Number-concentration of nanoparticles in liposomal and polymeric multiparticulate preparations: Empirical and calculation methods

被引:41
作者
Epstein, H
Afergan, E
Moise, T
Richter, Y
Rudich, Y [1 ]
Golomb, G
机构
[1] Weizmann Inst Sci, Dept Environm Sci & Energy Res, IL-76100 Rehovot, Israel
[2] Hebrew Univ Jerusalem, Fac Med, Sch Pharm, IL-91120 Jerusalem, Israel
[3] Biorest Ltd, Tel Aviv, Israel
关键词
particles; number concentration; nanoparticles; liposomes;
D O I
10.1016/j.biomaterials.2005.06.006
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
The actual number of particles in formulations of nanoparticles (NP) is of importance for quality assurance, comprehensive physicochemical characterization, and pharmacodynamics. Some calculation methods that have been previously employed are limited because they rely on several assumptions and are not applicable for certain preparations. Currently there are no validated experimental methods for determining the particle number-concentration (N-c)of liposomal and polymeric nanoparticulate preparations (< 500 nm). This study examines a new empirical method for counting the number of particles in nanoparticulate formulations including drug-containing liposomes and polymeric NP. In the new method, suspended NP are nebulized to form aerosol droplets which are dried and counted using a scanning mobility particle sizer (SMPS). Experiments were conducted with three different preparations, empty liposomes (200 and 400 nm), drug-loaded liposomes (200 nm), and polymeric NP (150 nm). It was verified that no detrimental morphological or structural changes of the formulations have been induced by the SMPS technique, and that the obtained N-c, values represent the original particles. It is concluded that nano-formulations with concentrations of up to 10, particles per 1 cm(3) air, corresponding to approximately 10(12) particles per 1 ml solution, can be directly counted within the size range of 30-900 nm. The measured values are compared to newly developed theoretical calculations to assess the viability of these calculations. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:651 / 659
页数:9
相关论文
共 33 条
[1]
Numerical simulations of surface plasmon resonance system for monitoring DNA hybridization and detecting protein lipid film interactions [J].
Caide, X ;
Sui, SF .
EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS, 1999, 28 (02) :151-157
[2]
Sustained delivery and expression of DNA encapsulated in polymeric nanoparticles [J].
Cohen, H ;
Levy, RJ ;
Gao, J ;
Fishbein, I ;
Kousaev, V ;
Sosnowski, S ;
Slomkowski, S ;
Golomb, G .
GENE THERAPY, 2000, 7 (22) :1896-1905
[3]
Novel PDGFβR antisense encapsulated in polymeric nanospheres for the treatment of restenosis [J].
Cohen-Sacks, H ;
Najajreh, Y ;
Tchaikovski, V ;
Gao, G ;
Elazer, V ;
Dahan, R ;
Gati, I ;
Kanaan, M ;
Waltenberger, J ;
Golomb, G .
GENE THERAPY, 2002, 9 (23) :1607-1616
[4]
Liposomal alendronate inhibits systemic innate immunity and reduces in-stent neointimal hyperplasia in rabbits [J].
Danenberg, HD ;
Golomb, G ;
Groothuis, A ;
Gao, JC ;
Epstein, H ;
Swaminathan, RV ;
Seifert, P ;
Edelman, ER .
CIRCULATION, 2003, 108 (22) :2798-2804
[5]
Systemic depletion of macrophages by liposomal bisphosphonates reduces neointimal formation following balloon-injury in the rat carotid artery [J].
Danenberg, HD ;
Fishbein, I ;
Epstein, H ;
Waltenberger, J ;
Moerman, E ;
Mönkkönen, J ;
Gao, XC ;
Gathi, I ;
Reichi, R ;
Golomb, G .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2003, 42 (05) :671-679
[6]
Macrophage depletion by clodronate-containing liposomes reduces neointimal formation after balloon injury in rats and rabbits [J].
Danenberg, HD ;
Fishbein, I ;
Gao, JC ;
Mönkkönen, J ;
Reich, R ;
Gati, I ;
Moerman, E ;
Golomb, G .
CIRCULATION, 2002, 106 (05) :599-605
[7]
de Lima MCP, 1999, MOL MEMBR BIOL, V16, P103
[8]
A peptide prodrug approach for improving bisphosphonate oral absorption [J].
Ezra, A ;
Hoffman, A ;
Breuer, E ;
Alferiev, IS ;
Mönkkönen, J ;
El Hanany-Rozen, N ;
Weiss, G ;
Stepensky, D ;
Gati, I ;
Cohen, H ;
Törmälehto, S ;
Amidon, GL ;
Golomb, G .
JOURNAL OF MEDICINAL CHEMISTRY, 2000, 43 (20) :3641-3652
[9]
Encapsulation of mithramycin in liposomes in response to a transmembrane gradient of calcium ions [J].
Frezard, F ;
GarnierSuillerot, A ;
Demicheli, C .
JOURNAL OF INCLUSION PHENOMENA AND MOLECULAR RECOGNITION IN CHEMISTRY, 1997, 28 (01) :51-62
[10]
Osmotic properties of poly(ethylene glycols): Quantitative features of brush and bulk scaling laws [J].
Hansen, PL ;
Cohen, JA ;
Podgornik, R ;
Parsegian, VA .
BIOPHYSICAL JOURNAL, 2003, 84 (01) :350-355