Hydroxypropyl-β-cyclodextrin-based fast dissolving carbamazepine printlets prepared by semisolid extrusion 3D printing. (1st October 2019)

• Record Type: Journal Article
• Authors: Conceição, Jaime; Farto-Vaamonde, Xián; Goyanes, Alvaro; Adeoye, Oluwatomide; Concheiro, Angel; Cabral-Marques, Helena; Sousa Lobo, José Manuel; Alvarez-Lorenzo, Carmen
• Is Part Of: Carbohydrate polymers. Volume 221(2019)
• Page Start: 55
• Page End: 62
• Publication Date: 2019-10-01
• Subjects: 3D printed tablets -- Semisolid extrusion -- Carbamazepine -- Hydroxypropyl-β-cyclodextrin -- Flash formulation -- Additive manufacturing; Polysaccharides -- Periodicals; Polysaccharides -- Periodicals; Polysaccharides -- Périodiques; Electronic journals; 547.78
• DOI: 10.1016/j.carbpol.2019.05.084
• Languages: English
• ISSNs: 0144-8617

Abstract

Graphical abstract: Highlights: HPβCD was used for the first time to prepare 3D printed formulations (printlets). Micro-extrusion printing enabled in situ formation of HPβCD-carbamazepine complexes. Orodispersible and immediate release printlets were successfully prepared. Small changes in cellulose ethers ratio allowed fine tuning of drug release profile. Abstract: This work aimed to explore for the first time the use of cyclodextrins to prepare printlets of poorly soluble drugs, such as carbamazepine, which require fine dose adjustment and rapid release. Orodispersible (flash) and immediate release formulations were 3D printed via semisolid extrusion of wet masses of hydroxypropyl-β-cyclodextrin (HPβCD) and cellulose ethers and regulating tablet porosity. Rheology of the wet masses allowed identifying printable compositions. Printing robustness was assessed evaluating weight, dimensions, hardness, drug content, and microstructure. Drug crystallinity, printlet disintegration and dissolution profiles were also characterized. The results highlight the feasibility of using HPβCD as excipient in printlets of poorly soluble drugs, and the possibilities of tuning drug release profiles through small changes in cellulose ethers nature and ratio. Semisolid extrusion-based 3D printing is revealed as a feasible approach to in situ form carbamazepine-HPβCD complexes and to produce printlets with suitable physical and drug release properties for oral delivery.