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Articles

Papers, explained in our own words

Every entry summarises what the study set out to test, what it found and why it changes how we design delivery systems. Browse research and reviews or search the collection.

586 articles

Showing 97–105 of 105 articles · Keyword: lipid nanoparticle Clear keyword

Nanoscale2014ReviewNon-viral Gene Delivery

97. Enhancing Endosomal Escape for Nanoparticle Mediated siRNA Delivery

Da Ma

siRNA-based gene therapy is a promising biotechnology for treating cancer and other diseases, but safe and efficient delivery is essential. Nanoparticle-mediated delivery must overcome multiple biological barriers, and endosomal escape is a critical rate-limiting barrier: nanoparticles are typically internalised via…

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2014ResearchDrug Delivery

98. Liposomes versus Lipid Nanoparticles Comparative Study of Lipid-Based Systems as Oryzalin Carriers for the Treatment of Leishmaniasis

Lopes Rm, Gaspar Mm, Pereira J, Eleuterio Cv, Carvalho M, Almeida Aj, Cruz Mem

Current leishmaniasis chemotherapy lacks options that combine high activity, low toxicity, and affordable cost. Oryzalin (ORZ), a dinitroaniline with in vitro antileishmanial activity, is limited by poor water solubility and low accumulation in diseased organs. Lipid-based nanocarriers may overcome these limitations…

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BioMed Research International.2014ReviewNon-viral Gene Delivery

99. Lipid Nanoparticles as Carriers for RNAi against Viral Infections Current Status and Future Perspectives

Torrecilla J, Rodríguez-Gascón A, Solinís Má, Del Pozo-Rodríguez A

Naked RNAi molecules are rapidly degraded by serum nucleases and cannot readily cross cell membranes because of their negative charge. Effective delivery systems are therefore required to exploit RNAi for antiviral therapy. Lipid nanoparticles (LNPs) are attractive because they are relatively safe, simple to produce…

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European Journal of Pharmaceutics and Biopharmaceutics.2014ReviewNon-viral Gene Delivery

100. Nanotoxicology applied to solid lipid nanoparticles and nanostructured lipid carriers – A systematic review of in vitro data

Slavomíra Doktorovová, Eliana B. Souto, Amélia Maria Silva

Solid lipid nanoparticles (SLN) and nanostructured lipid carriers (NLC) were developed as alternative colloidal carriers with better stability and tolerability than polymeric nanoparticles. However, in vitro toxicity data were scattered across many cell lines, assays, exposure times, concentrations, and formulations…

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Pharmaceutics2013ReviewNon-viral Gene Delivery

101. Advances in Lipid Nanoparticles for siRNA Delivery

Tam Yyc, Chen S, Cullis Pr

siRNA has broad therapeutic potential, but clinical translation is limited by rapid nuclease degradation, poor accumulation in target tissues, and inability to cross cell membranes to reach the cytoplasm. Lipid nanoparticles containing ionisable amino lipids are the leading systemic delivery system for siRNA, with…

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Drug Discovery Today.2013ReviewDrug Delivery

102. Recent advances in topical ophthalmic drug delivery with lipid-based nanocarriers

Gan L, Wang J, Jiang M, Bartlett H, Ouyang D, Eperjesi F, Liu J, Gan Y

Topical ocular drug delivery is limited by tear turnover, corneal and conjunctival barriers, efflux transporters, and poor water solubility of many drug candidates. Lipid-based nanocarriers may improve ocular bioavailability, prolong preocular residence, enhance corneal penetration, and provide controlled release…

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Pharmaceutical Research2011ReviewNon-viral Gene Delivery

103. Cancer Immunotherapy and Nanomedicine

Wei-Yun Sheng, Leaf Huang

The immune system can recognise and kill pre-cancer and cancer cells, but surviving tumour cells learn to escape immune surveillance after immunoselection. Cancer immunotherapy aims to overcome these escape mechanisms. Nanomedicine offers tools—nanodiagnostics and nanobiopharmaceuticals—to deliver antigens…

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2007ReviewNon-viral Gene Delivery

104. Lipid-based Nanoparticles for Nucleic Acid Delivery

Li W, Szoka Fc Jr

Systemic non-viral gene delivery is limited by rapid clearance, toxicity, and poor target-cell access. Cationic lipid–DNA lipoplexes are effective in vitro but perform poorly in vivo because they aggregate with serum proteins, are cleared by the reticuloendothelial system (RES), and accumulate mainly in lung and…

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Molecular Therapy2001ResearchNon-viral Gene Delivery

105. A Regulated, NFκB-Assisted Import of Plasmid DNA into Mammalian Cell Nuclei

Adi Mesika, Irina Grigoreva, Muriel Zohar, Ziv Reich

Transfection efficiency of nonviral gene delivery systems remains unacceptably low, largely due to the inability of plasmid DNA to effectively translocate through the nuclear pore complexes (NPCs). While substantial progress has been made in transcriptionally regulated vectors, control over nuclear targeting is…

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