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	<title>Delivery | Nano Publications</title>
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	<title>Delivery | Nano Publications</title>
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		<title>2011 &#8211; CLINAM Abstract &#8211; Thermosensitive Magnetoliposomes for MRI-Guided Drug Delivery &#8211; Meyr et al.</title>
		<link>https://bibliography.nanobiotix.com/2011-clinam-abstract-thermosensitive-magnetoliposomes-for-mri-guided-drug-delivery-meyr-et-al/</link>
					<comments>https://bibliography.nanobiotix.com/2011-clinam-abstract-thermosensitive-magnetoliposomes-for-mri-guided-drug-delivery-meyr-et-al/#respond</comments>
		
		<dc:creator><![CDATA[nano-pub]]></dc:creator>
		<pubDate>Tue, 07 Feb 2017 17:06:16 +0000</pubDate>
				<category><![CDATA[Congress Abstracts]]></category>
		<category><![CDATA[Miscellaneous]]></category>
		<category><![CDATA[Delivery]]></category>
		<category><![CDATA[Drug]]></category>
		<category><![CDATA[Encapsulate]]></category>
		<category><![CDATA[Liposome]]></category>
		<category><![CDATA[Nanocarrier]]></category>
		<category><![CDATA[Oxide]]></category>
		<category><![CDATA[Superparamagnetic]]></category>
		<category><![CDATA[Thermosensitive]]></category>
		<category><![CDATA[Treatment]]></category>
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					<description><![CDATA[<p>Congress: CLINAM, 23rd May 2011 – The development of new activatable drug nanocarriers, with multiple functionalities, presents a promising approach for cancer treatment. Improved drug delivery and controlled drug release at the tumor site may have considerable benefit by increasing treatment efficacy while reducing side effects and toxicity. Further, the possibility to monitor both nanocarrier accumulation and drug release via current clinical imaging techniques may be particularly relevant for an optimal treatment.</p>
The post <a href="https://bibliography.nanobiotix.com/2011-clinam-abstract-thermosensitive-magnetoliposomes-for-mri-guided-drug-delivery-meyr-et-al/">2011 – CLINAM Abstract – Thermosensitive Magnetoliposomes for MRI-Guided Drug Delivery – Meyr et al.</a> first appeared on <a href="https://bibliography.nanobiotix.com">Nano Publications</a>.]]></description>
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            </div><div class="az-box-icon-content az-font-custom az-font-color-custom" style="color: #ffffff;"><h3 class="az-box-icon-title">Authors</h3><p>Marie-Edith Meyre<span class="notes up">1</span>, Cyril Lorenzato<span class="notes up">2</span>, Matthieu Germain<span class="notes up">1</span>, Pierre Smirnov<span class="notes up">2</span>, Chrit Moonen<span class="notes up">2</span>, Agnès Pottier<span class="notes up">1</span> and Laurent Levy<span class="notes up">1</span><br />
<span class="notes">1 – Nanobiotix, Paris, France<br />
2 – Laboratoire Imagerie Moléculaire et Fonctionnelle. UMR 5231 CNRS / Université Bordeaux 2. France</span></p>
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<div class="az-content-element-wrapper az-empty-divider hidden-lg hidden-md" style="height: 60px;"></div></div></div></div><div data-animation-type="ani-in" data-animation-in="fadeInUp" data-animation-out="none" data-animation-speed="default" data-animation-delay="300" data-offset-down="90" data-offset-up="none" class="single-clms col-md-6 az-main-col-content az-module az-col-pos-middle az-v-space-clm animate-content az-module-bg-color"><div class="az-col az-clm-padding-105" >
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            </div><div class="az-box-icon-content"><h3 class="az-box-icon-title">Summary</h3><p><strong>Congress:</strong> CLINAM, 23rd May 2011</p>
<p><strong>Contents:</strong> The development of new activatable drug nanocarriers, with multiple functionalities, presents a promising approach for cancer treatment.</p>
<p>Improved drug delivery and controlled drug release at the tumor site may have considerable benefit by increasing treatment efficacy while reducing side effects and toxicity. Further, the possibility to monitor both nanocarrier accumulation and drug release via current clinical imaging techniques may be particularly relevant for an optimal treatment.</p>
<p>Within the European project “Sonodrugs”, we investigated the opportunity of triggering the drug release from new nanocarriers (temperature and pressure-sensitive) thanks to High Intensity Focused Ultrasounds (HIFU) and monitoring the release profile of the drug at the tumor site thanks to Magnetic Resonance Imaging (MRI) imaging.</p>
<p>A new versatile thermosensitive liposome has been designed and developed to efficiently encapsulate a drug (doxorubicin) and a contrast agent (superparamagnetic iron oxide nanoparticles).</p>
</div></div>
</div>
<div class="az-content-element-wrapper az-empty-divider hidden-lg hidden-md" style="height: 60px;"></div></div></div></div></div></div></div></div></div></div></div>The post <a href="https://bibliography.nanobiotix.com/2011-clinam-abstract-thermosensitive-magnetoliposomes-for-mri-guided-drug-delivery-meyr-et-al/">2011 – CLINAM Abstract – Thermosensitive Magnetoliposomes for MRI-Guided Drug Delivery – Meyr et al.</a> first appeared on <a href="https://bibliography.nanobiotix.com">Nano Publications</a>.]]></content:encoded>
					
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			</item>
		<item>
		<title>2010 &#8211; Combinations of proteins with Nano-Systems &#8211; Di Marco et al.</title>
		<link>https://bibliography.nanobiotix.com/2010-combinations-of-proteins-with-nano-systems-di-marco-et-al/</link>
					<comments>https://bibliography.nanobiotix.com/2010-combinations-of-proteins-with-nano-systems-di-marco-et-al/#respond</comments>
		
		<dc:creator><![CDATA[nano-pub]]></dc:creator>
		<pubDate>Mon, 06 Feb 2017 12:30:17 +0000</pubDate>
				<category><![CDATA[Miscellaneous]]></category>
		<category><![CDATA[NO-RIGHTS]]></category>
		<category><![CDATA[Publications]]></category>
		<category><![CDATA[Biomolecules]]></category>
		<category><![CDATA[Chemotherapeutic]]></category>
		<category><![CDATA[Delivery]]></category>
		<category><![CDATA[Design]]></category>
		<category><![CDATA[Drug]]></category>
		<category><![CDATA[Encapsulate]]></category>
		<category><![CDATA[Pharmacokinetics]]></category>
		<category><![CDATA[Protein]]></category>
		<category><![CDATA[Therapeutic]]></category>
		<category><![CDATA[Versatile]]></category>
		<guid isPermaLink="false">http://localhost:8888/nano-publications/?p=132</guid>

					<description><![CDATA[<p>The latest development of protein engineering allows the production of proteins having desired properties and large potential markets, but the clinical advances of therapeutical proteins are still limited by their fragility. Nanotechnology could provide optimal vectors able to protect from degradation therapeutical biomolecules such as proteins, enzymes or specific polypeptides.</p>
The post <a href="https://bibliography.nanobiotix.com/2010-combinations-of-proteins-with-nano-systems-di-marco-et-al/">2010 – Combinations of proteins with Nano-Systems – Di Marco et al.</a> first appeared on <a href="https://bibliography.nanobiotix.com">Nano Publications</a>.]]></description>
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            </div><div class="az-box-icon-content az-font-custom az-font-color-custom" style="color: #ffffff;"><h3 class="az-box-icon-title">Authors</h3><p>Mariagrazia Di Marco<span class="notes up">1</span>, Shaharum Shamsuddin<span class="notes up">2</span>, Khairunisak Abdul Razak<span class="notes up">3</span>, Azlan Abdul Aziz<span class="notes up">4</span>, Corinne Devaux<span class="notes up">1</span>, Elsa Borghi<span class="notes up">1</span>, Laurent Levy<span class="notes up">1</span>, Claudia Sadun<span class="notes up">5</span><br />
<span class="notes">1 – Nanobiotix, Paris, France<br />
2 – School of Health Sciences, Health Campus Universiti Sains Malaysia, Kelantan, Malaysia<br />
3 – School of Materials and Mineral Resources Engineering, Engineering Campus<br />
4 – School of Physics, Universiti Sains Malaysia, Penang, Malaysia<br />
5 – Department of Chemistry, Sapienza, University of Rome, Rome, Italy</span></p>
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<div class="az-content-element-wrapper az-empty-divider hidden-lg hidden-md" style="height: 60px;"></div></div></div></div><div data-animation-type="ani-in" data-animation-in="fadeInUp" data-animation-out="none" data-animation-speed="default" data-animation-delay="300" data-offset-down="90" data-offset-up="none" class="single-clms col-md-6 az-main-col-content az-module az-col-pos-middle az-v-space-clm animate-content az-module-bg-color"><div class="az-col az-clm-padding-105" >
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            </div><div class="az-box-icon-content"><h3 class="az-box-icon-title">Summary</h3><p><strong>Abstract:</strong> The latest development of protein engineering allows the production of proteins having desired properties and large potential markets, but the clinical advances of therapeutical proteins are still limited by their fragility. Nanotechnology could provide optimal vectors able to protect from degradation therapeutical biomolecules such as proteins, enzymes or specific polypeptides.</p>
<p>On the other hand, some proteins can be also used as active ligands to help nanoparticles loaded with chemotherapeutic or other drugs to reach particular sites in the body. The aim of this review is to provide an overall picture of the general aspects of the most successful approaches used to combine proteins with nanosystems. This combination is mainly achieved by absorption, bioconjugation and encapsulation. Interactions of nanoparticles with biomolecules and caveats related to protein denaturation are also pointed out. A clear understanding of nanoparticle-protein interactions could make possible the design of precise and versatile hybrid nanosystems. This could further allow control of their pharmacokinetics as well as activity, and safety.</p>
<p><strong>Keywords:</strong> nanoparticles, drug delivery, proteins, polypeptides, absorption, bioconjugation, encapsulation</p>
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<div class="az-content-element-wrapper az-empty-divider hidden-lg hidden-md" style="height: 60px;"></div></div></div></div></div></div></div></div></div></div></div>The post <a href="https://bibliography.nanobiotix.com/2010-combinations-of-proteins-with-nano-systems-di-marco-et-al/">2010 – Combinations of proteins with Nano-Systems – Di Marco et al.</a> first appeared on <a href="https://bibliography.nanobiotix.com">Nano Publications</a>.]]></content:encoded>
					
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