Literature DB >> 18361490

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

Jason M Zhao1, Yah-el Har-el, Michael T McMahon, Jinyuan Zhou, A Dean Sherry, George Sgouros, Jeff W M Bulte, Peter C M van Zijl.   

Abstract

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 microm/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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Year:  2008        PMID: 18361490      PMCID: PMC2759111          DOI: 10.1021/ja710159q

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  30 in total

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8.  The effect of lipid composition on the relaxivity of Gd-DTPA entrapped in lipid vesicles of defined size.

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  22 in total

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Review 7.  Diamagnetic chemical exchange saturation transfer (diaCEST) liposomes: physicochemical properties and imaging applications.

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8.  In vivo multicolor molecular MR imaging using diamagnetic chemical exchange saturation transfer liposomes.

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9.  Magnetization transfer contrast MRI for non-invasive assessment of innate and adaptive immune responses against alginate-encapsulated cells.

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