Edible solid foams as porous substrates for inkjet‐printable pharmaceuticals

Graphical abstract Figure. No Caption available. ABSTRACT The aim of this study was to investigate new porous flexible substrates, i.e., solid foams that would serve as a carrier with a high ink absorption potential for inkjet printable pharmaceuticals. Propranolol hydrochloride was used as a model active pharmaceutical ingredient (API). Pharmaceutically approved and edible cellulose derivatives and gums together with different additives were evaluated as a base for the substrate. Different methods for preparation of a solid foam such as freeze‐drying, vacuum oven drying and drying at room temperature were explored. Only freeze‐drying of the polymeric solutions resulted in the desired porous and flexible, but mechanically stable, soft sponge‐like substrates with hydroxypropyl methylcellulose (HPMC)‐based solid foams being the most suitable for the use in continuous inkjet printing. The plasticized HPMC foams had a superior absorption capacity and fast penetration speed for the different solvents due to the open cell pore structure and higher porosity as compared to nonplasticized additive‐free foams, although, the latter were less hygroscopic. The produced solid foams were well suited for inkjet printing of high volumes of API‐containing ink. The inkjet‐printed API was immediately released from the dosage forms upon contact with the dissolution medium. This work demonstrates that the fabricated solid foams, based on plasticized HPMC, show a great potential as porous carriers in the fabrication of high dose dosage forms by inkjet printing.

[1]  Maren Preis,et al.  Application of a colorimetric technique in quality control for printed pediatric orodispersible drug delivery systems containing propranolol hydrochloride. , 2016, International journal of pharmaceutics.

[2]  J. Rantanen,et al.  Electrospinnability of Poly Lactic-co-glycolic Acid (PLGA): the Role of Solvent Type and Solvent Composition , 2017, Pharmaceutical Research.

[3]  P. Modamio,et al.  Development and validation of liquid chromatography methods for the quantitation of propranolol, metoprolol, atenolol and bisoprolol: Application in solution stability studies , 1996 .

[4]  Niklas Sandler,et al.  Behavior of printable formulations of loperamide and caffeine on different substrates--effect of print density in inkjet printing. , 2013, International journal of pharmaceutics.

[5]  Abdul W. Basit,et al.  Personalised dosing: Printing a dose of one's own medicine. , 2015, International journal of pharmaceutics.

[6]  N. Schork Personalized medicine: Time for one-person trials , 2015, Nature.

[7]  Eric Allémann,et al.  Freeze-drying/Lyophilization of Pharmaceutical and Biological products , 2001 .

[8]  Jukka Rantanen,et al.  Social aspects in additive manufacturing of pharmaceutical products , 2017, Expert opinion on drug delivery.

[9]  J. Breitkreutz,et al.  Novel analytical methods for the characterization of oral wafers. , 2009, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[10]  A. Zimmer,et al.  Nanosuspensions as advanced printing ink for accurate dosing of poorly soluble drugs in personalized medicines. , 2011, International journal of pharmaceutics.

[11]  R. Dixit,et al.  Oral strip technology: overview and future potential. , 2009, Journal of controlled release : official journal of the Controlled Release Society.

[12]  Kaido Siimon,et al.  Mechanical characterization of electrospun gelatin scaffolds cross-linked by glucose , 2015, Journal of Materials Science: Materials in Medicine.

[13]  Laura Hirshfield,et al.  Dropwise additive manufacturing of pharmaceutical products for solvent-based dosage forms. , 2014, Journal of pharmaceutical sciences.

[14]  Bozena Michniak-Kohn,et al.  Electrodeless electrohydrodynamic drop-on-demand encapsulation of drugs into porous polymer films for fabrication of personalized dosage units. , 2012, Journal of pharmaceutical sciences.

[15]  Zhiqiang Su,et al.  Electrospinning design of functional nanostructures for biosensor applications. , 2017, Journal of materials chemistry. B.

[16]  Miguel Montenegro-Nicolini,et al.  Inkjet Printing of Proteins: an Experimental Approach , 2016, The AAPS Journal.

[17]  J. S. Vrentas,et al.  Surface concentration effects in the drying of solvent‐coated polymer films , 1996 .

[18]  Niklas Sandler,et al.  Tailoring controlled-release oral dosage forms by combining inkjet and flexographic printing techniques. , 2012, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

[19]  Niklas Sandler,et al.  Evaluation of different substrates for inkjet printing of rasagiline mesylate. , 2013, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[20]  Ana Filipa Borges,et al.  Oral films: Current status and future perspectives: I - Galenical development and quality attributes. , 2015, Journal of controlled release : official journal of the Controlled Release Society.

[21]  A. ElMeshad,et al.  Lyophilized Sustained Release Mucoadhesive Chitosan Sponges for Buccal Buspirone Hydrochloride Delivery: Formulation and In Vitro Evaluation , 2014, AAPS PharmSciTech.

[22]  J. Rantanen,et al.  Visualization and Non-Destructive Quantification of Inkjet-Printed Pharmaceuticals on Different Substrates Using Raman Spectroscopy and Raman Chemical Imaging , 2017, Pharmaceutical Research.

[23]  Abdul W. Basit,et al.  Preparation of Personalized-dose Salbutamol Sulphate Oral Films with Thermal Ink-Jet Printing , 2011, Pharmaceutical Research.

[24]  S. Hoag,et al.  Plasticizer Effects on Physical–Mechanical Properties of Solvent Cast Soluplus® Films , 2013, AAPS PharmSciTech.

[25]  Maren Preis,et al.  Development of Oromucosal Dosage Forms by Combining Electrospinning and Inkjet Printing. , 2017, Molecular pharmaceutics.

[26]  Howard L McLeod,et al.  Strategies for integrating personalized medicine into healthcare practice. , 2017, Personalized medicine.

[27]  J. Boateng,et al.  Characterisation of freeze-dried wafers and solvent evaporated films as potential drug delivery systems to mucosal surfaces. , 2010, International journal of pharmaceutics.

[28]  Rahamatullah Shaikh,et al.  Mucoadhesive drug delivery systems , 2011, Journal of pharmacy & bioallied sciences.

[29]  Boris Khusid,et al.  Electrodeless electrohydrodynamic printing of personalized medicines , 2010 .

[30]  Niklas Sandler,et al.  A step toward development of printable dosage forms for poorly soluble drugs. , 2013, Journal of pharmaceutical sciences.

[31]  Niklas Sandler,et al.  Printing technologies in fabrication of drug delivery systems , 2013, Expert opinion on drug delivery.

[32]  M. Peleg,et al.  Compressive Characteristics of Freeze‐Dried Agar and Alginate Gel Sponges , 1993 .

[33]  J. Boateng,et al.  In vitro drug release studies of polymeric freeze-dried wafers and solvent-cast films using paracetamol as a model soluble drug. , 2009, International journal of pharmaceutics.

[34]  Kunn Hadinoto,et al.  Combining inkjet printing and amorphous nanonization to prepare personalized dosage forms of poorly-soluble drugs. , 2015, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[35]  J. Boateng,et al.  Development and physico-mechanical characterisation of lyophilised chitosan wafers as potential protein drug delivery systems via the buccal mucosa. , 2012, Colloids and surfaces. B, Biointerfaces.

[36]  Hypromellose , 2019, Reactions Weekly.

[37]  J. Boateng,et al.  Development and physico-mechanical characterization of carrageenan and poloxamer-based lyophilized matrix as a potential buccal drug delivery system , 2014, Drug development and industrial pharmacy.

[38]  M. Bartolomei,et al.  Thermal studies on the polymorphic modifications of (R,S) propranolol hydrochloride , 1998 .

[39]  J. Amigo,et al.  Visualization and prediction of porosity in roller compacted ribbons with near-infrared chemical imaging (NIR-CI). , 2015, Journal of pharmaceutical and biomedical analysis.

[40]  J. Boateng,et al.  In vitro characterisation of chitosan based xerogels for potential buccal delivery of proteins. , 2012, Carbohydrate polymers.