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1.
J Geriatr Psychiatry Neurol ; 33(2): 103-108, 2020 03.
Article in English | MEDLINE | ID: mdl-31409182

ABSTRACT

OBJECTIVES: Previous studies have looked at the reasons for hospital admission in people with parkinsonism (PwP), yet few have looked at factors that precipitate admission. METHODS: People with parkinsonism with a diagnosis of idiopathic Parkinson disease of Hoehn and Yahr stage III-V and those with Parkinson plus syndromes were assessed for motor and nonmotor symptoms, quality of life, and functional performance. Logistic regression was used to investigate predictors of hospital admission over the subsequent 2 years. RESULTS: Overall, 162 patients consented to be part of the study. Seventy-one PwP (43.8%) had at least 1 hospital admission, and 17 (10.5%) patients had 3 or more admissions to hospital. Poorer cognition, more nonmotor symptoms, poorer quality of life, slower timed-up-and-go test scores, and abnormal swallow predicted a subsequent hospital admission. DISCUSSION: Our study emphasizes the importance of nonmotor symptoms in predicting admission. A cost-benefit analysis of early intervention to prevent admission should be considered.


Subject(s)
Data Collection/methods , Hospitalization/statistics & numerical data , Parkinsonian Disorders/therapy , Quality of Life/psychology , Aged , Aged, 80 and over , Female , Humans , Independent Living , Male , Middle Aged
2.
Contrast Media Mol Imaging ; 2018: 4617493, 2018.
Article in English | MEDLINE | ID: mdl-30046295

ABSTRACT

Novel probe development for positron emission tomography (PET) is leading to expanding the scope of molecular imaging. To begin responding to challenges, several biomaterials such as natural products and small molecules, peptides, engineered proteins including affibodies, and antibodies have been used in the development of targeted molecular imaging probes. To prepare radiotracers, a few bioactive materials are unique challenges to radiolabelling because of their complex structure, poor stability, poor solubility in aqueous or chemical organic solutions, and sensitivity to temperature and nonphysiological pH. To overcome these challenges, we developed a new radiolabelling strategy based on photoactivated 1,3-dipolar cycloaddition between alkene dipolarophile and tetrazole moiety containing compounds. Herein, we describe a light-triggered radiochemical synthesis via photoactivated click reaction to prepare 18F-radiolabelled PET tracers using small molecular and RGD peptide.


Subject(s)
Click Chemistry/methods , Isotope Labeling/methods , Positron-Emission Tomography/methods , Radiopharmaceuticals/chemical synthesis , Alkenes/chemistry , Animals , Cell Line, Tumor , Cycloaddition Reaction , Fluorine Radioisotopes/chemistry , Heterografts , Humans , Light , Molecular Probes/chemical synthesis , Rats , Tetrazoles/chemistry
3.
Chem Commun (Camb) ; 47(32): 9137-9, 2011 Aug 28.
Article in English | MEDLINE | ID: mdl-21750823

ABSTRACT

In a free solution of 10.0 mM Gly-Gly (pH 8.2), the flow directions of native-DNA and DNA molecules intercalated with the fluorescent dye YOYO-1 were reversed in the microchip channel. These results clearly showed that in a confined space and under specific environmental conditions, the fluorescent dye modified the original properties and behavior of the native-DNA molecule.


Subject(s)
Benzoxazoles/chemistry , DNA/chemistry , Fluorescent Dyes/chemistry , Intercalating Agents/chemistry , Microscopy, Interference/instrumentation , Oligonucleotide Array Sequence Analysis , Quinolinium Compounds/chemistry , Equipment Design , Glycylglycine/chemistry
4.
Lab Chip ; 11(2): 348-53, 2011 Jan 21.
Article in English | MEDLINE | ID: mdl-20957251

ABSTRACT

This study describes a simple and low cost method for fabricating enclosed transparent hydrophilic nanochannels by coating low-viscosity PDMS (monoglycidyl ether-terminated polydimethylsiloxane) as an adhesion layer onto the surface of the nanotrenches that are molded with a urethane-based UV-curable polymer, Norland Optical Adhesive (NOA 63). In detail, the nanotrenches made of NOA 63 were replicated from a Si master mold and coated with 6 nm thick layer of PDMS. These nanotrenches underwent an oxygen plasma treatment and finally were bound to a cover glass by chemical bonding between silanol and hydroxyl groups. Hydrophobic recovery that is observed in the bulk PDMS was not observed in the thin film of PDMS on the mold and the PDMS-coated nanochannel maintained its surface hydrophilicity for at least one month. The potentials of the nanochannels for bioapplications were demonstrated by stretching λ-DNA (48,502 bp) in the channels. Therefore, this fabrication approach provides a practical solution for the simple fabrication of the nanochannels for bioapplications.

5.
J Sep Sci ; 33(8): 1109-14, 2010 Apr.
Article in English | MEDLINE | ID: mdl-20175090

ABSTRACT

We report a diagnostic method for Anaplasma phagocytophilum (A. phagocytophilum) infection in cattle using a nested PCR and microchip electrophoresis (ME). A. phagocytophilum causes human granulocytic anaplasmosis and granulocytic ehrlichiosis, which are emerging tick-borne zoonotic diseases. Nested PCR was used to amplify genomic DNA samples extracted from cattle blood. The amplified PCR products were analyzed under a sieving gel matrix of 0.7% poly(ethyleneoxide) (M(r)=8,000,000) in a conventional glass microchip. In the ME assay, A. phagocytophilum was analyzed within 35 s with a relative standard deviation of 1.30% (n=5) using a programmed field strength gradient (PFSG) as follows: 615.3 V/cm for 0-24 s, 66.7 V/cm for 24-34 s, 615.3 V/cm for 34-100 s. The ME-PFSG assay was clinically validated by comparing the 16S rRNA gene levels obtained by this method with those measured using conventional slab gel electrophoresis performed with ten cattle blood samples suspected of A. phagocytophilum infection. In contrast to slab gel electrophoresis, the proposed ME-PFSG methodology had increased sensitivity (200-450 pg/microL), a faster analysis time (<35 s), and required a smaller sample volume (approximately 162 fL).


Subject(s)
Anaplasma phagocytophilum/isolation & purification , Anaplasmosis/diagnosis , Electrophoresis, Microchip/methods , Anaplasmosis/microbiology , Animals , Cattle , DNA, Bacterial/genetics , DNA, Bacterial/isolation & purification , Polymerase Chain Reaction , Time Factors
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