Counteracting Muscle Atrophy on Earth and in Space via Nanofluidics Delivery of Formoterol

被引:6
作者
Ballerini, Andrea [1 ,2 ]
Chua, Corrine Ying Xuan [1 ]
Rhudy, Jessica [1 ]
Susnjar, Antonia [1 ]
Di Trani, Nicola [1 ,3 ]
Jain, Priya R. [1 ]
Laue, Grit [4 ]
Lubicka, Danuta [5 ]
Shirazi-Fard, Yasaman [6 ]
Ferrari, Mauro [7 ]
Stodieck, Louis S. [8 ]
Cadena, Samuel M. [5 ]
Grattoni, Alessandro [1 ,9 ]
机构
[1] Houston Methodist Res Inst, Dept Nanomed, 6670 Bertner Ave, Houston, TX 77030 USA
[2] Univ Milan, Dept Med Biotechnol & Translat Med, Milan 20122, Italy
[3] Univ Chinese Acad Sci, Coll Mat Sci & Opta Elect Technol, 19 Yuquan Rd Beijing, Beijing 100049, Peoples R China
[4] Novartis Campus, Novartis Inst Biomed Res, Basel 4056, Switzerland
[5] Novartis Inst Biomed Res, 181 Massachusetts Ave, Cambridge, MA 02139 USA
[6] NASA, Ames Res Ctr, Space BioSci Div, Bone & Signaling Lab, Mail Stop 236-7, Moffett Field, CA 94035 USA
[7] Univ Washington, Box 357630H375 Hlth Sci Bldg, Seattle, WA 98195 USA
[8] Univ Colorado, Dept Aerosp Engn Sci, BioServe Space Technol, Boulder, CO 80309 USA
[9] Houston Methodist Res Inst, Dept Surg, 6670 Bertner Ave, Houston, TX 77030 USA
关键词
drug delivery; implantable devices; microgravity; muscle atrophy; nanofluidics; SKELETAL-MUSCLE; BETA(2)-ADRENOCEPTOR AGONISTS; RAT; MICROGRAVITY; SYSTEM; DRUG; BETA-2-ADRENOCEPTOR; NANOCHANNELS; MECHANISMS; MANAGEMENT;
D O I
10.1002/adtp.202000014
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Skeletal muscle atrophy is a critical health problem that affects quality of life and increases morbidity and mortality. At present, exercise training remains the only intervention and pharmaceutical treatments remain elusive. Formoterol (FMT), a beta 2-adrenergic receptor agonist, has emerged as a potential therapeutic by triggering skeletal muscle anabolism with daily dosing. Here, the efficacy of sustained FMT release is investigated via a subcutaneously implanted nanofluidic delivery system (nF) to prevent muscle wasting. Pharmacokinetics of nF-mediated sustained FMT delivery (nF-FMT) in healthy mice is assessed for 56 days, which demonstrates an anabolic effect on skeletal muscles. Using a hind limb suspension unloading mouse model, it is shown that nF-FMT treatment attenuates soleus mass loss in comparison to control mice. Further, the very first study of an implantable drug delivery device in microgravity in vivo is launched. The microgravity environment aboard the International Space Station is leveraged to assess the atrophy prevention capability of nF-FMT in mice for 29 and 55 days. Muscle hypertrophy is observed in both ground control and spaceflight mice treated with nF-FMT compared to their respective vehicle controls. Overall, the nF system is presented as a viable platform for sustained delivery of FMT for therapeutic intervention of skeletal muscle atrophy.
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页数:12
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