Fluorescence Correlation Spectroscopy Monitors the Fate of Degradable Nanocarriers in the Blood Stream

被引:16
作者
Schmitt, Sascha [1 ]
Huppertsberg, Anne [1 ]
Klefenz, Adrian [2 ,3 ]
Kaps, Leonard [2 ,3 ,4 ]
Mailaender, Volker [1 ,5 ]
Schuppan, Detlef [2 ,3 ,6 ]
Butt, Hans-Juergen [1 ]
Nuhn, Lutz [1 ]
Koynov, Kaloian [1 ]
机构
[1] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
[2] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Inst Translat Immunol, D-55131 Mainz, Germany
[3] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Res Ctr Immune Therapy, D-55131 Mainz, Germany
[4] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Dept Internal Med 1, D-55122 Mainz, Germany
[5] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Dept Dermatol, D-55122 Mainz, Germany
[6] Harvard Med Sch, Beth Israel Deaconess Med Ctr, Div Gastroenterol, Boston, MA 02115 USA
关键词
DELIVERY; NANOPARTICLES; PARTICLES; STABILITY; NANOGELS; CELLS; LIVER; RNA;
D O I
10.1021/acs.biomac.1c01407
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The use of nanoparticles as carriers to deliver pharmacologically active compounds to specific parts of the body via the bloodstream is a promising therapeutic approach for the effective treatment of various diseases. To reach their target sites, nanocarriers (NCs) need to circulate in the bloodstream for prolonged periods without aggregation, degradation, or cargo loss. However, it is very difficult to identify and monitor small-sized NCs and their cargo in the dense and highly complex blood environment. Here, we present a new fluorescence correlation spectroscopy-based method that allows the precise characterization of fluorescently labeled NCs in samples of less than 50 mu L of whole blood. The NC size, concentration, and loading efficiency can be measured to evaluate circulation times, stability, or premature drug release. We apply the new method to follow the fate of pH-degradable fluorescent cargo-loaded nanogels in the blood of live mice for periods of up to 72 h.
引用
收藏
页码:1065 / 1074
页数:10
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