Differences in physicochemical properties to consider in the design, evaluation and choice between microparticles and nanoparticles for drug delivery

被引:33
作者
Otto, Daniel P. [1 ]
Otto, Anja [2 ]
de Villiers, Melgardt M. [3 ]
机构
[1] North West Univ, Res Focus Area, Chem Resource Beneficiat Catalysis & Synth Res Gr, ZA-2531 Potchefstroom, South Africa
[2] North West Univ, Ctr Excellence Pharmaceut Sci, ZA-2531 Potchefstroom, South Africa
[3] Univ Wisconsin, Sch Med, Madison, WI 53705 USA
关键词
delivery; drug; micrometer; nanometer; DISSIPATIVE PARTICLE DYNAMICS; TISSUE DISTRIBUTION; IN-VIVO; NANO-PARTICLES; DISSOLUTION RATE; EX-VIVO; SIZE; MICRO; SOLUBILITY; DEPOSITION;
D O I
10.1517/17425247.2015.988135
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: The increase in the development of novel nanoparticle drug delivery systems makes the choice between micro- and nanoscale drug delivery systems ubiquitous. Changes in physical and chemical properties between micro- to nanosized particles give them different properties that influence their physiological, anatomical and clinical behavior and therefore potential application. Areas covered: This review focuses on the effect changes in the surface- to- volume ratio have on the thermal properties, solubility, dissolution and crystallization of micro- versus nanosized drug delivery systems. With these changes in the physicochemical properties in mind, the review covers computational and biophysical approaches to the design and evaluation of micro- and nano-delivery systems. The emphasis of the review is on the effect these properties have on clinical performance in terms of drug release, tissue retention, biodistribution, efficacy, toxicity and therefore choice of delivery system. Expert opinion: Ultimately, the choice between micro- and nanometer-sized delivery systems is not straightforward. However, if the fundamental differences in physical and chemical properties are considered, it can be much easier to make a rational choice of the appropriate drug delivery system size.
引用
收藏
页码:763 / 777
页数:15
相关论文
共 86 条
[1]   Micro and nanoparticle deposition in human nasal passage pre and post virtual maxillary sinus endoscopic surgery [J].
Abouali, Omid ;
Keshavarzian, Erfan ;
Ghalati, Pejman Farhadi ;
Faramarzi, Abolhasan ;
Ahmadi, Goodarz ;
Bagheri, Mohammad Hadi .
RESPIRATORY PHYSIOLOGY & NEUROBIOLOGY, 2012, 181 (03) :335-345
[2]   Evaluation of cytotoxic, genotoxic and inflammatory responses of micro- and nano-particles of granite on human lung fibroblast cell IMR-90 [J].
Ahmad, Iqbal ;
Khan, Mohd Imran ;
Patil, Govil ;
Chauhan, L. K. S. .
TOXICOLOGY LETTERS, 2012, 208 (03) :300-307
[3]   Nano-encapsulation of furosemide microcrystals for controlled drug release [J].
Ai, H ;
Jones, SA ;
de Villiers, MM ;
Lvov, YM .
JOURNAL OF CONTROLLED RELEASE, 2003, 86 (01) :59-68
[4]   Size-dependent disposition of nanoparticles and microparticles following subconjunctival administration [J].
Amrite, AC ;
Kompella, UB .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2005, 57 (12) :1555-1563
[5]   PHYSICOCHEMICAL ASPECTS OF DRUG RELEASE .7. THE EFFECT OF SURFACTANT CONCENTRATION AND DRUG PARTICLE-SIZE ON SOLUBILITY AND DISSOLUTION RATE OF FELODIPINE, A SPARINGLY SOLUBLE DRUG [J].
ANDERBERG, EK ;
BISRAT, M ;
NYSTROM, C .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1988, 47 (1-3) :67-77
[6]   Is the C60 fullerene molecule toxic?! [J].
Andrievsky, G ;
Klochkov, V ;
Derevyanchenko, L .
FULLERENES NANOTUBES AND CARBON NANOSTRUCTURES, 2005, 13 (04) :363-376
[7]   Inhalation toxicity and lung toxicokinetics of C60 fullerene nanoparticles and microparticles [J].
Baker, Gregory L. ;
Gupta, Amit ;
Clark, Mark L. ;
Valenzuela, Blandina R. ;
Staska, Lauren M. ;
Harbo, Sam J. ;
Pierce, Judy T. ;
Dill, Jeffery A. .
TOXICOLOGICAL SCIENCES, 2008, 101 (01) :122-131
[8]   Melting of nanostructured drugs embedded into a polymeric matrix [J].
Bergese, P ;
Colombo, I ;
Gervasoni, D ;
Depero, LE .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (40) :15488-15493
[9]   PHYSICOCHEMICAL ASPECTS OF DRUG RELEASE .8. THE RELATION BETWEEN PARTICLE-SIZE AND SURFACE SPECIFIC DISSOLUTION RATE IN AGITATED SUSPENSIONS [J].
BISRAT, M ;
NYSTROM, C .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1988, 47 (1-3) :223-231
[10]   Optimizing particle size for targeting diseased microvasculature: from experiments to artificial neural networks [J].
Boso, Daniela P. ;
Lee, Sei-Young ;
Ferrari, Mauro ;
Schrefler, Bernhard A. ;
Decuzzi, Paolo .
INTERNATIONAL JOURNAL OF NANOMEDICINE, 2011, 6 :1517-1526