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In vivo SPECT imaging of Tc-99m radiolabeled exosomes from human umbilical-cord derived mesenchymal stem cells in small animals.
Chung, Yi-Hsiu; Ho, Yi-Pei; Farn, Shiou-Shiow; Tsai, Wei-Cheng; Li, Zhi-Xiang; Lin, Tzou-Yien; Weng, Chi-Chang.
Afiliación
  • Chung YH; Department of Medical Research and Development, Research Division, Chang Gung Memorial Hospital at Linkou, Taoyuan, Taiwan.
  • Ho YP; Department of Medical Imaging and Radiological Sciences, Chang Gung University, Taoyuan, Taiwan; Healthy Aging Research Center, Chang GungUniversity, Taoyuan, Taiwan.
  • Farn SS; Department of Isotope Application Research, National Atomic Research Institute, Taoyuan, Taiwan.
  • Tsai WC; ExoOne Bio Co., Ltd., Taipei, Taiwan.
  • Li ZX; ExoOne Bio Co., Ltd., Taipei, Taiwan.
  • Lin TY; Department of Pediatrics, Division of Infectious Diseases, Chang Gung Memorial Hospital, Taoyuan, Taiwan; College of Medicine, Chang Gung University, Taoyuan, Taiwan. Electronic address: alinpid@gmail.com.
  • Weng CC; Department of Medical Research and Development, Research Division, Chang Gung Memorial Hospital at Linkou, Taoyuan, Taiwan; Department of Medical Imaging and Radiological Sciences, Chang Gung University, Taoyuan, Taiwan; Healthy Aging Research Center, Chang GungUniversity, Taoyuan, Taiwan. Electroni
Biomed J ; 47(5): 100721, 2024 Apr 16.
Article en En | MEDLINE | ID: mdl-38636899
ABSTRACT
Extracellular vesicles derived from human umbilical cord-derived mesenchymal stem cells (UCMSC-EVs) have been postulated to have therapeutic potential for various diseases. However, the biodistribution and pharmacokinetics of these vesicles are still unclear. For a better understanding of the in vivo properties of UCMSC-EVs, in the present study, these vesicles were first radiolabeled with Technetium-99m (99mTc-UCMSC-EVs) and evaluated using in vivo single photon emission computed tomography (SPECT) imaging and biodistribution experiments. SPECT images demonstrated that the liver and spleen tissues mainly took up the 99mTc-UCMSC-EVs. The biodistribution study observed slight uptake in the thyroid and stomach, indicating that 99mTc-UCMSC-EVs was stable at 24 h in vivo. The pharmacokinetic analyses of the blood half-life demonstrated the quick distribution phase (0.85 ± 0.28 min) and elimination phase (25.22 ± 20.76 min) in mice. This study provides a convenient and efficient method for 99mTc-UCMSC-EVs preparation without disturbing their properties. In conclusion, the biodistribution, quick elimination, and suitable stability in vivo of 99mTc-UCMSC-EVs were quantified by the noninvasive imaging and pharmacokinetic analyses, which provides useful information for indication selection, dosage protocol design, and toxicity assessment in future applications.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Biomed J Año: 2024 Tipo del documento: Article País de afiliación: Taiwán

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Biomed J Año: 2024 Tipo del documento: Article País de afiliación: Taiwán
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