Reetu Yadav1*, Ashutosh Kumar Yadav1, Anita Singh2
1K.R. Mangalam University, Sohna Road, Gurugram, Haryana 122103 India
2Sunderdeep Pharmacy College, NH-24, Delhi-Hapur Road, Dasna, Ghaziabad-201015 (U.P) India
*Address for Corresponding Author
Reetu Yadav
K.R. Mangalam University, Sohna Road, Gurugram, Haryana 122103 India
Abstract
Co-crystal is defined as a material which contains two or more discrete molecular entities in the crystal structure. Co-crystals of many compounds are known for years in solid state chemistry. Pharmaceutical co-crystals are important because they can improve many properties of the parent API like solubility, dissolution rate, stability, crystallinity and many more. Biopharmaceutics Classification System (BCS) of drugs classifies drugs into four major categories based on their solubility and permeability behavior. BCS Class II and Class IV drugs suffer from poor aqueous solubility. Co-crystallization enhances solubility of BCS class II and class IV drug, in addition to BCS of drugs. The aim of this review is to present an extensive overview of the co-crystallization methods, focusing in the specificities of each technique, its advantages and disadvantages.
Keywords: Cocrystal, solubility enhancement, co-crystallization method