Controlling the Vaterite CaCO3 Crystal Pores. Design of Tailor-Made Polymer Based Microcapsules by Hard Templating

被引:77
作者
Feoktistova, Natalia [1 ,2 ]
Rose, Juergen [3 ]
Prokopovic, Vladimir Z. [1 ]
Vikulina, Anna S. [1 ,4 ]
Skirtach, Andre [5 ]
Volodkin, Dmitry [1 ,2 ,4 ]
机构
[1] Fraunhofer Inst Cell Therapy & Immunol, Fraunhofer IZI BB, Branch Bioanalyt & Bioproc, Muehlenberg 13, D-14476 Potsdam, Germany
[2] Moscow MV Lomonosov State Univ, Dept Chem, Leninskiye Gory 1-3, Moscow 119991, Russia
[3] Univ Potsdam, Inst Biochem & Biol, Karl Liebknecht Str 24-25, D-14476 Potsdam, Germany
[4] Nottingham Trent Univ, Sch Sci & Technol, Clifton Lane, Nottingham NG11 8NS, England
[5] Univ Ghent, Dept Mol Biotechnol & NB Photon, Coupure Links 653, B-9000 Ghent, Belgium
关键词
CALCIUM-CARBONATE; PROTEIN PARTICLES; TRANSFORMATION MECHANISM; CRYSTALLIZATION; CAPSULES; PRECIPITATION; ENCAPSULATION; FABRICATION; NUCLEATION; ADDITIVES;
D O I
10.1021/acs.langmuir.6b00717
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The spherical vaterite CaCO3 microcrystals are nowadays widely used as sacrificial templates for fabrication of various microcarriers made of biopolymers (e.g., proteins, nucleic acids, enzymes) due to porous structure and mild template elimination conditions. Here, we demonstrated for the first time that polymer microcarriers with tuned internal nanoarchitecture can be designed by employing the CaCO3 crystals of controlled porosity. The layer-by-layer deposition has been utilized to assemble shell-like (hollow) and matrix-like (filled) polymer capsules due to restricted and free polymer diffusion through the crystal pores, respectively. The crystal pore size in the range of few tens of nanometers can be adjusted without any additives by variation of the crystal preparation temperature in the range 745 degrees C. The temperature-mediated growth mechanism is explained by the Ostwald ripening of nanocrystallites forming the crystal secondary structure. Various techniques including SEM, AFM, CLSM, Raman microscopy, nitrogen adsorptiondesorption, and XRD have been employed for crystal and microcapsule analysis. A three-dimensional model is introduced to describe the crystal internal structure and predict the pore cutoff and available surface for the pore diffusing molecules. Inherent biocompatibility of CaCO3 and a possibility to scale the porosity in the size range of typical biomacromolecules make the CaCO3 crystals extremely attractive tools for template assisted designing tailor-made biopolymer-based architectures in 2D to 3D targeted at drug delivery and other bioapplications.
引用
收藏
页码:4229 / 4238
页数:10
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