Design of thermally responsive, recombinant polypeptide carriers for targeted drug delivery

被引:214
作者
Chilkoti, A [1 ]
Dreher, MR [1 ]
Meyer, DE [1 ]
机构
[1] Duke Univ, Dept Biomed Engn, Durham, NC 27708 USA
关键词
artificial polypeptide; genetically encoded synthesis; elastin-like polypeptide; thermally responsive; drug delivery; thermal targeting; cancer therapy; block copolymers; nanoparticles; micelles;
D O I
10.1016/S0169-409X(02)00060-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In this article, we review recombinant DNA methods for the design and synthesis of amino acid-based biopolymers, and briefly summarize an approach, recursive directional ligation (RDL), that we have employed to synthesize oligomeric genes for such biopolymers. We then describe our ongoing research in the use of RDL to synthesize recombinant polypeptide carriers for the targeted delivery of radionuclides, chemotherapeutics and biomolecular therapeutics to tumors. The targeted delivery system uses a thermally responsive, elastin-like polypeptide (ELP) as the drug carrier to enhance the localization of ELP-drug conjugates within a solid tumor that is heated by regional hyperthermia. In the context of this drug delivery application, we discuss the design of ELPs and their recombinant synthesis, which enables the molecular weight and the thermal properties of the polypeptide to be precisely controlled. Finally, our results pertaining to the in vivo targeting of tumors with ELPs are briefly summarized. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:1093 / 1111
页数:19
相关论文
共 61 条
  • [1] Liposomal drug formulations - Rationale for development and what we can expect for the future
    Allen, TM
    [J]. DRUGS, 1998, 56 (05) : 747 - 756
  • [2] Spiropyran derivative of an elastin-like bioelastic polymer:: Photoresponsive molecular machine to convert sunlight into mechanical work
    Alonso, M
    Reboto, V
    Guiscardo, L
    San Martín, A
    Rodríguez-Cabello, JC
    [J]. MACROMOLECULES, 2000, 33 (26) : 9480 - 9482
  • [3] AOTA S, 1988, NUCLEIC ACIDS RES, V16, P315
  • [4] Cancer treatment by targeted drug delivery to tumor vasculature in a mouse model
    Arap, W
    Pasqualini, R
    Ruoslahti, E
    [J]. SCIENCE, 1998, 279 (5349) : 377 - 380
  • [5] Bioinspired polymeric materials: in-between proteins and plastics
    Barron, AE
    Zuckermann, RN
    [J]. CURRENT OPINION IN CHEMICAL BIOLOGY, 1999, 3 (06) : 681 - 687
  • [6] Nature's complex copolymers: Engineering design of oligopeptide materials
    Caplan, MR
    Lauffenburger, DA
    [J]. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2002, 41 (03) : 403 - 412
  • [7] GENETIC-ENGINEERING OF STRUCTURAL PROTEIN POLYMERS
    CAPPELLO, J
    CRISSMAN, J
    DORMAN, M
    MIKOLAJCZAK, M
    TEXTOR, G
    MARQUET, M
    FERRARI, F
    [J]. BIOTECHNOLOGY PROGRESS, 1990, 6 (03) : 198 - 202
  • [8] In-situ self-assembling protein polymer gel systems for administration, delivery, and release of drugs
    Cappello, J
    Crissman, JW
    Crissman, M
    Ferrari, FA
    Textor, G
    Wallis, O
    Whitledge, JR
    Zhou, X
    Burman, D
    Aukerman, L
    Stedronsky, ER
    [J]. JOURNAL OF CONTROLLED RELEASE, 1998, 53 (1-3) : 105 - 117
  • [9] ACTIVITY OF N-(2-HYDROXYPROPYL)METHACRYLAMIDE COPOLYMERS CONTAINING DAUNOMYCIN AGAINST A RAT-TUMOR MODEL
    CASSIDY, J
    DUNCAN, R
    MORRISON, GJ
    STROHALM, J
    PLOCOVA, D
    KOPECEK, J
    KAYE, SB
    [J]. BIOCHEMICAL PHARMACOLOGY, 1989, 38 (06) : 875 - 879
  • [10] Thermo-responsive drug delivery from polymeric micelles constructed using block copolymers of poly(N-isopropylacrylamide) and poly(butylmethacrylate)
    Chung, JE
    Yokoyama, M
    Yamato, M
    Aoyagi, T
    Sakurai, Y
    Okano, T
    [J]. JOURNAL OF CONTROLLED RELEASE, 1999, 62 (1-2) : 115 - 127