Literature DB >> 21608994

Polymeric vesicles: from drug carriers to nanoreactors and artificial organelles.

Pascal Tanner1, Patric Baumann, Ramona Enea, Ozana Onaca, Cornelia Palivan, Wolfgang Meier.   

Abstract

One strategy in modern medicine is the development of new platforms that combine multifunctional compounds with stable, safe carriers in patient-oriented therapeutic strategies. The simultaneous detection and treatment of pathological events through interactions manipulated at the molecular level offer treatment strategies that can decrease side effects resulting from conventional therapeutic approaches. Several types of nanocarriers have been proposed for biomedical purposes, including inorganic nanoparticles, lipid aggregates, including liposomes, and synthetic polymeric systems, such as vesicles, micelles, or nanotubes. Polymeric vesicles--structures similar to lipid vesicles but created using synthetic block copolymers--represent an excellent candidate for new nanocarriers for medical applications. These structures are more stable than liposomes but retain their low immunogenicity. Significant efforts have been made to improve the size, membrane flexibility, and permeability of polymeric vesicles and to enhance their target specificity. The optimization of these properties will allow researchers to design smart compartments that can co-encapsulate sensitive molecules, such as RNA, enzymes, and proteins, and their membranes allow insertion of membrane proteins rather than simply serving as passive carriers. In this Account, we illustrate the advances that are shifting these molecular systems from simple polymeric carriers to smart-complex protein-polymer assemblies, such as nanoreactors or synthetic organelles. Polymeric vesicles generated by the self-assembly of amphiphilic copolymers (polymersomes) offer the advantage of simultaneous encapsulation of hydrophilic compounds in their aqueous cavities and the insertion of fragile, hydrophobic compounds in their membranes. This strategy has permitted us and others to design and develop new systems such as nanoreactors and artificial organelles in which active compounds are simultaneously protected and allowed to act in situ. In recent years, we have created a variety of multifunctional, proteinpolymersomes combinations for biomedical applications. The insertion of membrane proteins or biopores into the polymer membrane supported the activity of co-encapsulated enzymes that act in tandem inside the cavity or of combinations of drugs and imaging agents. Surface functionalization of these nanocarriers permitted specific targeting of the desired biological compartments. Polymeric vesicles alone are relatively easy to prepare and functionalize. Those features, along with their stability and multifunctionality, promote their use in the development of new theranostic strategies. The combination of polymer vesicles and biological entities will serve as tools to improve the observation and treatment of pathological events and the overall condition of the patient.

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Year:  2011        PMID: 21608994     DOI: 10.1021/ar200036k

Source DB:  PubMed          Journal:  Acc Chem Res        ISSN: 0001-4842            Impact factor:   22.384


  67 in total

1.  Mechanical properties of drug loaded diblock copolymer bilayers: A molecular dynamics study.

Authors:  Damián A Grillo; Juan M R Albano; Esteban E Mocskos; Julio C Facelli; Mónica Pickholz; Marta B Ferraro
Journal:  J Chem Phys       Date:  2018-06-07       Impact factor: 3.488

2.  Fusion Domains Guide the Oriented Insertion of Light-Driven Proton Pumps into Liposomes.

Authors:  Noah Ritzmann; Johannes Thoma; Stephan Hirschi; David Kalbermatter; Dimitrios Fotiadis; Daniel J Müller
Journal:  Biophys J       Date:  2017-07-08       Impact factor: 4.033

3.  Nanoreactors based on DNAzyme-functionalized magnetic nanoparticles activated by magnetic field.

Authors:  Saira F Bakshi; Nataliia Guz; Andrey Zakharchenko; Han Deng; Alexei V Tumanov; Craig D Woodworth; Sergiy Minko; Dmitry M Kolpashchikov; Evgeny Katz
Journal:  Nanoscale       Date:  2018-01-18       Impact factor: 7.790

4.  Towards self-assembled hybrid artificial cells: novel bottom-up approaches to functional synthetic membranes.

Authors:  Roberto J Brea; Michael D Hardy; Neal K Devaraj
Journal:  Chemistry       Date:  2015-07-06       Impact factor: 5.236

5.  Redox-Responsive Self-Assembled Chain-Shattering Polymeric Therapeutics.

Authors:  Kaimin Cai; Jonathan Yen; Qian Yin; Yang Liu; Ziyuan Song; Stéphane Lezmi; Yanfeng Zhang; Xujuan Yang; William G Helferich; Jianjun Cheng
Journal:  Biomater Sci       Date:  2015-07       Impact factor: 6.843

Review 6.  The subcellular distribution of small molecules: from pharmacokinetics to synthetic biology.

Authors:  Nan Zheng; Hobart Ng Tsai; Xinyuan Zhang; Gus R Rosania
Journal:  Mol Pharm       Date:  2011-08-15       Impact factor: 4.939

7.  Supramolecular guests in solvent driven block copolymer assembly: From internally structured nanoparticles to micelles.

Authors:  Daniel Klinger; Maxwell J Robb; Jason M Spruell; Nathaniel A Lynd; Craig J Hawker; Luke A Connal
Journal:  Polym Chem       Date:  2013-10-07       Impact factor: 5.582

8.  Programmable Nanoassemblies from Non-Assembling Homopolymers Using Ad Hoc Electrostatic Interactions.

Authors:  Jiaming Zhuang; Matteo Garzoni; Diego Amado Torres; Ambata Poe; Giovanni M Pavan; S Thayumanavan
Journal:  Angew Chem Int Ed Engl       Date:  2017-03-13       Impact factor: 15.336

9.  Size-controlled self-assembly of superparamagnetic polymersomes.

Authors:  Robert J Hickey; Jason Koski; Xin Meng; Robert A Riggleman; Peijun Zhang; So-Jung Park
Journal:  ACS Nano       Date:  2014-01-02       Impact factor: 15.881

10.  Polyactives: controlled and sustained bioactive release via hydrolytic degradation.

Authors:  N D Stebbins; J J Faig; W Yu; R Guliyev; K E Uhrich
Journal:  Biomater Sci       Date:  2015-06-02       Impact factor: 6.843

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