Anti-bacterial performance of azithromycin nanoparticles as colloidal drug delivery system against different gram-negative and grampositive bacteria

被引:47
作者
Azhdarzadeh, Morteza [1 ,2 ]
Lotfipour, Farzaneh [3 ,4 ]
Zakeri-Milani, Parvin [3 ,5 ]
Mohammadi, Ghobad [6 ]
Valizadeh, Hadi [1 ,3 ]
机构
[1] Tabriz Univ Med Sci, Res Ctr Pharmaceut Nanotechnol, Tabriz, Iran
[2] Tabriz Univ Med Sci, Students Res Comm, Tabriz, Iran
[3] Tabriz Univ Med Sci, Fac Pharm, Tabriz, Iran
[4] Tabriz Univ Med Sci, Biotechnol Res Ctr, Tabriz, Iran
[5] Tabriz Univ Med Sci, Liver & Gastrointestinal Dis Res Ctr, Tabriz, Iran
[6] Kermanshah Univ Med Sci, Fac Pharm, Kermanshah, Iran
关键词
Azithromycin; PLGA; Nanoparticle; Modified quasi emulsion solvent-diffusion; Minimum inhibitory concentration;
D O I
10.5681/apb.2012.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Purpose: Azithromycin (AZI) is a new macrolide antibiotic with a better activity against intracellular gram negative bacteria in comparison with Erythromycin. The purpose of this research was to prepare AZI nanoparticles (NPs) using PLGA polymer and to compare the effectiveness of prepared nanoparticles with untreated AZI solution. Methods: AZI NPs were prepared by Modified Quasi-Emulsion Solvent Diffusion method. The antibacterial activities of prepared NPs in comparison with AZI solution were assayed against indicator bacteria of Escherichia coli (PTCC 1330), Haemophilus influenzae (PTCC 1623) and Streptococcus pneumoniae (PTCC 1240) using agar well diffusion. Inhibition zone diameters (IZD) of nano-formulation were compared to the corresponding untreated AZI. Mean Inhibitory Concentration (MIC) values of AZI were also determined using serial dilution method in nutrient broth medium. Results: Mean IZD of nano-formulations for all indicator bacteria were significantly higher than that of untreated AZI (P < 0.01). The enhanced antibacterial efficacy was more dominant in the gram positive species. The MIC values of NPs against the tested bacteria were reduced 8 times in comparison to those of untreated AZI. Conclusion: These results indicated an improved potency of AZI NPs which could be attributed to the modified surface characteristics as well as increased drug adsorption and uptake.
引用
收藏
页码:17 / 24
页数:8
相关论文
共 29 条
  • [1] Thermal treating as a tool for sustained release of indomethacin from Eudragit RS and RL matrices
    Azarmi, S
    Farid, J
    Nokhodchi, A
    Bahari-Saravi, SM
    Valizadeh, H
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2002, 246 (1-2) : 171 - 177
  • [2] SYNTHESIS AND RGD PEPTIDE MODIFICATION OF A NEW BIODEGRADABLE COPOLYMER - POLY(LACTIC ACID-CO-LYSINE)
    BARRERA, DA
    ZYLSTRA, E
    LANSBURY, PT
    LANGER, R
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (23) : 11010 - 11011
  • [3] The mechanism of uptake of biodegradable microparticles in Caco-2 cells is size dependent
    Desai, MP
    Labhasetwar, V
    Walter, E
    Levy, RJ
    Amidon, GL
    [J]. PHARMACEUTICAL RESEARCH, 1997, 14 (11) : 1568 - 1573
  • [4] Adhesion of PLGA or Eudragit®/PLGA nanoparticles to Staphylococcus and, Pseudomonas
    Dillen, Kathleen
    Bridts, Chris
    Van der Veken, Pieter
    Cos, Paul
    Vandervoort, Jo
    Augustyns, Koen
    Stevens, Wim
    Ludwig, Annick
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2008, 349 (1-2) : 234 - 240
  • [5] Preparation and antibacterial activity evaluation of rifampicin-loaded poly lactide-co-glycolide nanoparticles
    Esmaeili, Farnaz
    Hosseini-Nasr, Mahdi
    Rad-Malekshahi, Mazda
    Samadi, Nasrin
    Atyabi, Fatemeh
    Dinarvand, Rassoul
    [J]. NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, 2007, 3 (02) : 161 - 167
  • [6] TREATMENT OF EXPERIMENTAL SALMONELLOSIS IN MICE WITH AMPICILLIN-BOUND NANOPARTICLES
    FATTAL, E
    YOUSSEF, M
    COUVREUR, P
    ANDREMONT, A
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1989, 33 (09) : 1540 - 1543
  • [7] Ciprofloxacin-loaded polyisobutylcyanoacrylate nanoparticles: pharmacokinetics and in vitro antimicrobial activity
    Fawaz, F
    Bonini, F
    Maugein, J
    Lagueny, AM
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1998, 168 (02) : 255 - 259
  • [8] Preparation, characterization, and drug release behaviors of drug nimodipine-loaded poly(ε-caprolactone)-poly(ethylene oxide)-poly(ε-caprolactone) amphiphilic triblock copolymer micelles
    Ge, HX
    Hu, Y
    Jiang, XQ
    Cheng, DM
    Yuan, YY
    Bi, H
    Yang, CZ
    [J]. JOURNAL OF PHARMACEUTICAL SCIENCES, 2002, 91 (06) : 1463 - 1473
  • [9] Metabolic Limitations of the Use of Nucleoside Analogs in Cancer Therapy May Be Overcome by Application of Nanoparticles as Drug Carriers: A Review
    Hajdo, Lukasz
    Szulc, Aleksandra Beata
    Klajnert, Barbara
    Bryszewska, Maria
    [J]. DRUG DEVELOPMENT RESEARCH, 2010, 71 (07) : 383 - 394
  • [10] PLA Nanoparticles Loaded With an Active Lactone Form of Hydroxycamptothecin: Development, Optimization, and In Vitro-In Vivo Evaluation in Mice Bearing H22 Solid Tumor
    Hou, Zhenqing
    Zhou, Chunxiao
    Luo, Ying
    Zhan, Chuanming
    Wang, Yixiao
    Xie, Liya
    Zhang, Qiqing
    [J]. DRUG DEVELOPMENT RESEARCH, 2011, 72 (04) : 337 - 345