4.8 Article

Size-induced enhancement of chemical exchange saturation transfer (CEST) contrast in liposomes

期刊

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 130, 期 15, 页码 5178-5184

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ja710159q

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资金

  1. NCI NIH HHS [R01CA115531, R01 CA115531-03, R01 CA115531] Funding Source: Medline
  2. NCRR NIH HHS [P41 RR002584, P41 RR002584-216312, P41RR02584] Funding Source: Medline
  3. NIBIB NIH HHS [R21 EB005252, R21 EB005252-02, R21EB005252, K01 EB006394-02, K01EB006394, K01 EB006394, R01 EB015031] Funding Source: Medline
  4. NIDDK NIH HHS [P01DK058398, P01 DK058398-070006, P01 DK058398] Funding Source: Medline
  5. NINDS NIH HHS [R01 NS045062] Funding Source: Medline

向作者/读者索取更多资源

Liposome-based chemical exchange saturation transfer (lipoCEST) agents have shown great sensitivity and potential for molecular magnetic resonance imaging (MRI). Here we demonstrate that the size of liposomes can be exploited to enhance the lipoCEST contrast. A concise analytical model is developed to describe the contrast dependence on size for an ensemble of liposomes. The model attributes the increased lipoCEST contrast in smaller liposomes to their larger surface-to-volume ratio, causing an increased membrane water exchange rate. Experimentally measured rates correlate with size, in agreement with the model. The water permeability of liposomal membrane is found to be 1.11 +/- 0.14 mu m/s for the specific lipid composition at 22 degrees C. Availability of the model allows rational design of the size of liposomes and quantification of their properties. These new theoretical and experimental tools are expected to benefit applications of liposomes to sensing the cellular environment, targeting and imaging biological processes, and optimizing drug delivery properties.

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