Preface to Special Topic: Selected Papers from the 5th International Conference on Optofluidics

The 5th International Conference on Optofluidics (Optofluidics 2015) was held in Taipei, Taiwan, July 26–29, 2015. The aim of this conference was to provide a forum to promote scientific exchange and to foster closer networks and collaborative ties between leading international researchers in optics and micro/nanofluidics across various disciplines. The scope of Optofluidics 2015 was deliberately broad and interdisciplinary, encompassing the latest advances and the most innovative developments in micro/nanoscale science and technology. Topics ranged from fundamental research to its applications in chemistry, physics, biology, materials, and medicine.Approximately 300 delegates participated in Optofluidics 2015 from across the globe, including Australia, Canada, China, France, Germany, Hong Kong, India, Japan, Korea, Singapore, Taiwan, UK, and USA. In total, 242 presentations were arranged, including 10 plenary speeches, 27 keynote speeches, 65 invited talks, 33 contributed talks, and 107 poster presentations. This collection of twelve papers on this special topic spans both the fundamentals and the frontier applications of this interdisciplinary research field.Optical measurements of particle or flow and fluidic manipulation for optical applications were presented. Lin and Su¹ reported a novel method to measure the depth position of rapidly moving objects inside a microfluidic channel based on the chromatic aberration effect; the depth positions of label-free particles of diameter as small as 2 μm and erythrocytes of concentration 2 × 10³ cells/μl and velocity 2.78 mm/s were detected within a range ±25 μm in a simple and inexpensive manner. Sun and Huang² demonstrated the use of a microscopic circular polariscope to measure the flow-induced birefringence in a microfluidic device that represents the kinematics of fluid motion optically; CTAB:NaSal, CPyCl:NaSal, and CPyCl:NaSal:NaCl solutions were used to investigate the strain rate and the results were compared with the μPIV diagnosis. He et al.³ studied the fundamentals, especially the thinning and opening of the oil film within each pixel of an electrowetting display; to achieve repeatable oil movement and the resulting pixel performance, a new method to fill each pixel with a controllable oil volume using an oil-droplet emulsion created with a microfluidic device was demonstrated.This special topic includes papers also on particle manipulation. Weng et al.⁴ evaluated the size-dependent crossing frequency of dielectrophoretically driven particles; numerical simulation using a Maxwell stress tensor and a finite element method was reported to assess the size effect. In addition to electric manipulation, magnetic driving of the particles was demonstrated. Ido et al.⁵ examined microswimmers of magnetic particle chains in an oscillating magnetic field experimentally and analyzed numerically with a lattice Boltzmann method, an immersed boundary method, and a discrete particle method based on simplified Stokesian dynamics. Huang et al.⁶ described a technique to manipulate magnetic beads and achieved a great washing efficiency with zero bead loss using an appropriate electrode design and channel height of a digital microfluidic immunoassay; a model immunoassay of human soluble tumor necrosis factor receptor I (sTNF-RI) was performed to offer an improved limit of detection (3.14 pg/ml) with a small number of magnetic beads (25 beads), decreased reagent volumes (200 nl), and decreased duration of analysis (<1 h). Chiu et al.⁷ reported particle separation using cross-flow filtration enhanced with hydrodynamic focusing; label-free separation of particles of diameters 2.7 and 10.6 μm at a sample throughput 10 μl/min was performed; separation of spiked human prostate cancer cell lines (PC3) cells in whole blood was also demonstrated.Chemical sensors and biosensors are covered in this special topic. Cheng et al.⁸ measured the chemical compounds in third-hand smoke on varied clothing fibres with an analytical balance, or nicotine and 3-ethenylpyridine (3-EP) with a surface-acoustic-wave sensor composed of coated oxidized hollow mesoporous carbon nanospheres. Pu et al.⁹ described a continuous glucose monitoring microsystem consisting of a three-electrode electrochemical sensor in which the working electrode (WE) was covered with a single layer of graphene and gold nanoparticles to improve the sensor performance; the results of glucose measurement were linear below concentration 162 mg/dl with a detection limit 1.44 mg/dl. Li et al.¹⁰ implemented a microfluidic device measuring the glucose concentration with integrated fibre-optic surface plasmon resonance sensor and electrode pairs for volume quantification.Implantable devices and microneedles for drug delivery and liquid transport are addressed in this special topic. Zhang et al.¹¹ reported a flexible polyimide device seated under rabbit eyelids to deliver drug by iontophoresis; varied currents to release manganese ions (Mn²⁺) as tracers were investigated; the thermal effect on application of a current was studied. Lee et al.¹² presented a disposable Parylene microneedle array of large aspect ratio that vibrated with a piezoelectric actuator to mimic the vibrating motion of a mosquito''s proboscis and to decrease the insertion force by 40%. Song et al.¹³ demonstrated microinjection into a model organism, Caenorhabditis elegans (C. elegans) on an automated device capable of loading, immobilization, injection, and sorting; with 200 worms studied, injection speed 6.6 worm/min, injection success rate 77.5%, and sorting success rate 100% were obtained.We express our gratitude for the financial support from Ministry of Science and Technology (Taiwan), Bureau of Foreign Trade (Taiwan), National Taiwan University and Research Center for Applied Sciences of Academia Sinica, and for administrative support from Instrument Technology Research Center in making Optofluidics 2015 a successful conference. Our acknowledgements include Leslie Yeo, Frederick Kontur, Christine Urso, and all staff from Biomicrofluidics for their kind assistance during the preparation, and, most importantly, all authors who have contributed their work for this special topic.     

Preface to Special Topic: Microfluidics in Drug Delivery

In this special topic of Biomicrofluidics, the importance of microfluidics in the field of drug delivery is highlighted. Different aspects from cell-drug carrier interactions, delivery vehicle assembly to novel drug delivery devices are considered. The contributing reviews and original articles illustrate the synergistic outcomes between these two areas of research with the aim to have a positive impact on biomedical applications.Microfluidics is certainly one of the huge success stories when it comes to anticipated impact and fulfilled promises in academic research environments. Microfluidic approaches are game changers in many disciplines in natural science, including (bio)medical science. In the latter case, the fields of biosensing/diagnostics, tissue engineering, and drug discovery/delivery have benefited from concepts which allow for the fast throughput manipulation of fluids at the submillimeter length scale.A key aim in microfluidic-assisted drug discovery is the development of strategies which will facilitate the identification of potential “hits”—new drugs with the anticipated therapeutic benefit. In this context, “organ(disease)-on-chips” are considered as highly sophisticated in vitro models with lower cost and less ethical issues compared to extensive testing in animals. This technology is still very young with countless research challenges to be addressed and eventually overcome, but the few current reports are promising, and include “gut-on-chip,” “cancer-on-chip,” or “blood vessel-on-chip.” Additionally, intravenously injected drug delivery vehicles are exposed to the blood stream and the induced mechanical forces which are likely to affect their interaction with cells and tissue. Therefore, understanding the diffusion phenomena of biomolecules in microfluidic devices as reviewed by Yesil-Celiktas and coworkers in the current special content is crucial.¹ What is more, the contribution by Hosta-Rigau and colleagues provides a comprehensive overview over the interaction of drug carriers and cells in microfluidic-based systems which deliver a simple, but yet more realistic model of the dynamic in vivo situation.² Further, to illustrate the relevance of shear stress when assessing the potential of nanocarriers for drug delivery applications, we assembled novel block copolymers consisting of poly(cholesteryl acrylate) as the hydrophobic core and poly(N-isopropylacrylamide) as the hydrophilic extensions together with lipids into vesicles using the evaporation-rehydration method.³ Following on, we biologically evaluated the assemblies with applied shear stress using macrophages. In a related report by the Chakraborty group, a biocompatible acoustic microfluidic system was outlined including the effect of microbubbles with the applied acoustic field on biological cells.⁴From a different perspective, droplet microfluidics has become a popular method to assemble a huge diversity of particles of different size, shape, and morphology equipped with options for active or passive drug release. Microfluidics provides unique opportunities and flexibility to fabricate decent amounts of mono-disperse drug carriers using monomers, polymers, lipids, or inorganic precursor materials as building blocks. The assembly of size-tunable polymer/lipid particles by Sun et al.,⁵ and the fabrication of poly (lactic-co-glycolic acid) nanoparticles incorporated within poly (ethylene glycol) (PEG) microgels by the Chen group,⁶ provide interesting examples in this context. Further, artefacts associated with this technique have to be addressed and understood to avoid inaccurate and misleading data as reported by Litten et al.⁷ Microfluidic techniques can also be employed for cell encapsulation. Fan et al. demonstrated the trapping of human colon cancer cells in hydrogel particles with preserved viability and response to inflammatory stimuli.⁸Novel drug delivery devices which consider microfluidic concepts and set-ups are an interesting addition to traditional approaches. Implantable drug delivery systems provide an alternative to ensure constant drug level in blood without relying on the compliance of the patient while circumventing challenges involved in oral drug delivery coming from drug instability or limited absorbance among others. Yi and coworkers propose a reservoir approach in combination with a heat responsive valve towards the long term delivery of solid drugs.⁹ What is more, nebulizers, as alternative to inhalers for pulmonary drug delivery, suffer from miniaturization and drug degradation issues. Cortez-Jugo et al. report on a novel portable acoustomicrofluidic device, which successfully nebulized monoclonal antibodies into a fine aerosol mist including the first positive biological evaluation.¹⁰Further, combining microfluidics with sensing concepts as illustrated by Knoll and coworker¹¹ is of importance, since the design of drug delivery vehicles strongly relies on the fundamental understanding of the interaction between biomolecules, cells, and tissue.Taken together, these articles give an overview over the use of microfluidics in the area of drug delivery, which goes beyond the assembly of drug carries, but also provides a platform for their biological evaluation or the design of entirely new drug delivery devices. I hope that this collection of articles will stimulate new ideas and future collaborations between engineers/chemists/physicist and biologists towards the common goal to provide solutions for biomedical challenges. Finally, I would like to thank Professor Leslie Yeo for the invitation to be the guest editor for this special topic, and Christine Urso and other editorial and production staffs of Biomicrofluidics for making it a reality.     

Preface to Special Topic: Papers from the 13th International Conference on Surface and Colloid Science (ICSCS) and the 83rd ACS Colloid and Surface Science Symposium, Columbia University, New York, 2009

This Special Topic section is a compilation of several original contributions covering both fundamental and practical aspects of electrokinetic microfluidic phenomena that were presented during the Electrokinetics and Microfluidics sessions held at the conference.Electrokinetics is currently the mechanism of choice for the manipulation of fluids as well as colloidal and biological particles at microscale and nanoscale dimensions.¹ The popularity of electrokinetics is perhaps not so surprising as electrodes are easy to fabricate and embed into microfluidic chips, thus allowing the entire fluid and particle actuation mechanism to be completely integrated into the device. In addition, driving microfluidics with electric fields is relatively straightforward and allows for precise actuation. Nevertheless, considerable challenges remain in understanding the complex mechanisms associated with the hydrodynamics of conducting and dielectric fluids and particles under the influence of electric fields. Concomitantly, there has been an exponential increase in research and development in this field along both fundamental and applied themes in the past five years.This sustained growth in the microfluidics community of electrokinetics research has led to a sequel to the first Electrokinetic Phenomena and Microfluidics session at the 82nd ACS Colloid and Surface Science Symposium in Raleigh, NC, in 2008, and which we hope will now be a regular feature at successive ACS Colloid and Surface Science meetings. This year at the combined 2009 13th International Conference on Surface and Colloid Science (ICSCS) and the 83rd ACS Colloid and Surface Science Symposium in New York, the Electrokinetics and Microfluidics symposium proved to be extremely popular, with three keynote lectures presented by Professor Howard Stone, Professor Hsueh-Chia Chang, and Professor Thomas Healy, and 44 oral presentations. In both 2008 and 2009, Biomicrofluidics has organized a special issue to cover some of the contributions reported at these meetings.²The growing interest in using electric fields to manipulate biological entities such as cells, DNA, and even single molecules is reflected in this year’s collection of papers with dielectrophoretic (DEP) phenomena comprising the bulk of the contributions. In Ref. ³, a new theory to describe Stern layer conductance along the surface of nanocolloids is proposed, forming the basis for the derivation of a more accurate prediction of the DEP crossover frequency. This theory is then employed to determine the conformation and, hence, optimum coverage of oligonucleotides on the surface of nanocolloid functionalized molecular probes during DNA hybridization under the influence of DEP, which can be exploited for biomolecular sensing. Other fundamental DEP papers include the investigation of particle motion under DEP induced optically via a photoconductor, in which Zhu et al.⁴ characterized the frequency dependence of the motion through the synchronous velocity spectra of the particles, and a numerical study of particle trapping at the throat of converging-diverging microchannels under the influence of negative DEP using a transient arbitrary Lagrangian–Eulerian finite element method.⁵ A more practical implementation is, on the other hand, reported by Yang et al.⁶ in which the negative DEP is exploited to separate colorectal cancer cells from other cells in a microfluidic device as a demonstration of a portable cancer detection tool.Continuing along the separation theme, but with regard to DNA separation using pulsed-field gel electrophoresis aided by sparse but regularly ordered microfabricated arrays of nanoposts, is a Brownian dynamics simulation model reported by Ou et al.⁷ in which DNA channeling, which predicts that the motion of DNA is undisturbed by the presence of arrays for large spacing to DNA equilibrium size ratios and when the field lines are straight, is predicted, consistent with experimental observations. In another fundamental paper, a direct numerical simulation model is presented to predict the current-voltage relationship across conducting pores along cell membranes, which is of fundamental importance in the electroporation process.⁸We hope that you will enjoy reading the contributions in this special topic and that it encourages you to participate in future Electrokinetics and Microfluidics meetings at the ACS Colloid and Surface Science Symposia, which we definitely hope will continue on a regular basis.     

Preface to Special Topic: Microfluidics in cell biology and tissue engineering

In this special issue of Biomicrofluidics, a wide variety of applications of microfluidics to tissue engineering and cell biology are presented. The articles illustrate the benefits of using microfluidics for controlling the cellular environment in a precise yet high rate manner using minimum reagents. The topic is very timely and takes a stab at portraying a glimpse of what is to come in this exciting and emerging field of research.     

Preface to Special Topic: Papers from the 82nd American Chemical Society Colloid and Surface Science Symposium, Raleigh, North Carolina, 2008

This Special Topic section of Biomicrofluidics contains original contributions that were presented at the 82nd Colloid and Surface Science Symposium, which took place on 15–18 June 2008 at North Carolina State University. The Symposium covered a wide range of topics that are relevant to the fundamentals of fluidics and their application to biological systems.The recent interest in microfluidics and nanofluidics is constantly increasing due to the numerous applications that these techniques have to offer. They have been used for chemical and biomolecular sensing, separation of charged analytes, and single DNA molecule manipulation. These applications were facilitated by the significant increase in the range of advanced microfabrication and nanofabrication techniques. Improving and extending the range of applicability of micro- and nanofluidic techniques also requires better fundamental understanding of the physics of the transport at small length scales. The transport of fluids and solutes in microchannels and nanochannels usually occurs at very small Reynolds regime. The typical length scale and the surface forces (electrostatic, van der Waals, hydrophobic, hydration, etc.) may be comparable to the size of the channels. All these features often require the development of new experimental techniques and approaches for theoretical analysis.The importance and the substantial recent interest in micro- and nanofluidics prompted the organization of a special session on Electrokinetic Phenomena and Microfluidics as part of the program at the 82nd Colloid and Surface Science Symposium at North Carolina State University in June 2008. The collected papers in this issue of Biomicrofluidics cover some of the very important fundamental and engineering aspects of electrokinetic phenomena in micro- and nanofluidic channels. These include molecular dynamics simulation of biomolecules in confined spaces, analysis of the electric double layer effects on the fluid flow in nanochannels, hydrodynamic resistance to droplet motion in microchannels, electrophoresis in nanocomposite gels, and microfluidics for nanoparticle fabrication. The paper by Srivastava et al.¹ explores the possibility of using microfluidics for fabrication of Janus nanofibers. Chang² presented a theoretical analysis of the electro-osmosis on a salt-free microchannel by simultaneously solving the nonlinear Poisson–Boltzmann equation for the electrostatic potential distribution and the Navier–Stokes equations for the fluid flow. Trahan and Doyle³ reported theoretical analysis of DNA molecule interaction with obstacles in a microchannel. Finally, Labrot et al.⁴ presented studies on the droplet hydrodynamic resistance in a microfluidic channel.We hope that the reader will find the papers useful and informative.     

Preface to Special Topic: Biological microfluidics in tissue engineering and regenerative medicine

In this special issue of Biomicrofluidics, many manifestations of biological microfluidics have been highlighted that have significance to regenerative biology and medicine. The collated articles demonstrate the applicability of these biological microfluidics for studying a wide range of biomedical problems most useful for understanding and shining light on basic biology to those applications relevant to clinical medicine.     

从国际社会的评价看香港回归15年来的科技创新发展

香港回归15年来,特区政府相继出台一系列旨在提升科技创新能力的施政措施,并取得显著成效。本文从国际社会公认的几大主要评价报告中抽取出1997至2012年间香港以及台湾、新加坡和韩国的数据,按照时间坐标进行排列对比和分析,以求揭示15年来国际社会对香港在科技创新方面的评价及其演变趋势。最后基于香港科技创新能力优劣势分析,提出了相应的建议,以供相关部门和人员参考。     

粤港澳大湾区科技服务协同创新体系建设研究

科技服务协同创新体系是粤港澳大湾区创新资源高效配置的新范式。为回答“谁在协同,为谁协同,怎么协同”这一协同创新体系构建中迫切需要解决的理论问题,通过总结科技服务协同创新体系内涵与发展过程,基于粤港澳大湾区科技服务发展现状以及科技服务协同创新理论上的“黑箱”,构建以科技服务组织为核心驱动的,由高校知识生产体系、机构技术研发体系、创新企业发展体系、科技中介服务体系等4个子系统构成的科技服务协同创新体系,并基于主体联动的视角提出,通过加强科技服务机构与企业、研发机构和高校的协同,提升科技服务水平来推动粤港澳大湾区科技服务协同创新体系建设发展。     

论文合著视角下粤港科技合作的演变特征研究

[目的/意义]基于合著的视角,研究粤港科技论文合作的发展过程,明确粤港科技合作的特征。[方法/过程]采用社会网络分析方法,以科技论文的单位为节点,以合作关系为边,通过Netdraw分析工具绘制粤港科技合作网络,并进行相关统计分析。[结果/结论]首先,早期粤港合作水平不及京港与沪港,而2008年之后两地科技合作得到迅猛发展。其次,粤港科技论文合作网络呈现核心-边缘结构特征,如香港大学、香港中文大学、中山大学等实力较强的科研机构处于网络的中心地位,而实力较弱的则位于边缘位置。最后,粤港间合作的相对强度不及港粤,需进一步加强广东省同香港间的科技交流,通过两地科技优势互补,共同推动粤港澳大湾区科创中心建设。     

理工医类研究生发表论文的现状分析与思考——以暨南大学为例

采用发表论文数、研究生招生人数等指标,结合2008-2012年暨南大学理工医类研究生发表论文的相关数据,进行学科、期刊级别等方面横纵向对比分析。研究发现当前理工医类研究生发表论文质量有了一定的提升,但由于研究生培养机制和培养模式的滞后使得理工医类研究生科研能力仍有待加强。最后本文针对暨南大学和其他高校存在的问题提出提高科研能力的建议和途径。     

《科技管理研究》1981—2015 年刊文计量分析

知识图谱是一种用以对文献计量进行分析的工具。基于知识图谱的视角,借助CiteSpace 软件对《科技管理研 究》1981—2015 年的刊文进行文献计量分析,透析《科技管理研究》创刊35 年来所刊文研究的知识脉络、发文核 心作者与机构、热点关键词的演变、被引用等情况。     

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研究国际创新中心的概念内涵、主要特征、发展和演进,在此基础上深入研究国际科技创新中心的四大核心组成体系,并提出粤港澳大湾区国际科技创新中心建设的对策建议.