Alternative drug formulations of docetaxel: a review

被引:176
作者
Engels, Frederike K.
Mathot, Ron A. A.
Verweij, Jaap
机构
[1] Erasmus Univ, Med Ctr, Dept Med Oncol, Dr Daniel Den Hoed Canc Ctr, NL-3075 EA Rotterdam, Netherlands
[2] Erasmus Univ, Med Ctr, Dept Hosp Pharm & Clin Pharmacol, NL-3075 EA Rotterdam, Netherlands
关键词
docetaxel; drug formulations; liposomes; nanoparticles; polysorbate; 80; Taxotere; Tween; METASTATIC BREAST-CANCER; PHASE-III TRIAL; P-GLYCOPROTEIN; INTRAVENOUS-INFUSION; PEGYLATED LIPOSOMES; FLUID RETENTION; IN-VITRO; PLASMA PHARMACOKINETICS; UNBOUND DOCETAXEL; TAXOTERE RP-56976;
D O I
10.1097/CAD.0b013e3280113338
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The anticancer drug docetaxel (Taxotere) is formulated in the nonionic surfactant polysorbate 80 (Tween 80). Early in the clinical development of docetaxel, it became clear that docetaxel administration is associated with the occurrence of unpredictable (acute) hypersensitivity reactions and cumulative fluid retention. These side-effects have been attributed, in part, to the presence of polysorbate 80 and have consequently initiated research focused on the development of a less-toxic, better-to le rated polysorbate 80-free formulation of docetaxel. More recently, there is an increasing interest in developing a (polysorbate 80-free) docetaxel formulation that selectively targets malignant tissue, thereby increasing efficacy while decreasing the occurrence of side-effects related to wide and nonspecific body distribution. This review aims to discuss the preclinical and clinical results of pharmaceutical strategies [PEGylated (immuno)liposomal docetaxel, docetaxel-fibrinogen-coated olive oil droplets, docetaxel encapsulated nanoparticle-aptamer bioconjugates, submicronic dispersion formulation] to develop an alternative, solvent-free, delivery form for docetaxel characterized by increased efficacy and decreased toxicity.
引用
收藏
页码:95 / 103
页数:9
相关论文
共 70 条
  • [1] Non-allergic nature of docetaxel-induced acute hypersensitivity reactions
    Ardavanis, A
    Tryfonopoulos, D
    Yiotis, I
    Gerasimidis, G
    Baziotis, N
    Rigatos, G
    [J]. ANTI-CANCER DRUGS, 2004, 15 (06) : 581 - 585
  • [2] Relationship of systemic exposure to unbound docetaxel and neutropenia
    Baker, SD
    Li, J
    ten Tije, AJ
    Figg, WD
    Graveland, W
    Verweij, J
    Sparreboom, A
    [J]. CLINICAL PHARMACOLOGY & THERAPEUTICS, 2005, 77 (01) : 43 - 53
  • [3] The pathophysiological mechanism of fluid retention in advanced cancer patients treated with docetaxel, but not receiving corticosteroid comedication
    Behar, A
    PujadeLauraine, E
    Maurel, A
    Brun, MD
    Lagrue, G
    DeChauvin, FF
    OulidAissa, D
    Hille, D
    [J]. BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1997, 43 (06) : 653 - 658
  • [4] Contact allergenic activity of Tween(R) 80 before and after air exposure
    Bergh, M
    Magnusson, K
    Nilsson, JLG
    Karlberg, AT
    [J]. CONTACT DERMATITIS, 1997, 37 (01) : 9 - 18
  • [5] BISSETT D, 1993, CANCER RES, V53, P523
  • [6] Cytotoxic and antitumor effect of fibrinogen-methotrexate conjugate
    Boratynski, J
    Opolski, A
    Wietrzyk, J
    Górski, A
    Radzikowski, C
    [J]. CANCER LETTERS, 2000, 148 (02) : 189 - 195
  • [7] Population pharmacokinetics/pharmacodynamics of docetaxel in phase II studies in patients with cancer
    Bruno, R
    Hille, D
    Riva, A
    Vivier, N
    Huinnink, WWTB
    van Oosterom, AT
    Kaye, SB
    Verweij, J
    Fossella, FV
    Valero, V
    Rigas, JR
    Seidman, AD
    Chevallier, B
    Fumoleau, P
    Burris, HA
    Ravclin, PM
    Sheiner, LB
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (01) : 187 - 196
  • [8] PHASE-I CLINICAL-TRIAL OF TAXOTERE ADMINISTERED AS EITHER A 2-HOUR OR 6-HOUR INTRAVENOUS-INFUSION
    BURRIS, H
    IRVIN, R
    KUHN, J
    KALTER, S
    SMITH, L
    SHAFFER, D
    FIELDS, S
    WEISS, G
    ECKARDT, J
    RODRIGUEZ, G
    RINALDI, D
    WALL, J
    COOK, G
    SMITH, S
    VREELAND, F
    BAYSSAS, M
    LEBAIL, N
    VONHOFF, D
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (05) : 950 - 958
  • [9] CAMPONE M, 2002, P AN M AM SOC CLIN, V21, pA2152
  • [10] From conventional to stealth liposomes: a new frontier in cancer chemotherapy
    Cattel, L
    Ceruti, M
    Dosio, F
    [J]. JOURNAL OF CHEMOTHERAPY, 2004, 16 : 94 - 97