Nanomaterials in Cancer-Therapy Drug Delivery System

被引:103
|
作者
Zhang, Gen [1 ]
Zeng, Xin [2 ]
Li, Ping [2 ]
机构
[1] Nanjing Med Univ, Sch Basic Med Sci, Dept Cell Biol, Nanjing 210029, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Nanjing Matern & Child Hlth Care Hosp, Dept Gynecol Endocrine, State Key Lab Reprod Med, Nanjing 210029, Jiangsu, Peoples R China
关键词
Nanoparticles; Apoptosis; Drug Delivery; Biodistribution; Nanocomposites; IN-VITRO EVALUATION; DAUNORUBICIN INDUCE APOPTOSIS; IRON-OXIDE NANOPARTICLES; WALLED CARBON NANOTUBES; MAGNETIC NANOPARTICLES; SILVER NANOPARTICLES; MULTIDRUG-RESISTANCE; FE3O4; NANOPARTICLES; QUANTUM DOTS; POLYETHYLENE-GLYCOL;
D O I
10.1166/jbn.2013.1583
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Nanomaterials can enhance the delivery and treatment efficiency of anti-cancer drugs, and the mechanisms of the tumor-reducing activity of nanomaterials with cancer drug have been investigated. The task for drug to reach pathological areas has facilitated rapid advances in nanomedicine. Herein, we summarize promising findings with respect to cancer therapeutics based on nano-drug delivery vectors. Relatively high toxicity of uncoated nanoparticles restricts the use of these materials in humans. In order to reduce toxicity, many approaches have focused on the encapsulation of nanoparticles with biocompatible materials. Efficient delivery systems have been developed that utilized nanoparticles loaded with high dose of cancer drug in the presence of bilayer molecules. Well-established nanotechnologies have been designed for drug delivery with specific bonding. Surface-modified nanoparticles as vehicles for drug delivery system that contains multiple nano-components, each specially designed to achieve aimed task for the emerging application delivery of therapeutics. Drug-coated polymer nanoparticles could efficiently increase the intracellular accumulation of anti-cancer drugs. This review also introduces the nanomaterials with drug on the induction of apoptosis in cancer cells in vitro and in vivo. Direct interactions between the particles and cellular molecules to cause adverse biological responses are also discussed.
引用
收藏
页码:741 / 750
页数:10
相关论文
共 50 条
  • [1] Nanomaterials for Drug Delivery and Cancer Therapy
    Nicoletta, Fiore Pasquale
    Iemma, Francesca
    [J]. NANOMATERIALS, 2023, 13 (01)
  • [2] IMMUNOCONJUGATES - APPLICATIONS IN TARGETED DRUG DELIVERY FOR CANCER-THERAPY
    RAM, BP
    TYLE, P
    [J]. PHARMACEUTICAL RESEARCH, 1987, 4 (03) : 181 - 188
  • [3] Carbon Nanomaterials for Drug Delivery and Cancer Therapy
    Chakrabarti, Mrinmay
    Kiseleva, Raisa
    Vertegel, Alexey
    Ray, Swapan K.
    [J]. JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY, 2015, 15 (08) : 5501 - 5511
  • [4] SITE-SPECIFIC (TARGETED) DRUG DELIVERY IN CANCER-THERAPY
    POSTE, G
    KIRSH, R
    [J]. BIO-TECHNOLOGY, 1983, 1 (10): : 869 - 878
  • [5] Multifunctional Nanomaterials and Their Applications in Drug Delivery and Cancer Therapy
    Srinivasan, Mathangi
    Rajabi, Mehdi
    Mousa, Shaker A.
    [J]. NANOMATERIALS, 2015, 5 (04) : 1690 - 1703
  • [6] THE DRUG-IMMUNE SYSTEM INTERACTION IN CANCER-THERAPY
    GHIONE, M
    [J]. INTERNATIONAL JOURNAL OF TISSUE REACTIONS-EXPERIMENTAL AND CLINICAL ASPECTS, 1984, 6 (06): : 513 - 521
  • [7] Carbon nanomaterials: Types, synthesis strategies and their application as drug delivery system for cancer therapy
    Brindhadevi, Kathirvel
    Garalleh, Hakim A. L.
    Alalawi, Amr
    Al-Sarayreh, Ebtisam
    Pugazhendhi, Arivalagan
    [J]. BIOCHEMICAL ENGINEERING JOURNAL, 2023, 192
  • [8] GENETIC DELIVERY OF ENZYMES FOR CANCER-THERAPY
    DEONARAIN, MP
    SPOONER, RA
    EPENETOS, AA
    [J]. GENE THERAPY, 1995, 2 (04) : 235 - 244
  • [9] Peptide-stabilized nanomaterials for drug delivery and cancer therapy
    Dragulska, Sylwia
    Poursharifi, Mina
    Cheng, Ying
    Martignetti, John
    Mieszawska, Aneta
    [J]. FASEB JOURNAL, 2020, 34
  • [10] DRUG-MONITORING IN CANCER-THERAPY
    HANDE, KR
    [J]. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1991, 83 (21) : 1523 - 1524