Nanotechnology offers many advantages in various fields of science. In this regard, nanoparticles are the essential building blocks of nanotechnology. Recent advances in nanotechnology have proven that nanoparticles acquire a great potential in medical applications. Formation of stable interactions with ligands, variability in size and shape, high carrier capacity, and convenience of binding of both hydrophilic and hydrophobic substances make nanoparticles favorable platforms for the target-specific and controlled delivery of micro- and macromolecules in disease therapy. Nanoparticles combined with the therapeutic agents overcome problems associated with conventional therapy; however, some issues like side effects and toxicity are still debated and should be well concerned before their utilization in biological systems. It is therefore important to understand the specific properties of therapeutic nanoparticles and their delivery strategies. Here, we provide an overview on the unique features of nanoparticles in the biological systems. We emphasize on the type of clinically used nanoparticles and their specificity for therapeutic applications, as well as on their current delivery strategies for specific diseases such as cancer, infectious, autoimmune, cardiovascular, neurodegenerative, ocular, and pulmonary diseases. Understanding of the characteristics of nanoparticles and their interactions with the biological environment will enable us to establish novel strategies for the treatment, prevention, and diagnosis in many diseases, particularly untreatable ones.
The importance of high transfection efficiency has been emphasized in many studies investigating methods to improve gene delivery. Accordingly, non-viral transfection agents are widely used as transfection vectors to condense oligonucleotides, DNA, RNA, siRNA, deliver into the cell, and release the cargo. Polyethyleneimine (PEI) is one of the most popular non-viral transfection agents. However, the challenge between high transfection efficiency and toxicity of the polymers is not totally resolved. The delivery of necessary drugs and genes for patients and their transport under safe conditions require carefully designed and controlled delivery systems and constitute a critical stage of patients' treatment. Compact systems are considered as the strongest candidate for the preparation and delivery of drugs and genes under leak free and safe conditions because of their low energy consumption, low waste disposal, parallel and fast processing capabilities, removal of human factor, high mixing capabilities, enhanced safety, and low amount of reagents. Motivated by this need in the literature, a platform for gene delivery via magnetic actuation of nanoparticles was developed in this study. The use of PEI-SPION (Super paramagnetic ironoxide nanoparticles) as transfection agents in in vitro studies was investigated with the effect of varying magnetic fields provided by a special magnetic system design, which was used as magnetic actuator offering different magnet's turn speeds and directions in the system. Results obtained from magnetic actuator systems were compared to the experiments without actuation and significant enhancement was observed in the transfection efficacies.
Gene therapy is a developing method for the treatment of various diseases. For this purpose, the search for nonviral methods has recently accelerated to avoid toxic effects. A strong alternative method is magnetofection, which involves the use of superparamagnetic iron oxide nanoparticles (SPIONs) with a proper organic coating and external magnetic field to enhance the localization of SPIONs at the target site. In this study, a new magnetic actuation system consisting of four rare-earth magnets on a rotary table was designed and manufactured to obtain improved magnetofection. As a model, green fluorescent protein DNA-bearing polyethyleneimine-coated SPIONs were used. Magnetofection was tested on MCF7 cells. The system reduced the transfection time (down to 1 h) of the standard polyethyleneimine transfection protocol. As a result, we showed that the system could be effectively used for gene transfer.
occur at the second outlet of each channel. The efficiency of enrichment was observed in the microchannel with 500 µm width as high as 93 %. Our results suggest that these curved channels can be regarded as a prototype of a microfluidic diagnostic device due to their fast reaction time, relatively accurate results, low cost and miniaturized features.
Hydrodynamic cavitation is one of the major phase change phenomena and occurs with a sudden decrease in the local static pressure within a fluid. With the emergence of microelectromechanical systems (MEMS), high-speed microfluidic devices have attracted considerable attention and been implemented in many fields, including cavitation applications. In this study, a new generation of ‘cavitation-on-a-chip’ devices with eight parallel structured microchannels is proposed. This new device is designed with the motivation of decreasing the upstream pressure (input energy) required for facile hydrodynamic cavitation inception. Water and a poly(vinyl alcohol) (PVA) microbubble (MB) suspension are used as the working fluids. The results show that the cavitation inception upstream pressure can be reduced with the proposed device in comparison with previous studies with a single flow restrictive element. Furthermore, using PVA MBs further results in a reduction in the upstream pressure required for cavitation inception. In this new device, different cavitating flow patterns with various intensities can be observed at a constant cavitation number and fixed upstream pressure within the same device. Moreover, cavitating flows intensify faster in the proposed device for both water and the water–PVA MB suspension in comparison to previous studies. Due to these features, this next-generation ‘cavitation-on-a-chip’ device has a high potential for implementation in applications involving microfluidic/organ-on-a-chip devices, such as integrated drug release and tissue engineering.
During the last decade, hydrodynamic cavitation has been implemented in various applications such as energy harvesting and biomedical applications. Facile hydrodynamic cavitation methods are required for fulfilling the requirements in these applications. In this study, a new generation microfluidic device containing eight parallel micro-orifices with a new design was fabricated and tested with the purpose of intensifying the cavitating flows and early cavitation inception. The roughness elements in the micro-orifices facilitated cavitation inception. This study presents a general perspective of occurrence of different cavitating flow patterns in microscale and addresses the ambiguities about the conditions for the formation of a specific flow pattern. Cavitation inception occurred with the appearance of small bubbles emerging from roughness elements at a rather low upstream pressure in the open loop experimental setup. A reduction in the cavitation number resulted in the formation of different flow patterns such as cavitation clouds, twin cavities, sheet cavities, and bubbly flows. Having several flow patterns with different intensities all together within a single microfluidic device is the main advantage of the proposed device over the state of the art microfluidic devices. Generation of flow patterns with various released energy levels makes this proposed device a unique multi-functional platform, which can be implemented to a lab on a chip platform for applications such as nanoparticle synthesis and wound healing.
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