11.06.2013 Views

'X' ENCON,TRO NACIONAL DE FISICA DA MATERIA CONDENSADA

'X' ENCON,TRO NACIONAL DE FISICA DA MATERIA CONDENSADA

'X' ENCON,TRO NACIONAL DE FISICA DA MATERIA CONDENSADA

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

XX ENFMC - Resumos<br />

constituica"o de amostras que facilitam a determinacao<br />

da estrutura de membranas atraves de XSW.<br />

INTERAcAO <strong>DE</strong> FARMACOS COM<br />

SISTEMAS LIPi<strong>DE</strong>OS/AGUA: ESTUDO<br />

ESTRUTURAL<br />

LEI<strong>DE</strong> PASSOS CAVALCANTI, IRIS L. TORRIANI<br />

Institute de Fi'sica 'Gleb Wataghin', UNICAMP,<br />

Campinas, SP, Brasil<br />

Lipideos e sistemas lipideo/agua apresentam urn variado<br />

mesomorfismo. As mesofases lamelares de sistemas<br />

simples, como lipideos naturais ou sinteticos, sejam<br />

puros ou misturados, fornecem urn modelo racional,<br />

que serve de base para estudar sistemas mais cornplexos<br />

destinados a aplicacaes bioquimicas, medicas<br />

ou industriais. A relacao entre estrutura molecular<br />

e comportamento da mesofase em escudo e estabelecida,<br />

geralmente, atraves de diagramas de fase que representam<br />

a composicao relativa de fases coexistentes<br />

para uma temperatura dada. E importante determinar<br />

parametros composicionais que podem ser adotados na<br />

formulacao de farmacos encapsulados ou corn propricdades<br />

de liberacao controlada. Em experiencias anteriores<br />

estudamos os sistemas dipalmitoilfosfatidilcolina<br />

(DPPC)/cardiolipina (CL) corn incorporacEo de elipticina<br />

(ELPT), urn alcaloide de mac, anti-cancerigena,<br />

verificando que a presenca de lipideos anionicos, como<br />

a CL, favorecem a incorporacao da ELPT nos sistemas<br />

de lipideos mistos DPPC/CL. Neste trabalho utilizamos<br />

a difracao de raios-X para identificar e caracterizar<br />

estruturalmente as transigoes de fase encontradas<br />

nos sistemas DPPC/CL e DPPC/CL/ELPT, corn<br />

o objetivo de estabelecer relacOes estrutura-atividade<br />

do farmaco ern quest5o. As medidas foram realizadas<br />

em urn intervalo de temperatura de 25°C a 85°C corn<br />

urn arranjo experimental que permute obter as diagramas<br />

de difracao de raios-X "in-situ". Com esse arranjo<br />

foi possivel monitorar as reflexoes lamelares correspondentes<br />

a espacamentos da ordem de 60Ae o halo difuso<br />

devido a distancia entre as cadeias acilicas que sao indicadores<br />

da transican entre a fase gel e a fase liquidocristalina.<br />

CNPq.<br />

TEMPERATURE AND IONIC STRENGTH<br />

<strong>DE</strong>PEN<strong>DE</strong>NT LIGHT SCATTERING OF<br />

DMPG DISPERSIONS<br />

KARIN A. RISKE, MARIA TERESA LAMY-FREUND<br />

Institute of Physics, Universidade de Sao Paulo, SP<br />

MARIO J. POLITI<br />

Institute of Chemistry, Universidade de Scio Paulo, SP<br />

WAYNE F. REED<br />

Department of Physics, Tulane University, New Orleans,<br />

LA, USA<br />

The temperature dependence of the intensity of light<br />

scattered by aqueous dispersions of the anionic lipid<br />

DMPG (dimyristoyl phosphatidylglycerol) was studied<br />

at different ionic strengths. The lipid main transition,<br />

gel-liquid crystal, can be well monitored by a sharp decrease<br />

in turbidity. As expected, the temperature of<br />

the main transition (T m ) was found to increase with<br />

the increase of the ionic strength. For low ionic strength,<br />

a DMPG second temperature transition, named<br />

post-transition, can be monitored by both an increase<br />

in light scattering and a decrease in conductivity. Zimm<br />

plot analysis indicates that bellow T n, the liposomes<br />

tend to aggregate, yielding a negative second virial coefficient<br />

A2, and particles of large molecular weight. At<br />

the phase transition, parallel to the decrease in turbidity,<br />

there is an increase in the sample conductivity,<br />

A 2 becomes positive and the particle molecular weight<br />

decreases, indicating a non-aggregated state. Moreover,<br />

at the post-transition (T p ) A2 becomes very small,<br />

and the molecular weight increases again. Opposite to<br />

the main transition on the post-transition could not be<br />

detected by spin labels placed either at the membrane<br />

surface, or in the bilayer core. Considering an increase<br />

in area per lipid headgroup upon the main transition,<br />

and the Gouy-Chapman-Stern model, it was possible<br />

to show that the main transition increases the vesicle<br />

degree of dissociation, hence increasing the ion concentration<br />

in solution. However, within the framework of<br />

that simple model, it was necessary to consider different<br />

Na+-PG — association constants, in the gel and liquid<br />

phases, to explain an increase in vesicles repulsion<br />

upon the main transition. The mechanisms governing<br />

the post-transition are even less clear.<br />

23

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!