In the current study, superdisintegrants for fast-dissolving tablets (FDTs) have been examined using microcrystalline cellulose -polyethylene glycol conjugates. MCC was combined with polyethylene glycol (PEG) 200 and heated in the presence of a catalyst to create the PEGylated conjugate of microcrystalline cellulose (MCC). MCC-PEG conjugates were created, and the powdered conjugates were characterised using micromeritic investigations, FTIR, SEM, and powder XRD techniques. By using FT-IR, the conjugation of MCC and PEG was verified. Conjugate's physical and chemical characteristics were contrasted with MCC. The conjugate was evaluated for water vapour uptake isotherms, maximum water saturation, water penetration rate, disintegration duration, superdisintegration power, and dissolution studies. Through direct compression, the conjugates were employed to create Lurasidone hydrochloride FDTs, and the in vitro drug release was assessed. After comparing its results with that of commercial superdisintegrants, it can be concluded that MCC-PEG conjugate can prove to be an excellent superdisintegrant.
Introduction:Fast disintegrating tablets (FDTs) have gained popularity recently as popular dosage forms because of their quick disintegration in the mouth and quick commencement of action. Pre-gastric FDT absorption in the mouth and oesophagus reduces the amount of medication undergoing first-pass metabolism, improving bioavailability [1,2] . These dosage forms also provide a number of additional benefits, including accurate dosing, simple mobility, chemical and physical stability, and high patient convenience for elderly, young patients, bedridden patients, psychiatric patients and uncooperative patients [3] . They are frequently described as quick melt, orally disintegrating, melt in mouth, quick dissolve, rapid melt, oro-dispersible, fast dissolve and mouth dissolving tablets. Disintegrants are added to solid oral dosage forms to speed up the compacted mass breakdown and boost medication absorption. Superdisintegrants, more advanced disintegrants, are currently being researched. Compared to other disintegrants, these substances are used in low concentrations, typically 1-10% of the dosage form's overall weight. Standard super disintegrants like croscarmellose sodium, crospovidone, and sodium starch glycolate are used in a number of formulations [4] . The demand for a shorter disintegration time encouraged ongoing efforts to find new, more effective disintegrating agents. Superdisintegrants are substances that achieve disintegration far more quickly than the commonly used standard disintegrants. The basic modes of action for tablet disintegrants were discovered to be wicking and swelling, while other mechanisms, including deformation recovery, particle repulsion theory, heat of wetting, generation of a gas, etc., may also be involved in specific instances of tablet disintegration [5] . The water uptake induced by capillary forces is one of the most important variables in the disintegration processes of many formulations [6...