The in vivo performance of biomagnetic hydroxyapatite nanoparticles in cancer hyperthermia therapy

被引:206
作者
Hou, Chun-Han [1 ,2 ,3 ]
Hou, Sheng-Mou [1 ,2 ,4 ]
Hsueh, Yu-Sheng [1 ,2 ]
Lin, Jinn [4 ]
Wu, Hsi-Chin [1 ,2 ]
Lin, Feng-Huei [1 ,2 ]
机构
[1] Natl Taiwan Univ, Inst Biomed Engn, Coll Med, Taipei 100, Taiwan
[2] Natl Taiwan Univ, Coll Engn, Taipei 100, Taiwan
[3] Taiwan Univ Hosp, Dept Orthopaed Surg, Yun Lin Branch, Yun Lin Cty, Taiwan
[4] Natl Taiwan Univ Hosp, Dept Orthopaed Surg, Taipei, Taiwan
关键词
Hydroxyapatite; Hydroxyapatite composite; Nanocomposite; Nanoparticle; Chemotherapy; MR LYMPHOGRAPHY; PARTICLES; RELEASE; CARRIER; AGENTS; CELLS;
D O I
10.1016/j.biomaterials.2009.04.020
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Hyperthermia therapy for cancer has drawn more and more attention these days. In this study, we conducted an in vivo cancer hyperthermia study of the new magnetic hydroxyapatite nanoparticles by a mouse model. The magnetic hydroxyapatite nanoparticles were first made by co-precipitation method with the addition of Fe2+. Then, magnetic-HAP powder (mHAP) or pure HAP powder (HAP) was mixed with phosphate buffer solution (PBS), respectively. The mixture was injected around the tumor. In order to achieve hyperthermia. the mice were placed into an inductive heater with high frequency and alternating magnetic field. Only the mice which were injected with mHAP and had been treated inside the magnetic field showed dramatic reduction of tumor volume, in the 15-day observation period. No local recurrence was noted. The blood test of mice proved that mHAP powders possessed good biocompatibility and little toxicity when injected subcutaneously. Therefore, our new magnetic hydroxyapatite nanoparticles have demonstrated therapeutic effect in a mouse model with little toxicity. Further study should be done before its application inside the human body. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3956 / 3960
页数:5
相关论文
共 37 条
[1]
[Anonymous], ADV SCI TECHNOL
[2]
AOKI H, 1994, WHAT IS HYDROXYAPATI, P1
[3]
Biphasic materials for bone grafting and hyperthermia treatment of cancer [J].
Arcos, D ;
del Real, RP ;
Vallet-Regí, M .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2003, 65A (01) :71-78
[4]
AC-magnetic field controlled drug release from magnetoliposomes:: design of a method for site-specific chemotherapy [J].
Babincová, M ;
Cicmanec, P ;
Altanerová, V ;
Altaner, C ;
Babinec, P .
BIOELECTROCHEMISTRY, 2002, 55 (1-2) :17-19
[5]
SUPERPARAMAGNETIC IRON-OXIDES AS POSITIVE MR CONTRAST AGENTS - INVITRO AND INVIVO EVIDENCE [J].
CHAMBON, C ;
CLEMENT, O ;
LEBLANCHE, A ;
SCHOUMANCLAEYS, E ;
FRIJA, G .
MAGNETIC RESONANCE IMAGING, 1993, 11 (04) :509-519
[6]
Synthesis and surface engineering of iron oxide nanoparticles for biomedical applications [J].
Gupta, AK ;
Gupta, M .
BIOMATERIALS, 2005, 26 (18) :3995-4021
[7]
Isolation and transplantation of autologous peripheral CD34+ progenitor cells highly purified by magnetic-activated cell sorting [J].
Handgretinger, R ;
Lang, P ;
Schumm, M ;
Taylor, G ;
Neu, S ;
Koscielnak, E ;
Niethammer, D ;
Klingebiel, T .
BONE MARROW TRANSPLANTATION, 1998, 21 (10) :987-993
[8]
Medical application of functionalized magnetic nanoparticles [J].
Ito, A ;
Shinkai, M ;
Honda, H ;
Kobayashi, T .
JOURNAL OF BIOSCIENCE AND BIOENGINEERING, 2005, 100 (01) :1-11
[9]
USE OF MAGNETITE PARTICLES AS A CONTRAST AGENT FOR MR IMAGING OF THE LIVER [J].
KAWAMURA, Y ;
ENDO, K ;
WATANABE, Y ;
SAGA, T ;
NAKAI, T ;
HIKITA, H ;
KAGAWA, K ;
KONISHI, J .
RADIOLOGY, 1990, 174 (02) :357-360
[10]
Kubo T, 2000, INT J ONCOL, V17, P309