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      Resveratrol Enhances mRNA and siRNA Lipid Nanoparticles Primary CLL Cell Transfection

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          Abstract

          Chronic lymphocytic leukemia (CLL) is the most common adult leukemia in Western populations. Therapies such as mRNA and siRNA encapsulated in lipid nanoparticles (LNPs) represent a clinically advanced platform and are utilized for a wide variety of applications. Unfortunately, transfection of RNA into CLL cells remains a formidable challenge and a bottleneck for developing targeted therapies for this disease. Therefore, we aimed to elucidate the barriers to efficient transfection of RNA-encapsulated LNPs into primary CLL cells to advance therapies in the future. To this end, we transfected primary CLL patient samples with mRNA and siRNA payloads encapsulated in an FDA-approved LNP formulation and characterized the transfection. Additionally, we tested the potential of repurposing caffeic acid, curcumin and resveratrol to enhance the transfection of nucleic acids into CLL cells. The results demonstrate that the rapid uptake of LNPs is required for successful transfection. Furthermore, we demonstrate that resveratrol enhances the delivery of both mRNA and siRNA encapsulated in LNPs into primary CLL patient samples, overcoming inter-patient heterogeneity. This study points out the important challenges to consider for efficient RNA therapeutics for CLL patients and advocates the use of resveratrol in combination with RNA lipid nanoparticles to enhance delivery into CLL cells.

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          Progress and challenges towards targeted delivery of cancer therapeutics

          Targeted delivery approaches for cancer therapeutics have shown a steep rise over the past few decades. However, compared to the plethora of successful pre-clinical studies, only 15 passively targeted nanocarriers (NCs) have been approved for clinical use and none of the actively targeted NCs have advanced past clinical trials. Herein, we review the principles behind targeted delivery approaches to determine potential reasons for their limited clinical translation and success. We propose criteria and considerations that must be taken into account for the development of novel actively targeted NCs. We also highlight the possible directions for the development of successful tumor targeting strategies.
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            Lipid Nanoparticles Enabling Gene Therapies: From Concepts to Clinical Utility

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              On the Formation and Morphology of Lipid Nanoparticles Containing Ionizable Cationic Lipids and siRNA

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                Author and article information

                Journal
                Pharmaceutics
                Pharmaceutics
                pharmaceutics
                Pharmaceutics
                MDPI
                1999-4923
                07 June 2020
                June 2020
                : 12
                : 6
                : 520
                Affiliations
                [1 ]Laboratory of Precision NanoMedicine, Tel Aviv University, Tel Aviv 69978, Israel; edokon89@ 123456gmail.com (E.K.); hinbal@ 123456tauex.tau.ac.il (I.H.-H.); danielr0406@ 123456gmail.com (D.R.); nivcohenb@ 123456gmail.com (N.C.); sushmita.microbio@ 123456gmail.com (S.C.); nuphar.veiga@ 123456gmail.com (N.V.)
                [2 ]School of Molecular Cell Biology and Biotechnology, George S Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv 69978, Israel
                [3 ]Department of Materials Sciences and Engineering, Iby and Aladar Fleischman Faculty of Engineering, Tel Aviv University, Tel Aviv 69978, Israel
                [4 ]Center for Nanoscience and Nanotechnology, and Tel Aviv University, Tel Aviv 69978, Israel
                [5 ]Cancer Biology Research Center, Tel Aviv University, Tel Aviv 69978, Israel
                [6 ]Davidoff Cancer Center, Beilinson Hospital, Rabin Medical Center Petah Tiqva, Institute of Hematology, Petah Tikva 49100, Israel; Piar@ 123456clalit.org.il (P.R.); Osnatb@ 123456clalit.org.il (O.B.)
                [7 ]Chaim Sheba Medical Center, Tel-Hashomer, Ramat Gan 52621, Israel; Ohad.Benjamini@ 123456sheba.health.gov.il (O.B.); a.nagler@ 123456sheba.gov.il (A.N.)
                Author notes
                [* ]Correspondence: peer@ 123456tauex.tau.ac.il ; Tel.: +972-3-640-7925
                Author information
                https://orcid.org/0000-0001-8238-0673
                Article
                pharmaceutics-12-00520
                10.3390/pharmaceutics12060520
                7355647
                32517377
                456491db-43b0-40af-84eb-d22fe00efdcd
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 05 May 2020
                : 05 June 2020
                Categories
                Article

                endosomal escape,b lymphocyte,rna therapies,drug delivery,clinic,caffeic acid,curcumin

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