Inflammation is often accompanied by glioblastoma cells(GBMs)and is considered a key factor for GBM growth.This feature is believed to be connected with the tryptophan pathway mainly affected by intestinal microbes si...Inflammation is often accompanied by glioblastoma cells(GBMs)and is considered a key factor for GBM growth.This feature is believed to be connected with the tryptophan pathway mainly affected by intestinal microbes since the concept of gut-brain axis(GBA)has been proposed.Here we present a microchip model co-culturing intestinal cells(Caco2),microbes(E.coli),and GBM cells(U87)to study inflammatory responses of GBM by investigating the tryptophan metabolism.E.coli after encapsulating with alginate hydrogel microparticles(AHMPs)was seeded in the microchip where Caco2 was located,forming the simulated system of intestinal physiology and avoiding excessive reproduction of microbes.Continuous flow was applied to maintain the cell viability,induce the morphogenesis,and simulate the tryptophan transportation in GBA.The morphological alterations of Caco2 and U87 were characterized by fluorescence imaging and the tryptophan metabolism,especially the tryptophan-kynurenine pathway,was analyzed by LC-MS.Above these results of molecular analysis and cell behavior,we can conclude that GBM inflammation is induced by tryptophan accumulation.This microchip-based model generally provides an alternative method for in vitro research of interactions in GBA.展开更多
An integrated poly(dimethylsiloxane) (PDMS) microchip with two sharpened stretching has been presented. The sample was directly introduced into the separation channel through the stretching inlet tip without complicat...An integrated poly(dimethylsiloxane) (PDMS) microchip with two sharpened stretching has been presented. The sample was directly introduced into the separation channel through the stretching inlet tip without complicated power switching supplies and without injection cross-channel. Operations of running buffer refreshing or channel cleaning also becomes simple by vacuumed in one end and placed another tip into solution vial. The fabrication method can be easily applied in most analytical laboratories at low cost in the absence of soft lithography and plasma bonding equipments. Characteristics of the chips were tested and it can be used to separate fluorescence labeled molecules.展开更多
The textile industrial chain all over the world is facing a challenge of differentiating cashmere fiber from mixture of wool and other fibers in case cashmere stocks are adulterated with wool or other fibers. For iden...The textile industrial chain all over the world is facing a challenge of differentiating cashmere fiber from mixture of wool and other fibers in case cashmere stocks are adulterated with wool or other fibers. For identification of cashmere in such mixtures, the development of microchip based real-time PCR technology offers a very sensitive, specific, and accurate solution. The technology has been validated with cashmere and wool samples procured from distant farms, and from cashmere goats and sheep of different age and sex. Model samples with incremental raw cashmere or wool content were tested. The experimentally determined content was found to be comparable to the weighed content of the respective fibers in the samples. This technology may prove a cost cutter since it needs only 1.2 μl of the PCR reagent mix. It is substantially faster than traditional real-time PCR systems for being carried as miniature reaction volume in metal microchip. These features allow faster thermal equilibrium and thermal uniformity over the entire array of microreactors. For routine tests or in commercial set up, the microchips are available as ready-to-run with lyophilized reagents in its microreactors to which only 1 μl of the 10-fold diluted isolated DNA sample is added. The lyophilized microchips offer user-friendly handling in testing laboratories and help minimize human error.展开更多
External-cavity birefringence feedback effects of the microchip Nd：YAG laser are presented. When a birefringence element is placed in the external feedback cavity of the laser, two orthogonally polarized laser beams ...External-cavity birefringence feedback effects of the microchip Nd：YAG laser are presented. When a birefringence element is placed in the external feedback cavity of the laser, two orthogonally polarized laser beams with a phase difference are output. The phase difference is twice as large as the phase retardation in the external cavity along the two orthogonal directions. The variable extra-cavity birefringence, caused by rotation of the external-cavity birefringenee element, results in tunable phase difference between the two orthogonally polarized beams. This means that the roll angle information has been translated to phase difference of two output laser beams. A theoretical analysis based on the Fabry-Perot cavity equivalent model and refractive index ellipsoid is presented, which is in good agreement with the experimental results. This phenomenon has potential applications for roll angle measurement.展开更多
Giant liposome is an important lipid structure widely used in biological and medical fields. In its main preparation method, electroformation, many influencing factors must be optimized for good effect. How to collect...Giant liposome is an important lipid structure widely used in biological and medical fields. In its main preparation method, electroformation, many influencing factors must be optimized for good effect. How to collect the desired giant liposomes is another major issue. In this work, a microchip with a reactor chamber array was used to study the influences of multiple parameters, and a suitable condition could be achieved rapidly and efficiently. A tailor-made collection chamber was also integrated on the chip. Based on the multifactor and multilevel orthogonal experiment, optimal conditions of the lipid solution, buffer solution, and electric signal were achieved with high efficiency. More than one thousand giant liposomes could be formed in each microscale reactor chamber, and most of them were unilamellar. The on-chip collection ratio of giant liposome carriers could also approximate to 40%.展开更多
基金supported by the National Key R&D Program of China(No.2021YFF0600700)the National Natural Science Foundation of China(No.22034005)+1 种基金Research Projects of Putian University(No.2024172)the Startup Fund for Advanced Talents of Putian University(No.2024046)。
文摘Inflammation is often accompanied by glioblastoma cells(GBMs)and is considered a key factor for GBM growth.This feature is believed to be connected with the tryptophan pathway mainly affected by intestinal microbes since the concept of gut-brain axis(GBA)has been proposed.Here we present a microchip model co-culturing intestinal cells(Caco2),microbes(E.coli),and GBM cells(U87)to study inflammatory responses of GBM by investigating the tryptophan metabolism.E.coli after encapsulating with alginate hydrogel microparticles(AHMPs)was seeded in the microchip where Caco2 was located,forming the simulated system of intestinal physiology and avoiding excessive reproduction of microbes.Continuous flow was applied to maintain the cell viability,induce the morphogenesis,and simulate the tryptophan transportation in GBA.The morphological alterations of Caco2 and U87 were characterized by fluorescence imaging and the tryptophan metabolism,especially the tryptophan-kynurenine pathway,was analyzed by LC-MS.Above these results of molecular analysis and cell behavior,we can conclude that GBM inflammation is induced by tryptophan accumulation.This microchip-based model generally provides an alternative method for in vitro research of interactions in GBA.
文摘An integrated poly(dimethylsiloxane) (PDMS) microchip with two sharpened stretching has been presented. The sample was directly introduced into the separation channel through the stretching inlet tip without complicated power switching supplies and without injection cross-channel. Operations of running buffer refreshing or channel cleaning also becomes simple by vacuumed in one end and placed another tip into solution vial. The fabrication method can be easily applied in most analytical laboratories at low cost in the absence of soft lithography and plasma bonding equipments. Characteristics of the chips were tested and it can be used to separate fluorescence labeled molecules.
文摘The textile industrial chain all over the world is facing a challenge of differentiating cashmere fiber from mixture of wool and other fibers in case cashmere stocks are adulterated with wool or other fibers. For identification of cashmere in such mixtures, the development of microchip based real-time PCR technology offers a very sensitive, specific, and accurate solution. The technology has been validated with cashmere and wool samples procured from distant farms, and from cashmere goats and sheep of different age and sex. Model samples with incremental raw cashmere or wool content were tested. The experimentally determined content was found to be comparable to the weighed content of the respective fibers in the samples. This technology may prove a cost cutter since it needs only 1.2 μl of the PCR reagent mix. It is substantially faster than traditional real-time PCR systems for being carried as miniature reaction volume in metal microchip. These features allow faster thermal equilibrium and thermal uniformity over the entire array of microreactors. For routine tests or in commercial set up, the microchips are available as ready-to-run with lyophilized reagents in its microreactors to which only 1 μl of the 10-fold diluted isolated DNA sample is added. The lyophilized microchips offer user-friendly handling in testing laboratories and help minimize human error.
基金supported by the National Natural Science Foundation of China (Grant No 50575110)
文摘External-cavity birefringence feedback effects of the microchip Nd：YAG laser are presented. When a birefringence element is placed in the external feedback cavity of the laser, two orthogonally polarized laser beams with a phase difference are output. The phase difference is twice as large as the phase retardation in the external cavity along the two orthogonal directions. The variable extra-cavity birefringence, caused by rotation of the external-cavity birefringenee element, results in tunable phase difference between the two orthogonally polarized beams. This means that the roll angle information has been translated to phase difference of two output laser beams. A theoretical analysis based on the Fabry-Perot cavity equivalent model and refractive index ellipsoid is presented, which is in good agreement with the experimental results. This phenomenon has potential applications for roll angle measurement.
基金supported by the National Natural Science Foundation of China(Nos. 81501617,81871450,21827812)Science and Technology Planning Project of Yuzhong District, Chongqing, China(No. 20170122)+1 种基金the Program of International S&T Cooperation (No. 2014DFG31380)the Foundation for Higher Education Young Key Teacher of Chongqing, China
文摘Giant liposome is an important lipid structure widely used in biological and medical fields. In its main preparation method, electroformation, many influencing factors must be optimized for good effect. How to collect the desired giant liposomes is another major issue. In this work, a microchip with a reactor chamber array was used to study the influences of multiple parameters, and a suitable condition could be achieved rapidly and efficiently. A tailor-made collection chamber was also integrated on the chip. Based on the multifactor and multilevel orthogonal experiment, optimal conditions of the lipid solution, buffer solution, and electric signal were achieved with high efficiency. More than one thousand giant liposomes could be formed in each microscale reactor chamber, and most of them were unilamellar. The on-chip collection ratio of giant liposome carriers could also approximate to 40%.
