PLGA-based nanoparticles: Effect of chitosan in the aggregate stabilization. A dielectric relaxation spectroscopy study

被引:20
作者
Chronopoulou, L. [3 ]
Cutonilli, A. [3 ]
Cametti, C. [1 ,2 ]
Dentini, M. [3 ]
Palocci, C. [3 ]
机构
[1] Univ Roma La Sapienza, Dept Phys, I-00185 Rome, Italy
[2] Univ Roma La Sapienza, INFM CNR SOFT, I-00185 Rome, Italy
[3] Univ Roma La Sapienza, Dept Chem, I-00185 Rome, Italy
关键词
PLGA nanoparticles; Dielectric relaxation; Chitosan-induced aggregation; Drug release; CHARGED LIPOSOMES; COMPLEX; CONDUCTIVITY; DELIVERY; MICROPARTICLES; MICROSPHERES; POLYLYSINE; PARTICLES; POLYMERS; FACETS;
D O I
10.1016/j.colsurfb.2012.04.016
中图分类号
Q6 [生物物理学];
学科分类号
071011 [生物物理学];
摘要
Chitosan-modified polylactic-co-glycolic acid (PLGA) nanoparticles with average diameter of 200 nm in PBS buffer solution have been investigated by means of dielectric relaxation spectroscopy measurements in the frequency range (1 MHz-2 GHz) where interfacial polarizations occur. PLGA-based nanoparticles offer remarkable advantages in different biotechnological fields, such as their biocompatibility, easiness of administration and rather complete biodegradation. However, despite the use of these drug delivery systems is increasing, little is known about the basic process involved in the formation of complexes and in the subsequent release kinetics. In the present work, we have characterized the colloidal behavior of PLGA-based nanoparticles in the presence of oppositely charged chitosan polyelectrolyte by means of dynamic light scattering, electrophoretic mobility and radiowave dielectric relaxation measurements. In particular, we have emphasized how the presence of a coating layer at the nanoparticle surface could exert a marked slowing-down in the drug release. The consequence of this finding is briefly discussed at the light of some biological implications. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:117 / 123
页数:7
相关论文
共 37 条
[1]
Structure of poly(acrylic acid) in electrolyte solutions determined from simulations and viscosity measurements [J].
Adamczyk, Z. ;
Bratek, A. ;
Jachimska, B. ;
Jasinski, T. ;
Warszynski, P. .
JOURNAL OF PHYSICAL CHEMISTRY B, 2006, 110 (45) :22426-22435
[2]
Responsive polymers at the biology/materials science interface [J].
Alexander, Cameron ;
Shakesheff, Kevin M. .
ADVANCED MATERIALS, 2006, 18 (24) :3321-3328
[3]
MICROWAVE DIELECTRIC MEASUREMENTS OF ERYTHROCYTE SUSPENSIONS [J].
BAO, JZ ;
DAVIS, CC ;
SWICORD, ML .
BIOPHYSICAL JOURNAL, 1994, 66 (06) :2173-2180
[4]
Stimuli-responsive polymers and their applications in drug delivery [J].
Bawa, Priya ;
Pillay, Viness ;
Choonara, Yahya E. ;
du Toit, Lisa C. .
BIOMEDICAL MATERIALS, 2009, 4 (02)
[5]
Strong repulsive interactions in polyelectrolyte-liposome clusters close to the isoelectric point: A sign of an arrested state [J].
Bordi, F. ;
Cametti, C. ;
Sennato, S. ;
Truzzolillo, D. .
PHYSICAL REVIEW E, 2007, 76 (06)
[6]
Dielectric spectroscopy and conductivity of polyelectrolyte solutions [J].
Bordi, F ;
Cametti, C ;
Colby, RH .
JOURNAL OF PHYSICS-CONDENSED MATTER, 2004, 16 (49) :R1423-R1463
[7]
Determination of polyelectrolyte charge and interaction with water using dielectric spectroscopy [J].
Bordi, F ;
Cametti, C ;
Tan, JS ;
Boris, DC ;
Krause, WE ;
Plucktaveesak, N ;
Colby, RH .
MACROMOLECULES, 2002, 35 (18) :7031-7038
[8]
Electrical conductivity of polyelectrolyte solutions in the semidilute and concentrated regime: The role of counterion condensation [J].
Bordi, F ;
Colby, RH ;
Cametti, C ;
De Lorenzo, L ;
Gili, T .
JOURNAL OF PHYSICAL CHEMISTRY B, 2002, 106 (27) :6887-6893
[9]
Polyion-induced aggregation of oppositely charged liposomes and charged colloidal particles: The many facets of complex formation in low-density colloidal systems [J].
Cametti, C. .
CHEMISTRY AND PHYSICS OF LIPIDS, 2008, 155 (02) :63-73
[10]
Versatile electrostatic assembly of nanoparticles and polyelectrolytes: Coating, clustering and layer-by-layer processes [J].
Chapel, J. -P. ;
Berret, J. -F. .
CURRENT OPINION IN COLLOID & INTERFACE SCIENCE, 2012, 17 (02) :97-105