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2.
Cont Lens Anterior Eye ; 31(2): 89-94, 2008 Apr.
Article in English | MEDLINE | ID: mdl-17964212

ABSTRACT

PURPOSE: The purpose of this work was to evaluate the ability of four silicone-hydrogel contact lenses (galyfilcon A, balafilcon A, lotrafilcon A and lotrafilcon B) to retain their equilibrium water content before and after wear, through measurements of refractive index and compare with that of a conventional disposable hydrogel contact lens (etafilcon A). METHODS: The refractive indices of 115 contact lenses were measured using an automated refractometer (CLR 12-70, Index Instruments, Cambridge, U.K.) before and after a schedule of daily wear by 58 patients for 30 days in the case of silicone-hydrogel lenses and 15 days for the conventional contact lenses. RESULTS: In the silicone-hydrogel contact lenses the changes on the refractive indices were not statistically significant, however after being worn the refractive index of the conventional etalfilcon A hydrogel contact lens increased significantly (p<0.001). CONCLUSION: The results presented here show that after being worn the silicone-hydrogel contact lens, show more capacity to retain or to reach their initial equilibrium water content than conventional hydrogel contact lenses. This suggests that the silicone-hydrogel contact lenses are less susceptible to spoilation over time maintaining its biocompatibility and contributing to the clinical success of lens performance.


Subject(s)
Contact Lenses , Hydrogels , Refraction, Ocular , Refractive Errors/diagnosis , Refractive Errors/rehabilitation , Silicon , Equipment Design , Equipment Failure Analysis , Female , Humans , Male , Reproducibility of Results , Sensitivity and Specificity , Treatment Outcome
3.
J Fluoresc ; 18(2): 555-62, 2008 Mar.
Article in English | MEDLINE | ID: mdl-18157688

ABSTRACT

Lipoplexes are commonly used as delivery systems in vitro and in vivo, the role of a neutral lipid as helper being of extreme importance in these systems. Cationic liposomes composed of dioctadecyldimethylammonium bromide (DODAB) with monoolein (MO) as a helper, at different molar ratios (1:2; 1:1 and 1:0.5) were prepared, and subsequently titrated to DNA. The structural and physicochemical properties of the lipid/DNA complexes were assessed by ethidium bromide (EtBr) exclusion, 90 degrees static light scattering (90 degrees SLS) assays and fluorescence resonance energy transfer (FRET). In EtBr exclusion assays, the steady-state fluorescence spectra of EtBr were decomposed into the sum of two lognormal emissions, emanating from two different environments--H(2)O and DNA, and the effect of charge ratio (+/-) was observed. 90 degrees SLS assays gave an important contribution, detecting size variations in systems with different MO fractions on the lipoplexes. In FRET assays, 2-(3-(diphenylhexatrienyl)propanoyl)-1-hexadecanoyl-sn-glycero-3-phosphocholine (DPH-HPC) was used as donor and EtBr as acceptor. The DNA component previously calculated by EtBr exclusion, was used to determine the energy transfer efficiency, as an indirect measurement of the lipoplexes structural and physicochemical properties. Our results demonstrate that the inclusion of monoolein in the cationic liposomes formulation significantly modifies the rate of DNA complexation, being DODAB:MO (1:1) the system with higher DNA condensation efficiency.


Subject(s)
Glycerides/chemistry , Liposomes , Spectrometry, Fluorescence , DNA/metabolism , Ethidium/chemistry , Fluorescence Resonance Energy Transfer , Quaternary Ammonium Compounds/chemistry , Quaternary Ammonium Compounds/metabolism , Transfection
4.
J Liposome Res ; 13(2): 123-30, 2003 May.
Article in English | MEDLINE | ID: mdl-12855107

ABSTRACT

The objective of our work has been the microencapsulation of dyes with lecithin from soybean, with the formation of liposomes, as a substitute for synthetic auxiliaries so as to improve the quality of the effluent. Current scenarios promote the disintegration and leakage of the liposomes, such as, changes in temperature, pH, and the use of surfactants. Since dyeing process is a mix of all these parameters, we pretended to study each one separately. Changes in pH at constant temperature induce a release of dye similar with changes in temperature. In acid conditions, we found a very fast initial dye release which doesn't occur in basic conditions. Using carboxyfluorescein, as a pH fluorescence probe, we concluded that the liposome membrane doesn't protect the liposome interior from changes on the external pH.


Subject(s)
Fluorescent Dyes/chemistry , Liposomes/chemistry , Phosphatidylcholines , Rhodamines/chemistry , Drug Compounding , Fluoresceins , Hydrogen-Ion Concentration , Phosphatidylcholines/chemistry , Glycine max/chemistry , Spectrometry, Fluorescence
5.
J Liposome Res ; 13(2): 111-21, 2003 May.
Article in English | MEDLINE | ID: mdl-12855106

ABSTRACT

The objective of our work has been the microencapsulation of dyes with lecithin from soybean, with the formation of liposomes, as a substitute for synthetic auxiliaries so as to improve the quality of the effluent. Current scenarios promote the disintegration and leakage of the liposomes, such as, changes in temperature, pH and the use of surfactants. Since dyeing process is a mix of all these parameters, we pretended to study each one separately. Rhodamine 6G fluorescence is known to be concentration quenched through the formation of non-fluorescent dimmers and, additionally, through the energy transfer from rhodamine monomer to these dimmers (Baptista ALF, Coutinho PJG, Real Oliveira MECD, Gomes JINR. Proceedings of 13th International Symposium of Surfactants, SIS 2000, Gainesville, USA, 2000). The temperature, the surfactant and pH induce a release of the encapsulated dye resulting in rhodamine dilution and consequently alterations in the dimerization/binding equilibrium. The experimental spectra indicate that rhodamine binds almost completely to liposomes. The decomposition of the rhodamine fluorescence spectra allowed us to determine the percentage of released dye during a simulated dyeing process, and allowed us to conclude that the dimerization process occurs mainly at the inner interfaces. The amount of dye released induced by temperature changes was greater in the presence of surfactant.


Subject(s)
Fluorescent Dyes , Liposomes/chemistry , Phosphatidylcholines , Rhodamines/chemistry , Surface-Active Agents , Temperature , Drug Compounding , Hydrogen-Ion Concentration , Mathematics , Phosphatidylcholines/chemistry , Glycine max/chemistry , Spectrometry, Fluorescence
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