Literature DB >> 28804160

Smart Nanoscale Drug Delivery Platforms from Stimuli-Responsive Polymers and Liposomes.

Sang-Min Lee1,2, SonBinh T Nguyen1.   

Abstract

Since the 1960's, stimuli-responsive polymers have been utilized as functional soft materials for biological applications such as the triggered-release delivery of biologically active cargos. Over the same period, liposomes have been explored as an alternative drug delivery system with potentials to decrease the toxic side effects often associated with conventional small-molecule drugs. However, the lack of drug-release triggers and the instability of bare liposomes often limit their practical applications, causing short circulation time and low therapeutic efficacy. This perspective article highlights recent work in integrating these two materials together to achieve a targetable, triggerable nanoscale platform that fulfills all the characteristics of a near-ideal drug delivery system. Through a drop-in, post-synthesis modification strategy, a network of stimuli-responsive polymers can be integrated onto the surface of liposomes to form polymer-caged nanobins, a multifunctional nanoscale delivery platform that allows for multi-drug loading, targeted delivery, triggered drug-release, and theranostic capabilities.

Entities:  

Keywords:  drug delivery; liposomes; stimuli-responsive polymer gels; triggered release

Year:  2013        PMID: 28804160      PMCID: PMC5552073          DOI: 10.1021/ma401529w

Source DB:  PubMed          Journal:  Macromolecules        ISSN: 0024-9297            Impact factor:   5.985


  75 in total

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7.  Programmed supramolecular nanoassemblies: enhanced serum stability and cell specific triggered release of anti-cancer drugs.

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8.  Phospholipase A2-Responsive Phosphate Micelle-Loaded UCNPs for Bioimaging of Prostate Cancer Cells.

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9.  Elegant Approach to the Controllability of the Mechanical Properties of a Microgel via the Self-Assembly of Internal Molecules.

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10.  Polymeric Core-Shell Combinatorial Nanomedicine for Synergistic Anticancer Therapy.

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Journal:  ACS Omega       Date:  2019-11-11
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