Matches in SemOpenAlex for { <https://semopenalex.org/work/W2336521569> ?p ?o ?g. }
Showing items 1 to 64 of
64
with 100 items per page.
- W2336521569 abstract "Event Abstract Back to Event pH-sensitive surface charge-conversion nanomicelle for anti-tumor drug delivery Wei Wu1, 2*, Guixue Wang1* and Jianshu Li2* 1 Chongqing University, Bioengineering College, China 2 Sichuan University, College of Polymer Science and Engineering, China Introduction: During the last decade, tremendous efforts have been attained in the development of stimuli-responsive polymeric nanocarriers for the controlled delivery of various anti-cancerous drugs[1]. Physiological stimuli-responsive nanocarriers provide the feasible platforms for cancer therapy due to their improved anticancer efficiency as well as reduced systematic cytotoxicity via the tumor specific enhanced permeability and retention (EPR) effect[2]. It is interesting to note the pH-sensitive surface charge-conversion strategy, which is potential for enhancing tumor cell internalization efficiency. In this study, we attempt to engineer this smart tumor-acidity activated surface charge-conversion function into a biodegradable amphiphilic block copolymers for anticancer application. Materials and Methods: Poly(D, L-lactide)-block-poly(2-aminoethyl methacrylate) (PLA-b-PAEMA, MW 8900, PDI 1,24) was firstly synthesized through ring-opening polymerization (ROP) and subsequently atom transition radical polymerization method. PLA-b-PAEMA/DMMA was obtained by using 2,3-dimethykmaleic anhydride (DMMA) modified PLA-b-PAEMA. Results and Discussion: The well-defined PLA-b-PAEMA is further modified by DMMA and succinic anhydride (SA) to yield the tumor-acidity activated surface charge-conversional block copolymer (PLA-b-PAEMA/DMMA) and the control sample (PLA-b-PAEMA/SA). In this design, the biodegradable PLA block and the functional PAEMA/DMMA (or PAEMA/SA) block provide the amphiphilic driving force to self-assemble into nanocarriers, which have PLA aggregated hydrophobic inner core and PAEMA/DMMA (or PAEMA/SA) outer corona, in aqueous solution. As compared with the invariable negative surface charge of PAEMA/SA block, PAEMA/DMMA block shows the tumor-acidity activated surface charge-conversion feature, i.e., exhibiting negatively charged surface during the blood circulation time and positively charged surface in response to slight tumor acidic environment through the hydrolysis of DMMA functional agents. Thus, after the loading of positively charged doxorubicin hydrochloride (DOX·HCl) into the negatively charged corona structure through electrostatic attraction, the DOX·HCl-loaded PLA-b-PAEMA/DMMA carrier (PLA-b-PAEMA/DMMA@DOX·HCl) is expected to prolong blood circulation time because its “stealthy” negatively charged surface could effectively decrease the undesired consumption by the reticuloendothelial system (RES) and the protein adsorption in vivo, and promote the anti-cancer therapeutic efficiency though the tumor activated positively charged surface for enhanced tumor cell adhesion and targeted drug release (Scheme 1). Scheme1. Illustration of tumor-acidity activated carriers for enhanced cell uptake and targeted drug release. Conclusions: In summary, we construct a smart nanocarrier based on biodegradable PLA-b-PAEMA/DMMA copolymer, which could convert surface charge from negative to positive in response to the tumor-acidity. It exhibits various superiorities for tumor-specific drug delivery, including long blood circulation time, enhanced tumor-cell adhesion, tumor targeted drug release and additional cytotoxicity for tumor cells after the charge-conversion. Thus, this biodegradable smart carrier integrated high drug delivery efficiency and well-improved biocompatibility provides a feasible platform for the ideal anti-tumor therapy. Financial support from the National Natural Science Foundation of China (51322303); Financial support from the Foundations of Sichuan Province (2012JQ0009)References:[1] Mura S., Nicolas J., Couvreur P., stimuli-responsive nanocarriers for drug delivery [J], Nat. Mater., 2013(12): 991-1003.[2] Wu W., Wang J., Lin Z., tumor-acidity activated surface charge-conversion of polymeric nanocarriers for enhanced cell adhesion and targeted drug release [J], Macromol. Rapid Commun., 2014, 35 (19): 1679-1684. Keywords: Cell Adhesion, Drug delivery, stimuli-response, Biodegradable material Conference: 10th World Biomaterials Congress, Montréal, Canada, 17 May - 22 May, 2016. Presentation Type: Poster Topic: Biomaterials for therapeutic delivery Citation: Wu W, Wang G and Li J (2016). pH-sensitive surface charge-conversion nanomicelle for anti-tumor drug delivery. Front. Bioeng. Biotechnol. Conference Abstract: 10th World Biomaterials Congress. doi: 10.3389/conf.FBIOE.2016.01.01351 Copyright: The abstracts in this collection have not been subject to any Frontiers peer review or checks, and are not endorsed by Frontiers. They are made available through the Frontiers publishing platform as a service to conference organizers and presenters. The copyright in the individual abstracts is owned by the author of each abstract or his/her employer unless otherwise stated. Each abstract, as well as the collection of abstracts, are published under a Creative Commons CC-BY 4.0 (attribution) licence (https://creativecommons.org/licenses/by/4.0/) and may thus be reproduced, translated, adapted and be the subject of derivative works provided the authors and Frontiers are attributed. For Frontiers’ terms and conditions please see https://www.frontiersin.org/legal/terms-and-conditions. Received: 27 Mar 2016; Published Online: 30 Mar 2016. * Correspondence: Dr. Wei Wu, Chongqing University, Bioengineering College, Chongqing, China, Email1 Dr. Guixue Wang, Chongqing University, Bioengineering College, Chongqing, China, wanggx@cqu.edu.cn Dr. Jianshu Li, Sichuan University, College of Polymer Science and Engineering, Chengdu, China, jianshu_li@scu.edu.cn Login Required This action requires you to be registered with Frontiers and logged in. To register or login click here. Abstract Info Abstract The Authors in Frontiers Wei Wu Guixue Wang Jianshu Li Google Wei Wu Guixue Wang Jianshu Li Google Scholar Wei Wu Guixue Wang Jianshu Li PubMed Wei Wu Guixue Wang Jianshu Li Related Article in Frontiers Google Scholar PubMed Abstract Close Back to top Javascript is disabled. Please enable Javascript in your browser settings in order to see all the content on this page." @default.
- W2336521569 created "2016-06-24" @default.
- W2336521569 creator A5031039660 @default.
- W2336521569 creator A5071042021 @default.
- W2336521569 creator A5084952125 @default.
- W2336521569 date "2016-01-01" @default.
- W2336521569 modified "2023-09-27" @default.
- W2336521569 title "pH-sensitive surface charge-conversion nanomicelle for anti-tumor drug delivery" @default.
- W2336521569 doi "https://doi.org/10.3389/conf.fbioe.2016.01.01351" @default.
- W2336521569 hasPublicationYear "2016" @default.
- W2336521569 type Work @default.
- W2336521569 sameAs 2336521569 @default.
- W2336521569 citedByCount "0" @default.
- W2336521569 crossrefType "journal-article" @default.
- W2336521569 hasAuthorship W2336521569A5031039660 @default.
- W2336521569 hasAuthorship W2336521569A5071042021 @default.
- W2336521569 hasAuthorship W2336521569A5084952125 @default.
- W2336521569 hasBestOaLocation W23365215691 @default.
- W2336521569 hasConcept C127413603 @default.
- W2336521569 hasConcept C15920480 @default.
- W2336521569 hasConcept C171250308 @default.
- W2336521569 hasConcept C178790620 @default.
- W2336521569 hasConcept C18150654 @default.
- W2336521569 hasConcept C185592680 @default.
- W2336521569 hasConcept C188027245 @default.
- W2336521569 hasConcept C192562407 @default.
- W2336521569 hasConcept C2776743539 @default.
- W2336521569 hasConcept C2777735259 @default.
- W2336521569 hasConcept C2779820397 @default.
- W2336521569 hasConcept C42360764 @default.
- W2336521569 hasConcept C44228677 @default.
- W2336521569 hasConcept C521977710 @default.
- W2336521569 hasConceptScore W2336521569C127413603 @default.
- W2336521569 hasConceptScore W2336521569C15920480 @default.
- W2336521569 hasConceptScore W2336521569C171250308 @default.
- W2336521569 hasConceptScore W2336521569C178790620 @default.
- W2336521569 hasConceptScore W2336521569C18150654 @default.
- W2336521569 hasConceptScore W2336521569C185592680 @default.
- W2336521569 hasConceptScore W2336521569C188027245 @default.
- W2336521569 hasConceptScore W2336521569C192562407 @default.
- W2336521569 hasConceptScore W2336521569C2776743539 @default.
- W2336521569 hasConceptScore W2336521569C2777735259 @default.
- W2336521569 hasConceptScore W2336521569C2779820397 @default.
- W2336521569 hasConceptScore W2336521569C42360764 @default.
- W2336521569 hasConceptScore W2336521569C44228677 @default.
- W2336521569 hasConceptScore W2336521569C521977710 @default.
- W2336521569 hasLocation W23365215691 @default.
- W2336521569 hasOpenAccess W2336521569 @default.
- W2336521569 hasPrimaryLocation W23365215691 @default.
- W2336521569 hasRelatedWork W1595862141 @default.
- W2336521569 hasRelatedWork W1985204895 @default.
- W2336521569 hasRelatedWork W1989747786 @default.
- W2336521569 hasRelatedWork W2074731395 @default.
- W2336521569 hasRelatedWork W2100561888 @default.
- W2336521569 hasRelatedWork W2392360665 @default.
- W2336521569 hasRelatedWork W2791060554 @default.
- W2336521569 hasRelatedWork W3205587479 @default.
- W2336521569 hasRelatedWork W4311495042 @default.
- W2336521569 hasRelatedWork W4365813959 @default.
- W2336521569 hasVolume "4" @default.
- W2336521569 isParatext "false" @default.
- W2336521569 isRetracted "false" @default.
- W2336521569 magId "2336521569" @default.
- W2336521569 workType "article" @default.