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Effect of Liposomal Encapsulation on the Chemical Exchange Properties of Diamagnetic CEST Agents.

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TLDR
This is the first study in which a model has been constructed to measure the exchange properties of diamagnetic CEST agents encapsulated inside liposomes, and a concise analytical model is developed to describe the liposomal contrast dependence on several parameters such as pH, temperature, irradiation amplitude, and intraliposomal water content.
Abstract
Exogenous chemical exchange saturation transfer (CEST) contrast agents such as glucose or 2-deoxy-d-glucose (2-DG) have shown high sensitivities and significant potential for monitoring glucose uptake in tumors with MRI. Here, we show that liposome encapsulation of such agents can be exploited to enhance the CEST signal by reducing the overall apparent exchange rate. We have developed a concise analytical model to describe the liposomal contrast dependence on several parameters such as pH, temperature, irradiation amplitude, and intraliposomal water content. This is the first study in which a model has been constructed to measure the exchange properties of diamagnetic CEST agents encapsulated inside liposomes. Experimentally measured exchange rates of glucose and 2-DG in the liposomal system were found to be reduced due to the intermembrane exchange between the intra- and extraliposomal compartments because of restrictions in water transfer imposed by the lipid membrane. These new theoretical and experimental findings will benefit applications of diamagnetic liposomes to image biological processes. In addition, combining this analytical model with measurements of the CEST signal enhancement using liposomes as a model membrane system is an important new general technique for studying membrane permeability.

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Citations
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Journal ArticleDOI

Molecular imaging of tumors by chemical exchange saturation transfer MRI of glucose analogs

TL;DR: Preclinical data may help strengthen the translation of CEST MRI of glucose analogs into the clinic, improving cancer imaging to enable early intervention without the need for invasive techniques, and broaden the knowledge of fundamental biological processes.
Journal ArticleDOI

Repurposing Clinical Agents for Chemical Exchange Saturation Transfer Magnetic Resonance Imaging: Current Status and Future Perspectives.

TL;DR: The Chemical Exchange Saturation Transfer (CEST) MRI is emerging as an attractive approach with the capability of directly using low concentration, exchangeable protons-containing agents for generating quantitative MRI contrast.
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What do we know about dynamic glucose-enhanced (DGE) MRI and how close is it to the clinics? Horizon 2020 GLINT consortium report

TL;DR: In this paper , the authors summarized the progress made to date both by these groups and others in increasing our knowledge of the underlying mechanisms related to this technique as well as translating it into clinical practice.
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A snapshot of the vast array of diamagnetic CEST MRI contrast agents

TL;DR: A very extensive snapshot of the types of diamagnetic compounds that can generate CEST MRI contrast, together with guidance on their utility on typical preclinical and clinical scanners and review of the applications which might benefit the most from this new technology.
Journal ArticleDOI

Compartmentalized agents: A powerful strategy for enhancing the detection sensitivity of chemical exchange saturation transfer contrast

TL;DR: In this article , a semi-measurable barrier/membrane is proposed to separate the inner core from the MRI-detected bulk pool via a semipermeable barrier.
References
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Principles of nanoparticle design for overcoming biological barriers to drug delivery

TL;DR: By successively addressing each of the biological barriers that a particle encounters upon intravenous administration, innovative design features can be rationally incorporated that will create a new generation of nanotherapeutics, realizing a paradigmatic shift in nanoparticle-based drug delivery.
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Amphipathic polyethyleneglycols effectively prolong the circulation time of liposomes

TL;DR: The PEG‐PE's activity to prolong the circulation time of liposomes is greater than that of the ganglioside GM1, awell‐described glycolipid with this activity.
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Liposomes and nanoparticles: nanosized vehicles for drug delivery in cancer.

TL;DR: Current knowledge on liposome and nanoparticles offer increased precision in chemotherapeutic targeting of prostate cancer and new avenues for the treatment of breast cancer are reviewed.
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Chemical exchange saturation transfer (CEST): what is in a name and what isn't?

TL;DR: The focus of this review is on basic magnetic resonance principles underlying CEST and similarities to and differences with conventional magnetization transfer contrast.
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Direct measurements of forces between phosphatidylcholine and phosphatidylethanolamine bilayers in aqueous electrolyte solutions

TL;DR: Direct measurements of the full interbilayer force laws between bilayers of various phosphatidylcholines andosphatidylethanolamine in aqueous solutions concluded that bilayer fusion is not simply related to the interbilayers force law.
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