A review of therapeutic challenges and achievements of methotrexate delivery systems for treatment of cancer and rheumatoid arthritis

被引:204
作者
Abolmaali, Samira Sadat [1 ]
Tamaddon, Ali Mohammad [1 ]
Dinarvand, Rassoul [2 ]
机构
[1] Shiraz Univ Med Sci, Fac Pharm, Pharmaceut Nanotechnol & Biomat Res Ctr, Shiraz 71345, Iran
[2] Univ Tehran Med Sci, Fac Pharm, Nanotechnol Res Ctr, Tehran 14174, Iran
关键词
Methotrexate; Cancer; Rheumatoid arthritis; Drug delivery; Nanoparticle; Drug conjugate; Human serum albumin; Liposome; Microsphere; Dendrimer; LIPOSOMALLY CONJUGATED METHOTREXATE; TARGETED DRUG-DELIVERY; FOLATE RECEPTOR-BETA; IN-VITRO; ANTITUMOR-ACTIVITY; GELATIN MICROSPHERES; CONTROLLED-RELEASE; MOLECULAR-WEIGHT; ANTICANCER DRUG; INTRAARTICULAR DELIVERY;
D O I
10.1007/s00280-012-2062-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Methotrexate (MTX) is one of the most widely studied and effective therapeutics agents available to treat many solid tumors, hematologic malignancies, and autoimmune diseases such as rheumatoid arthritis; however, the poor pharmacokinetic and narrow safety margin of the drug limits the therapeutic outcomes of conventional drug delivery systems. For an improved delivery of MTX, several pathophysiological features such as angiogenesis, enhanced permeability and retention effects, acidosis, and expression of specific antigens and receptors can be used either as targets or as tools for drug delivery. There are many novel delivery systems developed to improve the pitfalls of MTX therapy ranged from polymeric conjugates such as human serum albumin, liposomes, microspheres, solid lipid nanoparticles, polymeric nanoparticles, dendrimers, polymeric micelles, in situ forming hydrogels, carrier erythrocyte, and nanotechnology-based vehicles such as carbon nanotubes, magnetic nanoparticles, and gold nanoparticles. Some are further modified with targeting ligands for active targeting purposes. Such delivery systems provide prolonged plasma profile, enhanced and specific activity in vitro and in vivo in animal models. Nevertheless, more complementary studies are needed before they can be applied in human. This review deals with the challenges of conventional systems and achievements of each pharmaceutical class of novel drug delivery vehicle.
引用
收藏
页码:1115 / 1130
页数:16
相关论文
共 127 条
[1]   Preparation and optimization of surface-treated methotrexate-loaded nanogels intended for brain delivery [J].
Azadi, Amir ;
Hamidi, Mehrdad ;
Khoshayand, Mohammad-Reza ;
Amini, Mohsen ;
Rouini, Mohammad-Reza .
CARBOHYDRATE POLYMERS, 2012, 90 (01) :462-471
[2]   Accumulation of methotrexate in systemic tissues after intrathecal administration [J].
Bleyer, WA ;
Nelson, JA ;
Kamen, BA .
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 1997, 19 (06) :530-532
[3]  
BLEYER WA, 1978, CANCER-AM CANCER SOC, V41, P36, DOI 10.1002/1097-0142(197801)41:1<36::AID-CNCR2820410108>3.0.CO
[4]  
2-I
[5]   Characterization and in vitro methotrexate release from methotrexate/gelatin conjugates of opposite conjugate bond polarity [J].
Bowman, BJ ;
Ofner, CM .
PHARMACEUTICAL RESEARCH, 2000, 17 (10) :1309-1315
[6]   Gelatin nanoparticles produced by a simple W/O emulsion as delivery system for methotrexate [J].
Cascone, MG ;
Lazzeri, L ;
Carmignani, C ;
Zhu, ZH .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2002, 13 (05) :523-526
[7]   THERMAL AND PHOTOLYTIC DECOMPOSITION OF METHOTREXATE IN AQUEOUS-SOLUTIONS [J].
CHATTERJI, DC ;
GALLELLI, JF .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1978, 67 (04) :526-531
[8]   Investigation of targeting mechanism of new dextran-peptide-methotrexate conjugates using biodistribution study in matrix-metalloproteinase-overexpressing tumor xenograft model [J].
Chau, Y ;
Dang, NM ;
Tan, FE ;
Langer, R .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2006, 95 (03) :542-551
[9]   Synthesis and characterization of dextran-peptide-methotrexate conjugates for tumor targeting via mediation by matrix metalloproteinase II and matrix metalloproteinase IX [J].
Chau, Y ;
Tan, FE ;
Langer, R .
BIOCONJUGATE CHEMISTRY, 2004, 15 (04) :931-941
[10]   Methotrexate conjugated to gold nanoparticles inhibits tumor growth in a syngeneic lung tumor model [J].
Chen, Yu-Hung ;
Tsai, Chiau-Yuang ;
Huang, Pon-Yu ;
Chang, Meng-Ya ;
Cheng, Pai-Chiao ;
Chou, Chen-Hsi ;
Chen, Dong-Hwang ;
Wang, Chrong-Reen ;
Shiau, Ai-Li ;
Wu, Chao-Liang .
MOLECULAR PHARMACEUTICS, 2007, 4 (05) :713-722