Influence of ultrasonic processing on the macromolecular properties of poly (D,L-lactide-co-glycolide) alone and in its biocomposite with hydroxyapatite

被引:6
作者
Vukomanovic, Marija [1 ]
Mitric, Miodrag [2 ]
Skapin, Sreco D. [3 ]
Zagar, Ema [4 ]
Plavec, Janez [4 ]
Ignjatovic, Nenad [1 ]
Uskokovic, Dragan [1 ]
机构
[1] Serbian Acad Arts & Sci, Inst Tech Sci, Belgrade 11000, Serbia
[2] Inst Nucl Sci Vinca, Belgrade, Serbia
[3] Jozef Stefan Inst, Ljubljana, Slovenia
[4] Natl Inst Chem, Ljubljana, Slovenia
关键词
Poly(D; L-lactide-co-glycolide); L-lactide-co-glycolide)/hydroxyapatite composite; Molar mass averages; Composition; Glass-transition temperature; Ultrasonic processing; CONTROLLED DRUG-DELIVERY; MOLECULAR-WEIGHT; DEGRADATION; NANOPARTICLES; MICROSPHERES; SYSTEMS; POLY(DL-LACTIDE-CO-GLYCOLIDE); MICROPARTICLES; EMULSIFICATION; NANOSPHERES;
D O I
10.1016/j.ultsonch.2010.01.007
中图分类号
O42 [声学];
学科分类号
070206 ; 082403 ;
摘要
In this work poly(D,L-lactide-co-glycolide) (PLGA) and a poly(D,L-lactide-co-glycolide)/hydroxyapatite (PLGA/HAp) composite processed in an ultrasonic field at higher (25 degrees C) and lower (8 degrees C) temperatures were studied with respect to the molecular properties of the obtained materials. The processing of the PLGA and the PLGA/HAp composite in an ultrasonic field resulted in a change of molar mass averages of the polymer/polymeric part of these materials, while an amorphous structure and a 50:50 lactide-to-glycolide co-monomer ratio were preserved without the formation of crystalline oligomers. However, mobility of polymeric chains obtained after ultrasonic processing was lower indicating ordering the structure of polymeric chains as a result of processing. Additionally, it was observed that the mobility of the PLGA macromolecules was lower within the composite in comparison with the mobility of the chains within the PLGA alone in the case when both were obtained after ultrasonic processing. This was a consequence of the structure formation through the interactions between the PLGA and the HAp. Based on these results different degradation rate of PLGA in composite can be expected, which is important in the application of this material for the controlled drug delivery of medicaments. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:902 / 908
页数:7
相关论文
共 42 条
[1]   Substitution of osteoporotic alveolar bone by biphasic calcium phosphate/poly-DL-lactide-co-glycolide biomaterials [J].
Ajdukovic, Zorica ;
Ignjatovic, Nenad ;
Petrovic, Dragan ;
Uskokovic, Dragan .
JOURNAL OF BIOMATERIALS APPLICATIONS, 2007, 21 (03) :317-328
[2]   Ultrasound-induced site-specific cleavage of azo-functionalized poly(ethylene glycol) [J].
Berkowski, KL ;
Potisek, SL ;
Hickenboth, CR ;
Moore, JS .
MACROMOLECULES, 2005, 38 (22) :8975-8978
[3]  
Billmeyer F.W., 1984, TXB POLYM SCI
[4]   Ketoprofen poly(lactide-co-glycolide) physical interaction [J].
Blasi, Paolo ;
Schoubben, Aurelie ;
Giovagnoli, Stefano ;
Perioli, Luana ;
Ricci, Maurizio ;
Rossi, Carlo .
AAPS PHARMSCITECH, 2007, 8 (02)
[5]   FULLPAT:: a full-pattern quantitative analysis program for X-ray powder diffraction using measured and calculated patterns [J].
Chipera, SJ ;
Bish, DL .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 2002, 35 :744-749
[6]   The energy efficiency of formation of photons, radicals and ions during single-bubble cavitation [J].
Didenko, YT ;
Suslick, KS .
NATURE, 2002, 418 (6896) :394-397
[7]   Factorial design, physicochemical characterisation and activity of ciprofloxacin-PLGA nanoparticles [J].
Dillen, K ;
Vandervoort, J ;
Van den Mooter, G ;
Verheyden, L ;
Ludwig, A .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2004, 275 (1-2) :171-187
[8]   INTERPARTICLE COLLISIONS DRIVEN BY ULTRASOUND [J].
DOKTYCZ, SJ ;
SUSLICK, KS .
SCIENCE, 1990, 247 (4946) :1067-1069
[9]   Flow-through ultrasonic emulsification combined with static micromixing for aseptic production of microspheres by solvent extraction [J].
Freitas, S ;
Rudolf, B ;
Merkle, HP ;
Gander, B .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2005, 61 (03) :181-187
[10]   Continuous contact- and contamination-free ultrasonic emulsification - a useful tool for pharmaceutical development and production [J].
Freitas, S ;
Hielscher, G ;
Merkle, HP ;
Gander, B .
ULTRASONICS SONOCHEMISTRY, 2006, 13 (01) :76-85