Synergistic effect of HPMA copolymer-bound doxorubicin and dexamethasone in vivo on mouse lymphomas

被引:23
作者
Kostkova, Hana [1 ]
Etrych, Tomas [1 ]
Rihova, Blanka [2 ]
Ulbrich, Karel [1 ]
机构
[1] Acad Sci Czech Republic, Inst Macromol Chem, VVI, Prague 16206 6, Czech Republic
[2] Acad Sci Czech Republic, Inst Microbiol, VVI, Prague 14220 4, Czech Republic
关键词
HPMA copolymer; doxorubicin; dexamethasone; drug delivery; combination therapy; B-cell lymphoma; T-cell lymphoma; PEGYLATED LIPOSOMAL DOXORUBICIN; REDUCED-DOSE DEXAMETHASONE; MULTIPLE-MYELOMA; COMBINATION THERAPY; CANCER-CHEMOTHERAPY; PHYSICOCHEMICAL CHARACTERIZATION; ANTITUMOR IMMUNITY; ELDERLY-PATIENTS; DRUG-RELEASE; THALIDOMIDE;
D O I
10.1177/0883911511406326
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
N-(2-Hydroxypropyl) methacrylamide (HPMA) copolymer-drug conjugates bearing the anti-inflammatory and anti-proliferative drug dexamethasone (DEX) and the anti-cancer drug doxorubicin (DOX) bound to either the polymer carrier separately or in combination, were synthesized. Both the in vitro and in vivo anti-cancer activity on mouse B-cell (38C13) and T-cell (EL4) lymphoma was studied. The conjugates were fairly stable in model buffers at pH 7.4, simulating blood pH, and the drug was released by chemical hydrolysis at pH values based on the endosomal and lysosomal environments in the target cells (pH 5-6). As a control, polymer conjugates containing only a single-drug (DOX or DEX) attached to the HPMA copolymer carrier were synthesized and tested. Contrary to the treatment with either single drug conjugate, where no significant long-term survival was observed, a synergistic effect of the two drugs was manifested in vivo. Treatment of mice bearing B-cell lymphoma 38C13 formulated as a mixture of both single drug-containing conjugates or a as a conjugate with both drugs in combination gave long-term survivors.
引用
收藏
页码:270 / 286
页数:17
相关论文
共 33 条
[1]  
ALEXANIAN R, 1992, BLOOD, V80, P887
[2]   Do HPMA copolymer conjugates have a future as clinically useful nanomedicines? A critical overview of current status and future opportunities [J].
Duncan, Ruth ;
Vicent, Maria J. .
ADVANCED DRUG DELIVERY REVIEWS, 2010, 62 (02) :272-282
[3]  
Etrych T, 2002, MACROMOL BIOSCI, V2, P43, DOI 10.1002/1616-5195(20020101)2:1<43::AID-MABI43>3.0.CO
[4]  
2-8
[5]   New HPMA copolymers containing doxorubicin bound via pH-sensitive linkage:: synthesis and preliminary in vitro and in vivo biological properties [J].
Etrych, T ;
Jelínková, M ;
Ríhová, B ;
Ulbrich, K .
JOURNAL OF CONTROLLED RELEASE, 2001, 73 (01) :89-102
[6]  
ETRYCH T, 2009, MACROMOL BIOSCI, V37, P405
[7]   N-(2-hydroxypropyl)methacrylamide-based polymer conjugates with pH-controlled activation of doxorubicin.: I.: New synthesis, physicochemical characterization and preliminary biological evaluation [J].
Etrych, Tomas ;
Mrkvan, Tomas ;
Chytil, Petr ;
Konak, Cestmir ;
Rihova, Blanka ;
Ulbrich, Karel .
JOURNAL OF APPLIED POLYMER SCIENCE, 2008, 109 (05) :3050-3061
[8]   HPMA Copolymer Conjugates of Paclitaxel and Docetaxel with pH-Controlled Drug Release [J].
Etrych, Tomas ;
Sirova, Milada ;
Starovoytova, L. ;
Rihova, Blanka ;
Ulbrich, Karel .
MOLECULAR PHARMACEUTICS, 2010, 7 (04) :1015-1026
[9]   The combination of thalidomide, cyclophosphamide and dexamethasone is potentially useful in highly resistant Hodgkin's lymphoma [J].
Garcia-Sanz, R. ;
Gonzalez-Lopez, T. J. ;
Vazquez, L. ;
Hermida, G. ;
Graciani, I. F. ;
San Miguel, J. F. .
EUROPEAN JOURNAL OF HAEMATOLOGY, 2010, 84 (03) :266-270
[10]   Weekly Bortezomib, Pegylated Liposomal Doxorubicin, and Dexamethasone Is a Safe and Effective Therapy for Elderly Patients With Relapsed/Refractory Multiple Myeloma [J].
Gozzetti, Alessandro ;
Fabbri, Alberto ;
Oliva, Stefania ;
Marchini, Elena ;
Bocchia, Monica ;
Defina, Marzia ;
Lauria, Francesco .
CLINICAL LYMPHOMA MYELOMA & LEUKEMIA, 2010, 10 (01) :68-72