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CROSPROVIDONE (POLYVINYLPYRROLIDONE)
Crospovidone is an advanced, insoluble, cross-linked polyvinylpyrrolidone polymer widely used as a superdisintegrant and binder in solid oral dosage forms. Its exceptional ability to rapidly absorb water and swell facilitates quick tablet disintegration, significantly enhancing the dissolution rate and bioavailability of active ingredients, thus optimizing the overall efficacy and absorption of supplements.
Description
Crospovidone, also known as insoluble polyvinylpyrrolidone (PVP), is a synthetic, highly cross-linked homopolymer of N-vinyl-2-pyrrolidone. This pharmaceutical-grade excipient is distinguished by its unique chemical structure, which renders it insoluble in water yet capable of rapid and extensive swelling. Its porous, particulate nature provides a large internal surface area, making it an exceptionally effective superdisintegrant and binder in solid oral dosage forms. Originating from the pyrrolidone monomer, its polymerization and subsequent cross-linking ensure a stable, inert material widely accepted across global pharmacopoeias, including USP/NF, EP, and JP. This non-toxic, non-absorbable polymer plays a critical role in ensuring the optimal performance and patient compliance of various supplement and pharmaceutical products by facilitating the swift breakdown of tablets and capsules upon ingestion. Its high purity and consistent particle size distribution are crucial characteristics for its reliable function in diverse formulations.
The primary functional benefit of Crospovidone lies in its unparalleled ability to enhance the disintegration and dissolution rates of active ingredients. Upon contact with aqueous media, such as gastric fluid, Crospovidone rapidly absorbs water, causing it to swell significantly and exert disruptive forces within the tablet matrix. This rapid swelling mechanism leads to the swift breakup of the dosage form into smaller particles, thereby increasing the surface area available for solvent contact. For many active compounds, particularly those with low aqueous solubility, an improved dissolution rate is a critical determinant of their bioavailability and subsequent therapeutic or physiological effect. Scientific studies have consistently demonstrated that formulations incorporating Crospovidone achieve faster drug release profiles compared to those utilizing conventional disintegrants, ensuring that the active ingredients are presented to the body in a more readily absorbable form. This mechanism is crucial for maximizing the efficacy and consistency of supplement delivery.
Crospovidone's versatility makes it an invaluable component in a wide array of supplement and pharmaceutical formulations, including tablets, capsules, and granules. Its dual functionality as both a superdisintegrant and a dry binder allows formulators to achieve robust tablets with excellent hardness while simultaneously ensuring rapid disintegration. Research, such as studies published in the International Journal of Pharmaceutics, frequently highlights Crospovidone's superior performance in accelerating dissolution, particularly for poorly water-soluble compounds, directly impacting their in vivo absorption. Quality considerations for Crospovidone involve stringent controls over particle morphology, specific surface area, and chemical purity to guarantee consistent performance and safety. Its inert nature ensures compatibility with a broad spectrum of active ingredients and excipients, minimizing potential interactions that could compromise product stability or efficacy. The selection of appropriate Crospovidone grades, based on particle size, further refines its application, providing tailored disintegration profiles for specific product requirements and contributing to overall product quality and consumer satisfaction.
Key Benefits
- Significantly enhances tablet and capsule disintegration upon ingestion.
- Improves the dissolution rate and bioavailability of active ingredients.
- Functions as an effective dry binder, contributing to robust dosage form integrity.
- Exhibits high chemical inertness and broad compatibility with diverse ingredients.
Primary Uses
- Superdisintegrant in tablet, capsule, and orally disintegrating tablet (ODT) formulations.
- Dry binder in direct compression and wet granulation processes.
- Enhancing the dissolution and release of poorly water-soluble active compounds.
- Formulations requiring rapid active ingredient release and improved bioavailability.
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