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1.
J Control Release ; 146(3): 341-8, 2010 Sep 15.
Article in English | MEDLINE | ID: mdl-20595029

ABSTRACT

Biomaterials have been shown to differentially support dendritic cell (DC) maturation, a prerequisite for an adjuvant effect. Treatment of DCs with poly(D,L-lactic-co-glycolic acid) (PLGA) films resulted in DC maturation but agarose films did not. In these studies, the biomaterial adjuvant effect was attenuated by material selection (PLGA or agarose scaffolds) or local delivery of an anti-inflammatory/immunosuppressive glucocorticoid, dexamethasone (DX), from PLGA scaffolds. Porous scaffolds (SCs) of PLGA or agarose were produced to deliver equivalent amounts of model antigen, ovalbumin (OVA). Alternatively, PLGA SCs with incorporated OVA were produced with or without DX. These SCs were implanted individually, subcutaneously, and dorsally in C57BL/6 mice. Blood was collected from mice at specific times over a 12-week duration for measurement of antibody production against OVA. Scaffolds were explanted at 12 weeks for histological examination of foreign body response. Scaffolds of PLGA, but not of agarose, were found to elicit higher antibody production against co-delivered OVA, than negative controls. Short-term delivery of DX from PLGA SCs delivering OVA temporarily delayed onset of anti-OVA antibody production. More sustained release of DX at an effective dose and with an appropriate time course is expected to extend the effect of DX on the biomaterial adjuvant effect. The immunomodulatory ability of biomaterials to affect the immune response to co-delivered antigen is demonstrated wherein this immunomodulatory ability correlates with the observed in vitro differential effects of biomaterials on DC maturation.


Subject(s)
Adjuvants, Immunologic/metabolism , Anti-Inflammatory Agents/administration & dosage , Biocompatible Materials/metabolism , Dexamethasone/administration & dosage , Immunity, Humoral , Lactic Acid/immunology , Adjuvants, Immunologic/chemistry , Animals , Anti-Inflammatory Agents/immunology , Biocompatible Materials/chemistry , Dendritic Cells/immunology , Dexamethasone/immunology , Male , Mice , Mice, Inbred C57BL , Ovalbumin/administration & dosage , Ovalbumin/immunology , Polyglycolic Acid , Polylactic Acid-Polyglycolic Acid Copolymer , Sepharose/immunology , Tissue Scaffolds/chemistry
2.
Anal Chem ; 79(2): 445-52, 2007 Jan 15.
Article in English | MEDLINE | ID: mdl-17222006

ABSTRACT

In vitro microdialysis glucose sampling was used to test the transient and steady-state suitability of antifouling hydrogel coatings, composed of 2-hydroxyethyl methacrylate, vinylpyrrolidinone, and poly(ethylene glycol). The in vitro glucose diffusion coefficients of bare microdialysis membranes and hydrogel coatings were determined experimentally to be 1.1 x 10-6 and 3.2 x 10-6 cm2/s, respectively. These values were used to numerically simulate the effect of the hydrogel on glucose transport across the microdialysis membrane using a convection-diffusion transport model. The times for dialysate at the exit of the bare and hydrogel-coated microdialysis probes to reach 95% of steady state were calculated to be 20 and 66 s, respectively. However, the experimental data showed that 95% of steady-state glucose recoveries were reached after 4-5 min. Numerical simulations incorporating the Taylor dispersion in the outlet tubing showed the time difference was caused almost completely by convective transport in the outlet tubing with negligible contribution from analyte profile broadening. These data indicated that the hydrogel coatings imposed 44% reduction in glucose permeability and consequently 26% reduction in the percent recovery. The effect of hydrogel coatings on the time to reach the steady-state recovery was insignificant compared with the time required for convection of glucose in the outlet tubing.


Subject(s)
Glucose/chemistry , Hydrogel, Polyethylene Glycol Dimethacrylate/chemistry , Membranes, Artificial , Microdialysis/instrumentation , Methacrylates/chemistry , Permeability , Polyethylene Glycols/chemistry , Pyrrolidinones/chemistry
3.
Pediatrics ; 118 Suppl 2: S141-6, 2006 Nov.
Article in English | MEDLINE | ID: mdl-17079616

ABSTRACT

OBJECTIVE: Five NICUs that participate in the Vermont Oxford Network Quality Improvement Collaborative have implemented several potentially better practices in an attempt to decrease nurse turnover by 50%. These potentially better practices focus on orientation, rewards and recognition, healthy work environment, nurse-physician collaboration, and nursing autonomy. METHODS: Each unit implemented some or all of the potentially better practices. An Excel spreadsheet tool for tracking turnover rates was developed and used to measure the impact of the potentially better practices on retention. Rates were measured quarterly. RESULTS: After implementation of the potentially better practices, turnover rates fell at all of the NICUs ranging from 13% to 64%. CONCLUSIONS: Nurse retention is multifactorial. Implementation of the potentially better practices had a positive influence on nurse satisfaction but a varied impact on nurse retention. The impact of larger issues such as pay and staffing levels is significant and may not be influenced at the unit level.


Subject(s)
Intensive Care Units, Neonatal/organization & administration , Personnel Staffing and Scheduling , Focus Groups , Humans , Inservice Training/methods , Job Satisfaction , Neonatal Nursing , Personnel Turnover , Physician-Nurse Relations , Professional Autonomy , Quality Assurance, Health Care , Reward , United States , Workplace
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