Translational considerations in nanomedicine: The oncology perspective

被引:34
作者
Gabizon, Alberto A. [1 ]
de Rosales, Rafael T. M. [2 ]
La-Beck, Ninh M. [3 ]
机构
[1] Hebrew Univ Jerusalem, Shaare Zedek Med Ctr, Nanooncol Res Ctr, Fac Med, Jerusalem, Israel
[2] Kings Coll London, St Thomas Hosp, Sch Biomed Engn & Imaging Sci, Dept Imaging Chem & Biol, London SE1 7EH, England
[3] Texas Tech Univ, Jerry H Hodge Sch Pharm, Dept Immunotherapeut & Biotechnol, Dept Pharm Practice,Hlth Sci Ctr, Abilene, TX USA
基金
英国工程与自然科学研究理事会;
关键词
PEGYLATED-LIPOSOMAL DOXORUBICIN; STERICALLY STABILIZED LIPOSOMES; HUMAN TUMOR XENOGRAFT; STEALTH LIPOSOMES; FOLATE RECEPTOR; PROTEIN CORONA; SOLID TUMORS; RADIOLABELED LIPOSOMES; ENHANCED PERMEABILITY; THERAPEUTIC-EFFICACY;
D O I
10.1016/j.addr.2020.05.012
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Nanoparticles can provide effective control of the release rate and tissue distribution of their drug payload, leading to major pharmacokinetic and pharmacodynamic changes vis-a-vis the conventional administration of free drugs. In the last two decades, we have witnessed major progress in the synthesis and characterization of engineered nanoparticles for imaging and treatment of cancers, resulting in the approval for clinical use of several products and in new and promising approaches. Despite these advances, clinical applications of nanoparticle-based therapeutic and imaging agents remain limited due to biological, immunological, and translational barriers. There is a need to make high impact advances toward translation. In this review, we address biological, toxicological, immunological, and translational aspects of nanomedicine and discuss approaches to move the field forward productively. Overcoming these barriers may dramatically improve the development potential and role of nanomedicines in the oncology field and help meet the high expectations. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:140 / 157
页数:18
相关论文
共 144 条
  • [31] Tumor cell targeting of liposome-entrapped drugs with phospholipid-anchored folic acid-PEG conjugates
    Gabizon, A
    Shmeeda, H
    Horowitz, AT
    Zalipsky, S
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 2004, 56 (08) : 1177 - 1192
  • [32] GABIZON A, 1990, CANCER RES, V50, P6371
  • [33] GABIZON A, 1983, CANCER RES, V43, P4730
  • [34] Pharmacokinetics of pegylated liposomal doxorubicin - Review of animal and human studies
    Gabizon, A
    Shmeeda, H
    Barenholz, Y
    [J]. CLINICAL PHARMACOKINETICS, 2003, 42 (05) : 419 - 436
  • [35] Dose dependency of pharmacokinetics and therapeutic efficacy of pegylated liposomal doxorubicin (DOXIL) in murine models
    Gabizon, A
    Tzemach, D
    Mak, L
    Bronstein, M
    Horowitz, AT
    [J]. JOURNAL OF DRUG TARGETING, 2002, 10 (07) : 539 - 548
  • [36] LIPOSOME FORMULATIONS WITH PROLONGED CIRCULATION TIME IN BLOOD AND ENHANCED UPTAKE BY TUMORS
    GABIZON, A
    PAPAHADJOPOULOS, D
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (18) : 6949 - 6953
  • [37] Gabizon A., 2008, J LIPOSOME RES, V1, P123
  • [38] Pegylated liposomal doxorubicin: Metamorphosis of an old drug into a new form of chemotherapy
    Gabizon, AA
    [J]. CANCER INVESTIGATION, 2001, 19 (04) : 424 - 436
  • [39] Pharmacological basis of pegylated liposomal doxorubicin: Impact on cancer therapy
    Gabizon, Alberto
    Shmeeda, Hilary
    Grenader, Tal
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2012, 45 (04) : 388 - 398
  • [40] Improved therapeutic activity of folate-targeted liposomal doxorubicin in folate receptor-expressing tumor models
    Gabizon, Alberto
    Tzemach, Dina
    Gorin, Jenny
    Mak, Lidia
    Amitay, Yasmine
    Shmeeda, Hilary
    Zalipsky, Samuel
    [J]. CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2010, 66 (01) : 43 - 52