Assessment of Collagen-Induced Arthritis Using Cyanine 5.5 Conjugated with Hydrophobically Modified Glycol Chitosan Nanoparticles: Correlation with 18F-Fluorodeoxyglucose Positron Emission Tomography Data

被引:8
作者
Cha, Ji Hyeon [1 ,2 ]
Lee, Sang Hoon [1 ,2 ]
Lee, Sheen-Woo [1 ,2 ]
Park, Kyeongsoon [4 ]
Moon, Dae Hyuk [3 ]
Kim, Kwangmeyung [4 ]
Biswal, Sandip [5 ]
机构
[1] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Radiol, Seoul 138736, South Korea
[2] Univ Ulsan, Coll Med, Asan Med Ctr, Res Inst Radiol, Seoul 138736, South Korea
[3] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Nucl Med, Seoul 138736, South Korea
[4] Korea Inst Sci & Technol, Biomed Res Ctr, Seoul 136791, South Korea
[5] Stanford Univ, Sch Med, Div Musculoskeletal Imaging, Dept Radiol, Stanford, CA 94305 USA
关键词
HGC-Cy5.5; F-18-FDG PET; Near-infrared fluorescence imaging; Rheumatoid arthritis; NEAR-INFRARED FLUORESCENCE; RHEUMATOID-ARTHRITIS; DISEASE-ACTIVITY; F-18-FDG PET; BLOOD-FLOW; MODEL; PATHOGENESIS; LIPOSOMES; ANTIBODY; DYES;
D O I
10.3348/kjr.2012.13.4.450
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Objective: To evaluate the potential and correlation between near-infrared fluorescence (NIRF) imaging using cyanine 5.5 conjugated with hydrophobically modified glycol chitosan nanoparticles (HGC-Cy5.5) and F-18-fluorodeoxyglucose-positron emission tomography (F-18-FDG-PET) imaging of collagen-induced arthritis (CIA). Materials and Methods: We used 10 CIA and 3 normal mice. Nine days after the injecting collagen twice, microPET imaging was performed 40 minutes after the intravenous injection of 9.3 MBq F-18-FDG in 200 mu L PBS. One day later, NIRF imaging was performed two hours after the intravenous injection of HGC-cy5.5 (5 mg/kg). We assessed the correlation between these two modalities in the knees and ankles of CIA mice. Results: The mean standardized uptake values of F-18-FDG for knees and ankles were 1.68 +/- 0.76 and 0.79 +/- 0.71, respectively, for CIA mice; and 0.57 +/- 0.17 and 0.54 +/- 0.20 respectively for control mice. From the NIRF images, the total photon counts per 30 mm(2) for knees and ankles were 2.32 +/- 1.54 x 10(5) and 2.75 +/- 1.51 x 10(5), respectively, for CIA mice, and 1.22 +/- 0.27 x 10(5) and 0.88 +/- 0.24 x 10(5), respectively, for control mice. These two modalities showed a moderate correlation for knees (r = 0.604, p = 0.005) and ankles (r = 0.464, p = 0.039). Moreover, both HGC-Cy5.5 (p = 0.002) and F-18-FDG-PET (p = 0.005) imaging also showed statistically significant differences between CIA and normal mice. Conclusion: NIRF imaging using HGC-Cy5.5 was moderately correlated with F-18-FDG-PET imaging in the CIA model. As such, HGC-Cy5.5 imaging can be used for the early detection of rheumatoid arthritis.
引用
收藏
页码:450 / 461
页数:12
相关论文
共 30 条
  • [1] Andersson SE, 1998, J RHEUMATOL, V25, P1778
  • [2] Beckers C, 2004, J NUCL MED, V45, P956
  • [3] Brancato R, 1998, Semin Ophthalmol, V13, P189, DOI 10.3109/08820539809056052
  • [4] Brenner W, 2004, J NUCL MED, V45, P927
  • [5] Bresnihan B, 1999, J RHEUMATOL, V26, P717
  • [6] CAESAR J, 1961, CLIN SCI, V21, P43
  • [7] Arthritis imaging using a near-infrared fluorescence folate-targeted probe
    Chen, WT
    Mahmood, U
    Weissleder, R
    Tung, CH
    [J]. ARTHRITIS RESEARCH & THERAPY, 2005, 7 (02) : R310 - R317
  • [8] 2-Deoxy-2-[F-18]fluoro-D-glucose joint uptake on positron emission tomography images: Rheumatoid arthritis versus osteoarthritis
    Elzinga, E. H.
    van der Laken, C. J.
    Comans, E. F. I.
    Lammertsma, A. A.
    Dijkmans, B. A. C.
    Voskuyl, A. E.
    [J]. MOLECULAR IMAGING AND BIOLOGY, 2007, 9 (06) : 357 - 360
  • [9] Assessment of unspecific near-infrared dyes in laser-induced fluorescence imaging of experimental arthritis
    Fischer, T
    Gemeinhardt, I
    Wagner, S
    von Stieglitz, D
    Schnorr, J
    Hermann, KGA
    Ebert, B
    Petzelt, D
    MacDonald, R
    Licha, K
    Schirner, M
    Krenn, V
    Kamradt, T
    Taupitz, M
    [J]. ACADEMIC RADIOLOGY, 2006, 13 (01) : 4 - 13
  • [10] Antibody-mediated side effects of recombinant proteins
    Frost, H
    [J]. TOXICOLOGY, 2005, 209 (02) : 155 - 160