Structural Characterization of Photopolymerizable Binary Liposomes Containing Diacetylenic and Saturated Phospholipids
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
20/10/2012
20/10/2012
2010
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Resumo |
The use of liposomes to encapsulate materials has received widespread attention for drug delivery, transfection, diagnostic reagent, and as immunoadjuvants. Phospholipid polymers form a new class of biomaterials with many potential applications in medicine and research. Of interest are polymeric phospholipids containing a diacetylene moiety along their acyl chain since these kinds of lipids can be polymerized by Ultra-Violet (UV) irradiation to form chains of covalently linked lipids in the bilayer. In particular the diacetylenic phosphatidylcholine 1,2-bis(10,12-tricosadiynoyl)- sn-glycero-3-phosphocholine (DC8,9PC) can form intermolecular cross-linking through the diacetylenic group to produce a conjugated polymer within the hydrocarbon region of the bilayer. As knowledge of liposome structures is certainly fundamental for system design improvement for new and better applications, this work focuses on the structural properties of polymerized DC8,9PC:1,2-dimyristoyl-sn-glycero-3-phusphocholine (DMPC) liposomes. Liposomes containing mixtures of DC8,9PC and DMPC, at different molar ratios, and exposed to different polymerization cycles, were studied through the analysis of the electron spin resonance (ESR) spectra of a spin label incorporated into the bilayer, and the calorimetric data obtained from differential scanning calorimetry (DSC) studies. Upon irradiation, if all lipids had been polymerized, no gel-fluid transition would be expected. However, even samples that went through 20 cycles of UV irradiation presented a DSC band, showing that around 80% of the DC8,9PC molecules were not polymerized. Both DSC and ESR indicated that the two different lipids scarcely mix at low temperatures, however few molecules of DMPC are present in DC8,9PC rich domains and vice versa. UV irradiation was found to affect the gel fluid transition of both DMPC and DC8,9PC rich regions, indicating the presence of polymeric units of DC8,9PC in both areas, A model explaining lipids rearrangement is proposed for this partially polymerized system. Universidade de São Paulo (USP) Universidade de São Paulo USP FAPESP[01/11721-3] Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) UNQ-MPBio UNQ-MPBio[53/1001(PUNQ0396/07)] CONICET Consejo Nacional de Investigaciones Científicas y Técnicas de Argentina (CONICET) Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) MTL (CNPq) ELD (EAPESP) ELD (EAPESP)[06/55493-8] S. del VA (CONICET) Consejo Nacional de Investigaciones Científicas y Técnicas de Argentina (CONICET) Ministério da Ciência, Tecnologia e Inovação do Brasil (MCTI) MCT (UNQ) CET (CONICET)[3100/08] Consejo Nacional de Investigaciones Científicas y Técnicas de Argentina (CONICET) [PIP 5832/05] |
Identificador |
LANGMUIR, v.26, n.12, p.10084-10092, 2010 0743-7463 http://producao.usp.br/handle/BDPI/29194 10.1021/la100214v |
Idioma(s) |
eng |
Publicador |
AMER CHEMICAL SOC |
Relação |
Langmuir |
Direitos |
restrictedAccess Copyright AMER CHEMICAL SOC |
Palavras-Chave | #DRUG-DELIVERY SYSTEMS #BILAYER-MEMBRANES #POLYMERIZATION #PRETRANSITION #STABILITY #TRANSITION #PARAMETERS #BEHAVIOR #CARRIERS #PROGRESS #Chemistry, Multidisciplinary #Chemistry, Physical #Materials Science, Multidisciplinary |
Tipo |
article original article publishedVersion |