There are significant differences of glucose retention in site-specificity and individuals. Sixty... more There are significant differences of glucose retention in site-specificity and individuals. Sixty-two 5-year-old nursery schoolchildren participated in this study on the relation between the viscosity of saliva and flow rate and glucose retention. Each child was instructed to rinse his/her mouth with a glucose solution (0.5 M, 5 ml) and then to spit out. Three minutes after rinsing, glucose retention was determined. Resting saliva was collected by a natural outflow method, then the flow rate was determined. A rotational viscometer was used to determine the viscosity. Glucose retention and flow rate were correlated at the left maxillary primary molars, and glucose retention and viscosity were correlated at the maxillary central primary incisors. It was concluded that glucose retention after glucose mouth rinsing was site-specific, and that glucose retention and the index of decayed, missing and filled primary teeth (dmft) were slightly correlated with the salivary viscosity and flow rate.
ABSTRACT A method for determining the profiles of biomass volume and glucan within plaque was dev... more ABSTRACT A method for determining the profiles of biomass volume and glucan within plaque was developed using depth-specific analysis of plaque. The profiles of biomass volume and glucan demonstrated a tendency to be higher in the plaque exposed to sucrose, suggesting that an evaluation of these two plaque indices would be important to see the cariogenicity in the diet. Key wordsdepth-specific analysis-glucan-biomass volume-dental plaque
Journal of Chromatography B Analytical Technologies in the Biomedical and Life Sciences, Oct 15, 2010
A microfluidic structure is presented where selective capture of proteins in complex samples, fol... more A microfluidic structure is presented where selective capture of proteins in complex samples, followed by clean-up, enzymatic processing, and MALDI-MS sample preparation of peptides generated, can be performed. The structure uses an affinity column to capture the protein while all other components in the sample are disposed of. The protein of interest is then eluted from the affinity column and captured on a second column on which the enzymatic processing is performed. Salts and hydrophilic contaminants are then removed before the products from the enzymatic reaction are eluted together with a suitable MALDI matrix and the solvent evaporated in a designated MALDI target structure. All steps can be performed automatically in 54 parallel microstructures on a microfluidic compact disc. The process is demonstrated by the selective capture and tryptic digest of recombinant IgG molecules from samples containing other proteins: an excess of bovine serum albumin or spent cell culture media.
Journal of The American Society for Mass Spectrometry, 2013
The serum clearance rate of therapeutic antibodies is important as it affects the clinical effica... more The serum clearance rate of therapeutic antibodies is important as it affects the clinical efficacy, required dose, and dose frequency. The glycosylation of antibodies has in some studies been shown to have an impact on the elimination rates in vivo. Monitoring changes to the glycan profiles in pharmacokinetics studies can reveal whether the clearance rates of the therapeutic antibodies depend on the different glycoforms, thereby providing useful information for improvement of the drugs. In this paper, a novel method for glycosylation analysis of therapeutic antibodies in serum samples is presented. A microfluidic compact-disc (CD) platform in combination with MALDI-MS was used to monitor changes to the glycosylation profiles of samples incubated in vitro. Antibodies were selectively purified from serum using immunoaffinity capture on immobilized target antigens. The glycans were enzymatically released, purified, and finally analyzed by MALDI-TOF-MS. To simulate changes to glycan profiles after administration in vivo, a therapeutic antibody was incubated in serum with the enzyme α1-2,3 mannosidase to artificially reduce the amount of the high mannose glycoforms. Glycan profiles were monitored at specific intervals during the incubation. The relative abundance of the high mannose 5 glycoform was clearly found to decrease and, simultaneously, that of high mannose 4 increased over the incubation period. The method can be performed in a rapid, parallel, and automated fashion for glycosylation profiling consuming low amounts of samples and reagents. This can contribute to less labor work and reduced cost of the studies of therapeutic antibodies glycosylation in vitro and in vivo.
Journal of Pharmaceutical and Biomedical Analysis, 2012
Optimal glycosylation with respect to the efficacy, serum half-life time, and immunogenic propert... more Optimal glycosylation with respect to the efficacy, serum half-life time, and immunogenic properties is essential in the generation of therapeutic antibodies. The glycosylation pattern can be affected by several different parameters during the manufacture of antibodies and may change significantly over cultivation time. Fast and robust methods for determination of the glycosylation patterns of therapeutic antibodies are therefore needed. We have recently presented an efficient method for the determination of glycans on therapeutic antibodies using a microfluidic CD platform for sample preparation prior to matrix-assisted laser-desorption mass spectrometry analysis. In the present work, this method is applied to analyse the glycosylation patterns of three commercially available therapeutic antibodies and one intended for therapeutic use. Two of the antibodies produced in mouse myeloma cell line (SP2/0) and one produced in Chinese hamster ovary (CHO) cells exhibited similar glycosylation patterns but could still be readily differentiated from each other using multivariate statistical methods. The two antibodies with most similar glycosylation patterns were also studied in an assessment of the method's applicability for quality control of therapeutic antibodies. The method presented in this paper is highly automated and rapid. It can therefore efficiently generate data that helps to keep a production process within the desired design space or assess that an identical product is being produced after changes to the process.
Recently, the conjugated polymer - inorganic nanocomposites have been increasingly studied due to... more Recently, the conjugated polymer - inorganic nanocomposites have been increasingly studied due to the potential applications of these advanced materials in developing optoelectronic devices. In this work nanocomposite materials thin films based on poly [2-methoxy-5-(2’-ethyl-hexyloxy)-1,4-phenylene vinylene] (MEH-PPV) and nanocrystalline TiO2 (nc-TiO2) have been fabricated. The photoluminescence (PL) spectra of pure MEH-PPV and nanohybrid films have shown that the excitation at a 470 nm wavelength leads to the strong quenching in photoluminescent intensity due to the compositions of TiO2 component. Current-voltage (I-V) characteristics of multi-layer device with structure of Al//MEH-PPV:nc-TiO2//PEDOT:PSS//ITO//glass were investigated. The obtained results suggest the application of the hybrid MEH-PPV:nc-TiO2 materials in polymeric solar cells.
There are significant differences of glucose retention in site-specificity and individuals. Sixty... more There are significant differences of glucose retention in site-specificity and individuals. Sixty-two 5-year-old nursery schoolchildren participated in this study on the relation between the viscosity of saliva and flow rate and glucose retention. Each child was instructed to rinse his/her mouth with a glucose solution (0.5 M, 5 ml) and then to spit out. Three minutes after rinsing, glucose retention was determined. Resting saliva was collected by a natural outflow method, then the flow rate was determined. A rotational viscometer was used to determine the viscosity. Glucose retention and flow rate were correlated at the left maxillary primary molars, and glucose retention and viscosity were correlated at the maxillary central primary incisors. It was concluded that glucose retention after glucose mouth rinsing was site-specific, and that glucose retention and the index of decayed, missing and filled primary teeth (dmft) were slightly correlated with the salivary viscosity and flow rate.
ABSTRACT A method for determining the profiles of biomass volume and glucan within plaque was dev... more ABSTRACT A method for determining the profiles of biomass volume and glucan within plaque was developed using depth-specific analysis of plaque. The profiles of biomass volume and glucan demonstrated a tendency to be higher in the plaque exposed to sucrose, suggesting that an evaluation of these two plaque indices would be important to see the cariogenicity in the diet. Key wordsdepth-specific analysis-glucan-biomass volume-dental plaque
Journal of Chromatography B Analytical Technologies in the Biomedical and Life Sciences, Oct 15, 2010
A microfluidic structure is presented where selective capture of proteins in complex samples, fol... more A microfluidic structure is presented where selective capture of proteins in complex samples, followed by clean-up, enzymatic processing, and MALDI-MS sample preparation of peptides generated, can be performed. The structure uses an affinity column to capture the protein while all other components in the sample are disposed of. The protein of interest is then eluted from the affinity column and captured on a second column on which the enzymatic processing is performed. Salts and hydrophilic contaminants are then removed before the products from the enzymatic reaction are eluted together with a suitable MALDI matrix and the solvent evaporated in a designated MALDI target structure. All steps can be performed automatically in 54 parallel microstructures on a microfluidic compact disc. The process is demonstrated by the selective capture and tryptic digest of recombinant IgG molecules from samples containing other proteins: an excess of bovine serum albumin or spent cell culture media.
Journal of The American Society for Mass Spectrometry, 2013
The serum clearance rate of therapeutic antibodies is important as it affects the clinical effica... more The serum clearance rate of therapeutic antibodies is important as it affects the clinical efficacy, required dose, and dose frequency. The glycosylation of antibodies has in some studies been shown to have an impact on the elimination rates in vivo. Monitoring changes to the glycan profiles in pharmacokinetics studies can reveal whether the clearance rates of the therapeutic antibodies depend on the different glycoforms, thereby providing useful information for improvement of the drugs. In this paper, a novel method for glycosylation analysis of therapeutic antibodies in serum samples is presented. A microfluidic compact-disc (CD) platform in combination with MALDI-MS was used to monitor changes to the glycosylation profiles of samples incubated in vitro. Antibodies were selectively purified from serum using immunoaffinity capture on immobilized target antigens. The glycans were enzymatically released, purified, and finally analyzed by MALDI-TOF-MS. To simulate changes to glycan profiles after administration in vivo, a therapeutic antibody was incubated in serum with the enzyme α1-2,3 mannosidase to artificially reduce the amount of the high mannose glycoforms. Glycan profiles were monitored at specific intervals during the incubation. The relative abundance of the high mannose 5 glycoform was clearly found to decrease and, simultaneously, that of high mannose 4 increased over the incubation period. The method can be performed in a rapid, parallel, and automated fashion for glycosylation profiling consuming low amounts of samples and reagents. This can contribute to less labor work and reduced cost of the studies of therapeutic antibodies glycosylation in vitro and in vivo.
Journal of Pharmaceutical and Biomedical Analysis, 2012
Optimal glycosylation with respect to the efficacy, serum half-life time, and immunogenic propert... more Optimal glycosylation with respect to the efficacy, serum half-life time, and immunogenic properties is essential in the generation of therapeutic antibodies. The glycosylation pattern can be affected by several different parameters during the manufacture of antibodies and may change significantly over cultivation time. Fast and robust methods for determination of the glycosylation patterns of therapeutic antibodies are therefore needed. We have recently presented an efficient method for the determination of glycans on therapeutic antibodies using a microfluidic CD platform for sample preparation prior to matrix-assisted laser-desorption mass spectrometry analysis. In the present work, this method is applied to analyse the glycosylation patterns of three commercially available therapeutic antibodies and one intended for therapeutic use. Two of the antibodies produced in mouse myeloma cell line (SP2/0) and one produced in Chinese hamster ovary (CHO) cells exhibited similar glycosylation patterns but could still be readily differentiated from each other using multivariate statistical methods. The two antibodies with most similar glycosylation patterns were also studied in an assessment of the method's applicability for quality control of therapeutic antibodies. The method presented in this paper is highly automated and rapid. It can therefore efficiently generate data that helps to keep a production process within the desired design space or assess that an identical product is being produced after changes to the process.
Recently, the conjugated polymer - inorganic nanocomposites have been increasingly studied due to... more Recently, the conjugated polymer - inorganic nanocomposites have been increasingly studied due to the potential applications of these advanced materials in developing optoelectronic devices. In this work nanocomposite materials thin films based on poly [2-methoxy-5-(2’-ethyl-hexyloxy)-1,4-phenylene vinylene] (MEH-PPV) and nanocrystalline TiO2 (nc-TiO2) have been fabricated. The photoluminescence (PL) spectra of pure MEH-PPV and nanohybrid films have shown that the excitation at a 470 nm wavelength leads to the strong quenching in photoluminescent intensity due to the compositions of TiO2 component. Current-voltage (I-V) characteristics of multi-layer device with structure of Al//MEH-PPV:nc-TiO2//PEDOT:PSS//ITO//glass were investigated. The obtained results suggest the application of the hybrid MEH-PPV:nc-TiO2 materials in polymeric solar cells.
Uploads
Papers by Tran Lam Thuy