FORMULATION AND EVALUATION OF MICROSPHERES CONTAINING LOSARTAN POTASSIUM BY SPRAY-DRYING TECHNIQUE

被引:0
作者
Balwierz, Radoslaw [1 ]
Jankowski, Andrzej [1 ]
Jasinska, Agata [2 ]
Marciniak, Dominik [3 ]
Pluta, Janusz [3 ]
机构
[1] Med Univ Silesia, Dept Appl Pharm, Inst Pharmaceut Technol, 3 Kasztanowa St, PL-41200 Sosnowiec, Poland
[2] City Hosp Chorzow, Dept Internal Med, 11 Strzelcow Bytomskich St, PL-41500 Chorzow, Poland
[3] Wroclaw Med Univ, Dept & Inst Pharmaceut Technol, 211 Borowska St, PL-50556 Wroclaw, Poland
来源
ACTA POLONIAE PHARMACEUTICA | 2016年 / 73卷 / 05期
关键词
losartan potassium; microspheres; spray drying; Eudragit L30D55; kinetics; EUDRAGIT MICROPARTICLES; DELIVERY; RELEASE; MICROENCAPSULATION; PARAMETERS;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Despite numerous applications of microspheres, few works devoted to the preparation of microspheres containing cardiac medications have been published. This study presents the potential of receiving microspheres containing losartan potassium, based on a matrix containing Eudragit L30D55. The study focuses on the possibilities of controlled release of losartan potassium from microspheres in order to reduce the dosage frequency, and also provides information on the effect of the addition of excipients to the quality of the microspheres. Microspheres are monolithic, porous or smooth microparticles ranging from 1 to 500 microns in size. For the preparation of microspheres containing losartan potassium, the spray-drying method was used. The performed study confirmed that the spray-drying technology used to obtain microspheres meets the criteria of size and morphology of the microparticles. The assessment of the kinetics of losartan potassium release from the examined microspheres demonstrated that the release profile followed the first- and/or zero-order kinetics. The use of spray-drying techniques as well as Eudragit L30D55 polymer matrix to obtain the microspheres containing losartan potassium makes it possible to obtain a product with the required particle morphology and particle size ensuring the release of the active substance up to 12 h.
引用
收藏
页码:1275 / 1286
页数:12
相关论文
共 38 条
  • [1] A new oral vaccine candidate based on the microencapsulation by spray-drying of inactivated Vibrio cholerae
    Ano, Gemma
    Esquisabel, Amaia
    Pastor, Marta
    Talavera, Arturo
    Cedre, Barbara
    Fernandez, Sonsire
    Sifontes, Sergio
    Aranguren, Yisabel
    Falero, Gustavo
    Garcia, Luis
    Lydia Solis, Rosa
    Luis Pedraz, Jose
    [J]. VACCINE, 2011, 29 (34) : 5758 - 5764
  • [2] Balcerkiewicz M., 2007, NOW LEK, V76, P384
  • [3] BALWIERZ R, 2013, FARM POL, V69, P375
  • [4] Biodegradable microspheres of novel segmented poly(ether-ester-amide)s based on poly(ε-caprolactone) for the delivery of bioactive compounds
    Barbato, F
    La Rotonda, MI
    Maglio, G
    Palumbo, R
    Quaglia, F
    [J]. BIOMATERIALS, 2001, 22 (11) : 1371 - 1378
  • [5] RELATION BETWEEN INDIVIDUAL AND ENSEMBLE RELEASE KINETICS OF INDOMETHACIN FROM MICROSPHERES
    BENITA, S
    BABAY, D
    HOFFMAN, A
    DONBROW, M
    [J]. PHARMACEUTICAL RESEARCH, 1988, 5 (03) : 178 - 182
  • [6] Spray Drying Technique. I: Hardware and Process Parameters
    Cal, Krzysztof
    Sollohub, Krzysztof
    [J]. JOURNAL OF PHARMACEUTICAL SCIENCES, 2010, 99 (02) : 575 - 586
  • [7] Dash S, 2010, ACTA POL PHARM, V67, P217
  • [8] A Model-Based Methodology for Spray-Drying Process Development
    Dobry, Dan E.
    Settell, Dana M.
    Baumann, John M.
    Ray, Rod J.
    Graham, Lisa J.
    Beyerinck, Ron A.
    [J]. JOURNAL OF PHARMACEUTICAL INNOVATION, 2009, 4 (03) : 133 - 142
  • [9] Production of Eudragit microparticles by spray-drying technique: Influence of experimental parameters on morphological and dimensional characteristics
    Esposito, E
    Roncarati, R
    Cortesi, R
    Cervellati, F
    Nastruzzi, C
    [J]. PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY, 2000, 5 (02) : 267 - 278
  • [10] Polymer microspheres for controlled drug release
    Freiberg, S
    Zhu, X
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2004, 282 (1-2) : 1 - 18