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      3D-Printed Mesoporous Carrier System for Delivery of Poorly Soluble Drugs

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          Abstract

          Fused deposition modelling (FDM) is the most extensively employed 3D-printing technique used in pharmaceutical applications, and offers fast and facile formulation development of personalized dosage forms. In the present study, mesoporous materials were incorporated into a thermoplastic filament produced via hot-melt extrusion and used to produce oral dosage forms via FDM. Mesoporous materials are known to be highly effective for the amorphization and stabilization of poorly soluble drugs, and were therefore studied in order to determine their ability to enhance the drug-release properties in 3D-printed tablets. Celecoxib was selected as the model poorly soluble drug, and was loaded into mesoporous silica (MCM-41) or mesoporous magnesium carbonate. In vitro drug release tests showed that the printed tablets produced up to 3.6 and 1.5 times higher drug concentrations, and up to 4.4 and 1.9 times higher release percentages, compared to the crystalline drug or the corresponding plain drug-loaded mesoporous materials, respectively. This novel approach utilizing drug-loaded mesoporous materials in a printed tablet via FDM shows great promise in achieving personalized oral dosage forms for poorly soluble drugs.

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          Ordered mesoporous molecular sieves synthesized by a liquid-crystal template mechanism

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            On a Theory of the van der Waals Adsorption of Gases

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              Drug Solubility: Importance and Enhancement Techniques

              Solubility, the phenomenon of dissolution of solute in solvent to give a homogenous system, is one of the important parameters to achieve desired concentration of drug in systemic circulation for desired (anticipated) pharmacological response. Low aqueous solubility is the major problem encountered with formulation development of new chemical entities as well as for the generic development. More than 40% NCEs (new chemical entities) developed in pharmaceutical industry are practically insoluble in water. Solubility is a major challenge for formulation scientist. Any drug to be absorbed must be present in the form of solution at the site of absorption. Various techniques are used for the enhancement of the solubility of poorly soluble drugs which include physical and chemical modifications of drug and other methods like particle size reduction, crystal engineering, salt formation, solid dispersion, use of surfactant, complexation, and so forth. Selection of solubility improving method depends on drug property, site of absorption, and required dosage form characteristics.

                Author and article information

                Contributors
                Role: Academic Editor
                Role: Academic Editor
                Role: Academic Editor
                Journal
                Pharmaceutics
                Pharmaceutics
                pharmaceutics
                Pharmaceutics
                MDPI
                1999-4923
                18 July 2021
                July 2021
                : 13
                : 7
                : 1096
                Affiliations
                Division of Nanotechnology and Functional Materials, Department of Materials Science and Engineering, Uppsala University, Box 35, SE-751 03 Uppsala, Sweden; christos.katsiotis@ 123456angstrom.uu.se (C.S.K.); michelle.ahlen@ 123456angstrom.uu.se (M.Å.); maria.stromme@ 123456angstrom.uu.se (M.S.)
                Author notes
                Author information
                https://orcid.org/0000-0002-0154-3627
                https://orcid.org/0000-0002-5496-9664
                https://orcid.org/0000-0003-4543-1130
                Article
                pharmaceutics-13-01096
                10.3390/pharmaceutics13071096
                8308994
                34371787
                96e98b42-703f-4354-982e-1374102c3dbe
                © 2021 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 15 June 2021
                : 14 July 2021
                Categories
                Article

                3d printing,fused deposition modelling,fdm,hot-melt extrusion,hme,mesoporous,mesoporous magnesium carbonate,mcm-41,poorly soluble drug,drug delivery

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