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									<identifier>oai:www.peertechzpublications.org:10.17352/ahr.000028</identifier>
									<datestamp>2021-01-28</datestamp>
									<setSpec>PTZ.AHR:VOL7</setSpec>
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									<oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:mml="http://www.w3.org/1998/Math/MathML" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
										<dc:title>
										Lipid nanoparticulate drug delivery system for the treatment of hepatic fibrosis
										</dc:title><dc:creator>Swarupananda Mukherjee</dc:creator><dc:creator> Ayon Dutta</dc:creator><dc:creator>Dipanjana Ash</dc:creator><dc:description>&lt;p&gt;Background: Irreversible hepatic fibrosis, an excessive production and accumulation of extra cellular matrix by hepatic stellate cells in the liver, becomes a remarkable economic burden in global health care system.Low therapeutic efficacy and undesirable systemic effect of conventional therapies limit their clinical applications to targethepatic stellate cells.&lt;/p&gt;&lt;p&gt;Method: Surface engineered lipid nano-particle becomes a potential candidate to deliver anti-fibrotic nutrients or Small interfering RNA (siRNA) of fibrogenic genes for treating hepatic disorders.&amp;nbsp;&lt;/p&gt;&lt;p&gt;Conclusion: This mini review focuses on different strategies of surface engineered organic lipid nanoparticles for the treatment of hepatic fibrosis by targeting specific and un-specific Hepatic Stellate Cells (HSCs).&lt;/p&gt;</dc:description>
										<dc:publisher>Archives of Hepatitis Research - Peertechz Publications</dc:publisher>
										<dc:date>2021-01-28</dc:date>
										<dc:type>Mini Review</dc:type>
										<dc:identifier>https://doi.org/10.17352/ahr.000028</dc:identifier>
										<dc:language>en</dc:language>
										<dc:rights>Copyright © Swarupananda Mukherjee et al.</dc:rights>
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