Stem cell transplantation has been recognized as a promising strategy to induce the regeneration of injured and diseased tissues and sustain therapeutic molecules for prolonged periods in vivo. However, stem cell-based therapy is often ineffective due to low survival, poor engraftment, and a lack of site-specificity. Hydrogels can offer several advantages as cell delivery vehicles, including cell stabilization and the provision of tissue-like environments with specific cellular signals; however, the administration of bulk hydrogels is still not appropriate to obtain safe and effective outcomes. Hence, stem cell encapsulation in uniform micro-sized hydrogels and their transplantation in vivo have recently garnered great attention for minimally invasive administration and the enhancement of therapeutic activities of the transplanted stem cells. Several important methods for stem cell microencapsulation are described in this review. In addition, various natural and synthetic polymers, which have been employed for the microencapsulation of stem cells, are reviewed in this article.

Stretching and folding, diffusion, and breakup are three basic processes that occur while mixing fluids. Although stretching and folding the interface of two fluids by rotation enables the mixing at microscale level in both low and high Reynolds number flows, rotation is not as effective at a low Reynolds number as at a high Reynolds number. Therefore, developing a rapid micromixer for microfluidic systems that can be used at a low Reynolds number is a challenging task, because it can demonstrate the full potential of microfluidic systems in commercial markets. Here, to enhance the mixing efficiency of a micromixer based on passive rotation, we present a breakup method. The breakup method not only generates interface actively but also enhances the diffusion process at the interface. With our novel design, over 70% mixing can be achieved only after passing through a 4 mm long microchannel. In this work, the mixer was easily fabricated with polydimethylsiloxane by soft lithography and a self-aligned bonding method with methanol. We analyzed the flow in the micromixer using the computational fluid dynamics method. Also, we conducted quantitative analyses using a confocal scanning microscope and image processing.

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Plants produce a myriad of specialized metabolites to overcome their sessile habit and combat biotic as well as abiotic stresses. Evolution has shaped the diversity of specialized metabolites, which then drives many other aspects of plant biodiversity. However, until recently, large-scale studies investigating the diversity of specialized metabolites in an evolutionary context have been limited by the impossibility of identifying chemical structures of hundreds to thousands of compounds in a time-feasible manner. Here we introduce a workflow for large-scale, semi-automated annotation of specialized metabolites and apply it to over 1000 metabolites of the cosmopolitan plant family Rhamnaceae. We enhance the putative annotation coverage dramatically, from 2.5% based on spectral library matches alone to 42.6% of total MS/MS molecular features, extending annotations from well-known plant compound classes into dark plant metabolomics. To gain insights into substructural diversity within this plant family, we also extract patterns of co-occurring fragments and neutral losses, so-called Mass2Motifs, from the dataset; for example, only the Ziziphoid clade developed the triterpenoid biosynthetic pathway, whereas the Rhamnoid clade predominantly developed diversity in flavonoid glycosides, including 7-O-methyltransferase activity. Our workflow provides the foundations for the automated, high-throughput chemical identification of massive metabolite spaces, and we expect it to revolutionize our understanding of plant chemoevolutionary mechanisms.

In this paper, we present a novel flow manipulation and signal detection scheme for a microfabricated fluorescence-