TY - JOUR
T1 - Tumor-homing multifunctional nanoparticles for cancer theragnosis
T2 - Simultaneous diagnosis, drug delivery, and therapeutic monitoring
AU - Kim, Kwangmeyung
AU - Kim, Jong Ho
AU - Park, Hyungkyu
AU - Kim, Yoo Shin
AU - Park, Kyeongsoon
AU - Nam, Heayun
AU - Lee, Seulki
AU - Park, Jae Hyung
AU - Park, Rang Woon
AU - Kim, In San
AU - Choi, Kuiwon
AU - Kim, Sang Yoon
AU - Park, Kinam
AU - Kwon, Ick Chan
N1 - Funding Information:
This work was financially supported by the Real-Time Molecular Imaging Project , F104AA01003-06A0101-00310 , the GRL Program of MEST, by a Korea Research Foundation Grant funded by the Korean Government (MOEHRD, Basic Research Promotion Fund) ( KRF-357-2007-1-D00130 ), by a grant to the Intramural Research Program of KIST (Theragnosis), by a grant of the Ministry of Health Welfare and Family Affairs ( A062254 ), and by the Advanced Medical Technology Cluster for Diagnosis and Prediction at Kyungpook National University, awarded by MOCIE.
PY - 2010/9
Y1 - 2010/9
N2 - Theragnostic multifunctional nanoparticles hold great promise in simultaneous diagnosis of disease, targeted drug delivery with minimal toxicity, and monitoring of treatment. One of the current challenges in cancer treatment is enhancing the tumor-specific targeting of both imaging probes and anticancer agents. Herein, we report tumor-homing chitosan-based nanoparticles (CNPs) that simultaneously execute cancer diagnosis and therapy (cancer theragnosis). These CNPs are unique for their three distinctive characteristics, such as stability in serum, deformability, and rapid uptake by tumor cells. These properties are critical in increasing their tumor targeting specificity and reducing their nonspecific uptake by normal tissues. To develop these CNPs into novel theragnostic nanoparticles, we labeled them with Cy5.5, a near-infrared fluorescent (NIRF) dye, for imaging and also loaded them with paclitaxel (PTX-CNPs), an anticancer drug, for cancer treatment. Cy5.5 labeled PTX-CNPs exhibited significantly increased tumor-homing ability with low nonspecific uptake by other tissues in SCC7 tumor-bearing mice. Theragnostic nanoparticles, Cy5.5 labeled PTX-CNPs, are highly useful for simultaneous diagnosis of early-stage cancer and drug delivery.
AB - Theragnostic multifunctional nanoparticles hold great promise in simultaneous diagnosis of disease, targeted drug delivery with minimal toxicity, and monitoring of treatment. One of the current challenges in cancer treatment is enhancing the tumor-specific targeting of both imaging probes and anticancer agents. Herein, we report tumor-homing chitosan-based nanoparticles (CNPs) that simultaneously execute cancer diagnosis and therapy (cancer theragnosis). These CNPs are unique for their three distinctive characteristics, such as stability in serum, deformability, and rapid uptake by tumor cells. These properties are critical in increasing their tumor targeting specificity and reducing their nonspecific uptake by normal tissues. To develop these CNPs into novel theragnostic nanoparticles, we labeled them with Cy5.5, a near-infrared fluorescent (NIRF) dye, for imaging and also loaded them with paclitaxel (PTX-CNPs), an anticancer drug, for cancer treatment. Cy5.5 labeled PTX-CNPs exhibited significantly increased tumor-homing ability with low nonspecific uptake by other tissues in SCC7 tumor-bearing mice. Theragnostic nanoparticles, Cy5.5 labeled PTX-CNPs, are highly useful for simultaneous diagnosis of early-stage cancer and drug delivery.
KW - Chitosan nanoparticle
KW - Drug delivery
KW - Non-invasive imaging
KW - Paclitaxel
KW - Theragnosis
KW - Tumor homing
UR - http://www.scopus.com/inward/record.url?scp=77955417363&partnerID=8YFLogxK
U2 - 10.1016/j.jconrel.2010.04.004
DO - 10.1016/j.jconrel.2010.04.004
M3 - Article
C2 - 20403397
AN - SCOPUS:77955417363
SN - 0168-3659
VL - 146
SP - 219
EP - 227
JO - Journal of Controlled Release
JF - Journal of Controlled Release
IS - 2
ER -