Literature DB >> 31686433

Chiral Supraparticles for Controllable Nanomedicine.

Jihyeon Yeom1, Pedro P G Guimaraes1,2, Hyo Min Ahn3, Bo-Kyeong Jung3, Quanyin Hu1, Kevin McHugh1, Michael J Mitchell1,4, Chae-Ok Yun3, Robert Langer1, Ana Jaklenec1.   

Abstract

Chirality is ubiquitous in nature and hard-wired into every biological system. Despite the prevalence of chirality in biological systems, controlling biomaterial chirality to influence interactions with cells has only recently been explored. Chiral-engineered supraparticles (SPs) that interact differentially with cells and proteins depending on their handedness are presented. SPs coordinated with d-chirality demonstrate greater than threefold enhanced cell membrane penetration in breast, cervical, and multiple myeloma cancer cells. Quartz crystal microbalance with dissipation and isothermal titration calorimetry measurements reveal the mechanism of these chiral-specific interactions. Thermodynamically, d-SPs show more stable adhesion to lipid layers composed of phospholipids and cholesterol compared to l-SPs. In vivo, d-SPs exhibit superior stability and longer biological half-lives likely due to opposite chirality and thus protection from endogenous proteins including proteases. This work shows that incorporating d-chirality into nanosystems enhances uptake by cancer cells and prolonged in vivo stability in circulation, providing support for the importance of chirality in biomaterials. Thus, chiral nanosystems may have the potential to provide a new level of control for drug delivery systems, tumor detection markers, biosensors, and other biomaterial-based devices.
© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  chirality; drug delivery systems; nanomedicine; self-assembly; supraparticles

Mesh:

Substances:

Year:  2019        PMID: 31686433      PMCID: PMC6986383          DOI: 10.1002/adma.201903878

Source DB:  PubMed          Journal:  Adv Mater        ISSN: 0935-9648            Impact factor:   30.849


  39 in total

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