Facile fabrication of uniform size-controlled microparticles and potentiality for tandem drug delivery system of micro/nanoparticles.

This article describes a rapid and facile method for manufacturing various size-controlled gel particles with utilizing inkjet printing technology. Generally, the size of droplets could be controlled by changing nozzle heads of inkjet printer, from which ink solution is ejected. However, this method uses drying process before gelling microparticles, and with that, the size of microparticles was easily controlled by only altering the concentration of ejected solution. When sodium alginate solution with various concentrations was ejected from inkjet printer, we found that the concentration of alginate solution vs. the volume of dried alginate particle showed an almost linear relationship in the concentration range from 0.1 to 3.0%. After dried alginate particles were soaked into calcium chloride solution, the size of microgel beads were obtained almost without increasing their size. The microparticles including various sizes of nanoparticles were easily manufactured by ejecting nanoparticle-dispersed alginate solution. The release of 25-nm sized nanoparticles from alginate microgel beads was finished in a relatively-rapid manner, whereas 100-nm sized nanoparticles were partially released from those ones. Moreover, most of 250-nm sized nanoparticles were not released from alginate microgel beads even after 24-h soaking. This particle fabricating method would enable the tandem drug delivery system with a combination of the release from nano and microparticles, and be expected for the biological and tissue engineering application.

[1]  Rashad Tawashi,et al.  Morphic features variation of solid particles after size reduction: sonification compared to jet mill grinding , 1988 .

[2]  M Nakamura,et al.  Biomatrices and biomaterials for future developments of bioprinting and biofabrication , 2010, Biofabrication.

[3]  N. F. de Rooij,et al.  Characterisation of a fL droplet generator for inhalation drug therapy , 2000 .

[4]  María Luján Ferreira,et al.  PLGA based drug delivery systems (DDS) for the sustained release of insulin: insight into the protein/polyester interactions and the insulin release behavior , 2010 .

[5]  Makoto Nakamura,et al.  New approaches for tissue engineering: three dimensional cell patterning using inkjet technology , 2008 .

[6]  J. Benoit,et al.  Why and how to prepare biodegradable, monodispersed, polymeric microparticles in the field of pharmacy? , 2011, International journal of pharmaceutics.

[7]  S. Garg,et al.  Bioadhesive microspheres as a controlled drug delivery system. , 2003, International journal of pharmaceutics.

[8]  Steven P Schwendeman,et al.  Principles of encapsulating hydrophobic drugs in PLA/PLGA microparticles. , 2008, International journal of pharmaceutics.

[9]  Gorka Orive,et al.  Microcapsules and microcarriers for in situ cell delivery. , 2010, Advanced drug delivery reviews.

[10]  E. Cevher,et al.  Topical drug delivery using chitosan nano- and microparticles , 2012, Expert opinion on drug delivery.

[11]  Teerapol Srichana,et al.  Development of a pH-responsive drug delivery system for enantioselective-controlled delivery of racemic drugs. , 2010, Journal of controlled release : official journal of the Controlled Release Society.

[12]  Romano Lapasin,et al.  Structural Characterization of Calcium Alginate Matrices by Means of Mechanical and Release Tests , 2009, Molecules.

[13]  Rita Ambrus,et al.  Study of the parameters influencing the co-grinding process for the production of meloxicam nanoparticles , 2011 .

[14]  Emanuela Fabiola Craparo,et al.  PHEA-graft-polybutylmethacrylate copolymer microparticles for delivery of hydrophobic drugs. , 2012, International journal of pharmaceutics.

[15]  Shintaroh Iwanaga,et al.  Three-dimensional inkjet biofabrication based on designed images , 2011, Biofabrication.

[16]  Motohiro Uo,et al.  Microparticle formation and its mechanism in single and double emulsion solvent evaporation. , 2004, Journal of controlled release : official journal of the Controlled Release Society.

[17]  Cory Berkland,et al.  Precise control of PLG microsphere size provides enhanced control of drug release rate. , 2002, Journal of controlled release : official journal of the Controlled Release Society.

[18]  B. Gander,et al.  Kinetics of solvent extraction/evaporation process for PLGA microparticle fabrication. , 2008, International journal of pharmaceutics.

[19]  Catarina P Reis,et al.  Review and current status of emulsion/dispersion technology using an internal gelation process for the design of alginate particles , 2006, Journal of microencapsulation.

[20]  Makoto Nakamura,et al.  Development of a three-dimensional bioprinter: construction of cell supporting structures using hydrogel and state-of-the-art inkjet technology. , 2009, Journal of biomechanical engineering.

[21]  Takeshi Shimizu,et al.  Nanogel DDS enables sustained release of IL-12 for tumor immunotherapy. , 2008, Biochemical and biophysical research communications.

[22]  C. Arpagaus,et al.  Nano and microparticle engineering of water insoluble drugs using a novel spray-drying process. , 2012, Colloids and surfaces. B, Biointerfaces.

[23]  T. Okano,et al.  Inner core segment design for drug delivery control of thermo-responsive polymeric micelles. , 2000, Journal of controlled release : official journal of the Controlled Release Society.

[24]  Kai Yang,et al.  Molecular modeling of the relationship between nanoparticle shape anisotropy and endocytosis kinetics. , 2012, Biomaterials.

[25]  Robert Gurny,et al.  Fluorescent biodegradable PLGA particles with narrow size distributions: preparation by means of selective centrifugation. , 2007, International journal of pharmaceutics.

[26]  I. Hutchings,et al.  How PEDOT:PSS solutions produce satellite-free inkjets , 2012 .

[27]  A. Braeuer,et al.  High-pressure microfluidics for the investigation into multi-phase systems using the supercritical fluid extraction of emulsions (SFEE) , 2012 .

[28]  Peggy P Y Chan,et al.  Production of monodisperse epigallocatechin gallate (EGCG) microparticles by spray drying for high antioxidant activity retention. , 2011, International journal of pharmaceutics.

[29]  Akiko Ishii-Watabe,et al.  Evaluation of intracellular trafficking and clearance from HeLa cells of doxorubicin-bound block copolymers. , 2012, International journal of pharmaceutics.

[30]  F. Mi,et al.  Chitin/PLGA blend microspheres as a biodegradable drug-delivery system: phase-separation, degradation and release behavior. , 2002, Biomaterials.

[31]  A. Karydas,et al.  PLGA-mPEG nanoparticles of cisplatin: in vitro nanoparticle degradation, in vitro drug release and in vivo drug residence in blood properties. , 2002, Journal of controlled release : official journal of the Controlled Release Society.

[32]  T. Jesionowski,et al.  Preparation of the hydrophilic/hydrophobic silica particles , 2002 .

[33]  Lai Wah Chan,et al.  Evaluation of sodium alginate as drug release modifier in matrix tablets. , 2006, International journal of pharmaceutics.

[34]  G. Golomb,et al.  The relationship between drug release rate, particle size and swelling of silicone matrices , 1990 .

[35]  P. Choong,et al.  The performance of doxorubicin encapsulated in chitosan-dextran sulphate microparticles in an osteosarcoma model. , 2010, Biomaterials.

[36]  Kazuaki Matsumura,et al.  In Vivo Cancer Targeting of Water-Soluble Taxol by Folic Acid , 2011 .

[37]  H. Montaseri,et al.  Preparation and characterization of biodegradable paclitaxel loaded alginate microparticles for pulmonary delivery. , 2010, Colloids and surfaces. B, Biointerfaces.

[38]  Kenji Nakamura,et al.  Development of an oral sustained release drug delivery system utilizing pH-dependent swelling of carboxyvinyl polymer. , 2006, Journal of controlled release : official journal of the Controlled Release Society.

[39]  Ilia Fishbein,et al.  Lipophilic drug loaded nanospheres prepared by nanoprecipitation: effect of formulation variables on size, drug recovery and release kinetics. , 2002, Journal of controlled release : official journal of the Controlled Release Society.

[40]  J. Siepmann,et al.  Effect of the size of biodegradable microparticles on drug release: experiment and theory. , 2004, Journal of controlled release : official journal of the Controlled Release Society.

[41]  Sang Yong Lee,et al.  Size prediction of drops formed by dripping at a micro T-junction in liquid–liquid mixing , 2011 .

[42]  Gaurav Sahay,et al.  Endocytosis of nanomedicines. , 2010, Journal of controlled release : official journal of the Controlled Release Society.

[43]  I. Jeon,et al.  New insights into respirable protein powder preparation using a nano spray dryer. , 2011, International journal of pharmaceutics.

[44]  Jianhong Xu,et al.  Correlations of droplet formation in T-junction microfluidic devices: from squeezing to dripping , 2008 .

[45]  Jianhong Xu,et al.  Preparation of 10 μm scale monodispersed particles by jetting flow in coaxial microfluidic devices , 2013 .

[46]  Huaizhi Li,et al.  Droplet formation and breakup dynamics in microfluidic flow-focusing devices: From dripping to jetting , 2012 .

[47]  Delie,et al.  Evaluation of nano- and microparticle uptake by the gastrointestinal tract. , 1998, Advanced drug delivery reviews.

[48]  Moritz Beck-Broichsitter,et al.  Characterization of novel spray-dried polymeric particles for controlled pulmonary drug delivery. , 2012, Journal of controlled release : official journal of the Controlled Release Society.

[49]  Ali Nokhodchi,et al.  Glucosamine HCl as a new carrier for improved dissolution behaviour: effect of grinding. , 2010, Colloids and surfaces. B, Biointerfaces.

[50]  G. Alderborn,et al.  Drug release from reservoir pellets compacted with some excipients of different physical properties. , 2003, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

[51]  Say Chye Joachim Loo,et al.  Fabrication and drug release study of double-layered microparticles of various sizes. , 2012, Journal of pharmaceutical sciences.

[52]  V. Dinca,et al.  Influence of solution properties in the laser forward transfer of liquids , 2012 .

[53]  Timm Weitkamp,et al.  Three-dimensional quantification of capillary networks in healthy and cancerous tissues of two mice. , 2012, Microvascular research.

[54]  Makoto Nakamura,et al.  Ink Jet Three-Dimensional Digital Fabrication for Biological Tissue Manufacturing: Analysis of Alginate Microgel Beads Produced by Ink Jet Droplets for Three Dimensional Tissue Fabrication , 2008 .

[55]  Hui Gao,et al.  A novel delivery system of doxorubicin with high load and pH-responsive release from the nanoparticles of poly (α,β-aspartic acid) derivative. , 2012, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

[56]  Cui Tang,et al.  Effects of particle size and surface charge on cellular uptake and biodistribution of polymeric nanoparticles. , 2010, Biomaterials.

[57]  Clemens Burda,et al.  Nanoparticle mediated non-covalent drug delivery. , 2013, Advanced drug delivery reviews.

[58]  Jenny Andersson,et al.  Influences of Material Characteristics on Ibuprofen Drug Loading and Release Profiles from Ordered Micro- and Mesoporous Silica Matrices , 2004 .

[59]  Mauro Ferrari,et al.  Multi-stage delivery nano-particle systems for therapeutic applications. , 2011, Biochimica et biophysica acta.