Transfection System of Amino-Functionalized Calcium Phosphate Nanoparticles: In Vitro Efficacy, Biodegradability, and Immunogenicity Study

被引:27
作者
Mostaghaci, Babak [1 ]
Susewind, Julia [3 ]
Kickelbick, Guido [2 ]
Lehr, Claus-Michael [1 ,3 ]
Loretz, Brigitta [1 ]
机构
[1] Univ Saarland, Dept Drug Delivery DDEL, HelmholtzInst Pharmaceut Res Saarland HIPS, Helmholtz Ctr Infect Res HZI, D-66123 Saarbrucken, Germany
[2] Univ Saarland, Inorgan Solid State Chem, D-66125 Saarbrucken, Germany
[3] Univ Saarland, Biopharm & Pharmaceut Technol, Dept Pharm, D-66123 Saarbrucken, Germany
关键词
aminosilane; biodegradation; gene delivery; nucleotides; complement activation; cytokine release; GENE DELIVERY-SYSTEMS; SILICA NANOPARTICLES; CYTOKINE RESPONSE; SIRNA DELIVERY; ACTIVATION; EFFICIENCY; CELLS; VIVO; DNA; CARRIERS;
D O I
10.1021/am507193a
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Many methods have been developed in order to use calcium phosphate (CaP) for delivering nucleotides into living cells. Surface functionalization of CaP nanoparticles (CaP NPs) with N-(2-aminoethyl)-3-aminopropyltrimethoxysilane was shown recently to achieve dispersed NPs with a positive surface charge, capable of transfection (Chem. Mater. 2013, 25 (18), 3667). In this study, different crystal structures of amino-modified CaP NPs (brushite and hydroxyapatite) were investigated for their interaction in cell culture systems in more detail. Qualitative (confocal laser scanning microscopy) and quantitative (flow cytometry) transfection experiments with two cell lines showed the higher transfection efficacy of brushite versus hydroxyapatite. The transfection also revealed a cell type dependency. HEK293 cells were easier to transfect compared to A549 cells. This result was supported by the cytotoxicity results. A549 cells showed a higher degree of tolerance toward the CaP NPs. Further, the impact of the surface modification on the interaction with macrophages and complement as two important components of the innate immune system were considered. The amine surface functionalization had an effect of decreasing the release of proinflammatory cytokines. The complement interaction investigated by a C3a complement activation assay did show no significant differences between CaP NPs without or with amine modification and overall weak interaction. Finally, the degradation of CaP NPs in biological media was studied with respect to the two crystal structures and at acidic and neutral pH. Both amino-modified CaP NPs disintegrate within days at neutral pH, with a notable faster disintegration of brushite NPs at acidic pH. In summary, the fair transfection capability of this amino functionalized CaP NPs together with the excellent biocompatibility, biodegradability, and low immunogenicity make them interesting candidates for further evaluation.
引用
收藏
页码:5124 / 5133
页数:10
相关论文
共 49 条
[1]   COMBINED EFFECTS OF HEPATIC ARTERIAL EMBOLIZATION USING DEGRADABLE STARCH MICROSPHERES (DSM) IN HYPERTHERMIA FOR LIVER-CANCER [J].
AKUTA, K ;
ABE, M ;
KONDO, M ;
YOSHIKAWA, T ;
TANAKA, Y ;
YOSHIDA, M ;
MIURA, T ;
NAKAO, N ;
ONOYAMA, Y ;
YAMADA, T ;
MUKOUJIMA, T ;
TSUKADA, K .
INTERNATIONAL JOURNAL OF HYPERTHERMIA, 1991, 7 (02) :231-242
[2]   How To Prevent the Loss of Surface Functionality Derived from Aminosilanes [J].
Asenath-Smith, Emily ;
Chen, Wei .
LANGMUIR, 2008, 24 (21) :12405-12409
[3]   Delivering the goods: viral and non-viral gene therapy systems and the inherent limits on cargo DNA and internal sequences [J].
Atkinson, Helen ;
Chalmers, Ronald .
GENETICA, 2010, 138 (05) :485-498
[4]   In vivo genome editing using a high-efficiency TALEN system [J].
Bedell, Victoria M. ;
Wang, Ying ;
Campbell, Jarryd M. ;
Poshusta, Tanya L. ;
Starker, Colby G. ;
Krug, Randall G., II ;
Tan, Wenfang ;
Penheiter, Sumedha G. ;
Ma, Alvin C. ;
Leung, Anskar Y. H. ;
Fahrenkrug, Scott C. ;
Carlson, Daniel F. ;
Voytas, Daniel F. ;
Clark, Karl J. ;
Essner, Jeffrey J. ;
Ekker, Stephen C. .
NATURE, 2012, 491 (7422) :114-U133
[5]   Multifunctional silica nanoparticles with potentials of imaging and gene delivery [J].
Bhakta, Gajadhar ;
Sharma, Rakesh Kumar ;
Gupta, Nikesh ;
Cool, Simon ;
Nurcombe, Victor ;
Maitra, Amarnath .
NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, 2011, 7 (04) :472-479
[6]   A VERSATILE VECTOR FOR GENE AND OLIGONUCLEOTIDE TRANSFER INTO CELLS IN CULTURE AND IN-VIVO - POLYETHYLENIMINE [J].
BOUSSIF, O ;
LEZOUALCH, F ;
ZANTA, MA ;
MERGNY, MD ;
SCHERMAN, D ;
DEMENEIX, B ;
BEHR, JP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) :7297-7301
[7]   Adenovirus: a blueprint for non-viral gene delivery [J].
Chailertvanitkul, V. Ann ;
Pouton, Colin W. .
CURRENT OPINION IN BIOTECHNOLOGY, 2010, 21 (05) :627-632
[8]  
Cheng Y., 2012, Dendrimer-Based Drug Delivery Systems: From Theory to Practice
[9]  
Csogör Z, 2003, MAT SCI ENG C-BIO S, V23, P93
[10]   Cellular delivery of polynucleotides by cationic cyclodextrin polyrotaxanes [J].
Dandekar, Prajakta ;
Jain, Ratnesh ;
Keil, Manuel ;
Loretz, Brigitta ;
Muijs, Leon ;
Schneider, Marc ;
Auerbach, Dagmar ;
Jung, Gregor ;
Lehr, Claus-Michael ;
Wenz, Gerhard .
JOURNAL OF CONTROLLED RELEASE, 2012, 164 (03) :387-393