animal origin | Chitosan | |
Hyaluronic acid | ||
Gelatin | ||
Microbial polymers | Gellan gum | |
Xanthan gum | ||
Synthetic polymers | Poloxamer | |
Polyacrylates | ||
Polyvinylpyrrolidone | ||
Polyethylene glycol |
Protheragen-ING can develop vaginal tablets to address a variety of gynecological conditions. Some common types of vaginal tablets include:
1. Formulation Development
Consideration of the specific therapeutic requirements, compatibility and stability of the API and excipient.
2. Blend or Granule Preparation
API and excipients are blended or granulated using suitable technology (e.g. direct compression or wet granulation).
3. Tabletting
The mixture or granules are pressed into tablet form using a specialized tablet press.
4. Coating (if required)
Some vaginal tablets may require coating to enhance stability, control release or improve aesthetics.
5. Quality Control
The vaginal tablets produced undergo rigorous quality control testing to ensure that they meet the required standards for potency, dissolution, homogeneity and stability.
6. Packaging and Labeling
The final vaginal tablets are packaged and labeled according to regulatory requirements and industry standards.
Contact us today to discuss your vaginal tablet development requirements and explore how we can help you realize your vision.
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