Biocompatible stabilizers in the preparation of PLGA nanoparticles: a factorial design study

被引:193
|
作者
Vandervoort, J [1 ]
Ludwig, A [1 ]
机构
[1] Univ Instelling Antwerp, Dept Pharmaceut Sci, Lab Pharmaceut Technol & Biopharm, B-2610 Antwerp, Belgium
关键词
PLGA; nanoparticles; emulsification solvent evaporation; stabilizer; experimental design; response surface;
D O I
10.1016/S0378-5173(02)00058-3
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Poly(lactic-co-glycolic-acid) nanoparticles are often produced using the w/o/w emulsification solvent evaporation method. In most cases poly(vinyl alcohol) (PVA) is used as stabilizer of the emulsion. The goal of this study was to compare a series of polymers to PVA in a 21 full factorial design study. The influence of the concentration of PVA and the polymers tested on particle size and zeta potential value was evaluated before and after freeze-drying of the prepared particles. Nanoparticles were obtained with most polymers when they were used in combination with PVA. Leaving PVA out of the formulation, however, increased the size of the particles over 1 mum. Two exceptions are poloxamer and carbopol, which can be considered as valuable alternatives to PVA. Zeta potential values were usually slightly negative, the most extreme zeta potential values were measured when poloxamer and carbopol were employed. The use of gelatin type A made it possible to achieve positive values. The original 2(2) full factorial design study was further expanded to a central composite design for poloxamer and carbopol, in order to fit the measured data to a quadratic model and to calculate response surfaces. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:77 / 92
页数:16
相关论文
共 50 条
  • [1] Preparation, characterization and optimization of sildenafil citrate loaded PLGA nanoparticles by statistical factorial design
    Ghasemian, Elham
    Vatanara, Alireza
    Najafabadi, Abdolhossein Rouholamini
    Rouini, Mohammad Reza
    Gilani, Kambiz
    Darabi, Majid
    DARU-JOURNAL OF PHARMACEUTICAL SCIENCES, 2013, 21
  • [2] Preparation, characterization and optimization of sildenafil citrate loaded PLGA nanoparticles by statistical factorial design
    Elham Ghasemian
    Alireza Vatanara
    Abdolhossein Rouholamini Najafabadi
    Mohammad Reza Rouini
    Kambiz Gilani
    Majid Darabi
    DARU Journal of Pharmaceutical Sciences, 21
  • [3] Preparation, optimization by 23 factorial design, characterization and in vitro release kinetics of lorazepam loaded PLGA nanoparticles
    Bohrey, S.
    Chourasiya, V.
    Pandey, A.
    POLYMER SCIENCE SERIES A, 2016, 58 (06) : 975 - 986
  • [4] Preparation, optimization by 23 factorial design, characterization and in vitro release kinetics of lorazepam loaded PLGA nanoparticles
    S. Bohrey
    V. Chourasiya
    A. Pandey
    Polymer Science Series A, 2016, 58 : 975 - 986
  • [5] Factorial design, physicochemical characterisation and activity of ciprofloxacin-PLGA nanoparticles
    Dillen, K
    Vandervoort, J
    Van den Mooter, G
    Verheyden, L
    Ludwig, A
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2004, 275 (1-2) : 171 - 187
  • [6] Preparation factors affecting the properties of polylactide nanoparticles: a factorial design study
    Vandervoort, J
    Ludwig, A
    PHARMAZIE, 2001, 56 (06): : 484 - 488
  • [7] Factorial design based preparation, optimization, characterization and in vitro drug release studies of olanzapine loaded PLGA nanoparticles
    Bohrey, Sarvesh
    Chourasiya, Vibha
    Pandey, Archna
    MATERIALS RESEARCH EXPRESS, 2016, 3 (12):
  • [8] Quality by Design as a Tool in the Optimisation of Nanoparticle Preparation-A Case Study of PLGA Nanoparticles
    Struzek, Anna-Maria
    Scherliess, Regina
    PHARMACEUTICS, 2023, 15 (02)
  • [9] Preparation of biocompatible magnetite-PLGA composite nanoparticles using supercritical fluid extraction of emulsions
    Furlan, Marco
    Kluge, Johannes
    Mazzotti, Marco
    Lattuada, Marco
    JOURNAL OF SUPERCRITICAL FLUIDS, 2010, 54 (03): : 348 - 356
  • [10] Preparation of biocompatible magnetite-PLGA composite nanoparticles using supercritical fluid extraction of emulsions
    ETH Zurich, Institute for Chemical- and Bioengineering, Wolfgang-Pauli-Strasse 10, 8093 Zurich, Switzerland
    不详
    J. Supercritical Fluids, 3 (348-356):