The molecular interaction of quercetin-3-O-palmitate (QP) with dimyristoylphosphatidylcholine (DMPC) has been studied. Film balance measurements of the average molecular area vs QP molar fraction in DMPC/QP mixed monolayers showed that relevant positive deviations from ideality, i.e.. a less dense monolayer packing, occurred for a temperature of 10 degreesC, below the critical melting transition temperature of DMPC monolayers (T-m(C) approximate to 22 degreesC), while ideal behavior was observed at 37 degreesC, above this phase transition temperature. The positive deviation observed at low temperatures in the average molecular area increased with the surface pressure. Scanning probe microscopy measurements performed on mixed monolayers transferred on mica showed that the deviations from ideality were connected to the formation of nanometric-scale QP-rich domains. However, the formation of aggregates was observed only for relatively high-QP molar fractions X-QP greater than or equal to 0.25 at 10 degreesC, while it was not observed at 37 degreesC, i.e., when the ideal mixing was found at the air/water interface. The observed effects are explained in terms of a temperature- and surface pressure-dependent phase-separation process based on the predominance at low temperature and low molecular mobility of QP-QP and DMPC-DMPC aggregation forces, prompting the formation of QP-rich domains embedded in a DMPC-rich matrix. High temperature prompts the QP/DMPC ideal mixing (C) 2003 Elsevier Inc. All rights reserved.

The molecular interaction of quercetin-3-O-palmitate (QP) with dimyristoylphosphatidylcholine (DMPC) has been studied. Film balance measurements of the average molecular area vs QP molar fraction in DMPC/QP mixed monolayers showed that relevant positive deviations from ideality, i.e.. a less dense monolayer packing, occurred for a temperature of 10 degreesC, below the critical melting transition temperature of DMPC monolayers (T-m(C) approximate to 22 degreesC), while ideal behavior was observed at 37 degreesC, above this phase transition temperature. The positive deviation observed at low temperatures in the average molecular area increased with the surface pressure. Scanning probe microscopy measurements performed on mixed monolayers transferred on mica showed that the deviations from ideality were connected to the formation of nanometric-scale QP-rich domains. However, the formation of aggregates was observed only for relatively high-QP molar fractions X-QP greater than or equal to 0.25 at 10 degreesC, while it was not observed at 37 degreesC, i.e., when the ideal mixing was found at the air/water interface. The observed effects are explained in terms of a temperature- and surface pressure-dependent phase-separation process based on the predominance at low temperature and low molecular mobility of QP-QP and DMPC-DMPC aggregation forces, prompting the formation of QP-rich domains embedded in a DMPC-rich matrix. High temperature prompts the QP/DMPC ideal mixing (C) 2003 Elsevier Inc. All rights reserved.

Temperature and pressure dependence of quercetin-3-O-palmitate interaction with a model phospholipid membrane: film balance and scanning probe microscopy study

CASTELLI, Francesco;SARPIETRO, MARIA GRAZIA;MARLETTA, Giovanni
2004-01-01

Abstract

The molecular interaction of quercetin-3-O-palmitate (QP) with dimyristoylphosphatidylcholine (DMPC) has been studied. Film balance measurements of the average molecular area vs QP molar fraction in DMPC/QP mixed monolayers showed that relevant positive deviations from ideality, i.e.. a less dense monolayer packing, occurred for a temperature of 10 degreesC, below the critical melting transition temperature of DMPC monolayers (T-m(C) approximate to 22 degreesC), while ideal behavior was observed at 37 degreesC, above this phase transition temperature. The positive deviation observed at low temperatures in the average molecular area increased with the surface pressure. Scanning probe microscopy measurements performed on mixed monolayers transferred on mica showed that the deviations from ideality were connected to the formation of nanometric-scale QP-rich domains. However, the formation of aggregates was observed only for relatively high-QP molar fractions X-QP greater than or equal to 0.25 at 10 degreesC, while it was not observed at 37 degreesC, i.e., when the ideal mixing was found at the air/water interface. The observed effects are explained in terms of a temperature- and surface pressure-dependent phase-separation process based on the predominance at low temperature and low molecular mobility of QP-QP and DMPC-DMPC aggregation forces, prompting the formation of QP-rich domains embedded in a DMPC-rich matrix. High temperature prompts the QP/DMPC ideal mixing (C) 2003 Elsevier Inc. All rights reserved.
2004
The molecular interaction of quercetin-3-O-palmitate (QP) with dimyristoylphosphatidylcholine (DMPC) has been studied. Film balance measurements of the average molecular area vs QP molar fraction in DMPC/QP mixed monolayers showed that relevant positive deviations from ideality, i.e.. a less dense monolayer packing, occurred for a temperature of 10 degreesC, below the critical melting transition temperature of DMPC monolayers (T-m(C) approximate to 22 degreesC), while ideal behavior was observed at 37 degreesC, above this phase transition temperature. The positive deviation observed at low temperatures in the average molecular area increased with the surface pressure. Scanning probe microscopy measurements performed on mixed monolayers transferred on mica showed that the deviations from ideality were connected to the formation of nanometric-scale QP-rich domains. However, the formation of aggregates was observed only for relatively high-QP molar fractions X-QP greater than or equal to 0.25 at 10 degreesC, while it was not observed at 37 degreesC, i.e., when the ideal mixing was found at the air/water interface. The observed effects are explained in terms of a temperature- and surface pressure-dependent phase-separation process based on the predominance at low temperature and low molecular mobility of QP-QP and DMPC-DMPC aggregation forces, prompting the formation of QP-rich domains embedded in a DMPC-rich matrix. High temperature prompts the QP/DMPC ideal mixing (C) 2003 Elsevier Inc. All rights reserved.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11769/11816
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