Glaucoma is a prevalent retinal neurodegenerative disease that is characterized by progressive visual field loss, leading to eventual blindness. The main risk factor for glaucoma is elevated intraocular pressure (IOP) which results in the damage and death of retinal ganglion cells (RGCs) and their axons. The endpoint of the disease is the death of these cells by apoptosis; therefore, blocking the activation of apoptosis was hypothesized to be an effective therapy. Magnetic microbeads were injected into the eyes of mice to induce a model of ocular hypertension. Apoptosis was targeted through viral-mediated ocular delivery of the X-linked inhibitor of apoptosis (XIAP) gene, a potent caspase inhibitor. XIAP overexpression resulted in significant protection of ganglion cell somal and axonal function in glaucomatous eyes, and their optic nerves showed preservation of axon density, counts, and myelination, suggesting XIAP was able to provide both structural and functional protection. The results of these experiments provide proof-of-principle for XIAP’s efficacy as a neuroprotective treatment for glaucoma and are an important step forward in evaluating its full therapeutic potential.

In this study, the carbon electrode of supercapacitor was fabricated by using mesocarbon microbeads. For finding the optimal processing parameters of carbon electrode, the effects of specific surface area of activated carbon, the amount of carbon black and binder, and various electrolytes on the capacitative properties of supercapacitor are investigated. To fabricate the composite electrode of supercapacitor, NiO and WO3 thin films were deposited respectively on the carbon electrode by electron beam evaporation. The influences of various scan rates of cyclic voltammograms (CV) on the characteristic of capacitance are studied. The charge-discharge efficiency and life time of the composite electrode are also discussed. Experimental results reveal that the optimum carbon electrode can be obtained using mesocarbon microbeads with high specific surface area (2685 m2/g) and larger pore volume (0.6 cm3/g) and adding 10 wt.% carbon black and 2wt.% binder. The specific capacitances of carbon electrodes in 1 M KOH and 1 M Et4NBF4 are 230.8 F/g and 221.5 F/g, respectively. Besides, the XRD and SEM results showed that NiO and WO3 thin films on composite electrode are sheet-liked crystal structure and stone-liked amorphous structure, respectively. The composite electrode exhibits better capacitance properties than those of carbon electrode at high scan rate by CV analysis. It reveals the promotion of the capacitative property of supercapacitor at higher power density and the improving of the decay property in capacitance at high scan rate. Finally, in the test of charge-discharge efficiency and life time, the charge-discharge efficiency is near 100% after 5000 cycles and it still retains good adhesion between electrode material and substrate.

Calcification is linked to a high prevalence of cardiovascular events and mortality due to arterial stiffness. Stiffening of the arteries in the case of medial calcification is due to hydroxyapatite mineral deposited in the artery thus leading to the loss of elastin. A possibility of removing this rogue mineral along the vessel walls could be the use of osteoclasts. Osteoclasts, a type of osteocyte, have the unique ability to absorb bone in the bone turnover process. It is proposed that in the future, osteoclasts be delivered to the site of mineralization through oxidized alginate-fibrin microbeads. Alginate hydrogels have proven great in drug delivery and could be a revolutionary cell delivery device to provide care for multitudes of people suffering from adjacent cardiovascular health problems such as arterial stiffness.

Antibiotic resistant infections are a growing health care concern, with many cases reported annually. Infections can cause irreversible bodily damage or death if they are not diagnosed in a timely matter. To rapidly diagnose antibiotic resistance in infections, it is important to be able to capture and isolate the DNA coding for the resistance genes. This is challenging because bacteria are present in blood in minute concentrations. To enrich the DNA to detectable levels, I modified magnetic microbeads with ssDNA sequences complementary to the target DNA to capture the DNA via hybridization. I compared DNA capture efficiency in three different methods: Co-flow, packed bead bed, and pre-hybridization. The pre-hybridized method worked better than the other two. Since pre-hybridization involved mixing, I chose to study mixing in a microfluidic device. The mixing chamber was a well carved out of PMMA placed between two electromagnets. To test the mixing well, beads and capture DNA were placed in it, and the electromagnets were subjected to different frequencies, including symmetric or asymmetric magnetic fields. For each condition the capture efficiency was determined by measuring the relative fluorescence units (RFU). A 100 Hz asymmetric magnetic field had the best capture efficiency out of all conditions. These results demonstrate a path for enriching low concentrations of DNA to detectable levels, and future work should be done to develop electromagnetic mixing in microfluidic devices.

Dentre as diferentes poluições presentes nos oceanos, o plástico é provavelmente, aquele que leva aos maiores impactos ambientais, sendo encontrado de praias e manguezais à giros no meio dos oceanos. Os macroplásticos, cujo tamanho é superior a 5mm, são maiores em volume e provocam um impacto socioambiental importante, porém os microplásticos, fragmentos menores que 5mm, estão em maior quantidade e podem provocar danos em organismos marinhos filtradores como mexilhões e ostras. Apesar da sua grande presença nos oceanos, ainda não se estabeleceu com clareza se causam efeitos somente físicos, por um aumento de material particulado não orgânico ingerido, ou se seus efeitos podem ser de origem química, devido à quantidade de contaminantes que possuem. Para estudar o impacto que essas partículas têm em organismos filtradores, o mexilhão Perna perna, espécie bioindicadora abundante na costa brasileira, foi exposto a partículas de polietileno encontradas em cosméticos nacionais. O microplástico foi adquirido diretamente da indústria e precisou ser identificado. A análise de FT−IR mostrou que o plástico era polietileno de baixa densidade. Os organismos então foram expostos ao polietileno, virgem ou lixiviado, em duas concentrações (0,5 g⁄L e 2,5 g⁄L) por diferentes períodos (12,24,48,96 e 144 horas). Após os experimentos, os mexilhões foram coletados e dissecados e a resposta de seis biomarcadores foi analisada: O Tempo de Retenção do Vermelho Neutro nos hemócitos, Danos ao DNA e Lipoperoxidação nas brânquias e os níveis de três proteínas de estresse (AIF−1, pP38−MAPK e HSP−70) nas glândulas digestivas. Todos os biomarcadores foram afetados pela exposição ao polietileno, porém um padrão no resultado não pôde ser observado. Os fatores de exposição analisados (Concentração, Período e Tratamento do Plástico) individualmente, ou combinados, levaram a respostas diferentes e até mesmo opostas em alguns casos. A coleta de indivíduos de P. perna in situ na região do Porto de Santos mostrou que todos os bancos naturais possuem organismos contaminados. Os resultados deste trabalho mostram que a fisiologia do mexilhão P. perna é modificada após a exposição aguda ao polietileno. Um maior número de biomarcadores deve ser analisado futuramente para elucidar quais vias estão efetivamente sendo ativadas ou inibidas. O alto nível de contaminação dos mexilhões da região do porto de Santos é um fator alarmante que deve ser discutido pela sociedade com o intuito de se criar soluções para o problema da poluição por plástico nos oceanos antes que este afete a saúde humana. / Among all different pollutants, plastic debris is one of the main environmental impacts, being found from beaches and mangrove to gyres in the middle of the oceans. Macroplastics, with size above 5mm, are larger in volume and are an important social and environmental problem, but microplastics, fragments less than 5mm can be most harmful for filter feeding animals such as mussels and oysters. However, it is still debatable if its effects are physical, due to the increase in indigestible material; or chemical, due to plastic additives such as phthalates or PCBs. To study the impact that these particles can have in those animals, the brown mussel Perna perna (Bivalvia) an abundant and an organism easy to maintain in the laboratory, was exposed to virgin or leached polyethylene (PE) microbeads, used as abrasives in Brazilian cosmetics. Polyethylene was acquired directly from the industry and therefore needed to be identified. Analysis of FT−IR showed that the plastic was Low Density Polyethylene. The microplastic exposure had two concentrations (0.5 and 2.5g⁄l) and different periods of time (12, 24, 48, 96 and 144 hours). After the experiment, the organisms were dissected and the levels of six biomarkers were analyzed: Neutral Red Retention Time by the Hemocytes, Lipid Peroxidation and DNA Damages in the Gills and the response levels of three stress proteins (pP38−MAPK, AIF−1 and HSP−70) in the Digestive Glands. All biomarkers were affected by the PE exposure, but the results did not follow a pattern. The exposure factors analyzed (Concentration, Period of Time and Plastic Treatment), alone or combined, led to different and sometimes opposite responses. In Situ collected samples in the Santos Harbour area showed that all natural mussel\'s beds analyzed had microplastics contaminated mussels. The results of this work showed that microplastics acute exposure in P. perna modifies its physiology. More biomarkers should be used to clarify which pathways are being activated or inhibited. The high levels of contamination of important commercial mussel\'s beds in the Santos Harbour area, is an alarming sign for the community, that should start working together to solve the plastic pollution problem in our oceans before starts to affect human health.

The absorption enhancing ability of chitosan, a linear polysaccharide, is mediated by protonated amino groups on the C-2 position of the molecules that induce interaction with the anionic sites on the cell membranes to subsequently alter tight junction integrity. In neutral and basic environments, such as those found in the small and large intestines, most chitosan molecules will lose their charge and precipitate from solution rendering it ineffective as an absorption enhancer. To increase the solubility of this polymer, methylation of the amino groups on the C- 2 position was proposed. A partially quaternised and water soluble derivative of chitosan, N-trimethyl chitosan chloride (TMC), which exhibits superior solubility in a basic environment compared with other chitosan salts was synthesised and included in a chitosan microbead solid drug delivery system. Two TMC derivatives were synthesised by reductive methylation from high and medium molecular weight Chitoclear™ chitosan respectively. The degree of quaternisation calculated from the 1H-NMR spectra for the medium molecular weight TMC (TMC-M) and the high molecular weight TMC (TMC-H) polymers were 74.7 % and 48.5 % respectively. The mean molecular weights of the synthesised TMC-M and TMC-H polymers were 64 100 g/mole and 233 700 g/mole respectively. The effect of different concentrations TMC-M and TMC-H on chitosan microbeads was studied with results obtained from scanning electron microscopy (SEM), TMC loading capacity and microbead swelling behaviour. After selection of the most suitable TMC concentration, the effect of varying concentration (0.1, 0.2 and 0.5 %) additives on TMC and ibuprofen release was studied. Commonly used modified cellulose gum (Ac-di-sol®(ADS)), sodium starch glycolate (Explotab®(EXP)) and ascorbic acid (AA) were added as disintegrants to different microbead formulations to promote release of both the ibuprofen as model drug and TMC from the beads. It was noticed that the loading (% drug loading capacity) of TMC-M was much lower than that obtained with TMC-H while the inclusion of different additives in varying concentrations did not seem to have a profound influence on the loading of either TMC-M or TMC-H. It was further noticed from the fit factors (f1 and f2) for dissolution profiles of eighteen chitosan microbead variations that the formulation containing TMC-H and 0.5% (w/v) ascorbic acid was the only formulation with a significantly higher ibuprofen and TMC-H release profile compared to all other formulations tested. The chitosan microbead formulation containing 2%(w/v) TMC-H and 0.5 % (w/v) ascorbic acid (H-AA-0.5) was used for in vitro absorption studies through rat intestine in Sweetana-Grass diffusion chambers. Chitosan containing TMC-H (no ascorbic acid) (CHIT-H) only and a plain chitosan microbead (CHIT) formulation was used as control formulations during the in vitro studies. Although the H-AA-0.5 formulation exhibited the highest transport rate for ibuprofen, the mean rate of transport (P app) obtained from the two formulations containing TMCH (CHIT-H and H-AA-0.5) showed no significant difference in the transport rate of ibuprofen. Compared to the CHlT formulation as control, both formulations containing TMC-H exhibited increased ibuprofen transport across in vitro rat jejunum. However, a statistical significant increase in transport was obtained only from the H-AA-0.5 formulation in comparison with the CHlT formulation. It can be concluded that the combination of high molecular weight TMC with a low degree of quaternisation and ascorbic acid (0.5% w/v) in a chitosan microbead lead to a statistical significant increase in the in vitro transport rate of ibuprofen through rat jejunum. / Thesis (Ph.D. (Pharmaceutics))--North-West University, Potchefstroom Campus, 2006.

The absorption enhancing ability of chitosan, a linear polysaccharide, is mediated by protonated amino groups on the C-2 position of the molecules that induce interaction with the anionic sites on the cell membranes to subsequently alter tight junction integrity. In neutral and basic environments, such as those found in the small and large intestines, most chitosan molecules will lose their charge and precipitate from solution rendering it ineffective as an absorption enhancer. To increase the solubility of this polymer, methylation of the amino groups on the C- 2 position was proposed. A partially quaternised and water soluble derivative of chitosan, N-trimethyl chitosan chloride (TMC), which exhibits superior solubility in a basic environment compared with other chitosan salts was synthesised and included in a chitosan microbead solid drug delivery system. Two TMC derivatives were synthesised by reductive methylation from high and medium molecular weight Chitoclear™ chitosan respectively. The degree of quaternisation calculated from the 1H-NMR spectra for the medium molecular weight TMC (TMC-M) and the high molecular weight TMC (TMC-H) polymers were 74.7 % and 48.5 % respectively. The mean molecular weights of the synthesised TMC-M and TMC-H polymers were 64 100 g/mole and 233 700 g/mole respectively. The effect of different concentrations TMC-M and TMC-H on chitosan microbeads was studied with results obtained from scanning electron microscopy (SEM), TMC loading capacity and microbead swelling behaviour. After selection of the most suitable TMC concentration, the effect of varying concentration (0.1, 0.2 and 0.5 %) additives on TMC and ibuprofen release was studied. Commonly used modified cellulose gum (Ac-di-sol®(ADS)), sodium starch glycolate (Explotab®(EXP)) and ascorbic acid (AA) were added as disintegrants to different microbead formulations to promote release of both the ibuprofen as model drug and TMC from the beads. It was noticed that the loading (% drug loading capacity) of TMC-M was much lower than that obtained with TMC-H while the inclusion of different additives in varying concentrations did not seem to have a profound influence on the loading of either TMC-M or TMC-H. It was further noticed from the fit factors (f1 and f2) for dissolution profiles of eighteen chitosan microbead variations that the formulation containing TMC-H and 0.5% (w/v) ascorbic acid was the only formulation with a significantly higher ibuprofen and TMC-H release profile compared to all other formulations tested. The chitosan microbead formulation containing 2%(w/v) TMC-H and 0.5 % (w/v) ascorbic acid (H-AA-0.5) was used for in vitro absorption studies through rat intestine in Sweetana-Grass diffusion chambers. Chitosan containing TMC-H (no ascorbic acid) (CHIT-H) only and a plain chitosan microbead (CHIT) formulation was used as control formulations during the in vitro studies. Although the H-AA-0.5 formulation exhibited the highest transport rate for ibuprofen, the mean rate of transport (P app) obtained from the two formulations containing TMCH (CHIT-H and H-AA-0.5) showed no significant difference in the transport rate of ibuprofen. Compared to the CHlT formulation as control, both formulations containing TMC-H exhibited increased ibuprofen transport across in vitro rat jejunum. However, a statistical significant increase in transport was obtained only from the H-AA-0.5 formulation in comparison with the CHlT formulation. It can be concluded that the combination of high molecular weight TMC with a low degree of quaternisation and ascorbic acid (0.5% w/v) in a chitosan microbead lead to a statistical significant increase in the in vitro transport rate of ibuprofen through rat jejunum. / Thesis (Ph.D. (Pharmaceutics))--North-West University, Potchefstroom Campus, 2006.

Dentre as diferentes poluições presentes nos oceanos, o plástico é provavelmente, aquele que leva aos maiores impactos ambientais, sendo encontrado de praias e manguezais à giros no meio dos oceanos. Os macroplásticos, cujo tamanho é superior a 5mm, são maiores em volume e provocam um impacto socioambiental importante, porém os microplásticos, fragmentos menores que 5mm, estão em maior quantidade e podem provocar danos em organismos marinhos filtradores como mexilhões e ostras. Apesar da sua grande presença nos oceanos, ainda não se estabeleceu com clareza se causam efeitos somente físicos, por um aumento de material particulado não orgânico ingerido, ou se seus efeitos podem ser de origem química, devido à quantidade de contaminantes que possuem. Para estudar o impacto que essas partículas têm em organismos filtradores, o mexilhão Perna perna, espécie bioindicadora abundante na costa brasileira, foi exposto a partículas de polietileno encontradas em cosméticos nacionais. O microplástico foi adquirido diretamente da indústria e precisou ser identificado. A análise de FT−IR mostrou que o plástico era polietileno de baixa densidade. Os organismos então foram expostos ao polietileno, virgem ou lixiviado, em duas concentrações (0,5 g⁄L e 2,5 g⁄L) por diferentes períodos (12,24,48,96 e 144 horas). Após os experimentos, os mexilhões foram coletados e dissecados e a resposta de seis biomarcadores foi analisada: O Tempo de Retenção do Vermelho Neutro nos hemócitos, Danos ao DNA e Lipoperoxidação nas brânquias e os níveis de três proteínas de estresse (AIF−1, pP38−MAPK e HSP−70) nas glândulas digestivas. Todos os biomarcadores foram afetados pela exposição ao polietileno, porém um padrão no resultado não pôde ser observado. Os fatores de exposição analisados (Concentração, Período e Tratamento do Plástico) individualmente, ou combinados, levaram a respostas diferentes e até mesmo opostas em alguns casos. A coleta de indivíduos de P. perna in situ na região do Porto de Santos mostrou que todos os bancos naturais possuem organismos contaminados. Os resultados deste trabalho mostram que a fisiologia do mexilhão P. perna é modificada após a exposição aguda ao polietileno. Um maior número de biomarcadores deve ser analisado futuramente para elucidar quais vias estão efetivamente sendo ativadas ou inibidas. O alto nível de contaminação dos mexilhões da região do porto de Santos é um fator alarmante que deve ser discutido pela sociedade com o intuito de se criar soluções para o problema da poluição por plástico nos oceanos antes que este afete a saúde humana. / Among all different pollutants, plastic debris is one of the main environmental impacts, being found from beaches and mangrove to gyres in the middle of the oceans. Macroplastics, with size above 5mm, are larger in volume and are an important social and environmental problem, but microplastics, fragments less than 5mm can be most harmful for filter feeding animals such as mussels and oysters. However, it is still debatable if its effects are physical, due to the increase in indigestible material; or chemical, due to plastic additives such as phthalates or PCBs. To study the impact that these particles can have in those animals, the brown mussel Perna perna (Bivalvia) an abundant and an organism easy to maintain in the laboratory, was exposed to virgin or leached polyethylene (PE) microbeads, used as abrasives in Brazilian cosmetics. Polyethylene was acquired directly from the industry and therefore needed to be identified. Analysis of FT−IR showed that the plastic was Low Density Polyethylene. The microplastic exposure had two concentrations (0.5 and 2.5g⁄l) and different periods of time (12, 24, 48, 96 and 144 hours). After the experiment, the organisms were dissected and the levels of six biomarkers were analyzed: Neutral Red Retention Time by the Hemocytes, Lipid Peroxidation and DNA Damages in the Gills and the response levels of three stress proteins (pP38−MAPK, AIF−1 and HSP−70) in the Digestive Glands. All biomarkers were affected by the PE exposure, but the results did not follow a pattern. The exposure factors analyzed (Concentration, Period of Time and Plastic Treatment), alone or combined, led to different and sometimes opposite responses. In Situ collected samples in the Santos Harbour area showed that all natural mussel\'s beds analyzed had microplastics contaminated mussels. The results of this work showed that microplastics acute exposure in P. perna modifies its physiology. More biomarkers should be used to clarify which pathways are being activated or inhibited. The high levels of contamination of important commercial mussel\'s beds in the Santos Harbour area, is an alarming sign for the community, that should start working together to solve the plastic pollution problem in our oceans before starts to affect human health.

No description available.

Many scientists and engineers are turning to lab-on-a-chip systems for cheaper and high throughput analysis of chemical reactions and biomolecular interactions. In this work, we developed several lab-on-a-chip modules based on novel manipulations of individual microbeads inside microchannels. The first manipulation method employs arrays of soft ferromagnetic patterns fabricated inside a microfluidic channel and subjected to an external rotating magnetic field. We demonstrated that the system can be used to assemble individual beads (1-3µm) from a flow of suspended beads into a regular array on the chip, hence improving the integrated electrochemical detection of biomolecules bound to the bead surface. In addition, the microbeads can follow the external magnet rotating at very high speeds and simultaneously orbit around individual soft magnets on the chip. We employed this manipulation mode for efficient sample mixing in continuous microflow. Furthermore, we discovered a simple but effective way of transporting the microbeads on-chip in the rotating field. Selective transport of microbeads with different size was also realized, providing a platform for effective sample separation on a chip. The second manipulation method integrates magnetic and dielectrophoretic manipulations of the same microbeads. The device combines tapered conducting wires and fingered electrodes to generate desirable magnetic and electric fields, respectively. By externally programming the magnetic attraction and dielectrophoretic repulsion forces, out-of-plane oscillation of the microbeads across the channel height was realized. Furthermore, we demonstrated the tweezing of microbeads in liquid with high spatial resolutions by fine-tuning the net force from magnetic attraction and dielectrophoretic repulsion of the beads. The high-resolution control of the out-of-plane motion of the microbeads has led to the invention of massively parallel biomolecular tweezers.