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      Control over Silica Particle Growth and Particle–Biomolecule Interactions Facilitates Silica Encapsulation of Mammalian Cells with Thickness Control

      , 1 ,
      ACS Biomaterials Science & Engineering
      American Chemical Society (ACS)

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          Abstract

          <p class="first" id="P1">Over the last twenty years, many strategies utilizing sol-gel chemistry to integrate biological cells into silica-based materials have been reported. One such strategy, Sol-Generating Chemical Vapor into Liquid (SG-CViL) deposition, shows promise as an efficient encapsulation technique due to the ability to vary the silica encapsulation morphology obtained by this process through variation of SG-CViL reaction conditions. In this report, we develop SG-CViL as a tunable, multi-purpose silica encapsulation strategy by investigating the mechanisms governing both silica particle generation and subsequent interaction with phospholipid assemblies (liposomes and living cells). Using Dynamic Light Scattering (DLS) measurements, linear and exponential silica particle growth dynamics were observed which were dependent on deposition buffer ion constituents and ion concentration. Silica particle growth followed a cluster-cluster growth mechanism at acidic pH, and a monomer-cluster growth mechanism at neutral to basic pH. Increasing silica sol aging temperature resulted in higher rates of particle growth and larger particles. DLS measurements employing PEG coated liposomes and cationic liposomes, serving as model phospholipid assemblies, revealed electrostatic interactions promote more stable liposome-silica interactions than hydrogen bonding and facilitate silica coating on suspension cells. However, continued silica reactivity leads to aggregation of silica coated suspensions cells, revealing the need for cell isolation to tune deposited silica thickness. Utilizing these mechanistic study insights, silica was deposited onto adherent HeLa cells under biocompatible conditions with micron scale control over silica thickness, minimal cell manipulation steps, and retained cell viability over several days. </p><p id="P2">Silica sols are generated via vapor deposition of tetramethylorthosilicate into buffer. By varying the buffer ionic consituents, concentration, pH, and sol aging temperature, silica particle size in silica sols can be controlled, facilitating deposition of silica layers with tunable thickness on mammalian HeLa cells (represented by red fluorescense). </p><p id="P3"> <div class="figure-container so-text-align-c"> <img alt="" class="figure" src="/document_file/1cc89887-cbf0-4a10-877e-af08f7e50139/PubMedCentral/image/nihms893086u1.jpg"/> </div> </p>

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          Author and article information

          Journal
          ACS Biomaterials Science & Engineering
          ACS Biomater. Sci. Eng.
          American Chemical Society (ACS)
          2373-9878
          2373-9878
          June 15 2017
          September 11 2017
          July 31 2017
          September 11 2017
          : 3
          : 9
          : 2098-2109
          Affiliations
          [1 ]Bioenergy and Biodefense Technologies, Sandia National Laboratories, Albuquerque, New Mexico 87185, United States
          Article
          10.1021/acsbiomaterials.7b00185
          5705094
          29202010
          2f114ab6-c34b-411b-bdc2-d9a2cf6a2823
          © 2017
          History

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