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dc.contributor.CRUESPUNIVERSIDADE DE ESTADUAL DE CAMPINASpt_BR
dc.typeArtigo de periódicopt_BR
dc.titleUse Of A Novel Method For Determination Of Partition Coefficients To Compare The Effect Of Local Anesthetics On Membrane Structurept_BR
dc.contributor.authorPaula E.d.pt_BR
dc.contributor.authorSchreier S.pt_BR
unicamp.authorPaula, E.d., Department of Biochemistry, Institute of Chemistry, Universidade de São Paulo, C.P. 26077, 05599-970 São Paulo, Brazil, Department of Biochemistry, Institute of Biology, Universidade Estadual de Campinas, São Paulo, Brazilpt_BR
unicamp.author.externalSchreier, S., Department of Biochemistry, Institute of Chemistry, Universidade de São Paulo, C.P. 26077, 05599-970 São Paulo, Brazilpt
dc.description.abstractA new, simple procedure for the determination of partition coefficients (P) was developed based on spectral effects caused upon addition of solutes to spin labeled model lipid membranes, and on the knowledge of their water solubility. Values of P were determined for nine local anesthetics (LA), amino-esters and amino-amides. The results were in good agreement with those found by phase separation and by a more complex, previously reported, methodology (Lissi et al. (1990) Biochim. Biophys. Acta 1021, 46-50) applied to either EPR or fluorescence spectra of probes incorporated in the bilayers. Both the present and the previously reported procedures make use of effects on membrane structure evaluated by spectroscopic techniques and offer the advantage of not requiring phase separation. The spectral effects, indicative of a decrease in bilayer organization increased with LA concentration, reaching a maximum at the drug water solubility, indicating that partitioning in the membrane is limited by saturation of the aqueous phase. A thermodynamic analysis of the partition data according to Hill (Hill, M.W. (1974) Biochim. Biophys. Acta 356, 117-124) showed that the LAs did not display ideal behavior. Knowledge of the partition coefficients allowed a comparison between effects at the same drug concentration in the membrane. Within a given family (esters, acyclic amides, cyclic amides) no clear proportionality was observed between effect and LA hydrophibicity, as reflected in the partition coefficient. Rather, the membrane perturbing ability is a result of steric effects originating in the mismatch between anesthetic and phospholipid shapes. © 1995.en
dc.relation.ispartofBBA - Biomembranespt_BR
dc.date.issued1995pt_BR
dc.identifier.citationBba - Biomembranes. , v. 1240, n. 1, p. 25 - 33, 1995.pt_BR
dc.language.isoenpt_BR
dc.description.volume1240pt_BR
dc.description.issuenumber1pt_BR
dc.description.firstpage25pt_BR
dc.description.lastpage33pt_BR
dc.rightsfechadopt_BR
dc.sourceScopuspt_BR
dc.identifier.issn52736pt_BR
dc.identifier.doi10.1016/0005-2736(95)00155-6pt_BR
dc.identifier.urlhttp://www.scopus.com/inward/record.url?eid=2-s2.0-0028818451&partnerID=40&md5=cce7d12f9a3fc56754821c8e29e7a4edpt_BR
dc.date.available2015-06-26T17:14:39Z
dc.date.available2015-11-26T14:20:41Z-
dc.date.accessioned2015-06-26T17:14:39Z
dc.date.accessioned2015-11-26T14:20:41Z-
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dc.description.provenanceMade available in DSpace on 2015-11-26T14:20:41Z (GMT). No. of bitstreams: 2 2-s2.0-0028818451.pdf: 816105 bytes, checksum: e92397d48b2fcc1c603ffb5ab451f818 (MD5) 2-s2.0-0028818451.pdf.txt: 41197 bytes, checksum: b928c13a91f116940923a55feab6351f (MD5) Previous issue date: 1995en
dc.identifier.urihttp://www.repositorio.unicamp.br/handle/REPOSIP/95964
dc.identifier.urihttp://repositorio.unicamp.br/jspui/handle/REPOSIP/95964-
dc.identifier.idScopus2-s2.0-0028818451pt_BR
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