Functional polymeric microparticles engineered from controllable microfluidic emulsions.

Functional polymeric microparticles with typical sizes of 1-1000 μm have received considerable attention for many applications. Especially in biomedical fields, polymeric microparticles with advanced functions such as targeted delivery, controlled encapsulation, or "capture and release" show great importance as delivery systems for active molecules and drugs, as imaging agents for analytics and diagnostics, as microreactors for confined bioreactions, and more. Generally, the functions of these microparticles rely on both their structures and the properties of their component materials. Thus, creating unique structures from functional materials provides an important strategy for developing advanced functional polymeric microparticles. Several methods, such as dispersion polymerization, precipitation polymerization, copolymer self-assembly, and phase-separated polymer precipitation can be used to make functional microparticles, but each has limitations, for example, their limited control over the particle size and structure. Using emulsions as templates, however, allows precise control over the size, shape, composition, and structure of the resulting microparticles by tuning those of the emulsions via specific emulsification techniques. Microfluidic methods offer excellent control of emulsion droplets, thereby providing a powerful platform for continuous, reproducible, scalable production of polymeric microparticles with unprecedented control over their monodispersity, structures, and compositions. This approach provides broad opportunities for producing polymeric microparticles with novel structure-property combinations and elaborately designed functions. In this Account, we highlight recent efforts in microfluidic fabrication of advanced polymeric microparticles with well-designed functions for potential biomedical applications, and we describe the development of microfluidic techniques for producing monodisperse and versatile emulsion templates. We begin by describing microparticles made from single emulsions and then describe those from complex multiple emulsions, showing how the resulting microparticles combine novel structures and material properties to achieve their advanced functions. Monodisperse emulsions enable production of highly uniform microparticles of desired sizes to achieve programmed release rates and passive targeting for drug delivery and diagnostic imaging. Phase-separated multiple emulsions allow combination of a variety of functional materials to generate compartmental microparticles including hollow, core-shell, multicore-shell, and hole-shell structures for controlled encapsulation and release, selective capture, and confined bioreaction. We envision that the versatility of microfluidics for microparticle synthesis could open new frontiers and provide promising and exciting opportunities for fabricating new functional microparticles with broad implications for myriad fields.

[1]  Alexander F. Routh,et al.  Formation of liquid core-polymer shell microcapsules. , 2006, Soft matter.

[2]  Yuanjin Zhao,et al.  Biodegradable core-shell carriers for simultaneous encapsulation of synergistic actives. , 2013, Journal of the American Chemical Society.

[3]  Younan Xia,et al.  Microscale polymer bottles corked with a phase-change material for temperature-controlled release. , 2013, Angewandte Chemie.

[4]  L. Chu,et al.  K(+)-recognition capsules with squirting release mechanisms. , 2011, Chemical communications.

[5]  A. Lamprecht,et al.  Effect of the microencapsulation of nanoparticles on the reduction of burst release. , 2007, International journal of pharmaceutics.

[6]  G. Whitesides,et al.  Soft Lithography. , 1998, Angewandte Chemie.

[7]  R Langer,et al.  Responsive polymeric delivery systems. , 2001, Advanced drug delivery reviews.

[8]  G. Whitesides,et al.  Poly(dimethylsiloxane) as a material for fabricating microfluidic devices. , 2002, Accounts of chemical research.

[9]  Liang-Yin Chu,et al.  Microfluidic fabrication of monodisperse microcapsules for glucose-response at physiological temperature , 2013 .

[10]  Wei Wang,et al.  A novel thermo-induced self-bursting microcapsule with magnetic-targeting property. , 2009, Chemphyschem : a European journal of chemical physics and physical chemistry.

[11]  Mansoor M Amiji,et al.  Gastrointestinal distribution and in vivo gene transfection studies with nanoparticles-in-microsphere oral system (NiMOS). , 2007, Journal of controlled release : official journal of the Controlled Release Society.

[12]  Ruba Khnouf,et al.  Stable, biocompatible lipid vesicle generation by solvent extraction-based droplet microfluidics. , 2011, Biomicrofluidics.

[13]  R. Langer,et al.  Drug delivery and targeting. , 1998, Nature.

[14]  D. Weitz,et al.  Monodisperse Double Emulsions Generated from a Microcapillary Device , 2005, Science.

[15]  Christian Holtze,et al.  High throughput production of single core double emulsions in a parallelized microfluidic device. , 2012, Lab on a chip.

[16]  Robert Langer,et al.  Preparation of monodisperse biodegradable polymer microparticles using a microfluidic flow-focusing device for controlled drug delivery. , 2009, Small.

[17]  Liang-Yin Chu,et al.  Smart thermo-triggered squirting capsules for nanoparticle delivery , 2010 .

[18]  L. Chu,et al.  Microfluidic Preparation of Multicompartment Microcapsules for Isolated Co-encapsulation and Controlled Release of Diverse Components , 2012 .

[19]  D. Weitz,et al.  Microfluidic synthesis of monodisperse porous microspheres with size-tunable pores , 2012 .

[20]  Shin‐Hyun Kim,et al.  Microfluidic fabrication of photo-responsive hydrogel capsules. , 2013, Chemical communications.

[21]  G. Whitesides The origins and the future of microfluidics , 2006, Nature.

[22]  B. Voit,et al.  Progress on multi-compartment polymeric capsules , 2013 .

[23]  V. Torchilin,et al.  Biodegradable long-circulating polymeric nanospheres. , 1994, Science.

[24]  I. Chen,et al.  Biomedical nanoparticle carriers with combined thermal and magnetic responses , 2009 .

[25]  B. Stoeber,et al.  Lung perfusion imaging with monosized biodegradable microspheres. , 2010, Biomacromolecules.

[26]  Mitsutoshi Nakajima,et al.  Production of uniform droplets using membrane, microchannel and microfluidic emulsification devices , 2012 .

[27]  K. Roy,et al.  Nano-inside-micro: Disease-responsive microgels with encapsulated nanoparticles for intracellular drug delivery to the deep lung. , 2012, Journal of controlled release : official journal of the Controlled Release Society.

[28]  Wei Wang,et al.  Controllable microfluidic production of multicomponent multiple emulsions. , 2011, Lab on a chip.

[29]  Ho Cheung Shum,et al.  Microfluidic melt emulsification for encapsulation and release of actives. , 2010, ACS applied materials & interfaces.

[30]  Wei Wang,et al.  Simple and cheap microfluidic devices for the preparation of monodisperse emulsions. , 2011, Lab on a chip.

[31]  U. Häfeli,et al.  Uniform polymer microspheres: monodispersity criteria, methods of formation and applications. , 2013, Nanomedicine.

[32]  Wei Wang,et al.  Monodisperse core-shell chitosan microcapsules for pH-responsive burst release of hydrophobic drugs , 2011 .

[33]  S. Wise Nanocarriers as an emerging platform for cancer therapy , 2007 .

[34]  Wei Wang,et al.  Hole-shell microparticles from controllably evolved double emulsions. , 2013, Angewandte Chemie.

[35]  Liang-Yin Chu,et al.  Designer emulsions using microfluidics , 2008 .

[36]  Liang-Yin Chu,et al.  Controllable monodisperse multiple emulsions. , 2007, Angewandte Chemie.

[37]  Shoji Takeuchi,et al.  Microfluidic formation of monodisperse, cell-sized, and unilamellar vesicles. , 2009, Angewandte Chemie.

[38]  Howard A. Stone,et al.  ENGINEERING FLOWS IN SMALL DEVICES , 2004 .