Your browser doesn't support javascript.
loading
Detection of glycosaminoglycan loss in articular cartilage by fluorescence lifetime imaging.
Zhou, Xiangnan; Haudenschild, Anne K; Sherlock, Benjamin E; Hu, Jerry C; Leach, J Kent; Athanasiou, Kyriacos A; Marcu, Laura.
Afiliação
  • Zhou X; University of California, Department of Biomedical Engineering, Davis, California, United States.
  • Haudenschild AK; University of California, Department of Biomedical Engineering, Davis, California, United States.
  • Sherlock BE; University of California, Department of Biomedical Engineering, Davis, California, United States.
  • Hu JC; University of California, Department of Biomedical Engineering, Irvine, California, United States.
  • Leach JK; University of California, Department of Biomedical Engineering, Davis, California, United States.
  • Athanasiou KA; UC Davis Health, Department of Orthopaedic Surgery, Sacramento, California, United States.
  • Marcu L; University of California, Department of Biomedical Engineering, Irvine, California, United States.
J Biomed Opt ; 23(12): 1-8, 2018 12.
Article em En | MEDLINE | ID: mdl-30578627
ABSTRACT
Glycosaminoglycan (GAG) loss is an early marker of osteoarthritis, which is a clinical late stage disease that affects millions of people worldwide. The goal of our study was to evaluate the ability of a fiber-based fluorescence lifetime imaging (FLIm) technique to detect GAG loss in articular cartilage. Native bovine cartilage explants (n = 20) were exposed to 0 (control), 0.5 (low), or 1 U / mL (high) concentrations of chondroitinase ABC (cABC) to create samples with different levels of GAG loss. FLIm assessment (excitation 355 nm; detection channel 1 375 to 410 nm, channel 2 450 to 485 nm, channel 3 530 to 565 nm) was conducted on depth-resolved cross-sections of the cartilage sample. FLIm images, validated with histology, revealed that loss of GAG resulted in a decrease of fluorescence lifetime values in channel 2 (Δ = 0.44 ns, p < 0.05) and channel 3 (Δ = 0.75 ns, p < 0.01) compared to control samples (channel 2 6.34 ns; channel 3 5.22 ns). Fluorescence intensity ratio values were lower in channel 1 (37%, p < 0.0001) and channel 2 (31% decrease, p < 0.0001) and higher in channel 3 (23%, p < 0.0001) relative to control samples. These results show that FLIm can detect the loss of GAG in articular cartilage and support further investigation into the feasibility of in vivo FLIm arthroscopy.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cartilagem Articular / Imagem Óptica / Glicosaminoglicanos Tipo de estudo: Diagnostic_studies Limite: Animals Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cartilagem Articular / Imagem Óptica / Glicosaminoglicanos Tipo de estudo: Diagnostic_studies Limite: Animals Idioma: En Ano de publicação: 2018 Tipo de documento: Article