다중혈관 관상동맥 환자에서 y-문합을 이용하여 양쪽 내흉동맥만을 사용한 우회술의 조기 성적

Surface topographical factors influencing bacterial attachment

Erratum : An Overview of Injectable Polymeric Hydrogels for Tissue Engineering

In it for the long haul: Clusters of Pt nanowires (3D Pt nanoassemblies, Pt NA) serve as an electrocatalyst for low-temperature fuel cells. These Pt nanoassemblies exhibit remarkably high stability following thousands of voltage cycles and good catalytic activity, when compared with a commercial Pt catalyst and 20 % wt Pt catalyst supported on carbon black (20 % Pt/CB).

Self-Supported Interconnected Pt Nanoassemblies as Highly Stable Electrocatalysts for Low-Temperatur

While the bulk of the finished microbial genomes sequenced to date are derived from cultured bacterial and archaeal representatives, the vast majority of microorganisms elude current culturing attempts, severely limiting the ability to recover complete or even partial genomes from these environmental species. Single cell genomics is a novel culture-independent approach, which enables access to the genetic material of an individual cell. No single cell genome has to our knowledge been closed and finished to date. Here we report the completed genome from an uncultured single cell of Candidatus Sulcia muelleri DMIN. Digital PCR on single symbiont cells isolated from the bacteriome of the green sharpshooter Draeculacephala minerva bacteriome allowed us to assess that this bacteria is polyploid with genome copies ranging from approximately 200-900 per cell, making it a most suitable target for single cell finishing efforts. For single cell shotgun sequencing, an individual Sulcia cell was isolated and whole genome amplified by multiple displacement amplification (MDA). Sanger-based finishing methods allowed us to close the genome. To verify the correctness of our single cell genome and exclude MDA-derived artifacts, we independently shotgun sequenced and assembled the Sulcia genome from pooled bacteriomes using a metagenomic approach, yielding a nearly identical genome. Four variations we detected appear to be genuine biological differences between the two samples. Comparison of the single cell genome with bacteriome metagenomic sequence data detected two single nucleotide polymorphisms (SNPs), indicating extremely low genetic diversity within a Sulcia population. This study demonstrates the power of single cell genomics to generate a complete, high quality, non-composite reference genome within an environmental sample, which can be used for population genetic analyzes.

One Bacterial Cell, One Complete Genome

Biomedical Applications of Diamond-Like Nanocomposite Thin Films

Metallic nanoparticles have found various biomedical applications due to their intrinsic physicochemical properties. As the size decreases, the high surface area of particles gives rise to distinctive features, which are entirely different from that of a macro-sized structure. Several methods are involved in synthesizing metallic nanoparticles, and in general, it can be categorized into either bottom-up or top-down approaches. The top-down method consists of cutting down the bulk materials into nano-sized particles through physical, chemical, or mechanical treatments, whereas, in a bottom-up approach, nanoparticles are formed by joining individual atoms or molecules. The top-down approach produces metallic nanoparticles in naked form, which can further agglomerate and hence not suitable for biomedical applications. The bottom-up approach involves solid-state, liquid state, gas phase, biological, microfluidic-technology based, and other methods. Chemical reduction in the bottom-up approach is the most common method of metallic nanoparticle synthesis, which is flexible, simpler, inexpensive, and produces particles in homogenous form. Recently biological method of nanoparticle synthesis has become popular due to its toxic-free nature, inexpensiveness, sustainability, and eco-friendly. In this chapter, we describe the top-down and bottom-up approach and current trends in the synthesis of metallic nanoparticles for biomedical purposes. Further, it explains how the parameters can be tuned to get metallic nanoparticles with the desired shape, size, morphology, composition and crystallinity.

Metallic nanoparticles for biomedical applications

Optical Manipulation of Cells

The introduction of foreign cargo into living cells with high delivery efficiency and cell viability is a challenge in cell biology and biomedical research. Here, we demonstrate a nanosecond pulse laser-activated photoporation for highly efficient intracellular delivery using titanium dioxide (TiO2) microspikes as a substratum. The TiO2 microspikes were formed on titanium (Ti) substrate using an electrochemical anodization process. Cells were cultured on top of the TiO2 microspikes as a monolayer, and the biomolecule was added. Due to pulse laser exposure of the TiO2 microspike-cell membrane interface, the microspikes heat up and induce cavitation bubbles, which rapidly grow, coalesce and collapse to induce explosion, resulting in very strong fluid flow at the cell membrane surface. Thus, the cell plasma membrane disrupts and creates transient nanopores, allowing delivery of biomolecules into cells by a simple diffusion process. By this technique, we successfully delivered propidium iodide (PI) dye in HeLa cells with high delivery efficiency (93%) and high cell viability (98%) using 7 mJ pulse energy at 650 nm wavelength. Thus, our TiO2 microspike-based platform is compact, easy to use, and potentially applicable for therapeutic and diagnostic purposes.

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Tuhin Subhra Santra

Papers

Biomedical Applications of Diamond-Like Nanocomposite Thin Films

Metallic nanoparticles for biomedical applications

Optical Manipulation of Cells

Fabrication of TiO2 microspikes for highly efficient intracellular delivery by pulse laser-assisted photoporation.

Electrochemical fabrication of TiO2 micro-flowers for an efficient intracellular delivery using nanosecond light pulse.